Documents in category 'Genome-wide association studies' (gwas)

TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies.
score: 5.7944021, Molecular psychiatry, 2011, Erhardt, A et. al.

Hundreds of variants clustered in genomic loci and biological pathways affect human height
score: 5.2131404, Nature, 2010, Lango Allen, Hana et. al.

Multiple Loci Are Associated with White Blood Cell Phenotypes
score: 4.9516007, PLoS Genetics, 2011, Nalls, Michael A. et. al.

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects
score: 4.4456372, American Journal of Medical Genetics, 2010, Rizzi, Thais S et. al.

Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot
score: 4.4447872, Human Molecular Genetics, 2013, Cordell, Heather J. et. al.

Genetic Structure of Europeans: A View from the North–East
score: 4.2576577, PLoS ONE, 2009, Nelis, Mari et. al.

Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
score: 4.231791, Human molecular genetics, 2013, Cordell, Heather J et. al.

Hundreds of variants clustered in genomic loci and biological pathways affect human height.
score: 4.1888425, Nature, 2010, Lango Allen, Hana et. al.

A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus.
score: 3.9622543, Nature genetics, 2009, Gateva, Vesela et. al.

Pathway-based genome-wide association analysis identified the importance of regulation-of-autophagy pathway for ultradistal radius BMD.
score: 3.9258989, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2010, Zhang, Lishu et. al.

Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited
score: 3.893573, Aging Cell, 2011, Deelen, Joris et. al.

Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease
score: 3.8885342, PLoS Genetics, 2011,

Genomic insights into early-onset obesity
score: 3.8817761, Genome Medicine, 2010, Choquet, Hélène; Meyre, David

Pathway-Based Genome-Wide Association Analysis Identified the Importance of Regulation-of-Autophagy Pathway for Ultradistal Radius BMD
score: 3.8772388, Journal of Bone and Mineral Research, 2010, Zhang, Lishu et. al.

Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways
score: 3.8257968, Age, 2011, Deelen, Joris et. al.

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci
score: 3.7983026, The American Journal of Human Genetics, 2012, Asselbergs, Folkert W. et. al.

Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis.
score: 3.7842276, Genes and immunity, 2007, Steer, S et. al.

Genome-wide association Scan of dental caries in the permanent dentition
score: 3.7108053, BMC Oral Health, 2012, Wang, Xiaojing et. al.

Myelin Basic Protein as a Novel Genetic Risk Factor in Rheumatoid Arthritis—A Genome-Wide Study Combined with Immunological Analyses
score: 3.6931881, PLoS ONE, 2011, Terao, Chikashi et. al.

Swedish Population Substructure Revealed by Genome-Wide Single Nucleotide Polymorphism Data
score: 3.6118391, PLoS ONE, 2011, Salmela, Elina et. al.

Genome-wide Association and Population Genetic Analysis of C-Reactive Protein in African American and Hispanic American Women
score: 3.5896495, The American Journal of Human Genetics, 2012, Reiner, Alex P. et. al.

Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays
score: 3.5084268, BMC Genetics, 2011, Gross, Arnd et. al.

From Disease Association to Risk Assessment: An Optimistic View from Genome-Wide Association Studies on Type 1 Diabetes
score: 3.5039335, PLoS Genetics, 2009, Wei, Zhi et. al.

Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals.
score: 3.4703996, Human molecular genetics, 2013, Guo, Yiran et. al.

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
score: 3.4469915, Nature, 2011, International Multiple Sclerosis Genetics Consortium, et. al.

Refined QTLs of osteoporosis-related traits by linkage analysis with genome-wide SNPs: Framingham SHARe
score: 3.442442, Bone, 2010, Karasik, David et. al.

Abstracts of the AABB Annual Meeting, October 20-23, 2007, Anaheim, California, USA.
score: 3.4168838, Transfusion, 2007,

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.
score: 3.4112447, Genetic epidemiology, 2011, Zuvich, Rebecca L et. al.

Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project
score: 3.4036552, The American Journal of Human Genetics, 2012, Auer, Paul L. et. al.

Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project
score: 3.4036552, The American Journal of Human Genetics, 2012, Auer, Paul L. et. al.

Abstracts of the 60th Annual Scientific Meeting of the Gerontological Society of America, November 16-20, 2007, San Francisco, California, USA.
score: 3.3680814, The Gerontologist, 2007,

A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis.
score: 3.3228594, Genes and immunity, 2010, Bronson, P G et. al.

Poor replication of candidate genes for major depressive disorder using genome-wide association data.
score: 3.3205541, Molecular psychiatry, 2011, Bosker, F J et. al.

Implication of European-derived adiposity loci in African Americans.
score: 3.2921378, International journal of obesity (2005), 2012, Hester, J M et. al.

On Genome-wide Association Studies for Family-Based Designs: An Integrative Analysis Approach Combining Ascertained Family Samples with Unselected Controls
score: 3.2645054, The American Journal of Human Genetics, 2010, Lasky-Su, Jessica et. al.

Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NLHBI GO Exome Sequencing Project
score: 3.2472219, The American Journal of Human Genetics, 2012, Auer, Paul L. et. al.

A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease
score: 3.2362096, PLoS Genetics, 2011,

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
score: 3.233729, Breast Cancer Research : BCR, 2012, Antoniou, Antonis C et. al.

Evaluation of candidate genes in a genome-wide association study of childhood asthma in Mexicans
score: 3.2254086, The Journal of Allergy and Clinical Immunology, 2010, Wu, Hao et. al.

Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci
score: 3.1938503, The American Journal of Human Genetics, 2012, Asselbergs, Folkert W. et. al.

Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci
score: 3.1938503, The American Journal of Human Genetics, 2012, Asselbergs, Folkert W. et. al.

Extended Analysis of a Genome-Wide Association Study in Primary Sclerosing Cholangitis Detects Multiple Novel Risk Loci
score: 3.1703972, Journal of Hepatology, 2012, Folseraas, Trine et. al.

Forty-Three Loci Associated with Plasma Lipoprotein Size, Concentration, and Cholesterol Content in Genome-Wide Analysis
score: 3.1592775, PLoS Genetics, 2009, Chasman, Daniel I. et. al.

Analyses of shared genetic factors between asthma and obesity in children
score: 3.1087243, The Journal of Allergy and Clinical Immunology, 2010, Melén, Erik et. al.

Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci
score: 3.0954951, Journal of Hepatology, 2012, Folseraas, Trine et. al.

Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci
score: 3.0954951, Journal of Hepatology, 2012, Folseraas, Trine et. al.

Global Analysis of the Impact of Environmental Perturbation on cis -Regulation of Gene Expression
score: 3.0875568, PLoS Genetics, 2011, Grundberg, Elin et. al.

Common genetic variation contributes significantly to the risk of childhood B-cell precursor acute lymphoblastic leukemia.
score: 3.0749251, Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K, 2012, Enciso-Mora, V et. al.

Phosphodiesterase 8B Gene Variants Are Associated with Serum TSH Levels and Thyroid Function
score: 3.0612509, The American Journal of Human Genetics, 2008, Arnaud-Lopez, Lisette et. al.

Genome-wide Copy-Number-Variation Study Identified a Susceptibility Gene, UGT2B17, for Osteoporosis
score: 3.0129314, The American Journal of Human Genetics, 2008, Yang, Tie-Lin et. al.

Integrating Genome-Wide Genetic Variations and Monocyte Expression Data Reveals Trans -Regulated Gene Modules in Humans
score: 3.0118821, PLoS Genetics, 2011, Rotival, Maxime et. al.

Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility
score: 3.0072042, The Journal of Allergy and Clinical Immunology, 2009, Haller, Gabe et. al.

New genetic associations detected in a host response study to hepatitis B vaccine.
score: 3.0061843, Genes and immunity, 2010, Davila, S et. al.

Pathway-based analysis of genetic susceptibility to cervical cancer in situ: HLA-DPB1 affects risk in Swedish women.
score: 2.9838709, Genes and immunity, 2011, Ivansson, E L; Juko-Pecirep, I; Erlich, H A; Gyllensten, U B

The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits
score: 2.9588641, PLoS ONE, 2011, Min, Josine L. et. al.

Targeting 160 Candidate Genes for Blood Pressure Regulation with a Genome-Wide Genotyping Array
score: 2.9522617, PLoS ONE, 2009, Sõber, Siim et. al.

Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
score: 2.9509583, Human Molecular Genetics, 2011, Spain, Sarah L. et. al.

Comparison of the Performance of Two Commercial Genome-Wide Association Study Genotyping Platforms in Han Chinese Samples
score: 2.9497905, G3: Genes|Genomes|Genetics, 2013, Jiang, Lei et. al.

Imputation of exome sequence variants into population-based samples identifies blood cell trait-associated loci in African Americans: the NLHBI GO Exome Sequencing Project
score: 2.9480716, The American Journal of Human Genetics, 2012, Auer, Paul L. et. al.

Genome-wide Ancestry Association Testing Identifies a Common European Variant on 6q14.1 as a Risk Factor for Asthma in African Americans
score: 2.9195325, The Journal of Allergy and Clinical Immunology, 2012, Torgerson, Dara G. et. al.

Abstracts of the 26th International Conference on Pharmacoepidemiology & Therapeutic Risk Management. August 19-22, 2010. Brighton, United Kingdom.
score: 2.9119021, Pharmacoepidemiology and drug safety, 2010,

Genome-wide association meta-analysis identifies new endometriosis risk loci
score: 2.8963127, Nature genetics, 2012, Nyholt, Dale R. et. al.

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
score: 2.8911791, Nature, 2011, Sawcer, Stephen et. al.

Basic statistical analysis in genetic case-control studies.
score: 2.8813002, Nature protocols, 2011, Clarke, Geraldine M et. al.

IPGWAS: An integrated pipeline for rational quality control and association analysis of genome-wide genetic studies
score: 2.880629, Biochemical and Biophysical Research Communications, 2012, Fan, Yan-Hui; Song, You-Qiang

Genome-wide association analysis of cardiovascular-related quantitative traits in the Framingham Heart Study
score: 2.8701423, BMC Proceedings, 2009, Roslin, Nicole M et. al.

Trans -eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA
score: 2.8530918, PLoS Genetics, 2011, Fehrmann, Rudolf S. N. et. al.

Transferability and Fine Mapping of genome-wide associated loci for lipids in African Americans
score: 2.8480076, BMC Medical Genetics, 2012, Adeyemo, Adebowale et. al.

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.
score: 2.8438524, Human molecular genetics, 2013, Chen, Zhao et. al.

Meta-analysis of genome-wide association studies for panic disorder in the Japanese population
score: 2.8434862, Translational Psychiatry, 2012, Otowa, T et. al.

Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics
score: 2.8226799, The American Journal of Human Genetics, 2010, Biffi, Alessandro et. al.

Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis.
score: 2.8020997, Genes and immunity, 2012, Invernizzi, P et. al.

Genetic risk profiles for depression and anxiety in adult and elderly cohorts
score: 2.773792, Molecular Psychiatry, 2010, Demirkan, A et. al.

Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as Susceptibility Loci for Systemic Lupus Erythematosus in a Large-Scale Multiracial Replication Study
score: 2.764913, The American Journal of Human Genetics, 2012, Lessard, Christopher J. et. al.

Population-specific coding variant underlies genome-wide association with adiponectin level.
score: 2.7477744, Human molecular genetics, 2012, Croteau-Chonka, Damien C et. al.

A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis.
score: 2.7364945, Molecular biology and evolution, 2012, Cagliani, R et. al.

Genome-wide association scan allowing for epistasis in type 2 diabetes.
score: 2.7354189, Annals of human genetics, 2011, Bell, Jordana T et. al.

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium
score: 2.7325752, Human Genetics, 2012, Verhoeven, Virginie J. M. et. al.

Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects
score: 2.7173338, The Journal of Allergy and Clinical Immunology, 2012, Torgerson, Dara G. et. al.

Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects
score: 2.7173338, The Journal of Allergy and Clinical Immunology, 2012, Torgerson, Dara G. et. al.

Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans
score: 2.7126547, Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2010, Saykin, Andrew J. et. al.

Common genetic factors for hematological traits in humans.
score: 2.7038358, Journal of human genetics, 2012, Okada, Yukinori; Kamatani, Yoichiro

Resequencing and Analysis of Variation in the TCF7L2 Gene in African Americans Suggests That SNP rs7903146 Is the Causal Diabetes Susceptibility Variant
score: 2.7032048, Diabetes, 2011, Palmer, Nicholette D. et. al.

Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family.
score: 2.6892985, Arthritis and rheumatism, 2010, Chen, Hsiang-Cheng et. al.

Unraveling Multiple MHC Gene Associations with Systemic Lupus Erythematosus: Model Choice Indicates a Role for HLA Alleles and Non-HLA Genes in Europeans
score: 2.6864823, The American Journal of Human Genetics, 2012, Morris, David L. et. al.

Unraveling Multiple MHC Gene Associations with Systemic Lupus Erythematosus: Model Choice Indicates a Role for HLA Alleles and Non-HLA Genes in Europeans
score: 2.6864823, The American Journal of Human Genetics, 2012, Morris, David L. et. al.

Genetics Analysis Workshop 16 Problem 2: the Framingham Heart Study data
score: 2.6838561, BMC Proceedings, 2009, Cupples, L Adrienne et. al.

Identification of new SLE-associated genes with a two-step Bayesian study design.
score: 2.6655503, Genes and immunity, 2009, Armstrong, D L et. al.

Multistage analysis of variants in the inflammation pathway and lung cancer risk in smokers.
score: 2.6652254, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Spitz, Margaret R et. al.

Genome-wide and gene-based association implicates FRMD6 in Alzheimer disease.
score: 2.6539791, Human mutation, 2012, Hong, Mun-Gwan et. al.

A framework for interpreting genome-wide association studies of psychiatric disorders.
score: 2.6525426, Molecular psychiatry, 2009, Psychiatric GWAS Consortium Steering Committee,

Identity-by-Descent Mapping to Detect Rare Variants Conferring Susceptibility to Multiple Sclerosis
score: 2.6211397, PLoS ONE, 2013, Lin, Rui et. al.

Large Scale Replication Study of the Association between HLA Class II/ BTNL2 Variants and Osteoarthritis of the Knee in European-Descent Populations
score: 2.6161958, PLoS ONE, 2011, Valdes, Ana M. et. al.

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility.
score: 2.6144756, Nature genetics, 2011, Stacey, Simon N et. al.

Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS)
score: 2.5989554, Neurobiology of Aging, 2012, Shi, Hui et. al.

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.
score: 2.5793185, Molecular psychiatry, 2012, Ayalew, M et. al.

Estimating Kinship in Admixed Populations
score: 2.57782, The American Journal of Human Genetics, 2012, Thornton, Timothy et. al.

Distinct Variants at LIN28B Influence Growth in Height from Birth to Adulthood
score: 2.5680324, The American Journal of Human Genetics, 2010, Widén, Elisabeth et. al.

Identification of shared genetic susceptibility locus for coronary artery disease, type 2 diabetes and obesity: a meta-analysis of genome-wide studies
score: 2.556496, Cardiovascular Diabetology, 2012, Wu, Chaoneng et. al.

Genetic risk profiles for depression and anxiety in adult and elderly cohorts.
score: 2.5512913, Molecular psychiatry, 2011, Demirkan, A et. al.

Meta-analysis of gene-based genome-wide association studies of bone mineral density in Chinese and European subjects
score: 2.5340421, Osteoporosis International, 2011, Cheung, C.-L. et. al.

Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis.
score: 2.5307068, Genes and immunity, 2010, Briggs, F B S et. al.

Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort
score: 2.5250248, BMC Genomics, 2012, Valsesia, Armand et. al.

A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE
score: 2.5220481, European Journal of Human Genetics, 2010, Sandling, Johanna K et. al.

Case-control admixture mapping in Latino populations enriches for known asthma-associated genes
score: 2.5125683, The Journal of Allergy and Clinical Immunology, 2012, Torgerson, Dara G. et. al.

The genetics of alcohol dependence: Advancing towards systems-based approaches
score: 2.5114697, Drug and Alcohol Dependence, 2012, Palmer, R.H.C. et. al.

Genetic Background of Patients from a University Medical Center in Manhattan: Implications for Personalized Medicine
score: 2.5086841, PLoS ONE, 2011, Tayo, Bamidele O. et. al.

Detection, Imputation, and Association Analysis of Small Deletions and Null Alleles on Oligonucleotide Arrays
score: 2.5044163, The American Journal of Human Genetics, 2008, Franke, Lude et. al.

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
score: 2.5013384, Lancet, 2012, Voight, Benjamin F et. al.

Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level
score: 2.4917721, Genome Biology, 2010, Harismendy, Olivier et. al.

European Bone Mineral Density Loci Are Also Associated with BMD in East-Asian Populations
score: 2.4898646, PLoS ONE, 2010, Styrkarsdottir, Unnur et. al.

Stratification-score matching improves correction for confounding by population stratification in case-control association studies.
score: 2.4803056, Genetic epidemiology, 2012, Epstein, Michael P et. al.

ProbABEL package for genome-wide association analysis of imputed data
score: 2.4790308, BMC Bioinformatics, 2010, Aulchenko, Yurii S et. al.

Abstracts of the 27th International Conference on Pharmacoepidemiology & Therapeutic Risk Management. Chicago, Illinois, USA. August 14-17, 2011.
score: 2.4784884, Pharmacoepidemiology and drug safety, 2011,

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
score: 2.4760583, Nature genetics, 2012, Estrada, Karol et. al.

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
score: 2.4730355, The Lancet, 2012, Voight, Benjamin F et. al.

Association of Common Polymorphisms in GLUT9 Gene with Gout but Not with Coronary Artery Disease in a Large Case-Control Study
score: 2.4574456, PLoS ONE, 2008, Stark, Klaus et. al.

European lactase persistence genotype shows evidence of association with increase in body mass index
score: 2.450462, Human Molecular Genetics, 2009, Kettunen, Johannes et. al.

Molecular Basis of Obesity: Current Status and Future Prospects
score: 2.4501357, Current Genomics, 2011, Choquet, Hélène; Meyre, David

A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis.
score: 2.4404213, Genes and immunity, 2012, Vandenbroeck, K et. al.

LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer.
score: 2.4361194, Cancer research, 2011, Permuth-Wey, Jennifer et. al.

A High Density SNP Array for the Domestic Horse and Extant Perissodactyla: Utility for Association Mapping, Genetic Diversity, and Phylogeny Studies
score: 2.4255982, PLoS Genetics, 2012, McCue, Molly E. et. al.

Mining gold dust under the genome wide significance level: a two-stage approach to analysis of GWAS.
score: 2.4211685, Genetic epidemiology, 2011, Shi, Gang et. al.

Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study.
score: 2.4178149, European journal of human genetics : EJHG, 2010, Newby, Paul R et. al.

Genome-wide Linkage and Association Analyses Implicate FASN in Predisposition to Uterine Leiomyomata
score: 2.410683, The American Journal of Human Genetics, 2012, Eggert, Stacey L. et. al.

Statistical colocalization of monocyte gene expression and genetic risk variants for type 1 diabetes
score: 2.4088572, Human Molecular Genetics, 2012, Wallace, Chris et. al.

Identification of the UBP1 Locus as a Critical Blood Pressure Determinant Using a Combination of Mouse and Human Genetics
score: 2.4037128, PLoS Genetics, 2009, Koutnikova, Hana et. al.

Knowledge-Driven Multi-Locus Analysis Reveals Gene-Gene Interactions Influencing HDL Cholesterol Level in Two Independent EMR-Linked Biobanks
score: 2.403544, PLoS ONE, 2011, Turner, Stephen D. et. al.

The Role of Genetic Variation Near Interferon-Kappa in Systemic Lupus Erythematosus
score: 2.3998575, Journal of Biomedicine and Biotechnology, 2010, Harley, Isaac T. W. et. al.

Genetic Association for Renal Traits among Participants of African Ancestry Reveals New Loci for Renal Function
score: 2.3992122, PLoS Genetics, 2011, Liu, Ching-Ti et. al.

Susceptibility genes for osteoporotic fracture in postmenopausal chinese women.
score: 2.3991587, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2012, Wang, Chun et. al.

Spoiling the Whole Bunch: Quality Control Aimed at Preserving the Integrity of High-Throughput Genotyping
score: 2.3933165, The American Journal of Human Genetics, 2010, Pluzhnikov, Anna et. al.

Risk of breast and prostate cancer is not associated with increased homozygosity in outbred populations.
score: 2.3908652, European journal of human genetics : EJHG, 2010, Enciso-Mora, Victor; Hosking, Fay J; Houlston, Richard S

Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy
score: 2.3908432, Molecular Vision, 2009, Bessho, Hiroaki et. al.

Comprehensive Linkage and Association Analyses Identify Haplotype, Near to the TNFSF15 Gene, Significantly Associated with Spondyloarthritis
score: 2.3897769, PLoS Genetics, 2009, Zinovieva, Elena et. al.

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease.
score: 2.3763019, Movement disorders : official journal of the Movement Disorder Society, 2011, Latourelle, Jeanne C et. al.

The success of the genome-wide association approach: a brief story of a long struggle.
score: 2.3756928, European journal of human genetics : EJHG, 2008, Seng, Ku Chee; Seng, Chia Kee

Three periods of one and a half decade of ischemic stroke susceptibility gene research: lessons we have learned
score: 2.3654748, Genome Medicine, 2010, Maasz, Anita; Melegh, Bela

Replication of Previous Genome-wide Association Studies of Bone Mineral Density in Premenopausal American Women
score: 2.3578021, Journal of Bone and Mineral Research, 2010, Ichikawa, Shoji et. al.

Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder
score: 2.3554866, Translational Psychiatry, 2012, Lee, P H et. al.

IPGWAS: An integrated pipeline for rational quality control and association analysis of genome-wide genetic studies
score: 2.3553168, Biochemical and Biophysical Research Communications, 2012, Fan, Yan-Hui; Song, You-Qiang

IPGWAS: An integrated pipeline for rational quality control and association analysis of genome-wide genetic studies
score: 2.3553168, Biochemical and Biophysical Research Communications, 2012, Fan, Yan-Hui; Song, You-Qiang

IPGWAS: An integrated pipeline for rational quality control and association analysis of genome-wide genetic studies
score: 2.3553168, Biochemical and Biophysical Research Communications, 2012, Fan, Yan-Hui; Song, You-Qiang

Evaluation of Candidate Stromal Epithelial Cross-Talk Genes Identifies Association between Risk of Serous Ovarian Cancer and TERT , a Cancer Susceptibility “Hot-Spot”
score: 2.3542648, PLoS Genetics, 2010, Johnatty, Sharon E. et. al.

Study Designs for Genome‐Wide Association Studies
score: 2.3526106, Advances in Genetics, 2008, Kraft, Peter; Cox, David G.

Study Designs for Genome‐Wide Association Studies
score: 2.3526106, Advances in Genetics, 2008, Kraft, Peter; Cox, David G.

Genome-wide association database developed in the Japanese Integrated Database Project.
score: 2.351862, Journal of human genetics, 2009, Koike, Asako et. al.

Evidence for More than One Parkinson's Disease-Associated Variant within the HLA Region
score: 2.3501407, PLoS ONE, 2011, Hill-Burns, Erin M. et. al.

Genome-Wide Association Scan of Korean Autism Spectrum Disorders with Language Delay: A Preliminary Study
score: 2.350006, Psychiatry Investigation, 2011, Cho, Soo-Churl et. al.

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
score: 2.3451705, Nature genetics, 2012, Estrada, Karol et. al.

Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions
score: 2.3447159, BMC Medical Genetics, 2009, Casselbrant, Margaretha L et. al.

Genome-wide association study identifies common variants at TNFRSF13B associated with IgG level in a healthy Chinese male population.
score: 2.3415608, Genes and immunity, 2012, Liao, M et. al.

Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci
score: 2.3258978, Human Molecular Genetics, 2009,

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
score: 2.3240909, Nature, 2010, Walters, R G et. al.

A Genome-Wide Integrative Genomic Study Localizes Genetic Factors Influencing Antibodies against Epstein-Barr Virus Nuclear Antigen 1 (EBNA-1)
score: 2.3177275, PLoS Genetics, 2013, Rubicz, Rohina et. al.

Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects.
score: 2.3149394, Journal of human genetics, 2009, Saito, Akira; Kawamoto, Manabu; Kamatani, Naoyuki

A Novel, Functional and Replicable Risk Gene Region for Alcohol Dependence Identified by Genome-Wide Association Study
score: 2.299706, PLoS ONE, 2011, Zuo, Lingjun et. al.

Genome-Wide Association Studies in Nephrology Research
score: 2.2985671, American Journal of Kidney Diseases, 2010, Köttgen, Anna

Meta-Analysis Followed by Replication Identifies Loci in or nearCDKN1B,TET3,CD80,DRAM1, andARID5Bas Associated with Systemic Lupus Erythematosus in Asians
score: 2.295284, The American Journal of Human Genetics, 2013, Yang, Wanling et. al.

Genome-wide "pleiotropy scan" identifies HNF1A region as a novel pancreatic cancer susceptibility locus.
score: 2.2914548, Cancer research, 2011, Pierce, Brandon L; Ahsan, Habibul

The genetics of addiction—a translational perspective
score: 2.2889277, Translational Psychiatry, 2012, Agrawal, A et. al.

Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1 , BMP4 , and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer
score: 2.2873953, PLoS Genetics, 2011, Tomlinson, Ian P. M. et. al.

Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain
score: 2.2847347, Neurobiology of Disease, 2012, Hernandez, Dena G. et. al.

Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain
score: 2.2847347, Neurobiology of Disease, 2012, Hernandez, Dena G. et. al.

Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain
score: 2.2847347, Neurobiology of Disease, 2012, Hernandez, Dena G. et. al.

Estimating Kinship in Admixed Populations
score: 2.2840435, The American Journal of Human Genetics, 2012, Thornton, Timothy et. al.

Genetic Risk Factors for Type 2 Diabetes: A Trans-Regulatory Genetic Architecture?
score: 2.2746962, The American Journal of Human Genetics, 2012, Elbein, Steven C. et. al.

Mendelian Randomization Study of B-Type Natriuretic Peptide and Type 2 Diabetes: Evidence of Causal Association from Population Studies
score: 2.2736381, PLoS Medicine, 2011, Pfister, Roman et. al.

Quick, “Imputation-free” meta-analysis with proxy-SNPs
score: 2.2718616, BMC Bioinformatics, 2012, Meesters, Christian et. al.

Thymic stromal lymphopoietin (TSLP) is associated with allergic rhinitis in children with asthma
score: 2.2685651, Clinical and Molecular Allergy : CMA, 2011, Bunyavanich, Supinda et. al.

The Population Reference Sample, POPRES: A Resource for Population, Disease, and Pharmacological Genetics Research
score: 2.2583765, The American Journal of Human Genetics, 2008, Nelson, Matthew R. et. al.

Genome-wide association study of copy number variation identified gremlin1 as a candidate gene for lean body mass.
score: 2.2567621, Journal of human genetics, 2012, Hai, Rong et. al.

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
score: 2.2559121, Human Molecular Genetics, 2011, Wood, Andrew R. et. al.

Rare, Low-Frequency, and Common Variants in the Protein-Coding Sequence of Biological Candidate Genes from GWASs Contribute to Risk of Rheumatoid Arthritis
score: 2.2554397, The American Journal of Human Genetics, 2013, Diogo, Dorothée et. al.

Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies
score: 2.2384356, Journal of the American College of Cardiology, 2010, Assimes, Themistocles L. et. al.

A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE.
score: 2.2354842, European journal of human genetics : EJHG, 2011, Sandling, Johanna K et. al.

Differences in Candidate Gene Association between European Ancestry and African American Asthmatic Children
score: 2.2263448, PLoS ONE, 2011, Baye, Tesfaye M. et. al.

A Genome-wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases
score: 2.2248761, The American Journal of Human Genetics, 2010, Glessner, Joseph T. et. al.

Runs of Homozygosity in European Populations
score: 2.2155938, The American Journal of Human Genetics, 2008, McQuillan, Ruth et. al.

Implications for health and disease in the genetic signature of the Ashkenazi Jewish population
score: 2.2142458, Genome Biology, 2012, Guha, Saurav et. al.

A two-phase case–control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22
score: 2.2131398, British Journal of Cancer, 2011, Abulí, A et. al.

A genome-wide linkage study of mammographic density, a risk factor for breast cancer
score: 2.212515, Breast Cancer Research : BCR, 2011, Greenwood, Celia MT et. al.

A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene.
score: 2.2096766, European journal of human genetics : EJHG, 2012, Gregersen, Noomi et. al.

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
score: 2.2054287, Nature, 2011, Jacquemont, Sébastien et. al.

Genome-Wide Interaction-Based Association Analysis Identified Multiple New Susceptibility Loci for Common Diseases
score: 2.2054006, PLoS Genetics, 2011, Liu, Yang et. al.

Evaluating the Evidence for Transmission Distortion in Human Pedigrees
score: 2.2039961, Genetics, 2012, Meyer, Wynn K. et. al.

Pathway-based genome-wide association analysis identified the importance of EphrinA–EphR pathway for femoral neck bone geometry
score: 2.2012531, Bone, 2010, Chen, Yuan et. al.

Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population
score: 2.1948047, Molecular Vision, 2010, Zhao, Fuxin et. al.

Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at MSH5, HLA-DPB1 and HLA-G
score: 2.1939959, Annals of the Rheumatic Diseases, 2012, Fernando, Michelle M A et. al.

A Comprehensive Analysis of Shared Loci between Systemic Lupus Erythematosus (SLE) and Sixteen Autoimmune Diseases Reveals Limited Genetic Overlap
score: 2.1936806, PLoS Genetics, 2011, Ramos, Paula S. et. al.

Resequencing Candidate Genes Implicates Rare Variants in Asthma Susceptibility
score: 2.1886999, The American Journal of Human Genetics, 2012, Torgerson, Dara G. et. al.

IL-1 receptor–associated kinase 3 gene (IRAK3) variants associate with asthma in a replication study in the Spanish population
score: 2.1804092, The Journal of Allergy and Clinical Immunology, 2012, Pino-Yanes, María et. al.

Comprehensive evaluation of imputation performance in African Americans.
score: 2.1640683, Journal of human genetics, 2012, Chanda, Pritam et. al.

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies
score: 2.161165, Lancet Neurology, 2012, Traylor, Matthew et. al.

More CLEC16A gene variants associated with multiple sclerosis.
score: 2.1591251, Acta neurologica Scandinavica, 2011, Nischwitz, S et. al.

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies
score: 2.1517865, Lancet Neurology, 2012, Traylor, Matthew et. al.

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies
score: 2.1517865, Lancet Neurology, 2012, Traylor, Matthew et. al.

Reply
score: 2.1408656, The Journal of Pediatrics, 1997, Urlesberger, Berndt

A genome-wide association study using international breeding-evaluation data identifies major loci affecting production traits and stature in the Brown Swiss cattle breed
score: 2.1387728, BMC Genetics, 2012, Guo, Jiazhong; Jorjani, Hossein; Carlborg, Örjan

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association.
score: 2.135726, Human molecular genetics, 2011, Wood, Andrew R et. al.

A common variant in the CDKN2B gene on chromosome 9p21 protects against coronary artery disease in Americans of African ancestry.
score: 2.1308456, Journal of human genetics, 2011, Kral, Brian G et. al.

A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples
score: 2.1290464, BMC Genetics, 2008, Sebastiani, Paola et. al.

Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus.
score: 2.1256635, Nature genetics, 2011, Adrianto, Indra et. al.

Genetic Associations in the Vitamin D Receptor and Colorectal Cancer in African Americans and Caucasians
score: 2.1232377, PLoS ONE, 2011, Kupfer, Sonia S. et. al.

A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder
score: 2.121368, Schizophrenia Research, 2010, Wang, Ke-Sheng; Liu, Xue-Feng; Aragam, Nagesh

Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder.
score: 2.1090163, Molecular psychiatry, 2011, Williams, H J et. al.

Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene.
score: 2.107456, Genes and immunity, 2010, Pointon, J J et. al.

On the Replication of Genetic Associations: Timing Can Be Everything!
score: 2.0997342, The American Journal of Human Genetics, 2008, Lasky-Su, Jessica et. al.

Association of skin barrier genes within the PSORS4 locus is enriched in Singaporean Chinese with early-onset psoriasis.
score: 2.0923759, The Journal of investigative dermatology, 2009, Chen, Huijia et. al.

Gain-of-Function Lipoprotein Lipase Variant rs13702 Modulates Lipid Traits through Disruption of a MicroRNA-410 Seed Site
score: 2.0911948, The American Journal of Human Genetics, 2013, Richardson, Kris et. al.

Oligoclonal Band Status in Scandinavian Multiple Sclerosis Patients Is Associated with Specific Genetic Risk Alleles
score: 2.0892135, PLoS ONE, 2013, Mero, Inger-Lise et. al.

Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.
score: 2.0870221, Molecular psychiatry, 2013, Gamazon, E R et. al.

Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus.
score: 2.0787672, Genes and immunity, 2011, Mero, I-L et. al.

Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis.
score: 2.0787134, European journal of human genetics : EJHG, 2012, Babron, Marie-Claude et. al.

Examination of Type 2 Diabetes Loci Implicates CDKAL1 as a Birth Weight Gene
score: 2.0669695, Diabetes, 2009, Zhao, Jianhua et. al.

Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism.
score: 2.0587564, Journal of thrombosis and haemostasis : JTH, 2011, Heit, J A et. al.

A regulatory SNP in AKAP13 is associated with blood pressure in Koreans.
score: 2.0586785, Journal of human genetics, 2011, Hong, Kyung-Won; Lim, Ji-Eun; Oh, Bermseok

Genetic determinants of von Willebrand factor plasma levels and the risk of stroke: the Rotterdam Study.
score: 2.0513857, Journal of thrombosis and haemostasis : JTH, 2012, Van Schie, M C et. al.

Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.
score: 2.0513155, Human molecular genetics, 2010, International Multiple Sclerosis Genetics Consortium (IMSGC), et. al.

Conditional meta-analysis stratifying on detailed HLA genotypes identifies a novel type 1 diabetes locus around TCF19 in the MHC
score: 2.046216, Human Genetics, 2010, Cheung, Yee Him; Watkinson, John; Anastassiou, Dimitris

Variance component model to account for sample structure in genome-wide association studies.
score: 2.0452432, Nature genetics, 2010, Kang, Hyun Min et. al.

Multistage genomewide association study identifies a locus at 1q41 associated with rate of HIV-1 disease progression to clinical AIDS.
score: 2.0439718, The Journal of infectious diseases, 2010, Herbeck, Joshua T et. al.

Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study
score: 2.0436687, BMC Proceedings, 2009, Lantieri, Francesca et. al.

Prioritizing Genetic Variants for Causality on the Basis of Preferential Linkage Disequilibrium
score: 2.0428364, The American Journal of Human Genetics, 2012, Zhu, Qianqian et. al.

Simultaneous Genotype Calling and Haplotype Phasing Improves Genotype Accuracy and Reduces False-Positive Associations for Genome-wide Association Studies
score: 2.0422793, The American Journal of Human Genetics, 2009, Browning, Brian L.; Yu, Zhaoxia

Classical HLA-DRB1 and DPB1 Alleles Account for HLA Associations with Primary Biliary Cirrhosis
score: 2.0385197, Genes and immunity, 2012, Invernizzi, Pietro et. al.

Confirmation of the novel association at the BTNL2 locus with ulcerative colitis.
score: 2.0343833, Tissue antigens, 2009, Pathan, S et. al.

Genome-wide association analysis identifies three new breast cancer susceptibility loci.
score: 2.0319728, Nature genetics, 2012, Ghoussaini, Maya et. al.

Gene-centric Association Signals for Lipids and Apolipoproteins Identified via the HumanCVD BeadChip
score: 2.0272619, The American Journal of Human Genetics, 2009, Talmud, Philippa J. et. al.

The Genetic Structure of the Swedish Population
score: 2.0267311, PLoS ONE, 2011, Humphreys, Keith et. al.

Identification of QTL genes for BMD variation using both linkage and gene-based association approaches
score: 2.025555, Human Genetics, 2011, Li, Gloria Hoi-Yee et. al.

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis
score: 2.0224116, Human Molecular Genetics, 2010, Jarick, Ivonne et. al.

Genetic analyses of interferon pathway-related genes reveal multiple new loci associated with systemic lupus erythematosus.
score: 2.0190828, Arthritis and rheumatism, 2011, Ramos, Paula S et. al.

Regions of homozygosity in three Southeast Asian populations.
score: 2.0172947, Journal of human genetics, 2012, Teo, Shu-Mei et. al.

Support for association of HSPG2 with tardive dyskinesia in Caucasian populations.
score: 2.0102678, The pharmacogenomics journal, 2012, Greenbaum, L; Alkelai, A; Zozulinsky, P; Kohn, Y; Lerer, B

The Genetic Association of Variants in CD6 , TNFRSF1A and IRF8 to Multiple Sclerosis: A Multicenter Case-Control Study
score: 2.0013566, PLoS ONE, 2011,

Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
score: 2.0013194, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Couch, Fergus J et. al.

Replication of previous genome-wide association studies of bone mineral density in premenopausal American women.
score: 1.9976083, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2010, Ichikawa, Shoji et. al.

Meta-analysis of genome-wide and replication association studies on prostate cancer.
score: 1.9973388, The Prostate, 2011, Liu, Hong; Wang, Bo; Han, Chunsheng

Genome-Wide Association Study Link Novel Loci to Endometriosis
score: 1.995415, PLoS ONE, 2013, Albertsen, Hans M. et. al.

CIITA is not associated with risk of developing rheumatoid arthritis.
score: 1.9950756, Genes and immunity, 2011, Bronson, P G et. al.

Thursday Abstracts
score: 1.9902328, Biological Psychiatry, 2012,

Association Analysis of the FTO Gene with Obesity in Children of Caucasian and African Ancestry Reveals a Common Tagging SNP
score: 1.988162, PLoS ONE, 2008, Grant, Struan F. A. et. al.

Exploration of 16 candidate genes identifies the association of IDE with Alzheimer's disease in Han Chinese
score: 1.9854173, Neurobiology of Aging, 2012, Wang, Fen et. al.

Population Genetic Structure of the People of Qatar
score: 1.9816214, The American Journal of Human Genetics, 2010, Hunter-Zinck, Haley et. al.

A Systems Genetics Approach Provides a Bridge from Discovered Genetic Variants to Biological Pathways in Rheumatoid Arthritis
score: 1.9790096, PLoS ONE, 2011, Nakaoka, Hirofumi et. al.

Leprosy and the Adaptation of Human Toll-Like Receptor 1
score: 1.9769163, PLoS Pathogens, 2010, Wong, Sunny H. et. al.

Polymorphisms in Toll-like receptor genes influence antibody responses to cytomegalovirus glycoprotein B vaccine
score: 1.9763852, BMC Research Notes, 2012, Arav-Boger, Ravit et. al.

VKORC1 Common Variation and Bone Mineral Density in the Third National Health and Nutrition Examination Survey
score: 1.9729997, PLoS ONE, 2010, Crawford, Dana C.; Brown-Gentry, Kristin; Rieder, Mark J.

A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies.
score: 1.9704929, Genetic epidemiology, 2010, Lee, Sang Hong et. al.

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers.
score: 1.9608988, Human mutation, 2012, Ramus, Susan J et. al.

A New Statistic to Evaluate Imputation Reliability
score: 1.9547928, PLoS ONE, 2010, Lin, Peng et. al.

An Evolutionary Analysis of RAC2 Identifies Haplotypes Associated with Human Autoimmune Diseases.
score: 1.9531882, Molecular biology and evolution, 2011, Sironi, Manuela et. al.

Synthetic associations in the context of genome-wide association scan signals
score: 1.9503017, Human Molecular Genetics, 2010, Orozco, Gisela; Barrett, Jeffrey C.; Zeggini, Eleftheria

Genome-Wide Analysis of Single Nucleotide Polymorphisms Uncovers Population Structure in Northern Europe
score: 1.9483294, PLoS ONE, 2008, Salmela, Elina et. al.

Abstracts
score: 1.9428749, European Journal of Pediatrics, 2006,

Genetic interactions associated with 12-month atrophy in hippocampus and entorhinal cortex in Alzheimer's Disease Neuroimaging Initiative
score: 1.9260792, Neurobiology of Aging, 2013, Meda, Shashwath A. et. al.

Copy Number Variation across European Populations
score: 1.9237393, PLoS ONE, 2011, Chen, Wanting et. al.

Exome Sequencing Followed by Large-Scale Genotyping Fails to Identify Single Rare Variants of Large Effect in Idiopathic Generalized Epilepsy
score: 1.9225242, The American Journal of Human Genetics, 2012, Heinzen, Erin L. et. al.

Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans.
score: 1.921111, Genes, brain, and behavior, 2010, Saccone, N L et. al.

Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis.
score: 1.9206366, Genes and immunity, 2012, Lin, C P et. al.

Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population.
score: 1.9177125, Journal of human genetics, 2010, Liu, Xiaoxi et. al.

Association of the IL2RA/CD25 Gene With Juvenile Idiopathic Arthritis
score: 1.9138092, Arthritis and Rheumatism, 2009, Hinks, Anne et. al.

Gene expression endophenotypes: a novel approach for gene discovery in Alzheimer's disease
score: 1.9103234, Molecular Neurodegeneration, 2011, Ertekin-Taner, Nilüfer

Recapitulation of two genomewide association studies on blood pressure and essential hypertension in the Korean population.
score: 1.9068933, Journal of human genetics, 2010, Hong, Kyung-Won et. al.

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies
score: 1.9015539, BMC Genetics, 2009, Hao, Ke; Chudin, Eugene; McElwee, Joshua; Schadt, Eric E

A Genetic Risk Score Combining Ten Psoriasis Risk Loci Improves Disease Prediction
score: 1.8994752, PLoS ONE, 2011, Chen, Haoyan et. al.

“Higher order” addiction molecular genetics: Convergent data from genome-wide association in humans and mice
score: 1.8974941, Biochemical Pharmacology, 2008, Uhl, George R. et. al.

A two-phase case-control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22.
score: 1.894031, British journal of cancer, 2011, Abulí, A et. al.

Thursday Abstracts
score: 1.893686, Biological Psychiatry, 2009,

The regulation-of-autophagy pathway may influence Chinese stature variation: evidence from elder adults.
score: 1.8828579, Journal of human genetics, 2010, Pan, Feng et. al.

A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts.
score: 1.8809666, Human molecular genetics, 2010, Kalsi, Gursharan et. al.

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.
score: 1.880066, Molecular psychiatry, 2011, Chen, X et. al.

Conditional analyses on the T1DGC MHC dataset: novel associations with type 1 diabetes around HLA-G and confirmation of HLA-B.
score: 1.8772411, Genes and immunity, 2009, Eike, M C; Becker, T; Humphreys, K; Olsson, M; Lie, B A

Integrating common and rare genetic variation in diverse human populations.
score: 1.876451, Nature, 2010, International HapMap 3 Consortium, et. al.

Characterization of Genome-Wide Association-Identified Variants for Atrial Fibrillation in African Americans
score: 1.8740728, PLoS ONE, 2012, Delaney, Jessica T. et. al.

Rethinking the genetic basis for comorbidity of schizophrenia and type 2 diabetes
score: 1.8732987, Schizophrenia Research, 2010, Lin, P.I.; Shuldiner, A.R.

Polymorphisms in the Receptor Tyrosine Kinase MERTK Gene Are Associated with Multiple Sclerosis Susceptibility
score: 1.8697443, PLoS ONE, 2011, Ma, Gerry Z. M. et. al.

Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans.
score: 1.8664088, Genetic epidemiology, 2012, Murray, Tanda et. al.

Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes
score: 1.8596968, PLoS Genetics, 2011, Maranville, Joseph C. et. al.

Evaluating the effective numbers of independent tests and significant p -value thresholds in commercial genotyping arrays and public imputation reference datasets
score: 1.8568578, Human Genetics, 2011, Li, Miao-Xin et. al.

Application of principal component analysis to pharmacogenomic studies in Canada.
score: 1.8566731, The pharmacogenomics journal, 2009, Visscher, H et. al.

Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23
score: 1.8554757, Human Molecular Genetics, 2009, Orozco, Gisela et. al.

Ascertainment biases in SNP chips affect measures of population divergence.
score: 1.8546167, Molecular biology and evolution, 2010, Albrechtsen, Anders; Nielsen, Finn Cilius; Nielsen, Rasmus

Genetic variants near the MGAT1 gene are associated with body weight, BMI and fatty acid metabolism among adults and children
score: 1.8501557, International Journal of Obesity (2005), 2011, Jacobsson, J A et. al.

hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets
score: 1.8492856, Genome Biology, 2011, Johnson, Todd A et. al.

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.
score: 1.8477239, Molecular psychiatry, 2010, Carroll, L S et. al.

Expanding the range of ZNF804A variants conferring risk of psychosis.
score: 1.8472121, Molecular psychiatry, 2011, Steinberg, S et. al.

Genetics of Type 1 Diabetes: What's Next?
score: 1.8432697, Diabetes, 2010, Pociot, Flemming et. al.

Meta-analysis of sex-specific genome-wide association studies.
score: 1.8423523, Genetic epidemiology, 2010, Magi, Reedik; Lindgren, Cecilia M; Morris, Andrew P

Risk Alleles for Systemic Lupus Erythematosus in a Large Case-Control Collection and Associations with Clinical Subphenotypes
score: 1.8419642, PLoS Genetics, 2011, Taylor, Kimberly E. et. al.

WWOX gene is associated with HDL cholesterol and triglyceride levels
score: 1.8399264, BMC Medical Genetics, 2010, Sáez, María E et. al.

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1
score: 1.8373883, Neurobiology of Aging, 2013,

Genes Involved in Vasoconstriction and Vasodilation System Affect Salt-Sensitive Hypertension
score: 1.8365215, PLoS ONE, 2011, Citterio, Lorena et. al.

CD226 Gly307Ser association with multiple autoimmune diseases.
score: 1.8351482, Genes and immunity, 2009, Hafler, J P et. al.

Genetic Contributions to Clinical Pain and Analgesia: Avoiding Pitfalls in Genetic Research
score: 1.8338508, Journal of Pain, 2009, Kim, Hyungsuk; Clark, David; Dionne, Raymond A.

TTC7B emerges as a novel risk factor for ischemic stroke through the convergence of several genome-wide approaches.
score: 1.8325599, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2012, Krug, Tiago et. al.

MicroRNA-3148 Modulates Allelic Expression of Toll-Like Receptor 7 Variant Associated with Systemic Lupus Erythematosus
score: 1.8299028, PLoS Genetics, 2013, Deng, Yun et. al.

HYST: A Hybrid Set-Based Test for Genome-wide Association Studies, with Application to Protein-Protein Interaction-Based Association Analysis
score: 1.8288312, The American Journal of Human Genetics, 2012, Li, Miao-Xin; Kwan, Johnny S.H.; Sham, Pak C.

Genomewide Analysis of Inherited Variation Associated with Phosphorylation of PI3K/AKT/mTOR Signaling Proteins
score: 1.8260697, PLoS ONE, 2011, Hutz, Janna E. et. al.

Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment
score: 1.8259014, European Journal of Clinical Pharmacology, 2008, Brockmöller, Jürgen; Tzvetkov, Mladen V.

The association of a nonsynonymous single-nucleotide polymorphism in TNFAIP3 with systemic lupus erythematosus and rheumatoid arthritis in the Japanese population.
score: 1.8258951, Arthritis and rheumatism, 2010, Shimane, Kenichi et. al.

The role of non-HLA single nucleotide polymorphisms in multiple sclerosis susceptibility
score: 1.8238008, Journal of Neuroimmunology, 2010, Bahreini, Seyed Amir et. al.

High Differentiation among Eight Villages in a Secluded Area of Sardinia Revealed by Genome-Wide High Density SNPs Analysis
score: 1.8233905, PLoS ONE, 2009, Pistis, Giorgio et. al.

Replication of the TNFSF4 (OX40L) promoter region association with systemic lupus erythematosus.
score: 1.8221653, Genes and immunity, 2009, Delgado-Vega, A M et. al.

Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2.
score: 1.8192879, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Prokunina-Olsson, Ludmila et. al.

Genome-wide association analyses of North American Rheumatoid Arthritis Consortium and Framingham Heart Study data utilizing genome-wide linkage results
score: 1.8169003, BMC Proceedings, 2009, Yoo, Yun Joo et. al.

Replicating genotype-phenotype associations.
score: 1.8153919, Nature, 2007, NCI-NHGRI Working Group on Replication in Association Studies, et. al.

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)
score: 1.814918, Human Genetics, 2012, Xu, Jianfeng et. al.

Identification of a Shared Genetic Susceptibility Locus for Coronary Heart Disease and Periodontitis
score: 1.8122044, PLoS Genetics, 2009, Schaefer, Arne S. et. al.

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
score: 1.8098566, The American Journal of Human Genetics, 2007, Purcell, Shaun et. al.

Region-based analysis in genome-wide association study of Framingham Heart Study blood lipid phenotypes
score: 1.8084661, BMC Proceedings, 2009, Asimit, Jennifer L et. al.

9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium.
score: 1.8039614, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Warren, Helen et. al.

Evaluation of genetic loci influencing adult height in the Japanese population.
score: 1.7965398, Journal of human genetics, 2009, Takeuchi, Fumihiko et. al.

Phenotype harmonization and cross-study collaboration in GWAS consortia: the GENEVA experience.
score: 1.7958484, Genetic epidemiology, 2011, Bennett, Siiri N et. al.

Unravelling the genetic basis of renal diseases; from single gene to multifactorial disorders.
score: 1.7953526, The Journal of pathology, 2010, McKnight, Amy J; Currie, Diane; Maxwell, Alexander P

Comprehensive assessment of rheumatoid arthritis susceptibility loci in a large psoriatic arthritis cohort
score: 1.7889039, Annals of the Rheumatic Diseases, 2012, Bowes, John et. al.

Genome-wide association studies: progress and potential for drug discovery and development.
score: 1.7866923, Nature reviews. Drug discovery, 2008, Kingsmore, Stephen F et. al.

Assessing batch effects of genotype calling algorithm BRLMM for the Affymetrix GeneChip Human Mapping 500 K array set using 270 HapMap samples
score: 1.7852062, BMC Bioinformatics, 2008, Hong, Huixiao et. al.

Coexpression Network Analysis in Abdominal and Gluteal Adipose Tissue Reveals Regulatory Genetic Loci for Metabolic Syndrome and Related Phenotypes
score: 1.7836601, PLoS Genetics, 2012, Min, Josine L. et. al.

Single nucleotide polymorphisms in sFRP4 are associated with bone and body composition related parameters in Danish but not in Belgian men
score: 1.7784059, Molecular Genetics and Metabolism, 2012, Boudin, Eveline et. al.

Single nucleotide polymorphisms in sFRP4 are associated with bone and body composition related parameters in Danish but not in Belgian men
score: 1.7784059, Molecular Genetics and Metabolism, 2012, Boudin, Eveline et. al.

Single nucleotide polymorphisms in sFRP4 are associated with bone and body composition related parameters in Danish but not in Belgian men
score: 1.7784059, Molecular Genetics and Metabolism, 2012, Boudin, Eveline et. al.

Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS
score: 1.774721, PLoS Genetics, 2010, Nicolae, Dan L. et. al.

An Open Access Database of Genome-wide Association Results
score: 1.7730059, BMC Medical Genetics, 2009, Johnson, Andrew D; O'Donnell, Christopher J

Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.
score: 1.7715246, Genes and immunity, 2009, Morris, D L et. al.

The type I diabetes association of the IL2RA locus.
score: 1.7697725, Genes and immunity, 2009, Qu, H-Q et. al.

Evaluating the evidence for transmission distortion in human pedigrees.
score: 1.7682118, Genetics, 2012, Meyer, Wynn K et. al.

A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM)
score: 1.7648865, American Journal of Obstetrics and Gynecology, 2010, Romero, Roberto et. al.

Association analyses identify six new psoriasis susceptibility loci in the Chinese population.
score: 1.7639315, Nature genetics, 2010, Sun, Liang-Dan et. al.

Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.
score: 1.7562223, Molecular psychiatry, 2012, Badner, J A et. al.

Replication of GWAS associations for GAK and MAPT in Parkinson's disease.
score: 1.7547363, Annals of human genetics, 2011, Rhodes, Shannon L et. al.

A Genome-Wide Scan for Breast Cancer Risk Haplotypes among African American Women
score: 1.7528467, PLoS ONE, 2013, Song, Chi et. al.

A Network-Based Approach to Prioritize Results from Genome-Wide Association Studies
score: 1.7482292, PLoS ONE, 2011, Akula, Nirmala et. al.

Insights into the Genetic Architecture of Early Stage Age-Related Macular Degeneration: A Genome-Wide Association Study Meta-Analysis
score: 1.7471874, PLoS ONE, 2013, Holliday, Elizabeth G. et. al.

The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study
score: 1.7462938, PLoS Medicine, 2011, Do, Ron et. al.

Rheumatoid arthritis-associated polymorphisms are not protective against Alzheimer's disease
score: 1.7447387, Molecular Neurodegeneration, 2011, Simmons, Christopher R et. al.

Identification of KIF3A as a Novel Candidate Gene for Childhood Asthma Using RNA Expression and Population Allelic Frequencies Differences
score: 1.7413906, PLoS ONE, 2011, Butsch Kovacic, Melinda et. al.

Mammographic breast density and breast cancer: evidence of a shared genetic basis.
score: 1.7410709, Cancer research, 2012, Varghese, Jajini S et. al.

The SH2D2A gene and susceptibility to multiple sclerosis
score: 1.7397128, Journal of Neuroimmunology, 2008, Lorentzen, Åslaug R. et. al.

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes
score: 1.7368752, Human Molecular Genetics, 2009, Perry, John R.B. et. al.

Evaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk
score: 1.7350583, Molecular Neurodegeneration, 2011, Simmons, Christopher R et. al.

The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports
score: 1.7346538, BMC Medical Genetics, 2007, Cupples, L Adrienne et. al.

Unifying Candidate Gene and GWAS Approaches in Asthma
score: 1.7342424, PLoS ONE, 2010, Michel, Sven et. al.

Effect of Genome-Wide Genotyping and Reference Panels on Rare Variants Imputation
score: 1.7339717, Journal of Genetics and Genomics, 2012, Zheng, Hou-Feng et. al.

Effect of Genome-Wide Genotyping and Reference Panels on Rare Variants Imputation
score: 1.7339717, Journal of Genetics and Genomics, 2012, Zheng, Hou-Feng et. al.

Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping
score: 1.7291998, BMC Genetics, 2008, Olshen, Adam B et. al.

Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort
score: 1.726046, Human Genetics, 2012, Browning, Sharon R.; Browning, Brian L.

Common Variants Show Predicted Polygenic Effects on Height in the Tails of the Distribution, Except in Extremely Short Individuals
score: 1.7251681, PLoS Genetics, 2011, Chan, Yingleong et. al.

A genomewide linkage scan of cocaine dependence and major depressive episode in two populations.
score: 1.7151724, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Yang, Bao-Zhu et. al.

Fine Mapping of Five Loci Associated with Low-Density Lipoprotein Cholesterol Detects Variants That Double the Explained Heritability
score: 1.7134557, PLoS Genetics, 2011, Sanna, Serena et. al.

Genetic association of the major histocompatibility complex with rheumatoid arthritis implicates two non-DRB1 loci.
score: 1.7129005, Arthritis and rheumatism, 2009, Vignal, Charlotte et. al.

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease
score: 1.7112064, Neuroimage, 2010, Stein, Jason L. et. al.

Evaluating aggregate effects of rare and common variants in the 1000 Genomes Project exon sequencing data using latent variable structural equation modeling
score: 1.7089781, BMC Proceedings, 2011, Nock, NL; Zhang, LX

CTLA4/ICOS gene variants and haplotypes are associated with rheumatoid arthritis and primary biliary cirrhosis in the Canadian population.
score: 1.7082614, Arthritis and rheumatism, 2009, Walker, Erin J et. al.

A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample
score: 1.7067447, PLoS ONE, 2011, Obeidat, Ma'en et. al.

Genetic Heterogeneity in Colorectal Cancer Associations Between African and European Americans
score: 1.7065022, Gastroenterology, 2010, Kupfer, Sonia S. et. al.

Exploring the interaction between SNP genotype and postmenopausal hormone therapy effects on stroke risk
score: 1.7036704, Genome Medicine, 2012, Huang, Ying et. al.

Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18
score: 1.700778, PLoS ONE, 2010, Scerri, Thomas S. et. al.

Unidentified genetic variants influence pancreatic cancer risk: an analysis of polygenic susceptibility in the PanScan study.
score: 1.6997683, Genetic epidemiology, 2012, Pierce, Brandon L; Tong, Lin; Kraft, Peter; Ahsan, Habibul

Maternal and Fetal Genetic Associations of PTGER3 and PON1 with Preterm Birth
score: 1.6967331, PLoS ONE, 2010, Ryckman, Kelli K. et. al.

Batch effects in the BRLMM genotype calling algorithm influence GWAS results for the Affymetrix 500K array.
score: 1.6960668, The pharmacogenomics journal, 2010, Miclaus, K et. al.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
score: 1.6958773, Human Genetics, 2011, Casey, Jillian P. et. al.

Correlation between Genetic and Geographic Structure in Europe
score: 1.6908044, Current Biology, 2008, Lao, Oscar et. al.

Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples.
score: 1.6881715, Molecular psychiatry, 2010, Le Hellard, S et. al.

Genotype imputation for genome-wide association studies.
score: 1.6875773, Nature reviews. Genetics, 2010, Marchini, Jonathan; Howie, Bryan

Association of NCF2 , IKZF1 , IRF8 , IFIH1 , and TYK2 with Systemic Lupus Erythematosus
score: 1.6859901, PLoS Genetics, 2011, Cunninghame Graham, Deborah S. et. al.

Polymorphisms in inflammation-related genes are associated with susceptibility to major depression and antidepressant response.
score: 1.6851247, Molecular psychiatry, 2008, Wong, M-L; Dong, C; Maestre-Mesa, J; Licinio, J

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population
score: 1.6812649, European Journal of Human Genetics, 2011, Villanueva, Pia et. al.

Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis.
score: 1.6807257, Genes and immunity, 2012, Achkar, J-P et. al.

A Common Variant in the CDKN2B Gene on Chromosome 9p21 Protects Against Coronary Artery Disease in Americans of African Ancestry
score: 1.6802553, Journal of human genetics, 2011, Kral, Brian G. et. al.

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
score: 1.6783997, Lancet, 2010, Williams, Nigel M et. al.

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
score: 1.6783997, The Lancet, 2010, Williams, Nigel M et. al.

Validating, augmenting and refining genome-wide association signals.
score: 1.6739681, Nature reviews. Genetics, 2009, Ioannidis, John P A; Thomas, Gilles; Daly, Mark J

Statistical colocalization of monocyte gene expression and genetic risk variants for type 1 diabetes.
score: 1.6703437, Human molecular genetics, 2012, Wallace, Chris et. al.

Genome-wide detection and characterization of mating asymmetry in human populations.
score: 1.6695911, Genetic epidemiology, 2011, Bourgey, Mathieu et. al.

Evaluation of Clustering and Genotype Distribution for Replication in Genome Wide Association Studies: The Age-Related Eye Disease Study
score: 1.6689894, PLoS ONE, 2008, Edwards, Albert O. et. al.

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L – DOCK4 gene region in autism susceptibility
score: 1.6674204, Molecular Psychiatry, 2009, Maestrini, E et. al.

Integrated detection and population-genetic analysis of SNPs and copy number variation.
score: 1.6623325, Nature genetics, 2008, McCarroll, Steven A et. al.

SNP mistyping in genotyping arrays--an important cause of spurious association in case-control studies.
score: 1.6619104, Genetic epidemiology, 2011, Mitry, D et. al.

Differential co-expression analysis of obesity-associated networks in human subcutaneous adipose tissue
score: 1.661512, International Journal of Obesity (2005), 2011, Walley, A.J. et. al.

Interactions of Dietary Whole-Grain Intake With Fasting Glucose– and Insulin-Related Genetic Loci in Individuals of European Descent
score: 1.6612041, Diabetes Care, 2010, Nettleton, Jennifer A. et. al.

Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22.
score: 1.6595018, International journal of cancer. Journal international du cancer, 2011, Cropp, Cheryl D et. al.

Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease
score: 1.6589071, Human Mutation, 2008, Srinivasan, Balaji S et. al.

A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus.
score: 1.658065, Genes and immunity, 2012, Wang, S et. al.

A variant near the interleukin-6 gene is associated with fat mass in Caucasian men.
score: 1.6579239, International journal of obesity (2005), 2010, Andersson, N et. al.

Insights into Colon Cancer Etiology via a Regularized Approach to Gene Set Analysis of GWAS Data
score: 1.6578415, The American Journal of Human Genetics, 2010, Chen, Lin S. et. al.

EPHA2 Is Associated with Age-Related Cortical Cataract in Mice and Humans
score: 1.6563693, PLoS Genetics, 2009, Jun, Gyungah et. al.

Protective effect of human endogenous retrovirus K dUTPase variants on psoriasis susceptibility.
score: 1.6563316, The Journal of investigative dermatology, 2012, Lai, Olivia Y et. al.

UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study
score: 1.6533584, Neurobiology of Aging, 2013, Chiò, Adriano et. al.

Identity by descent estimation with dense genome-wide genotype data.
score: 1.6520467, Genetic epidemiology, 2011, Han, Lide; Abney, Mark

Pathway-Based Association Analyses Identified TRAIL Pathway for Osteoporotic Fractures
score: 1.643791, PLoS ONE, 2011, Zhang, Yin-Ping et. al.

Association of FTO gene variants with body composition in UK twins.
score: 1.6422099, Annals of human genetics, 2012, Livshits, Gregory et. al.

Caucasian and Asian Specific Rheumatoid Arthritis Risk Loci Reveal Limited Replication and Apparent Allelic Heterogeneity in North Indians
score: 1.6391863, PLoS ONE, 2012, Prasad, Pushplata et. al.

A common variant associated with prostate cancer in European and African populations.
score: 1.638523, Nature genetics, 2006, Amundadottir, Laufey T et. al.

OPG and RANK Polymorphisms Are Both Associated with Cortical Bone Mineral Density: Findings from a Metaanalysis of the Avon Longitudinal Study of Parents and Children and Gothenburg Osteoporosis and Obesity Determinants Cohorts
score: 1.6384898, The Journal of Clinical Endocrinology and Metabolism, 2010, Paternoster, L. et. al.

Effects of covariates and interactions on a genome-wide association analysis of rheumatoid arthritis
score: 1.6360635, BMC Proceedings, 2009, Arya, Rector et. al.

HMGA2 is confirmed to be associated with human adult height.
score: 1.6279662, Annals of human genetics, 2010, Yang, Tie-Lin et. al.

SNP-based analysis of the HLA locus in Japanese multiple sclerosis patients.
score: 1.6274406, Genes and immunity, 2011, McElroy, J P et. al.

Abstracts for the 20th EFI (European Federation for Immunogenetics) Conference, Oslo, Norway, 8-11 June, 2006.
score: 1.6273776, Tissue antigens, 2006,

Evidence for Polygenic Susceptibility to Multiple Sclerosis—The Shape of Things to Come
score: 1.62659, The American Journal of Human Genetics, 2010, The International Multiple Sclerosis Genetics Consortium (IMSGC), et. al.

Polymorphisms in Genes Involved in the NF-κB Signalling Pathway Are Associated with Bone Mineral Density, Geometry and Turnover in Men
score: 1.6251076, PLoS ONE, 2011, Roshandel, Delnaz et. al.

G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes
score: 1.624502, Diabetes, 2008, Trégouet, David-Alexandre et. al.

Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure
score: 1.6231875, PLoS Genetics, 2012, Gaál, Emília Ilona et. al.

How to deal with the early GWAS data when imputing and combining different arrays is necessary
score: 1.6219398, European Journal of Human Genetics, 2011, Uh, Hae-Won et. al.

The Genome-wide Patterns of Variation Expose Significant Substructure in a Founder Population
score: 1.615626, The American Journal of Human Genetics, 2008, Jakkula, Eveliina et. al.

Genetic architecture of circulating lipid levels.
score: 1.6062444, European journal of human genetics : EJHG, 2011, Demirkan, Ayşe et. al.

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.
score: 1.6034876, European journal of human genetics : EJHG, 2011, Villanueva, Pia et. al.

Copy Number Variation in CNP267 Region May Be Associated with Hip Bone Size
score: 1.5923982, PLoS ONE, 2011, Liu, Shan-Lin et. al.

Similarity-based multimarker association tests for continuous traits.
score: 1.5920317, Annals of human genetics, 2012, Lin, Wan-Yu et. al.

EVI5 is a risk gene for multiple sclerosis.
score: 1.5905981, Genes and immunity, 2008, Hoppenbrouwers, I A et. al.

Improved Heritability Estimation from Genome-wide SNPs
score: 1.5864203, The American Journal of Human Genetics, 2012, Speed, Doug et. al.

Improved Heritability Estimation from Genome-wide SNPs
score: 1.5864203, The American Journal of Human Genetics, 2012, Speed, Doug et. al.

The genetics of type 2 diabetes: what have we learned from GWAS?
score: 1.5815644, Annals of the New York Academy of Sciences, 2010, Billings, Liana K; Florez, Jose C

A Case Control Association Study and Cognitive Function Analysis of Neuropilin and Tolloid-Like 1 Gene and Schizophrenia in the Japanese Population
score: 1.581557, PLoS ONE, 2011, Banno, Masahiro et. al.

MicroRNA Expression in Abdominal and Gluteal Adipose Tissue Is Associated with mRNA Expression Levels and Partly Genetically Driven
score: 1.5800863, PLoS ONE, 2011, Rantalainen, Mattias et. al.

Influence of Polymorphisms in the RANKL/RANK/OPG Signaling Pathway on Volumetric Bone Mineral Density and Bone Geometry at the Forearm in Men
score: 1.5759786, Calcified Tissue International, 2011, Roshandel, Delnaz et. al.

Examination of All Type 2 Diabetes GWAS Loci Reveals HHEX-IDE as a Locus Influencing Pediatric BMI
score: 1.575624, Diabetes, 2009, Zhao, Jianhua et. al.

Association of variants in genes involved in pancreatic β-cell development and function with type 2 diabetes in North Indians.
score: 1.57481, Journal of human genetics, 2011, Chavali, Sreenivas et. al.

Genomic approaches to coronary artery disease
score: 1.5744087, The Indian Journal of Medical Research, 2010, Padmanabhan, Sandosh et. al.

An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population.
score: 1.5737012, European journal of human genetics : EJHG, 2009, Lu, Timothy Tehua et. al.

Comprehensive association study of genetic variants in the IL-1 gene family in systemic juvenile idiopathic arthritis.
score: 1.5697323, Genes and immunity, 2008, Stock, C J W et. al.

Turkish Population Structure and Genetic Ancestry Reveal Relatedness among Eurasian Populations.
score: 1.5651538, Annals of human genetics, 2012, Hodoğlugil, Uğur; Mahley, Robert W

Whole-genome association study for fatty acid composition of oleic acid in Japanese Black cattle.
score: 1.5643359, Animal genetics, 2010, Uemoto, Y et. al.

A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males.
score: 1.5641314, Journal of human genetics, 2011, Ratanajaraya, Chanavee et. al.

Testing for genetic association taking into account phenotypic information of relatives
score: 1.5629767, BMC Proceedings, 2009, Uh, Hae-Won et. al.

Association of Genetic Variants at 3q22 with Nephropathy in Patients with Type 1 Diabetes Mellitus
score: 1.562964, The American Journal of Human Genetics, 2009, He, Bing et. al.

Geographical genomics of human leukocyte gene expression variation in southern Morocco.
score: 1.5591074, Nature genetics, 2010, Idaghdour, Youssef et. al.

Comprehensive assessment of variation at the transforming growth factor beta type 1 receptor locus and colorectal cancer predisposition.
score: 1.5589581, Proceedings of the National Academy of Sciences of the United States of America, 2010, Carvajal-Carmona, Luis G et. al.

An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes.
score: 1.5580943, Kidney international, 2011, Pezzolesi, Marcus G et. al.

Moderation of adult depression by a polymorphism in the FKBP5 gene and childhood physical abuse in the general population.
score: 1.5554695, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Appel, Katja et. al.

Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses
score: 1.5552757, BMC Proceedings, 2009, Cupples, L Adrienne et. al.

Variants in linkage disequilibrium with the late cornified envelope gene cluster deletion are associated with susceptibility to psoriatic arthritis
score: 1.5543147, Annals of the Rheumatic Diseases, 2010, Bowes, John et. al.

Composite likelihood-based meta-analysis of breast cancer association studies.
score: 1.5541918, Journal of human genetics, 2011, Politopoulos, Ioannis et. al.

Extent of Height Variability Explained by Known Height-Associated Genetic Variants in an Isolated Population of the Adriatic Coast of Croatia
score: 1.5534152, PLoS ONE, 2011, Zhang, Ge et. al.

QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders.
score: 1.5523483, Molecular psychiatry, 2013, Lu, A T-H; Yoon, J; Geschwind, D H; Cantor, R M

GWAMA: software for genome-wide association meta-analysis
score: 1.5522322, BMC Bioinformatics, 2010, Mägi, Reedik; Morris, Andrew P

The renal urate transporter SLC17A1 locus: confirmation of association with gout
score: 1.5510147, Arthritis Research & Therapy, 2012, Hollis-Moffatt, Jade E et. al.

Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium
score: 1.5506073, European Heart Journal, 2012, Fedorowski, Artur et. al.

Interleukin-4/interleukin-4 receptor gene polymorphisms in hand osteoarthritis
score: 1.5496953, Osteoarthritis and Cartilage, 2010, Vargiolu, M. et. al.

Genome-wide association study identified three major QTL for carcass weight including the PLAG1-CHCHD7 QTN for stature in Japanese Black cattle
score: 1.5477683, BMC Genetics, 2012, Nishimura, Shota et. al.

Genetic polymorphisms in key methotrexate pathway genes are associated with response to treatment in rheumatoid arthritis patients.
score: 1.5476898, The pharmacogenomics journal, 2012, Owen, S A et. al.

A Genome-Wide Association Study Primer for Clinicians
score: 1.5457506, Taiwanese Journal of Obstetrics & Gynecology, 2009, Wang, Tzu-Hao; Wang, Hsin-Shih

Fine-mapping classical HLA variation associated with durable host control of HIV-1 infection in African Americans.
score: 1.5454203, Human molecular genetics, 2012, McLaren, Paul J et. al.

Genetic predictors of medically refractory ulcerative colitis.
score: 1.5447339, Inflammatory bowel diseases, 2010, Haritunians, Talin et. al.

Implication of Genetic Variants Near TCF7L2 , SLC30A8 , HHEX , CDKAL1 , CDKN2A/B , IGF2BP2 , and FTO in Type 2 Diabetes and Obesity in 6,719 Asians
score: 1.5387209, Diabetes, 2008, Ng, Maggie C.Y. et. al.

Variation in Human Recombination Rates and Its Genetic Determinants
score: 1.5357838, PLoS ONE, 2011, Fledel-Alon, Adi et. al.

Recombination rates in admixed individuals identified by ancestry-based inference.
score: 1.5340704, Nature genetics, 2011, Wegmann, Daniel et. al.

Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls
score: 1.5335986, Nature, 2010,

Racial/Ethnic Differences in Association of Fasting Glucose–Associated Genomic Loci With Fasting Glucose, HOMA-B, and Impaired Fasting Glucose in the U.S. Adult Population
score: 1.5299045, Diabetes Care, 2010, Yang, Quanhe et. al.

Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers.
score: 1.5291478, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Spurdle, Amanda B et. al.

Human longevity and variation in GH/IGF-1/insulin signaling, DNA damage signaling and repair and pro/antioxidant pathway genes: Cross sectional and longitudinal studies
score: 1.528485, Experimental Gerontology, 2012, Soerensen, Mette et. al.

Human longevity and variation in GH/IGF-1/insulin signaling, DNA damage signaling and repair and pro/antioxidant pathway genes: Cross sectional and longitudinal studies
score: 1.528485, Experimental Gerontology, 2012, Soerensen, Mette et. al.

Genome-wide association study of skin complex diseases
score: 1.5249328, Journal of Dermatological Science, 2012, Zhang, Xuejun

Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers
score: 1.5220705, Breast Cancer Research : BCR, 2012, Maia, Ana-Teresa et. al.

Child development and molecular genetics: 14 years later.
score: 1.521512, Child development, 2013, Plomin, Robert

HLA-DPB1-COL11A2 and three additional xMHC loci are independently associated with RA in a UK cohort.
score: 1.5202345, Genes and immunity, 2011, Orozco, G et. al.

A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing Study
score: 1.5176134, BMC Medical Genetics, 2011, Roshandel, Delnaz et. al.

Detecting gene-gene interactions that underlie human diseases.
score: 1.5136553, Nature reviews. Genetics, 2009, Cordell, Heather J

Family-based analysis of tumor necrosis factor and lymphotoxin-α tag polymorphisms with type 1 diabetes in the population of South Croatia
score: 1.5106562, Human Immunology, 2009, Boraska, Vesna et. al.

Detecting gene-by-smoking interactions in a genome-wide association study of early-onset coronary heart disease using random forests
score: 1.5104114, BMC Proceedings, 2009, Maenner, Matthew J et. al.

Positive association of common variants in CD36 with neovascular age-related macular degeneration
score: 1.510403, Aging, 2009, Kondo, Naoshi; Honda, Shigeru; Kuno, Shin-ichi; Negi, Akira

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
score: 1.5097852, Breast Cancer Research : BCR, 2011, Mulligan, Anna Marie et. al.

A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.
score: 1.5096427, Molecular psychiatry, 2013, Allebrandt, K V et. al.

Thursday Abstracts
score: 1.5095915, Biological Psychiatry, 2008,

A novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2
score: 1.503215, Nature, 2009, Walters, R. G. et. al.

Unraveling the Regulatory Mechanisms Underlying Tissue-Dependent Genetic Variation of Gene Expression
score: 1.5002385, PLoS Genetics, 2012, Fu, Jingyuan et. al.

Genome-wide association studies and the genetic dissection of complex traits.
score: 1.4996784, American journal of hematology, 2009, Sebastiani, Paola et. al.

Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population
score: 1.4959265, BMC Genetics, 2010, Andiappan, Anand Kumar et. al.

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
score: 1.4952272, Nature, 2010, Wellcome Trust Case Control Consortium, et. al.

Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations
score: 1.4925771, BMC Medical Genetics, 2009, Mocci, Evelina et. al.

On the Use of General Control Samples for Genome-wide Association Studies: Genetic Matching Highlights Causal Variants
score: 1.4898907, The American Journal of Human Genetics, 2008, Luca, Diana et. al.

Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a Japanese population.
score: 1.485046, Journal of human genetics, 2009, Hotta, Kikuko et. al.

Identification of novel genetic susceptibility loci in African American lupus patients in a candidate gene association study.
score: 1.4828542, Arthritis and rheumatism, 2011, Sánchez, Elena et. al.

RGMA and IL21R show association with experimental inflammation and multiple sclerosis.
score: 1.4818168, Genes and immunity, 2010, Nohra, R et. al.

Validation of genome-wide prostate cancer associations in men of African descent.
score: 1.4800764, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Chang, Bao-Li et. al.

EphB2 SNPs and Sporadic Prostate Cancer Risk in African American Men
score: 1.4749788, PLoS ONE, 2011, Robbins, Christiane M. et. al.

Genetics of Sputum Gene Expression in Chronic Obstructive Pulmonary Disease
score: 1.4744783, PLoS ONE, 2011, Qiu, Weiliang et. al.

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
score: 1.4737956, Molecular psychiatry, 2010, Maestrini, E et. al.

Gene discovery through imaging genetics: identification of two novel genes associated with schizophrenia.
score: 1.4715829, Molecular psychiatry, 2009, Potkin, S G et. al.

SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy
score: 1.4608022, Molecular Vision, 2009, Kondo, Naoshi; Bessho, Hiroaki; Honda, Shigeru; Negi, Akira

Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate.
score: 1.4599451, Birth defects research. Part A, Clinical and molecular teratology, 2012, Wu, Tao et. al.

Ultrahigh-dimensional variable selection method for whole-genome gene-gene interaction analysis
score: 1.4590214, BMC Bioinformatics, 2012, Ueki, Masao; Tamiya, Gen

High-Density SNP Screening of the Major Histocompatibility Complex in Systemic Lupus Erythematosus Demonstrates Strong Evidence for Independent Susceptibility Regions
score: 1.4575218, PLoS Genetics, 2009, Barcellos, Lisa F. et. al.

Program-Abstracts
score: 1.4573853, Cancer Microenvironment, 2009,

Accuracy of CNV Detection from GWAS Data
score: 1.4569729, PLoS ONE, 2011, Zhang, Dandan et. al.

Investigating association of four gene regions (GABRB3, MAOB, PAH, and SLC6A4) with five symptoms in schizophrenia
score: 1.4550722, Psychiatry Research, 2012, Sun, Jingchun et. al.

An ICA with reference approach in identification of genetic variation and associated brain networks
score: 1.4484567, Frontiers in Human Neuroscience, 2012, Liu, Jingyu et. al.

Fine-mapping of prostate cancer aggressiveness loci on chromosome 7q22-35.
score: 1.4482231, The Prostate, 2011, Liu, Xin et. al.

Genome-wide significant association between a ‘negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1
score: 1.4471566, Translational Psychiatry, 2012, Meier, S et. al.

COGENT (COlorectal cancer GENeTics) revisited.
score: 1.4433846, Mutagenesis, 2012, Houlston, Richard S; members of COGENT,

Identification of the Genetic Basis for Complex Disorders by Use of Pooling-Based Genomewide Single-Nucleotide–Polymorphism Association Studies
score: 1.4403804, The American Journal of Human Genetics, 2007, Pearson, John V. et. al.

A follow-up study for left ventricular mass on chromosome 12p11 identifies potential candidate genes
score: 1.4389428, BMC Medical Genetics, 2011, Della-Morte, David et. al.

Identification of gene-gene interaction using principal components
score: 1.4355207, BMC Proceedings, 2009, Li, Jia; Tang, Rui; Biernacka, Joanna M; de Andrade, Mariza

Mutations in BRIP1 confer high risk of ovarian cancer.
score: 1.4341266, Nature genetics, 2011, Rafnar, Thorunn et. al.

C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect
score: 1.4322551, Neurobiology of Aging, 2012, Ratti, Antonia et. al.

SNPLims: a data management system for genome wide association studies
score: 1.4315644, BMC Bioinformatics, 2008, Orro, Alessandro et. al.

A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE)
score: 1.4315548, Schizophrenia Research, 2009, Djurovic, S. et. al.

Autoimmune Disease Classification by Inverse Association with SNP Alleles
score: 1.4301456, PLoS Genetics, 2009, Sirota, Marina et. al.

Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays
score: 1.4300395, BMC Research Notes, 2010, Schosser, Alexandra et. al.

Linkage disequilibrium and age of HLA region SNPs in relation to classic HLA gene alleles within Europe.
score: 1.4297822, European journal of human genetics : EJHG, 2010, Evseeva, Irina et. al.

African ancestry and lung function in Puerto Rican children
score: 1.4287172, The Journal of Allergy and Clinical Immunology, 2012, Brehm, John M. et. al.

African ancestry and lung function in Puerto Rican children
score: 1.4287172, The Journal of Allergy and Clinical Immunology, 2012, Brehm, John M. et. al.

Using linkage analysis to identify quantitative trait loci for sleep apnea in relationship to body mass index.
score: 1.428061, Annals of human genetics, 2008, Larkin, E K et. al.

Analysis of potential genomic confounding in genetic association studies and an online genomic confounding browser (GCB).
score: 1.4247727, Annals of human genetics, 2011, Raistrick, Christopher A et. al.

Genetic Control of Individual Differences in Gene-Specific Methylation in Human Brain
score: 1.4226595, The American Journal of Human Genetics, 2010, Zhang, Dandan et. al.

IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci.
score: 1.4220847, Genes and immunity, 2010, International Multiple Sclerosis Genetics Conssortium (IMSGC), et. al.

Single and multivariate associations of MSR1, ELAC2, and RNASEL with prostate cancer in an ethnic diverse cohort of men.
score: 1.4213362, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Beuten, Joke et. al.

Characterization of gene-environment interactions for colorectal cancer susceptibility loci.
score: 1.421148, Cancer research, 2012, Hutter, Carolyn M et. al.

Genomic Dissection of Population Substructure of Han Chinese and Its Implication in Association Studies
score: 1.4195836, The American Journal of Human Genetics, 2009, Xu, Shuhua et. al.

Genome-wide association studies of atrial fibrillation: past, present, and future.
score: 1.4190547, Cardiovascular research, 2011, Sinner, Moritz F et. al.

ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry.
score: 1.416559, Molecular psychiatry, 2012, Bierut, L J et. al.

Statistical Epistasis and Functional Brain Imaging Support a Role of Voltage-Gated Potassium Channels in Human Memory
score: 1.4151335, PLoS ONE, 2011, Heck, Angela et. al.

Genetic association of cyclic AMP signaling genes with bipolar disorder
score: 1.4146779, Translational Psychiatry, 2012, McDonald, M-L; MacMullen, C; Liu, D J; Leal, S M; Davis, R L

FTO gene polymorphisms and obesity risk: a meta-analysis
score: 1.414621, BMC Medicine, 2011, Peng, Sihua et. al.

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.
score: 1.4145749, Nature genetics, 2011, Raychaudhuri, Soumya et. al.

Replication of a genome-wide association study of panic disorder in a Japanese population.
score: 1.4142929, Journal of human genetics, 2010, Otowa, Takeshi et. al.

Assessing and managing risk when sharing aggregate genetic variant data.
score: 1.4124791, Nature reviews. Genetics, 2011, Craig, David W et. al.

Germ-line sequence variants of PTEN do not have an important role in hereditary and non-hereditary prostate cancer susceptibility.
score: 1.4122357, Journal of human genetics, 2011, Xie, Chunmei C et. al.

TDP-43 Is Not a Common Cause of Sporadic Amyotrophic Lateral Sclerosis
score: 1.4111375, PLoS ONE, 2008, Guerreiro, Rita J. et. al.

Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes.
score: 1.4109193, Genes and immunity, 2012, Hirschfield, G M et. al.

Application of Bayesian network structure learning to identify causal variant SNPs from resequencing data
score: 1.4077119, BMC Proceedings, 2011, Schlosberg, Christopher E et. al.

Exploring the diabetogenicity of the HLA-B18-DR3 CEH: independent association with T1D genetic risk close to HLA-DOA.
score: 1.4072468, Genes and immunity, 2009, Santin, I et. al.

Using Functional Annotation for the Empirical Determination of Bayes Factors for Genome-Wide Association Study Analysis
score: 1.4071592, PLoS ONE, 2011, Knight, Jo et. al.

Human genetic variation and its contribution to complex traits.
score: 1.4069206, Nature reviews. Genetics, 2009, Frazer, Kelly A et. al.

Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis
score: 1.4013872, BMC Medical Genetics, 2010, Kerkhof, Hanneke JM et. al.

Building Genetic Scores to Predict Risk of Complex Diseases in Humans: Is It Possible?
score: 1.4010374, Diabetes, 2010, Liu, Simin; Song, Yiqing

Genome-wide association study of skin complex diseases
score: 1.4009271, Journal of Dermatological Science, 2012, Zhang, Xuejun

Using CSF biomarkers to replicate genetic associations in Alzheimer's disease
score: 1.4002682, Neurobiology of Aging, 2012, Schott, Jonathan M.

DNA microarray as a tool in establishing genetic relatedness—Current status and future prospects
score: 1.3943283, Forensic Science International: Genetics, 2012, Kling, Daniel et. al.

A systematic review of replication studies of prostate cancer susceptibility genetic variants in high-risk men originally identified from genome-wide association studies.
score: 1.3915067, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Ishak, Miriam B; Giri, Veda N

Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations
score: 1.3910454, Diabetes, 2008, Orho-Melander, Marju et. al.

Detecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analyses
score: 1.3897114, BMC Bioinformatics, 2009, Wongseree, Waranyu et. al.

Genome-wide association analysis of osteochondrosis of the tibiotarsal joint in Norwegian Standardbred trotters.
score: 1.3894495, Animal genetics, 2010, Lykkjen, S et. al.

Detectable clonal mosaicism from birth to old age and its relationship to cancer.
score: 1.3892019, Nature genetics, 2012, Laurie, Cathy C et. al.

Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions.
score: 1.3879102, The pharmacogenomics journal, 2009, Nelson, M R et. al.

Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors
score: 1.3875092, The American Journal of Human Genetics, 2013, Andreassen, Ole A. et. al.

Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors.
score: 1.3870434, Molecular psychiatry, 2012, Wong, M-L; Dong, C; Andreev, V; Arcos-Burgos, M; Licinio, J

Association of FOXO3A variation with human longevity confirmed in German centenarians.
score: 1.385905, Proceedings of the National Academy of Sciences of the United States of America, 2009, Flachsbart, Friederike et. al.

Genetic variants of the HLA-A, HLA-B and AIF1 loci show independent associations with type 1 diabetes in Norwegian families.
score: 1.3847366, Genes and immunity, 2009, Eike, M C et. al.

Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate.
score: 1.3845416, Genetic epidemiology, 2011, Beaty, Terri H et. al.

MPDA: Microarray pooled DNA analyzer
score: 1.3832089, BMC Bioinformatics, 2008, Yang, Hsin-Chou et. al.

A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.
score: 1.3815163, Genes and immunity, 2010, Ban, M et. al.

Allelotyping of pooled DNA with 250 K SNP microarrays
score: 1.3813169, BMC Genomics, 2007, Wilkening, Stefan et. al.

Genetic Variants in ER Cofactor Genes and Endometrial Cancer Risk
score: 1.3810014, PLoS ONE, 2012, Li, Yuqing et. al.

Effect of population stratification on the identification of significant single-nucleotide polymorphisms in genome-wide association studies
score: 1.3805939, BMC Proceedings, 2009, Sarasua, Sara M et. al.

The Potential for Enhancing the Power of Genetic Association Studies in African Americans through the Reuse of Existing Genotype Data
score: 1.3785242, PLoS Genetics, 2010, Chen, Gary K. et. al.

Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population.
score: 1.3767429, European journal of human genetics : EJHG, 2011, Sorice, Rossella et. al.

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
score: 1.3758529, Nature genetics, 2012, Morris, Andrew P et. al.

A unified framework for multi-locus association analysis of both common and rare variants
score: 1.3744561, BMC Genomics, 2011, Shriner, Daniel; Vaughan, Laura Kelly

Analysis and Application of European Genetic Substructure Using 300 K SNP Information
score: 1.3740889, PLoS Genetics, 2008, Tian, Chao et. al.

Susceptibility Genes for Age-Related Maculopathy on Chromosome 10q26
score: 1.3731001, The American Journal of Human Genetics, 2005, Jakobsdottir, Johanna et. al.

Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.
score: 1.3724386, Human molecular genetics, 2009, Kallio, Suvi P et. al.

Further evidence of association between two NET single-nucleotide polymorphisms with ADHD.
score: 1.3721072, Molecular psychiatry, 2008, Kim, J W et. al.

Evaluation of C1q genomic region in minority racial groups of lupus.
score: 1.370568, Genes and immunity, 2009, Namjou, B et. al.

A genome-wide linkage study of individuals with high scores on NEO personality traits.
score: 1.3701348, Molecular psychiatry, 2012, Amin, N et. al.

Discovery of Sexual Dimorphisms in Metabolic and Genetic Biomarkers
score: 1.3633399, PLoS Genetics, 2011, Mittelstrass, Kirstin et. al.

Gastric inhibitory polypeptide receptor: association analyses for obesity of several polymorphisms in large study groups
score: 1.3621528, BMC Medical Genetics, 2009, Vogel, Carla IG et. al.

WW-Domain-Containing Oxidoreductase Is Associated with Low Plasma HDL-C Levels
score: 1.3619147, The American Journal of Human Genetics, 2008, Lee, Jenny C. et. al.

Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels
score: 1.3608684, Human Genetics, 2011, Parikh, Hemang et. al.

ANK3 and CACNA1C – Missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples
score: 1.360386, Journal of Psychiatric Research, 2012, Kloiber, Stefan et. al.

ANK3 and CACNA1C – Missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples
score: 1.360386, Journal of Psychiatric Research, 2012, Kloiber, Stefan et. al.

ANK3 and CACNA1C – Missing genetic Link for bipolar disorder and major depressive disorder in two German case–control samples
score: 1.360386, Journal of Psychiatric Research, 2012, Kloiber, Stefan et. al.

A genome-wide survey over the ChIP-on-chip identified androgen receptor-binding genomic regions identifies a novel prostate cancer susceptibility locus at 12q13.13.
score: 1.360381, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Feng, Junjie et. al.

A Weighted False Discovery Rate Control Procedure Reveals Alleles at FOXA2 that Influence Fasting Glucose Levels
score: 1.3572274, The American Journal of Human Genetics, 2010, Xing, Chao; Cohen, Jonathan C.; Boerwinkle, Eric

A broad analysis of IL1 polymorphism and rheumatoid arthritis.
score: 1.3569618, Arthritis and rheumatism, 2008, Johnsen, Alyssa K et. al.

Investigation of genetic susceptibility factors for human longevity – A targeted nonsynonymous SNP study
score: 1.353693, Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 2010, Flachsbart, Friederike et. al.

North African Influences and Potential Bias in Case-Control Association Studies in the Spanish Population
score: 1.3533155, PLoS ONE, 2011, Pino-Yanes, María et. al.

The genetics and epigenetics of autoimmune diseases
score: 1.3508351, Journal of Autoimmunity, 2009, Hewagama, Anura; Richardson, Bruce

A hidden two-locus disease association pattern in genome-wide association studies
score: 1.3506208, BMC Bioinformatics, 2011, Yang, Can et. al.

Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: A study of 3,310 subjects from India and the US
score: 1.3490784, BMC Medical Genetics, 2011, Been, Latonya F et. al.

Variation in the upstream region of P-Selectin ( SELP ) is a risk factor for SLE
score: 1.3474766, Genes and Immunity, 2009, Morris, D L et. al.

Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci.
score: 1.3399631, International journal of obesity (2005), 2009, Kettunen, J et. al.

Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
score: 1.3390007, The American Journal of Psychiatry, 2012, Williams, Nigel M. et. al.

Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases
score: 1.3360033, Genetic Epidemiology, 2012, Mägi, Reedik et. al.

Amyloid pathway-based candidate gene analysis of [ 11 C]PiB-PET in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort
score: 1.3338026, Brain Imaging and Behavior, 2011, Swaminathan, Shanker et. al.

Development of a Panel of Genome-Wide Ancestry Informative Markers to Study Admixture Throughout the Americas
score: 1.3326439, PLoS Genetics, 2012, Galanter, Joshua Mark et. al.

Progress and promise of genome-wide association studies for human complex trait genetics.
score: 1.3323937, Genetics, 2011, Stranger, Barbara E; Stahl, Eli A; Raj, Towfique

Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome
score: 1.3323235, BMC Medical Genetics, 2011, Morgan, Thomas M et. al.

Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study
score: 1.3320354, Molecular Neurodegeneration, 2011, Carrasquillo, Minerva M et. al.

Interpretation of Association Signals and Identification of Causal Variants from Genome-wide Association Studies
score: 1.3301746, The American Journal of Human Genetics, 2010, Wang, Kai et. al.

Polymorphisms in GRIK4, HTR2A, and FKBP5 show interactive effects in predicting remission to antidepressant treatment.
score: 1.330144, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2010, Horstmann, Sonja et. al.

Support for calcium channel gene defects in autism spectrum disorders
score: 1.3295166, Molecular Autism, 2012, Lu, Ake Tzu-Hui et. al.

A common variant in Myosin - 18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults
score: 1.3287572, Translational Psychiatry, 2013, Ludwig, K U et. al.

Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors
score: 1.3281328, Molecular Psychiatry, 2012, Wong, M-L; Dong, C; Andreev, V; Arcos-Burgos, M; Licinio, J

Genome-wide association of mood-incongruent psychotic bipolar disorder
score: 1.3280989, Translational Psychiatry, 2012, Goes, F S et. al.

Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility
score: 1.3267852, Schizophrenia Research, 2012, Li, Ming et. al.

Identification of Two Independent Risk Factors for Lupus within the MHC in United Kingdom Families
score: 1.3254959, PLoS Genetics, 2007, Fernando, Michelle M. A et. al.

Novel tree-based method to generate markers from rare variant data
score: 1.324986, BMC Proceedings, 2011, Jiang, Yuan et. al.

Evaluation of IL12B as a candidate type I diabetes susceptibility gene using data from the Type I Diabetes Genetics Consortium.
score: 1.32413, Genes and immunity, 2009, Morahan, G et. al.

Child Development and Molecular Genetics: 14 Years Later
score: 1.3212021, Child Development, 2012, Plomin, Robert

Strategies and utility of imputed SNP genotypes for genomic analysis in dairy cattle
score: 1.3209311, BMC Genomics, 2012, Khatkar, Mehar S et. al.

ANK3 and CACNA1C – Missing Genetic Link for Bipolar Disorder and Major Depressive Disorder in two German case-control samples
score: 1.3200872, Journal of Psychiatric Research, 2012, Kloiber, Stefan et. al.

Replication of association of the PTPRC gene with response to anti-tumor necrosis factor therapy in a large UK cohort.
score: 1.3189428, Arthritis and rheumatism, 2012, Plant, Darren et. al.

Association between Parkinson's disease and the HLA-DRB1 locus.
score: 1.316794, Movement disorders : official journal of the Movement Disorder Society, 2012, Ahmed, Ismaïl et. al.

Genetic Variation and Recent Positive Selection in Worldwide Human Populations: Evidence from Nearly 1 Million SNPs
score: 1.3166169, PLoS ONE, 2009, López Herráez, David et. al.

Single nucleotide polymorphisms in genes that are associated with a modified response to statin therapy: the Rotterdam Study.
score: 1.3157096, The pharmacogenomics journal, 2011, de Keyser, C E et. al.

Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression.
score: 1.3155335, Nature genetics, 2012, Schödel, Johannes et. al.

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
score: 1.3139878, Nature genetics, 2008, Sharp, Andrew J et. al.

Promoter Variant of PIK3C3 Is Associated with Autoimmunity against Ro and Sm Epitopes in African-American Lupus Patients
score: 1.3127565, Journal of Biomedicine and Biotechnology, 2010, Kariuki, Silvia N. et. al.

Copy Number Variants in Extended Autism Spectrum Disorder Families Reveal Candidates Potentially Involved in Autism Risk
score: 1.3114325, PLoS ONE, 2011, Salyakina, Daria et. al.

Genetic Structure of the Han Chinese Population Revealed by Genome-wide SNP Variation
score: 1.3096018, The American Journal of Human Genetics, 2009, Chen, Jieming et. al.

Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami.
score: 1.3083535, European journal of human genetics : EJHG, 2010, Huyghe, Jeroen R et. al.

Interferon regulatory factor 5 ( IRF5 ) gene variants are associated with multiple sclerosis in three distinct populations
score: 1.3080126, Journal of Medical Genetics, 2008, Kristjansdottir, G et. al.

Gemcitabine and Arabinosylcytosin Pharmacogenomics: Genome-Wide Association and Drug Response Biomarkers
score: 1.3073025, PLoS ONE, 2009, Li, Liang et. al.

DNA Methylation Signatures in Development and Aging of the Human Prefrontal Cortex
score: 1.3070488, The American Journal of Human Genetics, 2012, Numata, Shusuke et. al.

The pursuit of genome-wide association studies: where are we now?
score: 1.3061175, Journal of human genetics, 2010, Ku, Chee Seng; Loy, En Yun; Pawitan, Yudi; Chia, Kee Seng

Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study
score: 1.3055196, International Journal of Alzheimer's Disease, 2011, Swaminathan, Shanker et. al.

Genetic Determinants of Lipid Traits in Diverse Populations from the Population Architecture using Genomics and Epidemiology (PAGE) Study
score: 1.3037833, PLoS Genetics, 2011, Dumitrescu, Logan et. al.

Abstracts of the 2009 Annual Scientific Meeting of the American Geriatric Society. April 29-May 3, 2009. Chicago, Illinois, USA.
score: 1.3037286, Journal of the American Geriatrics Society, 2009,

Linkage-Disequilibrium-Based Binning Affects the Interpretation of GWASs
score: 1.3034983, The American Journal of Human Genetics, 2012, Christoforou, Andrea et. al.

Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment
score: 1.3020944, Annals of the Rheumatic Diseases, 2010, Tan, Rachael J L et. al.

Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations.
score: 1.3020898, The pharmacogenomics journal, 2013, Wheeler, H E et. al.

Inference of Relationships in Population Data Using Identity-by-Descent and Identity-by-State
score: 1.3008415, PLoS Genetics, 2011, Stevens, Eric L. et. al.

Possible association between Interleukin-1beta gene and schizophrenia in a Japanese population
score: 1.3005061, Behavioral and Brain Functions : BBF, 2011, Sasayama, Daimei et. al.

Convergent evidence that choline acetyltransferase gene variation is associated with prospective smoking cessation and nicotine dependence.
score: 1.3000429, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2010, Ray, Riju et. al.

Common variants in P2RY11 are associated with narcolepsy.
score: 1.299393, Nature genetics, 2011, Kornum, Birgitte R et. al.

Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.
score: 1.2939459, Molecular psychiatry, 2011, Jablensky, A et. al.

Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes.
score: 1.290497, Nature genetics, 2007, Göring, Harald H H et. al.

The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans.
score: 1.2897042, Cancer research, 2009, Saccone, Nancy L et. al.

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk
score: 1.2889963, Human Molecular Genetics, 2012, Chapman, Jade et. al.

Meta-analysis of 32 genome-wide linkage studies of schizophrenia.
score: 1.2864494, Molecular psychiatry, 2009, Ng, M Y M et. al.

Genetic markers of ovarian follicle number and menopause in women of multiple ethnicities
score: 1.2861898, Human Genetics, 2012, Schuh-Huerta, Sonya M. et. al.

A candidate gene association study of alcohol consumption in young women.
score: 1.2849113, Alcoholism, clinical and experimental research, 2011, Agrawal, Arpana et. al.

Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease
score: 1.2849095, Brain, 2011, Schmidt, Helena et. al.

The Architecture of Long-Range Haplotypes Shared within and across Populations.
score: 1.2836968, Molecular biology and evolution, 2012, Gusev, Alexander et. al.

The MTAP-CDKN2A locus confers susceptibility to a naturally occurring canine cancer.
score: 1.2811198, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Shearin, Abigail L et. al.

Gene–environment interactions and obesity—Further aspects of genomewide association studies
score: 1.279427, Nutrition, 2009, Andreasen, Camilla H.; Andersen, Gitte

The common FTO variant rs9939609 is not associated with BMI in a longitudinal study on a cohort of Swedish men born 1920-1924
score: 1.2765576, BMC Medical Genetics, 2009, Jacobsson, Josefin A et. al.

Genetic variants near the MGAT1 gene are associated with body weight, BMI and fatty acid metabolism among adults and children.
score: 1.274981, International journal of obesity (2005), 2012, Jacobsson, J A et. al.

Significant Association of Estrogen Receptor Binding Site Variation with Bipolar Disorder in Females
score: 1.2739896, PLoS ONE, 2012, Graae, Lisette; Karlsson, Robert; Paddock, Silvia

Risk of Ovarian Cancer and Inherited Variants in Relapse-Associated Genes
score: 1.2720413, PLoS ONE, 2010, Peedicayil, Abraham et. al.

Combined effect of low-penetrant SNPs on breast cancer risk.
score: 1.2702831, British journal of cancer, 2012, Harlid, S et. al.

The era of genome-wide association studies: opportunities and challenges for asthma genetics.
score: 1.2698266, Journal of human genetics, 2009, Zhang, Guicheng; Goldblatt, Jack; LeSouëf, Peter

A Common CNR1 (Cannabinoid Receptor 1) Haplotype Attenuates the Decrease in HDL Cholesterol That Typically Accompanies Weight Gain
score: 1.2677541, PLoS ONE, 2010, Feng, Qiping et. al.

Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus
score: 1.2669705, PLoS Genetics, 2008, Taylor, Kimberly E. et. al.

Thursday Abstracts
score: 1.2663212, Biological Psychiatry, 2010,

DNA variations in human and medical genetics: 25 years of my experience.
score: 1.2645771, Journal of human genetics, 2009, Nakamura, Yusuke

Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 ( GRID1) gene promoter
score: 1.2626222, Schizophrenia Research, 2009, Treutlein, Jens et. al.

Case-control genome-wide association study of rheumatoid arthritis from Genetic Analysis Workshop 16 using penalized orthogonal-components regression-linear discriminant analysis
score: 1.2622945, BMC Proceedings, 2009, Zhang, Min et. al.

Rapid and Accurate Multiple Testing Correction and Power Estimation for Millions of Correlated Markers
score: 1.2586848, PLoS Genetics, 2009, Han, Buhm; Kang, Hyun Min; Eskin, Eleazar

Functional impact of global rare copy number variation in autism spectrum disorders.
score: 1.2573329, Nature, 2010, Pinto, Dalila et. al.

Association of ABCB1 genetic variants with renal function in Africans and in Caucasians
score: 1.2565779, BMC Medical Genomics, 2008, Bochud, Murielle et. al.

Evidence for genetic association of RORB with bipolar disorder
score: 1.2564417, BMC Psychiatry, 2009, McGrath, Casey L et. al.

Association of LY9 in UK and Canadian SLE families.
score: 1.2553415, Genes and immunity, 2008, Cunninghame Graham, D S et. al.

Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants
score: 1.2545415, BMC Medical Genomics, 2012, Volckmar, Anna-Lena et. al.

Fine-scale estimation of location of birth from genome-wide single-nucleotide polymorphism data.
score: 1.253974, Genetics, 2012, Hoggart, Clive J et. al.

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration
score: 1.2521257, Nature Genetics, 2011, Raychaudhuri, Soumya et. al.

The genetic contribution to non-syndromic human obesity.
score: 1.2517058, Nature reviews. Genetics, 2009, Walley, Andrew J; Asher, Julian E; Froguel, Philippe

The contribution of FTO and UCP - 1 SNPs to extreme obesity, diabetes and cardiovascular risk in Brazilian individuals
score: 1.2513371, BMC Medical Genetics, 2012, Ramos, Adauto V et. al.

11th Meeting of the Irish Society of Human Genetics, Friday 12th September 2008
score: 1.2513062, The Ulster Medical Journal, 2009,

Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies
score: 1.2509832, BMC Genomics, 2008, Duggal, Priya et. al.

Polymorphisms in the Hsp70 gene locus are genetically associated with systemic lupus erythematosus
score: 1.2504101, Annals of the Rheumatic Diseases, 2010, Fürnrohr, Barbara G et. al.

A genome-wide association study of early menopause and the combined impact of identified variants
score: 1.2498991, Human Molecular Genetics, 2013, Perry, John R. B. et. al.

Evaluation of seven common lipid associated loci in a large Indian sib pair study
score: 1.2490167, Lipids in Health and Disease, 2012, Rafiq, Sajjad et. al.

No interaction between alcohol consumption and HDL-related genes on HDL cholesterol levels
score: 1.2476232, Atherosclerosis, 2010, Marques-Vidal, Pedro et. al.

Population Substructure and Control Selection in Genome-Wide Association Studies
score: 1.24662, PLoS ONE, 2008, Yu, Kai et. al.

European population substructure correlates with systemic lupus erythematosus endophenotypes in North Americans of European descent.
score: 1.2458534, Genes and immunity, 2010, Richman, I B et. al.

A two-stage evaluation of genetic variation in immune and inflammation genes with risk of non-Hodgkin lymphoma identifies new susceptibility locus in 6p21.3 region.
score: 1.2443428, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Cerhan, James R et. al.

Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.
score: 1.2442024, Genes and immunity, 2009, McCauley, J L et. al.

Cross-disorder analysis of bipolar risk genes: further evidence of DGKH as a risk gene for bipolar disorder, but also unipolar depression and adult ADHD.
score: 1.2417919, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Weber, Heike et. al.

Genetic polymorphisms in adaptive immunity genes and childhood acute lymphoblastic leukemia.
score: 1.2413826, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Chang, Jeffrey S et. al.

Unrecognized sequence homologies may confound genome-wide association studies.
score: 1.2401123, Nucleic acids research, 2012, Galichon, Pierre et. al.

Common variants of FTO and the risk of obesity and type 2 diabetes in Indians.
score: 1.2399762, Journal of human genetics, 2011, Chauhan, Ganesh et. al.

Lack of association of the HMGA1 IVS5-13insC variant with type 2 diabetes in an ethnically diverse hypertensive case control cohort
score: 1.2361061, Journal of Translational Medicine, 2013, Karnes, Jason H et. al.

Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance.
score: 1.2356279, The Journal of investigative dermatology, 2012, Jagielska, Dagny et. al.

FTO Genetic Variation and Association With Obesity in West Africans and African Americans
score: 1.2343319, Diabetes, 2010, Adeyemo, Adebowale et. al.

Reproducible association with type 1 diabetes in the extended class I region of the major histocompatibility complex.
score: 1.233553, Genes and immunity, 2009, Viken, M K et. al.

Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population.
score: 1.2325981, Nature genetics, 2008, Suzuki, Akari et. al.

ANKRD55 and DHCR7 are novel multiple sclerosis risk loci.
score: 1.2274116, Genes and immunity, 2012, Alloza, I et. al.

Convergence of miRNA Expression Profiling, α-Synuclein Interacton and GWAS in Parkinson's Disease
score: 1.2272046, PLoS ONE, 2011, Martins, Madalena et. al.

The estrogen hypothesis of Schizophrenia implicates glucose metabolism: Association study in three independent samples
score: 1.227158, BMC Medical Genetics, 2008, Olsen, Line et. al.

African Ancestry Is Associated with Asthma Risk in African Americans
score: 1.2241934, PLoS ONE, 2012, Flores, Carlos et. al.

Fine mapping and conditional analysis identify a new mutation in the autoimmunity susceptibility gene BLK that leads to reduced half-life of the BLK protein
score: 1.2237115, Annals of the Rheumatic Diseases, 2012, Delgado-Vega, Angélica M et. al.

Association of FTO gene variants with body composition in UK twins
score: 1.2185055, Annals of Human Genetics, 2012, Livshits, Gregory et. al.

The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus.
score: 1.2180057, Genes and immunity, 2011, Bronson, P G et. al.

The utility of copy number variation (CNV) in studies of hypertension-related left ventricular hypertrophy (LVH): rationale, potential and challenges
score: 1.2170539, Molecular Cytogenetics, 2013, BoonPeng, Hoh; Yusoff, Khalid

Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD
score: 1.214549, PLoS Genetics, 2011, Böger, Carsten A. et. al.

Evaluation of genome-wide association study-identified type 2 diabetes loci in African Americans.
score: 1.2126125, American journal of epidemiology, 2012, Long, Jirong et. al.

Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data
score: 1.2117363, BMC Proceedings, 2009, Ling, Hua et. al.

Classification tree for detection of single-nucleotide polymorphism (SNP)-by-SNP interactions related to heart disease: Framingham Heart Study
score: 1.2113767, BMC Proceedings, 2009, Yao, Li et. al.

Tissue Effect on Genetic Control of Transcript Isoform Variation
score: 1.2106992, PLoS Genetics, 2009, Kwan, Tony et. al.

The Heritability of Ocular Traits
score: 1.2095452, Survey of Ophthalmology, 2010, Sanfilippo, Paul G. et. al.

A two-stage case-control association study of the dihydropyrimidinase-like 2 gene (DPYSL2) with schizophrenia in Japanese subjects.
score: 1.206635, Journal of human genetics, 2010, Koide, Takayoshi et. al.

Variation in TP63 is associated with lung adenocarcinoma in the UK population.
score: 1.2064713, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Wang, Yufei et. al.

Sex Differential Genetic Effect of Chromosome 9p21 on Subclinical Atherosclerosis
score: 1.2058208, PLoS ONE, 2010, Lin, Hsiu-Fen et. al.

Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study
score: 1.2052434, BMC Cancer, 2012, Niu, Nifang et. al.

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain.
score: 1.2049109, Molecular psychiatry, 2012, Richards, A L et. al.

Combined effect of low-penetrant SNPs on breast cancer risk
score: 1.2040868, British Journal of Cancer, 2011, Harlid, S et. al.

A Versatile Gene-Based Test for Genome-wide Association Studies
score: 1.2031449, The American Journal of Human Genetics, 2010, Liu, Jimmy Z. et. al.

Kernel machine SNP-set analysis for censored survival outcomes in genome-wide association studies.
score: 1.2010679, Genetic epidemiology, 2011, Lin, Xinyi et. al.

How to deal with the early GWAS data when imputing and combining different arrays is necessary.
score: 1.2005315, European journal of human genetics : EJHG, 2012, Uh, Hae-Won et. al.

Genotype imputation for African Americans using data from HapMap phase II versus 1000 genomes projects.
score: 1.2005292, Genetic epidemiology, 2012, Sung, Yun J et. al.

PNPLA3 variants specifically confer increased risk for histologic nonalcoholic fatty liver disease but not metabolic disease.
score: 1.2003614, Hepatology (Baltimore, Md.), 2010, Speliotes, Elizabeth K et. al.

Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium.
score: 1.1998338, Cancer research, 2011, Shete, Sanjay et. al.

Prioritizing GWAS Results: A Review of Statistical Methods and Recommendations for Their Application
score: 1.1984104, The American Journal of Human Genetics, 2010, Cantor, Rita M.; Lange, Kenneth; Sinsheimer, Janet S.

Commercially Available Outbred Mice for Genome-Wide Association Studies
score: 1.1976796, PLoS Genetics, 2010, Yalcin, Binnaz et. al.

Smoking and smoking cessation in disadvantaged women: Assessing genetic contributions
score: 1.1929869, Drug and Alcohol Dependence, 2009, Uhl, George R. et. al.

Evidence to support IL-13 as a risk locus for psoriatic arthritis but not psoriasis vulgaris
score: 1.1917684, Annals of the Rheumatic Diseases, 2011, Bowes, John et. al.

Replication of the BANK1 genetic association with systemic lupus erythematosus in a European-derived population.
score: 1.1914813, Genes and immunity, 2009, Guo, L et. al.

Sex-Specific Role for Adenylyl Cyclase Type 7 in Alcohol Dependence
score: 1.1892663, Biological Psychiatry, 2011, Desrivières, Sylvane et. al.

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer.
score: 1.1877992, Nature genetics, 2008, Stacey, Simon N et. al.

Linkage-Disequilibrium-Based Binning Misleads the Interpretation of Genome-wide Association Studies
score: 1.1872012, The American Journal of Human Genetics, 2012, Zhu, Xiaofeng; Feng, Tao; Elston, Robert C.

Linkage-Disequilibrium-Based Binning Misleads the Interpretation of Genome-wide Association Studies
score: 1.1872012, The American Journal of Human Genetics, 2012, Zhu, Xiaofeng; Feng, Tao; Elston, Robert C.

Genetic association of recovery from eating disorders: the role of GABA receptor SNPs.
score: 1.1860492, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Bloss, Cinnamon S et. al.

Replication of genetic variants from genome-wide association studies with metabolic traits in an island population of the Adriatic coast of Croatia.
score: 1.1838419, European journal of human genetics : EJHG, 2011, Karns, Rebekah et. al.

Abstracts of the Annual Scientific Meeting of the American Geriatrics Society. May 2-5, 2012. Seattle, Washington, USA.
score: 1.1800904, Journal of the American Geriatrics Society, 2012,

Multifactor Dimensionality Reduction as a Filter-Based Approach for Genome Wide Association Studies
score: 1.1783416, Frontiers in Genetics, 2011, Oki, Noffisat O.; Motsinger-Reif, Alison A.

Genetic Analysis of 103 Candidate Genes for Coronary Artery Disease and Associated Phenotypes in a Founder Population Reveals a New Association between Endothelin-1 and High-Density Lipoprotein Cholesterol
score: 1.1774172, The American Journal of Human Genetics, 2007, Paré, Guillaume et. al.

Evaluating the Effects of Imputation on the Power, Coverage, and Cost Efficiency of Genome-wide SNP Platforms
score: 1.1732107, The American Journal of Human Genetics, 2008, Anderson, Carl A. et. al.

Analysis of FTO gene variants with obesity and glucose homeostasis measures in the multiethnic Insulin Resistance Atherosclerosis Study cohort.
score: 1.1714595, International journal of obesity (2005), 2011, Wing, M R et. al.

A Common Complement C3 Variant Is Associated with Protection against Wet Age-Related Macular Degeneration in a Japanese Population
score: 1.1694596, PLoS ONE, 2011, Yanagisawa, Suiho et. al.

A novel Germline mutation in HOXB13 is associated with prostate cancer risk in Chinese men.
score: 1.1685756, The Prostate, 2012, Lin, Xiaoling et. al.

A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility.
score: 1.1677023, Genes and immunity, 2011, Bush, W S et. al.

Genetic variations in the dopaminergic system and alcohol use: a system-level analysis.
score: 1.1667751, Addiction biology, 2012, Chen, Chunhui et. al.

CHRNB2 promoter region: association with subjective effects to nicotine and gene expression differences.
score: 1.1641245, Genes, brain, and behavior, 2011, Hoft, N R; Stitzel, J A; Hutchison, K E; Ehringer, M A

A meta-analysis of genome-wide association studies of follicular lymphoma
score: 1.1616648, BMC Genomics, 2012, Skibola, Christine F et. al.

The EBMT activity survey 2008: impact of team size, team density and new trends.
score: 1.1611913, Bone marrow transplantation, 2011, Gratwohl, A et. al.

Family-based association of FKBP5 in bipolar disorder.
score: 1.1608536, Molecular psychiatry, 2009, Willour, V L et. al.

Insights to the Genetics of Diabetic Nephropathy Through a Genome-Wide Association Study of the GoKinD Collection
score: 1.1601685, Seminars in Nephrology, 2010, Pezzolesi, Marcus G. et. al.

A Polymorphism in the HLA-DPB1 Gene Is Associated with Susceptibility to Multiple Sclerosis
score: 1.158546, PLoS ONE, 2010, Field, Judith et. al.

The genetics of multiple sclerosis: SNPs to pathways to pathogenesis.
score: 1.1575406, Nature reviews. Genetics, 2008, Oksenberg, Jorge R et. al.

A General Framework for Two-Stage Analysis of Genome-wide Association Studies Has Application to Case-Control Studies
score: 1.1571946, The American Journal of Human Genetics, 2012, Wason, James M.S.; Dudbridge, Frank

Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset
score: 1.1566031, BMC Research Notes, 2011, Gui, Hongsheng; Li, Miaoxin; Sham, Pak C; Cherny, Stacey S

Association study of CSF2RB with schizophrenia in Irish family and case - control samples.
score: 1.1562797, Molecular psychiatry, 2008, Chen, Q et. al.

Common nonsynonymous variants in PCSK1 confer risk of obesity.
score: 1.1560662, Nature genetics, 2008, Benzinou, Michael et. al.

GDF5 single-nucleotide polymorphism rs143383 is associated with lumbar disc degeneration in Northern European women.
score: 1.1557859, Arthritis and rheumatism, 2011, Williams, F M K et. al.

Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays
score: 1.1556403, Nucleic Acids Research, 2008, Macgregor, Stuart et. al.

What will whole genome searches for susceptibility genes for common complex disease offer to clinical practice?
score: 1.1545993, Journal of internal medicine, 2008, Lango, H; Weedon, M N

A SNAP25 promoter variant is associated with early-onset bipolar disorder and a high expression level in brain.
score: 1.1545409, Molecular psychiatry, 2010, Etain, B et. al.

A second generation human haplotype map of over 3.1 million SNPs.
score: 1.1543861, Nature, 2007, International HapMap Consortium, et. al.

Genome Wide Linkage Analysis of 972 Bipolar Pedigrees Using Single Nucleotide Polymorphisms
score: 1.1530619, Molecular psychiatry, 2011, Badner, Judith A et. al.

The OPRD1 and OPRK1 loci in alcohol or drug dependence: OPRD1 variation modulates substance dependence risk.
score: 1.1495237, Molecular psychiatry, 2008, Zhang, H; Kranzler, H R; Yang, B-Z; Luo, X; Gelernter, J

Linkage and association studies in African- and Caucasian-American populations demonstrate that SHC3 is a novel susceptibility locus for nicotine dependence.
score: 1.147741, Molecular psychiatry, 2007, Li, M D; Sun, D; Lou, X-Y; Beuten, J; Payne, T J; Ma, J Z

Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility
score: 1.1475214, Schizophrenia Research, 2012, Li, Ming et. al.

Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility
score: 1.1475214, Schizophrenia Research, 2012, Li, Ming et. al.

Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility
score: 1.1475214, Schizophrenia Research, 2012, Li, Ming et. al.

Investigation of Crohn's Disease Risk Loci in Ulcerative Colitis Further Defines Their Molecular Relationship
score: 1.1470323, Gastroenterology, 2009, Anderson, Carl A. et. al.

A targeted association study in systemic lupus erythematosus identifies multiple susceptibility alleles.
score: 1.1443532, Genes and immunity, 2011, Budarf, M L et. al.

Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2.
score: 1.1436497, British journal of cancer, 2011, Osorio, A et. al.

Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk
score: 1.1424294, Human Molecular Genetics, 2009, Drenos, Fotios et. al.

Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia.
score: 1.1423803, Journal of human genetics, 2010, Sillén, Anna et. al.

Genetic Control of Human Brain Transcript Expression in Alzheimer Disease
score: 1.1423263, The American Journal of Human Genetics, 2009, Webster, Jennifer A. et. al.

Association of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish population.
score: 1.141172, Molecular psychiatry, 2007, Thomson, P A et. al.

Identifying Signatures of Natural Selection in Tibetan and Andean Populations Using Dense Genome Scan Data
score: 1.1408135, PLoS Genetics, 2010, Bigham, Abigail et. al.

Gene-Based Testing of Interactions in Association Studies of Quantitative Traits
score: 1.138902, PLoS Genetics, 2013, Ma, Li; Clark, Andrew G.; Keinan, Alon

A novel prostate cancer susceptibility locus at 19q13.
score: 1.137197, Cancer research, 2009, Hsu, Fang-Chi et. al.

A polymorphism in the thyroid hormone receptor gene is associated with bronchodilator response in asthmatics.
score: 1.1366063, The pharmacogenomics journal, 2012, Duan, Q L et. al.

Gene by Sex Interaction for Measures of Obesity in the Framingham Heart Study
score: 1.1359476, Journal of Obesity, 2010, Benjamin, Ashlee M. et. al.

Neuronal Genes for Subcutaneous Fat Thickness in Human and Pig Are Identified by Local Genomic Sequencing and Combined SNP Association Study
score: 1.1345395, PLoS ONE, 2011, Lee, Kyung-Tai et. al.

Genetic Determinants of Height Growth Assessed Longitudinally from Infancy to Adulthood in the Northern Finland Birth Cohort 1966
score: 1.1335157, PLoS Genetics, 2009, Sovio, Ulla et. al.

Dopamine D1 receptor (DRD1) genetic polymorphism: pleiotropic effects on heritable renal traits.
score: 1.1333656, Kidney international, 2009, Fung, Maple M et. al.

Variation in LPA Is Associated with Lp(a) Levels in Three Populations from the Third National Health and Nutrition Examination Survey
score: 1.1320531, PLoS ONE, 2011, Dumitrescu, Logan et. al.

PSEA: Phenotype Set Enrichment Analysis--a new method for analysis of multiple phenotypes.
score: 1.1291214, Genetic epidemiology, 2012, Ried, Janina S et. al.

The EBMT activity survey: 1990-2010.
score: 1.1284469, Bone marrow transplantation, 2012, Passweg, J R et. al.

Analysis of multiple phenotypes.
score: 1.1272671, Genetic epidemiology, 2009, Kent, Jack W

Mammalian NPC1 genes may undergo positive selection and human polymorphisms associate with type 2 diabetes
score: 1.1248939, BMC Medicine, 2012, Al-Daghri, Nasser M et. al.

Comparison of genome-wide variation between Malawians and African ancestry HapMap populations.
score: 1.1231693, Journal of human genetics, 2010, Joubert, Bonnie R et. al.

Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers
score: 1.1229394, Human Genetics, 2008, Yeager, Meredith et. al.

Predicting human height by Victorian and genomic methods.
score: 1.1205222, European journal of human genetics : EJHG, 2009, Aulchenko, Yurii S et. al.

Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms
score: 1.1185808, Genome Biology, 2012, Lu, James T; Wang, Yi; Gibbs, Richard A; Yu, Fuli

The Impact of Phenocopy on the Genetic Analysis of Complex Traits
score: 1.1173347, PLoS ONE, 2010, Lescai, Francesco; Franceschi, Claudio

Evidence for two independent associations with type 1 diabetes at the 12q13 locus.
score: 1.1162602, Genes and immunity, 2012, Keene, K L et. al.

Abraham's Children in the Genome Era: Major Jewish Diaspora Populations Comprise Distinct Genetic Clusters with Shared Middle Eastern Ancestry
score: 1.1162572, The American Journal of Human Genetics, 2010, Atzmon, Gil et. al.

Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants.
score: 1.1131758, Human molecular genetics, 2012, Juran, Brian D et. al.

Systematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic information
score: 1.1121833, BMC Medical Genomics, 2010, Zhang, Yonqing et. al.

Rule-based induction method for haplotype comparison and identification of candidate disease loci
score: 1.1121198, Genome Medicine, 2012, Karinen, Sirkku et. al.

Variability in GWAS analysis: the impact of genotype calling algorithm inconsistencies.
score: 1.1106733, The pharmacogenomics journal, 2010, Miclaus, K et. al.

Investigation of the fine structure of European populations with applications to disease association studies.
score: 1.1080493, European journal of human genetics : EJHG, 2008, Heath, Simon C et. al.

Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications
score: 1.1067799, Molecular Neurodegeneration, 2012, Allen, Mariet et. al.

Genetic variants on chromosome 6p21.1 and 6p22.3 are associated with type 2 diabetes risk: a case-control study in Han Chinese.
score: 1.1065027, Journal of human genetics, 2012, Lu, Feng et. al.

The MAP2K5-linked SNP rs2241423 is associated with BMI and obesity in two cohorts of Swedish and Greek children
score: 1.1055329, BMC Medical Genetics, 2012, Rask-Andersen, Mathias et. al.

MTNR1B G24E Variant Associates With BMI and Fasting Plasma Glucose in the General Population in Studies of 22,142 Europeans
score: 1.1055088, Diabetes, 2010, Andersson, Ehm A. et. al.

Peakwide Mapping on Chromosome 3q13 Identifies the Kalirin Gene as a Novel Candidate Gene for Coronary Artery Disease
score: 1.1051912, The American Journal of Human Genetics, 2007, Wang, Liyong et. al.

A risk variant in an miR-125b binding site in BMPR1B is associated with breast cancer pathogenesis.
score: 1.1027745, Cancer research, 2009, Saetrom, Pål et. al.

A genome wide association study for backfat thickness in Italian Large White pigs highlights new regions affecting fat deposition including neuronal genes
score: 1.1026963, BMC Genomics, 2012, Fontanesi, Luca et. al.

Identification of Susceptibility Genes for Cancer in a Genome-wide Scan: Results from the Colon Neoplasia Sibling Study
score: 1.1022199, The American Journal of Human Genetics, 2008, Daley, Denise et. al.

Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan.
score: 1.100904, Molecular psychiatry, 2009, Glatt, S J et. al.

Microarray-Based Maps of Copy-Number Variant Regions in European and Sub-Saharan Populations
score: 1.1000228, PLoS ONE, 2010, Vogler, Christian et. al.

Genome-wide association analysis of copy number variation in recurrent depressive disorder.
score: 1.0986657, Molecular psychiatry, 2011, Rucker, J J H et. al.

Genetics of disease
score: 1.0971608, Current Opinion in Genetics & Development, 1997,

Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design?
score: 1.0950694, PLoS Genetics, 2009, Heid, Iris M. et. al.

Finding common susceptibility variants for complex disease: past, present and future
score: 1.0939355, Briefings in Functional Genomics and Proteomics, 2009, Panoutsopoulou, Kalliope; Zeggini, Eleftheria

Inherited variation in immune genes and pathways and glioblastoma risk
score: 1.0929372, Carcinogenesis, 2010, Schwartzbaum, Judith A. et. al.

Replication of TCF4 through Association and Linkage Studies in Late-Onset Fuchs Endothelial Corneal Dystrophy
score: 1.0923157, PLoS ONE, 2011, Li, Yi-Ju et. al.

Mapping genes that predict treatment outcome in admixed populations.
score: 1.0918665, The pharmacogenomics journal, 2010, Baye, T M; Wilke, R A

Measures of Autozygosity in Decline: Globalization, Urbanization, and Its Implications for Medical Genetics
score: 1.0911591, PLoS Genetics, 2009, Nalls, Michael A. et. al.

Confirmation of Genetic Associations at ELMO1 in the GoKinD Collection Supports Its Role as a Susceptibility Gene in Diabetic Nephropathy
score: 1.0908238, Diabetes, 2009, Pezzolesi, Marcus G. et. al.

Association Analysis of 94 Candidate Genes and Schizophrenia-Related Endophenotypes
score: 1.0903561, PLoS ONE, 2012, Greenwood, Tiffany A. et. al.

Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24
score: 1.0891327, Journal of Medical Genetics, 2012, Jones, Angela M et. al.

Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population.
score: 1.0883903, Proceedings of the National Academy of Sciences of the United States of America, 2010, Bray, Steven M et. al.

C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect
score: 1.0863629, Neurobiology of Aging, 2012, Ratti, Antonia et. al.

Differential coexpression analysis of obesity-associated networks in human subcutaneous adipose tissue.
score: 1.0862446, International journal of obesity (2005), 2012, Walley, A J et. al.

Association of acid phosphatase locus 1*C allele with the risk of cardiovascular events in rheumatoid arthritis patients
score: 1.0859963, Arthritis Research & Therapy, 2011, Teruel, María et. al.

Assessment of variability in GWAS with CRLMM genotyping algorithm on WTCCC coronary artery disease.
score: 1.085109, The pharmacogenomics journal, 2010, Zhang, L et. al.

Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data
score: 1.0849204, BMC Proceedings, 2011, Saad, Mohamad et. al.

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions.
score: 1.0847672, Genetic epidemiology, 2010, Cornelis, Marilyn C et. al.

Elucidating the Chromosome 9 Association with AS; CARD9 is a Candidate Gene
score: 1.0842383, Genes and immunity, 2010, Pointon, Jennifer J et. al.

IL2RA Genetic Heterogeneity in Multiple Sclerosis and Type 1 Diabetes Susceptibility and Soluble Interleukin-2 Receptor Production
score: 1.0841185, PLoS Genetics, 2009, Maier, Lisa M. et. al.

Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression
score: 1.0826036, PLoS Genetics, 2010, Cunnington, Michael S. et. al.

A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility
score: 1.0803186, Genes and immunity, 2010, Bush, William S. et. al.

The impact of FADS genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans
score: 1.0802096, BMC Genetics, 2011, Mathias, Rasika A et. al.

Development of admixture mapping panels for African Americans from commercial high-density SNP arrays
score: 1.0800821, BMC Genomics, 2010, Chen, Guanjie et. al.

Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes
score: 1.079892, American Journal of Obstetrics and Gynecology, 2010, Romero, Roberto et. al.

Common SNPs explain a large proportion of the heritability for human height.
score: 1.075875, Nature genetics, 2010, Yang, Jian et. al.

Inherited variants in mitochondrial biogenesis genes may influence epithelial ovarian cancer risk.
score: 1.0751886, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Permuth-Wey, Jennifer et. al.

Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers
score: 1.074092, Breast Cancer Research : BCR, 2010, Walker, Logan C et. al.

Gene--gene interaction among cytokine polymorphisms influence susceptibility to aggressive periodontitis.
score: 1.0724435, Genes and immunity, 2011, Scapoli, C et. al.

Confirmation of TNIP1 and IL23A as susceptibility loci for psoriatic arthritis
score: 1.0708791, Annals of the Rheumatic Diseases, 2011, Bowes, John et. al.

Association of TMEM18 variants with BMI and waist circumference in children and correlation of mRNA expression in the PFC with body weight in rats.
score: 1.0708215, European journal of human genetics : EJHG, 2012, Rask-Andersen, Mathias et. al.

Genome-wide linkage scan for loci influencing plasma triglycerides
score: 1.0704722, Clinica Chimica Acta, 2006, Middelberg, Rita P. et. al.

Knowledge gaining by human genetic studies on tuberculosis susceptibility.
score: 1.069226, Journal of human genetics, 2011, Qu, Hui-Qi; Fisher-Hoch, Susan P; McCormick, Joseph B

Multi-locus Test Conditional on Confirmed Effects Leads to Increased Power in Genome-wide Association Studies
score: 1.0692171, PLoS ONE, 2010, Ma, Li; Han, Shizhong; Yang, Jing; Da, Yang

Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation.
score: 1.0677446, Molecular psychiatry, 2010, Bates, T C et. al.

Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study)
score: 1.0673378, BMC Medical Genetics, 2011, Hertel, Jens K et. al.

G-allele of Intronic rs10830963 in MTNR1B Confers Increased Risk of Impaired Fasting Glycemia and Type 2 Diabetes Through an Impaired Glucose-Stimulated Insulin Release
score: 1.0663605, Diabetes, 2009, Sparsø, Thomas et. al.

The Fat Mass and Obesity Associated Gene, FTO, Is Also Associated with Osteoporosis Phenotypes
score: 1.0641279, PLoS ONE, 2011, Guo, Yan et. al.

Japanese Population Structure, Based on SNP Genotypes from 7003 Individuals Compared to Other Ethnic Groups: Effects on Population-Based Association Studies
score: 1.0629944, The American Journal of Human Genetics, 2008, Yamaguchi-Kabata, Yumi et. al.

Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene.
score: 1.0610273, Molecular psychiatry, 2008, Buxbaum, J D et. al.

Association of COL25A1 with Comorbid Antisocial Personality Disorder and Substance Dependence
score: 1.0606449, Biological Psychiatry, 2012, Li, Dawei et. al.

Genetic variability of smoking persistence in African Americans.
score: 1.059282, Cancer prevention research (Philadelphia, Pa.), 2011, Hamidovic, Ajna et. al.

ParseCNV integrative copy number variation association software with quality tracking
score: 1.0571152, Nucleic Acids Research, 2013, Glessner, Joseph T.; Li, Jin; Hakonarson, Hakon

Genetic Variation at the FTO Locus Influences RBL2 Gene Expression
score: 1.0556343, Diabetes, 2009, Jowett, Jeremy B.M. et. al.

A 6-bp deletion in the TYRP1 gene causes the brown colouration phenotype in Chinese indigenous pigs.
score: 1.0536989, Heredity, 2011, Ren, J; Mao, H; Zhang, Z; Xiao, S; Ding, N; Huang, L

Association to the Glypican-5 gene in multiple sclerosis
score: 1.0517127, Journal of Neuroimmunology, 2010, Lorentzen, Åslaug R. et. al.

Exome sequencing and complex disease: practical aspects of rare variant association studies
score: 1.0516553, Human Molecular Genetics, 2012, Do, Ron; Kathiresan, Sekar; Abecasis, Gonçalo R.

On the follow-up of genome-wide association studies: an overall test for the most promising SNPs.
score: 1.0512935, Genetic epidemiology, 2011, Lipman, Peter J et. al.

Genome-wide association studies for hematological traits in swine.
score: 1.0511218, Animal genetics, 2013, Wang, J Y et. al.

Using New Tools to Define the Genetic Underpinnings of Risky Traits Associated With Coronary Artery Disease: The SardiNIA Study
score: 1.0504738, Trends in Cardiovascular Medicine, 2009, Strait, James B. et. al.

No association of the IRS1 and PAX4 genes with type I diabetes.
score: 1.05034, Genes and immunity, 2009, Bergholdt, R et. al.

Beyond genome-wide association studies: genetic heterogeneity and individual predisposition to cancer
score: 1.0484064, Trends in Genetics, 2010, Galvan, Antonella; Ioannidis, John P.A.; Dragani, Tommaso A.

Invited Lectures
score: 1.0473649, Purinergic Signalling, 2006,

Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk.
score: 1.0440019, Nature genetics, 2009, Raychaudhuri, Soumya et. al.

Genome-wide association studies for common diseases and complex traits.
score: 1.0432087, Nature reviews. Genetics, 2005, Hirschhorn, Joel N; Daly, Mark J

Polygenic susceptibility to prostate and breast cancer: implications for personalised screening.
score: 1.0418504, British journal of cancer, 2011, Pashayan, N et. al.

Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R , Using Linkage, Haplotype Sharing, and Association Analysis
score: 1.0412288, PLoS Genetics, 2011, Haataja, Ritva et. al.

Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population.
score: 1.039907, Journal of human genetics, 2011, Low, Siew-Kee et. al.

Genetics of disease
score: 1.0390349, Current Opinion in Genetics & Development, 1996,

Association between theSPRY1gene polymorphism and obesity-related traits and osteoporosis in Korean women
score: 1.0380011, Molecular Genetics and Metabolism, 2013, Jin, Hyun-Seok et. al.

Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder
score: 1.0368855, Molecular Autism, 2012, Ramos, Paula S et. al.

Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles
score: 1.0365455, PLoS ONE, 2011, Chen, Pei-Lung et. al.

Genetic Association and Altered Gene Expression of Mir-155 in Multiple Sclerosis Patients
score: 1.0347484, International Journal of Molecular Sciences, 2011, Paraboschi, Elvezia Maria et. al.

Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism.
score: 1.0321635, Molecular psychiatry, 2005, Philippi, A et. al.

Association Analysis of Type 2 Diabetes Loci in Type 1 Diabetes
score: 1.0319283, Diabetes, 2008, Qu, Hui-Qi et. al.

An integrated approach of comparative genomics and heritability analysis of pig and human on obesity trait: evidence for candidate genes on human chromosome 2
score: 1.0315389, BMC Genomics, 2012, Kim, Jaemin et. al.

Association of two independent functional risk haplotypes in TNIP1 with systemic lupus erythematosus.
score: 1.0299836, Arthritis and rheumatism, 2012, Adrianto, Indra et. al.

Common Genetic Variants Are Associated with Accelerated Bone Mineral Density Loss after Hematopoietic Cell Transplantation
score: 1.0298101, PLoS ONE, 2011, Yao, Song et. al.

The EBMT activity survey 2007 with focus on allogeneic HSCT for AML and novel cellular therapies.
score: 1.0297454, Bone marrow transplantation, 2009, Gratwohl, A et. al.

Association of chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression.
score: 1.0294376, The pharmacogenomics journal, 2012, Duarte, J D et. al.

Transferability and Fine-Mapping of Genome-Wide Associated Loci for Adult Height across Human Populations
score: 1.0291733, PLoS ONE, 2009, Shriner, Daniel et. al.

The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts
score: 1.0276427, BMC Medical Genetics, 2009, Bressler, Jan et. al.

Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis
score: 1.0264171, Genes and immunity, 2009, McCauley, Jacob L. et. al.

Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.
score: 1.0244532, Genes and immunity, 2011, Cavanillas, M L et. al.

A Transcription Factor Map as Revealed by a Genome-Wide Gene Expression Analysis of Whole-Blood mRNA Transcriptome in Multiple Sclerosis
score: 1.0237225, PLoS ONE, 2010, Riveros, Carlos et. al.

Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk.
score: 1.0235239, British journal of cancer, 2011, Stevens, K N et. al.

A Novel Statistic for Genome-Wide Interaction Analysis
score: 1.0219737, PLoS Genetics, 2010, Wu, Xuesen et. al.

A survey of ABCA1 sequence variation confirms association with dementia.
score: 1.0214898, Human mutation, 2009, Reynolds, Chandra A et. al.

Analyses and Comparison of Imputation-Based Association Methods
score: 1.0214439, PLoS ONE, 2010, Pei, Yu-Fang; Zhang, Lei; Li, Jian; Deng, Hong-Wen

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication.
score: 1.020244, Molecular psychiatry, 2010, Arcos-Burgos, M et. al.

Study of the common genetic background for rheumatoid arthritis and systemic lupus erythematosus
score: 1.0188923, Annals of the Rheumatic Diseases, 2010, Orozco, Gisela et. al.

Common Variation in Vitamin D Pathway Genes Predicts Circulating 25-Hydroxyvitamin D Levels among African Americans
score: 1.0181403, PLoS ONE, 2011, Signorello, Lisa B. et. al.

Discovery and Fine Mapping of Serum Protein Loci through Transethnic Meta-analysis
score: 1.0163944, The American Journal of Human Genetics, 2012, Franceschini, Nora et. al.

Optimized selection of unrelated subjects for whole-genome sequencing studies of rare high-penetrance alleles.
score: 1.015479, Genetic epidemiology, 2012, Edwards, Todd L; Li, Chun

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder
score: 1.0148557, Schizophrenia Research, 2012, Mühleisen, Thomas W. et. al.

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder
score: 1.0148557, Schizophrenia Research, 2012, Mühleisen, Thomas W. et. al.

Gene Expression Profiling in Monocytes and SNP Association Suggest the Importance of the Gene for Osteoporosis in Both Chinese and Caucasians
score: 1.0123764, Journal of Bone and Mineral Research, 2009, Chen, Xiang-Ding et. al.

Pharmacogenetic analysis of genes implicated in rodent models of antidepressant response: association of TREK1 and treatment resistance in the STAR(*)D study.
score: 1.0096554, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008, Perlis, Roy H et. al.

Risk estimation and risk prediction using machine-learning methods
score: 1.0091817, Human Genetics, 2012, Kruppa, Jochen; Ziegler, Andreas; König, Inke R.

Genome-wide homozygosity and multiple sclerosis in Orkney and Shetland Islanders.
score: 1.0067579, European journal of human genetics : EJHG, 2012, McWhirter, Rebekah E et. al.

Genetics of age-related white matter lesions from linkage to genome wide association studies
score: 1.0064401, Journal of the Neurological Sciences, 2012, Freudenberger, Paul; Schmidt, Reinhold; Schmidt, Helena

Genetics of age-related white matter lesions from linkage to genome wide association studies
score: 1.0064401, Journal of the Neurological Sciences, 2012, Freudenberger, Paul; Schmidt, Reinhold; Schmidt, Helena

Genetics of age-related white matter lesions from linkage to genome wide association studies
score: 1.0064401, Journal of the Neurological Sciences, 2012, Freudenberger, Paul; Schmidt, Reinhold; Schmidt, Helena

Recent Developments in Genomewide Association Scans: A Workshop Summary and Review
score: 1.0060673, The American Journal of Human Genetics, 2005, Thomas, Duncan C.; Haile, Robert W.; Duggan, David

The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis
score: 1.0046466, Lancet, 2012,

The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis
score: 1.0046466, The Lancet, 2012,

The lp13.3 genomic region -rs599839- is associated with endothelial dysfunction in patients with rheumatoid arthritis
score: 1.0041103, Arthritis Research & Therapy, 2012, López-Mejías, Raquel et. al.

The genetics of attention deficit/hyperactivity disorder in adults, a review
score: 1.0040813, Molecular Psychiatry, 2011, Franke, B et. al.

Genetic Loci Implicated in Erythroid Differentiation and Cell Cycle Regulation Are Associated With Red Blood Cell Traits
score: 1.0039331, Mayo Clinic Proceedings, 2012, Ding, Keyue et. al.

A Genomewide Scan for Type 1–Diabetes Susceptibility in Scandinavian Families: Identification of New Loci with Evidence of Interactions
score: 1.002259, The American Journal of Human Genetics, 2001,

The EBMT activity survey 2009: trends over the past 5 years.
score: 1.001968, Bone marrow transplantation, 2011, Baldomero, H et. al.

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.
score: 0.99805361, Cancer research, 2010, Antoniou, Antonis C et. al.

Clustering by genetic ancestry using genome-wide SNP data
score: 0.99731823, BMC Genetics, 2010, Solovieff, Nadia et. al.

Linkage Analysis Followed by Association Show NRG1 Associated with Cannabis Dependence in African Americans
score: 0.99683619, Biological Psychiatry, 2012, Han, Shizhong et. al.

Linkage Analysis Followed by Association Show NRG1 Associated with Cannabis Dependence in African Americans
score: 0.99683619, Biological Psychiatry, 2012, Han, Shizhong et. al.

Protocol for investigating genetic determinants of posttraumatic stress disorder in women from the Nurses' Health Study II
score: 0.99625574, BMC Psychiatry, 2009, Koenen, Karestan C et. al.

GENETICS OF GENE EXPRESSION IN PRIMARY IMMUNE CELLS IDENTIFIES CELL-SPECIFIC MASTER REGULATORS AND ROLES OF HLA ALLELES
score: 0.99477688, Nature genetics, 2012, Fairfax, Benjamin P et. al.

Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia
score: 0.99405641, The American Journal of Human Genetics, 2003, Lewis, Cathryn M. et. al.

Beta2-adrenergic receptor gene polymorphisms as systemic determinants of healthy aging in an evolutionary context
score: 0.99265381, Mechanisms of Ageing and Development, 2010, Kulminski, Alexander M. et. al.

The genetics of multiple sclerosis: An update 2010
score: 0.99188657, Molecular and Cellular Probes, 2010, Hoffjan, Sabine; Akkad, Denis A.

Genetic association study of individual symptoms in depression
score: 0.9903932, Psychiatry Research, 2012, Myung, Woojae et. al.

Genetic association study of individual symptoms in depression
score: 0.9903932, Psychiatry Research, 2012, Myung, Woojae et. al.

KCNJ6 is associated with adult alcohol dependence and involved in gene × early life stress interactions in adolescent alcohol drinking.
score: 0.99004781, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Clarke, Toni-Kim et. al.

Association Between Schizophrenia and Common Variation in Neurocan (NCAN), a Genetic Risk Factor for Bipolar Disorder
score: 0.98952016, Schizophrenia Research, 2012, Mühleisen, Thomas W. et. al.

LIPC variants in the promoter and intron 1 modify HDL-C levels in a sex-specific fashion
score: 0.98911996, Atherosclerosis, 2009, Feitosa, Mary F. et. al.

No association between ADCYAP1R1 and post-traumatic stress disorder in two independent samples.
score: 0.98885741, Molecular psychiatry, 2012, Chang, S-C et. al.

Additive Effects of Genetic Variation in GCK and G6PC2 on Insulin Secretion and Fasting Glucose
score: 0.98719874, Diabetes, 2009, Li, Xia et. al.

Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers.
score: 0.98546408, Journal of human genetics, 2009, Nakabayashi, Kazuhiko et. al.

Determination of the Loss of Function Complement C4 Exon 29 CT Insertion Using a Novel Paralog-Specific Assay in Healthy UK and Spanish Populations
score: 0.98510892, PLoS ONE, 2011, Boteva, Lora et. al.

Genetic variants in thymic stromal lymphopoietin are associated with atopic dermatitis and eczema herpeticum
score: 0.98415431, The Journal of Allergy and Clinical Immunology, 2010, Gao, Pei-Song et. al.

Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2 , with Schizophrenia in an Arab-Israeli Family Sample
score: 0.98223461, PLoS ONE, 2012, Alkelai, Anna et. al.

Genome-Wide Association Study Identifies Genetic Loci Associated with Iron Deficiency
score: 0.98038433, PLoS ONE, 2011, McLaren, Christine E. et. al.

Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain
score: 0.9802785, Journal of Neuroimmunology, 2010, Swaminathan, Bhairavi et. al.

Hip geometry variation is associated with bone mineralization pathway gene variants: The Framingham Study.
score: 0.98000627, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2010, Cheung, Ching-Lung et. al.

Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.
score: 0.97850146, The Journal of investigative dermatology, 2010, Duffy, David L et. al.

Investigation of the HIN200 locus in UK SLE families identifies novel copy number variants.
score: 0.97804605, Annals of human genetics, 2011, Fernando, Michelle M A et. al.

Endophenotypes in normal brain morphology and Alzheimer's disease: a review
score: 0.97691393, Neuroscience, 2009, Reitz, C.; Mayeux, R.

Bivariate genome-wide association study suggests fatty acid desaturase genes and cadherin DCHS2 for variation of both compressive strength index and appendicular lean mass in males
score: 0.97665426, Bone, 2012, Han, Yingying et. al.

Bivariate genome-wide association study suggests fatty acid desaturase genes and cadherin DCHS2 for variation of both compressive strength index and appendicular lean mass in males
score: 0.97665426, Bone, 2012, Han, Yingying et. al.

CONAN: copy number variation analysis software for genome-wide association studies
score: 0.97558118, BMC Bioinformatics, 2010, Forer, Lukas et. al.

Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)
score: 0.97497209, PLoS ONE, 2012, Hein, Rebecca et. al.

Low-Frequency Variants in HMGA1 Are Not Associated With Type 2 Diabetes Risk
score: 0.97483426, Diabetes, 2012, Marquez, Marcel et. al.

Gene-centric analysis of serum cotinine levels in African and European American populations.
score: 0.97317599, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2012, Hamidovic, Ajna et. al.

Genome-Wide Association Study of Irritable vs. Elated Mania Suggests Genetic Differences between Clinical Subtypes of Bipolar Disorder
score: 0.97230633, PLoS ONE, 2013, Greenwood, Tiffany A.; Kelsoe, John R.

Identification of a new prostate cancer susceptibility locus on chromosome 8q24.
score: 0.97183893, Nature genetics, 2009, Yeager, Meredith et. al.

Protective Effect of Human Endogenous Retrovirus K dUTPase Variants on Psoriasis Susceptibility
score: 0.97126111, The Journal of Investigative Dermatology, 2012, Lai, Olivia Y. et. al.

Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIalpha gene (PIP5K2A) with schizophrenia.
score: 0.97039397, Molecular psychiatry, 2006, Schwab, S G et. al.

Genetic clustering of European cancer patients indicates that opioid-mediated pain relief is independent of ancestry.
score: 0.96936344, The pharmacogenomics journal, 2012, Galvan, A et. al.

Genetic variation in TRPS1 may regulate hip geometry as well as bone mineral density
score: 0.96926942, Bone, 2012, Ackert-Bicknell, Cheryl L. et. al.

Genomewide Significant Linkage to Migrainous Headache on Chromosome 5q21
score: 0.96860401, The American Journal of Human Genetics, 2005, Nyholt, Dale R. et. al.

Common sequence variation in FLNB regulates bone structure in women in the general population and FLNB mRNA expression in osteoblasts in vitro.
score: 0.96752932, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2009, Wilson, Scott G et. al.

Colorectal cancer susceptibility quantitative trait loci in mice as a novel approach to detect low-penetrance variants in humans: a two-stage case-control study.
score: 0.96640433, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Fernández-Rozadilla, Ceres et. al.

Variation in regulator of G-protein signaling 17 gene ( RGS17 ) is associated with multiple substance dependence diagnoses
score: 0.96600204, Behavioral and Brain Functions : BBF, 2012, Zhang, Huiping et. al.

The chromosome 7q region association with rheumatoid arthritis in females in a British population is not replicated in a North American case-control series.
score: 0.96581234, Arthritis and rheumatism, 2009, Korman, Benjamin D et. al.

Performance of Single Nucleotide Polymorphisms versus Haplotypes for Genome-Wide Association Analysis in Barley
score: 0.96510125, PLoS ONE, 2010, Lorenz, Aaron J.; Hamblin, Martha T.; Jannink, Jean-Luc

Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae.
score: 0.96334513, Proceedings of the National Academy of Sciences of the United States of America, 2009, Kenny, Eimear E et. al.

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia
score: 0.96324852, Molecular Psychiatry, 2011, Lips, E S et. al.

Filaggrin mutations that confer risk of atopic dermatitis confer greater risk for eczema herpeticum
score: 0.96191253, The Journal of Allergy and Clinical Immunology, 2009, Gao, Pei-Song et. al.

Polymorphisms in seizure 6-like gene are associated with bipolar disorder I: Evidence of gene×gender interaction
score: 0.96173555, Journal of Affective Disorders, 2013, Xu, Chun et. al.

Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium.
score: 0.96112169, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2008, Kote-Jarai, Zsofia et. al.

In Vitro Whole-Genome Analysis Identifies a Susceptibility Locus for HIV-1
score: 0.96076553, PLoS Biology, 2008, Loeuillet, Corinne et. al.

Complex nature of SNP genotype effects on gene expression in primary human leucocytes
score: 0.96039057, BMC Medical Genomics, 2009, Heap, Graham A et. al.

A Genomewide Scan for Loci Predisposing to Type 2 Diabetes in a U.K. Population (The Diabetes UK Warren 2 Repository): Analysis of 573 Pedigrees Provides Independent Replication of a Susceptibility Locus on Chromosome 1q
score: 0.95973576, The American Journal of Human Genetics, 2001, Wiltshire, Steven et. al.

Genome-wide association analyses of quantitative traits: the GAW16 experience.
score: 0.95956192, Genetic epidemiology, 2009, Ghosh, Saurabh

Autoimmune disease risk variant of IFIH1 is associated with increased sensitivity to IFN-α and serologic autoimmunity in lupus patients.
score: 0.95688046, Journal of immunology (Baltimore, Md. : 1950), 2011, Robinson, Talin et. al.

Assessment of heterogeneity between European Populations: a Baltic and Danish replication case-control study of SNPs from a recent European ulcerative colitis genome wide association study
score: 0.95455194, BMC Medical Genetics, 2011, Andersen, Vibeke et. al.

A review of software for microarray genotyping
score: 0.95432396, Human Genomics, 2011, Lamy, Philippe; Grove, Jakob; Wiuf, Carsten

Replication of Association Between Working Memory and Reelin, a Potential Modifier Gene in Schizophrenia
score: 0.95350353, Biological Psychiatry, 2010, Wedenoja, Juho et. al.

Genetic Structure of the Spanish Population
score: 0.95264758, BMC Genomics, 2010, Gayán, Javier et. al.

Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer.
score: 0.95151719, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Milne, Roger L et. al.

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature
score: 0.95063998, BMC Medical Genetics, 2010, Zhao, Jianhua et. al.

Data quality control in genetic case-control association studies.
score: 0.95031224, Nature protocols, 2010, Anderson, Carl A et. al.

Evaluation of Association of HNF1B Variants with Diverse Cancers: Collaborative Analysis of Data from 19 Genome-Wide Association Studies
score: 0.95028282, PLoS ONE, 2010, Elliott, Katherine S. et. al.

A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search
score: 0.94936763, The American Journal of Human Genetics, 2002, Angius, Andrea et. al.

Variants of the elongator protein 3 ( ELP3 ) gene are associated with motor neuron degeneration
score: 0.94900279, Human Molecular Genetics, 2008, Simpson, Claire L. et. al.

Genotyping Platforms for Mass‐Throughput Genotyping with SNPs, Including Human Genome‐Wide Scans
score: 0.94816652, Advances in Genetics, 2008, Maresso, Karen; Broeckel, Ulrich

Genotyping Platforms for Mass‐Throughput Genotyping with SNPs, Including Human Genome‐Wide Scans
score: 0.94816652, Advances in Genetics, 2008, Maresso, Karen; Broeckel, Ulrich

Power of selective genotyping in genome-wide association studies of quantitative traits
score: 0.94740121, BMC Proceedings, 2009, Xing, Chao; Xing, Guan

A common variant in ERBB4 regulates GABA concentrations in human cerebrospinal fluid.
score: 0.94732977, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2012, Luykx, Jurjen J et. al.

A High-Density SNP Genomewide Linkage Scan for Chronic Lymphocytic Leukemia–Susceptibility Loci
score: 0.94668176, The American Journal of Human Genetics, 2005, Sellick, Gabrielle S. et. al.

Application of collapsing methods for continuous traits to the Genetic Analysis Workshop 17 exome sequence data
score: 0.946065, BMC Proceedings, 2011, Sung, Yun Ju; Rice, Treva K; Rao, Dabeeru C

A new association test based on Chi-square partition for case-control GWA studies.
score: 0.94596189, Genetic epidemiology, 2011, Chen, Zhongxue

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.
score: 0.94543804, Molecular psychiatry, 2006, Brookes, K et. al.

Family-Based Association Tests for Genomewide Association Scans
score: 0.94454319, The American Journal of Human Genetics, 2007, Chen, Wei-Min; Abecasis, Gonçalo R.

GDF5 single-nucleotide polymorphism rs143383 is associated with lumbar disc degeneration in Northern European women
score: 0.9445399, Arthritis and Rheumatism, 2011, Williams, F M K et. al.

Utilizing Genotype Imputation for the Augmentation of Sequence Data
score: 0.94296409, PLoS ONE, 2010, Fridley, Brooke L. et. al.

Genetic Variation of Promoter Sequence Modulates XBP1 Expression and Genetic Risk for Vitiligo
score: 0.94183066, PLoS Genetics, 2009, Ren, Yunqing et. al.

Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone.
score: 0.9402127, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2010, Chung, Pui Yan Jenny et. al.

Evaluation of DOK5 as a susceptibility gene for type 2 diabetes and obesity in North Indian population
score: 0.93920255, BMC Medical Genetics, 2010, Tabassum, Rubina et. al.

Non-HLA genes modulate the risk of rheumatoid arthritis associated with HLA-DRB1 in a susceptible North American Native population.
score: 0.93891943, Genes and immunity, 2011, El-Gabalawy, H S et. al.

Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort.
score: 0.93838049, Genes and immunity, 2011, Namjou, B et. al.

HECTD2 Is Associated with Susceptibility to Mouse and Human Prion Disease
score: 0.93777945, PLoS Genetics, 2009, Lloyd, Sarah E. et. al.

SNPpy - Database Management for SNP Data from Genome Wide Association Studies
score: 0.93577239, PLoS ONE, 2011, Mitha, Faheem et. al.

Association of Variants at 1q32 and STAT3 with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease
score: 0.93564585, PLoS Genetics, 2010, Danoy, Patrick et. al.

Analysis of candidate genes on chromosome 20q12-13.1 reveals evidence for BMI mediated association of PREX1 with type 2 diabetes in European Americans
score: 0.93521071, Genomics, 2010, Lewis, Joshua P. et. al.

Accounting for multiple comparisons in a genome-wide association study (GWAS)
score: 0.93401817, BMC Genomics, 2010, Johnson, Randall C et. al.

Genotype, haplotype and copy-number variation in worldwide human populations.
score: 0.93304503, Nature, 2008, Jakobsson, Mattias et. al.

Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits
score: 0.93279299, BMC Proceedings, 2011, Zhang, Qunyuan et. al.

Genome Wide Association Study to predict severe asthma exacerbations in children using random forests classifiers
score: 0.93244304, BMC Medical Genetics, 2011, Xu, Mousheng et. al.

Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease.
score: 0.9317908, Inflammatory bowel diseases, 2010, Dubinsky, Marla C et. al.

Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms.
score: 0.93083893, Genes, chromosomes & cancer, 2008, Gunnarsson, Rebeqa et. al.

Evidence for an association between KIBRA and late-onset Alzheimer's disease
score: 0.93004415, Neurobiology of Aging, 2010, Corneveaux, Jason J. et. al.

IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.
score: 0.92991729, Genes and immunity, 2008, Weber, F et. al.

Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP.
score: 0.92941632, The Journal of investigative dermatology, 2011, Birlea, Stanca A et. al.

Variations in the FTO gene are associated with severe obesity in the Japanese
score: 0.92637773, Journal of Human Genetics, 2008, Hotta, Kikuko et. al.

Genetics of Sjögren’s syndrome in the genome-wide association era
score: 0.92325611, Journal of Autoimmunity, 2012, Ice, John A. et. al.

Genetics of Sjögren’s syndrome in the genome-wide association era
score: 0.92325611, Journal of Autoimmunity, 2012, Ice, John A. et. al.

Common Variants in CRP and LEPR Influence High Sensitivity C-Reactive Protein Levels in North Indians
score: 0.92223356, PLoS ONE, 2011, Mahajan, Anubha et. al.

The use of race, ethnicity and ancestry in human genetic research
score: 0.92206142, The HUGO Journal, 2011, Ali-Khan, Sarah E. et. al.

Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression.
score: 0.92144684, Journal of human genetics, 2009, Cha, Pei-Chieng et. al.

Applicability of DNA pools on 500 K SNP microarrays for cost-effective initial screens in genomewide association studies
score: 0.91958573, BMC Genomics, 2007, Docherty, Sophia J et. al.

Identification of Genetic and Epigenetic Marks Involved in Population Structure
score: 0.91774718, PLoS ONE, 2010, Liu, Jingyu et. al.

Multi-ethnic studies in complex traits
score: 0.91628982, Human Molecular Genetics, 2011, Fu, Jingyuan; Festen, Eleonora A.M.; Wijmenga, Cisca

Robust joint analysis allowing for model uncertainty in two-stage genetic association studies
score: 0.91623249, BMC Bioinformatics, 2011, Pan, Dongdong et. al.

A Genomewide Scan for Early-Onset Coronary Artery Disease in 438 Families: The GENECARD Study
score: 0.91604292, The American Journal of Human Genetics, 2004, Hauser, Elizabeth R. et. al.

Association of CDX1 binding site of periostin gene with bone mineral density and vertebral fracture risk
score: 0.91436877, Osteoporosis International, 2012, Xiao, S.-M. et. al.

Associations of markers in 11 obesity candidate genes with maximal weight loss and weight regain in the SOS bariatric surgery cases.
score: 0.91383509, International journal of obesity (2005), 2011, Sarzynski, M A et. al.

Incorporating biological knowledge in the search for gene × gene interaction in genome-wide association studies
score: 0.91364973, BMC Proceedings, 2009, Manning, Alisa K et. al.

A haplotype analysis is consistent with the role of functional HTR1B variants in alcohol dependence
score: 0.91330122, Drug and Alcohol Dependence, 2012, Contini, Verônica et. al.

An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males
score: 0.91241337, Molecular Autism, 2011, Chung, Ren-Hua et. al.

Amino Acid Position 11 of HLA-DRβ1 is a Major Determinant of Chromosome 6p Association with Ulcerative Colitis
score: 0.91144892, Genes and Immunity, 2011, Achkar, Jean-Paul et. al.

Evaluation of Haplotype Inference Using Definitive Haplotype Data Obtained from Complete Hydatidiform Moles, and Its Significance for the Analyses of Positively Selected Regions
score: 0.90855904, PLoS Genetics, 2009, Higasa, Koichiro et. al.

Genome-wide scan for adiposity-related phenotypes in adults from American Samoa.
score: 0.90685268, International journal of obesity (2005), 2007, Dai, F et. al.

Association of the DTNBP1 Locus with Schizophrenia in a U.S. Population
score: 0.90336191, The American Journal of Human Genetics, 2004, Funke, Birgit et. al.

Replication and functional genomic analyses of the breast cancer susceptibility locus at 6q25.1 generalize its importance in women of chinese, Japanese, and European ancestry.
score: 0.90291589, Cancer research, 2011, Cai, Qiuyin et. al.

Polymorphisms in the Estrogen Receptor 1 and Vitamin C and Matrix Metalloproteinase Gene Families Are Associated with Susceptibility to Lymphoma
score: 0.90232343, PLoS ONE, 2008, Skibola, Christine F. et. al.

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder
score: 0.90205321, Schizophrenia Research, 2012, Mühleisen, Thomas W. et. al.

Variance heterogeneity analysis for detection of potentially interacting genetic loci: method and its limitations
score: 0.90119154, BMC Genetics, 2010, Struchalin, Maksim V et. al.

Comprehensive genetic assessment of a functional TLR9 promoter polymorphism: no replicable association with asthma or asthma-related phenotypes
score: 0.90055136, BMC Medical Genetics, 2011, Lange, Nancy E et. al.

Circadian polymorphisms associated with affective disorders
score: 0.89950978, Journal of Circadian Rhythms, 2009, Kripke, Daniel F et. al.

Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis
score: 0.89949633, Journal of Medical Genetics, 2012, Alcina, Antonio et. al.

Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing.
score: 0.89669418, Genes and immunity, 2009, Douglas, K B et. al.

Rapid and robust resampling-based multiple-testing correction with application in a genome-wide expression quantitative trait loci study.
score: 0.89591997, Genetics, 2012, Zhang, Xiang; Huang, Shunping; Sun, Wei; Wang, Wei

A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis.
score: 0.89421807, European journal of human genetics : EJHG, 2010, Mero, Inger-Lise et. al.

C-Reactive protein gene variants are associated with postoperative C-reactive protein levels after coronary artery bypass surgery
score: 0.89371265, BMC Medical Genetics, 2009, Perry, Tjörvi E et. al.

Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations.
score: 0.89336507, Proceedings of the National Academy of Sciences of the United States of America, 2010, Bryc, Katarzyna et. al.

Evaluating the performance of Affymetrix SNP Array 6.0 platform with 400 Japanese individuals
score: 0.89135936, BMC Genomics, 2008, Nishida, Nao et. al.

Identification of AF4/FMR2 family, member 3 ( AFF3 ) as a novel rheumatoid arthritis susceptibility locus and confirmation of two further pan-autoimmune susceptibility genes
score: 0.89130794, Human Molecular Genetics, 2009, Barton, Anne et. al.

A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis
score: 0.8907191, Annals of the Rheumatic Diseases, 2010, Skinningsrud, Beate et. al.

Association and Haplotype Analyses of Positional Candidate Genes in Five Genomic Regions Linked to Scrotal Hernia in Commercial Pig Lines
score: 0.89054057, PLoS ONE, 2009, Du, Zhi-Qiang et. al.

Case-control study for colorectal cancer genetic susceptibility in EPICOLON: previously identified variants and mucins
score: 0.89028178, BMC Cancer, 2011, Abulí, Anna et. al.

Extension of Type 2 Diabetes Genome-Wide Association Scan Results in the Diabetes Prevention Program
score: 0.88990937, Diabetes, 2008, Moore, Allan F. et. al.

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.
score: 0.88921823, Molecular psychiatry, 2012, Priebe, L et. al.

The Relationship of DNA Methylation with Age, Gender and Genotype in Twins and Healthy Controls
score: 0.88917885, PLoS ONE, 2009, Boks, Marco P. et. al.

BDNF is not associated with schizophrenia: Data from a Japanese population study and meta-analysis
score: 0.88872753, Schizophrenia Research, 2009, Kawashima, Kunihiro et. al.

Predicting white matter integrity from multiple common genetic variants.
score: 0.88678211, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2012, Kohannim, Omid et. al.

Comparison of methods for correcting population stratification in a genome-wide association study of rheumatoid arthritis: principal-component analysis versus multidimensional scaling
score: 0.88596771, BMC Proceedings, 2009, Wang, Dai et. al.

Genetics of subcortical vascular dementia
score: 0.88583139, Experimental Gerontology, 2012, Schmidt, Helena et. al.

Genetics of subcortical vascular dementia
score: 0.88583139, Experimental Gerontology, 2012, Schmidt, Helena et. al.

Case-Control Study of Six Genes Asymmetrically Expressed in the Two Cerebral Hemispheres: Association of BAIAP2 with Attention-Deficit/Hyperactivity Disorder
score: 0.88506807, Biological Psychiatry, 2009, Ribasés, Marta et. al.

Genetic Determinants of Variability in Glycated Hemoglobin (HbA 1c ) in Humans: Review of Recent Progress and Prospects for Use in Diabetes Care
score: 0.88308863, Current Diabetes Reports, 2011, Soranzo, Nicole

Common variants in FTO are not significantly associated with obesity-related phenotypes among Samoans of Polynesia.
score: 0.88270957, Annals of human genetics, 2012, Karns, Rebekah et. al.

Angiogenin Levels and ANG Genotypes: Dysregulation in Amyotrophic Lateral Sclerosis
score: 0.88133695, PLoS ONE, 2010, McLaughlin, Russell Lewis et. al.

Localization of a Susceptibility Gene for Type 2 Diabetes to Chromosome 5q34–q35.2
score: 0.88113189, The American Journal of Human Genetics, 2003, Reynisdottir, Inga et. al.

Pooled DNA genotyping on Affymetrix SNP genotyping arrays
score: 0.88111156, BMC Genomics, 2006, Kirov, George et. al.

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.
score: 0.88071742, Molecular psychiatry, 2012, Visscher, P M; Goddard, M E; Derks, E M; Wray, N R

Segmental copy-number gain within the region of isopentenyl diphosphate isomerase genes in sporadic amyotrophic lateral sclerosis
score: 0.87902845, Biochemical and Biophysical Research Communications, 2010, Kato, Takeo et. al.

Association of coagulation-related and inflammation-related genes and factor VIIc levels with stroke: the Cardiovascular Health Study.
score: 0.87856749, Journal of thrombosis and haemostasis : JTH, 2011, Zakai, N A et. al.

Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study.
score: 0.87845679, Molecular psychiatry, 2011, Voyiaziakis, E et. al.

Evaluation of 15 Functional Candidate Genes for Association with Chronic Otitis Media with Effusion and/or Recurrent Otitis Media (COME/ROM)
score: 0.87783066, PLoS ONE, 2011, Sale, Michèle M. et. al.

A General Framework for Two-Stage Analysis of Genome-wide Association Studies and Its Application to Case-Control Studies
score: 0.87732872, The American Journal of Human Genetics, 2012, Wason, James M.S.; Dudbridge, Frank

Genome partitioning of genetic variation for complex traits using common SNPs.
score: 0.87681138, Nature genetics, 2011, Yang, Jian et. al.

The EBMT activity survey 2006 on hematopoietic stem cell transplantation: focus on the use of cord blood products.
score: 0.87620754, Bone marrow transplantation, 2008, Gratwohl, A et. al.

Association of the Sirtuin and Mitochondrial Uncoupling Protein Genes with Carotid Plaque
score: 0.87567756, PLoS ONE, 2011, Dong, Chuanhui et. al.

The pitfalls of platform comparison: DNA copy number array technologies assessed
score: 0.8753881, BMC Genomics, 2009, Curtis, Christina et. al.

Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2: association with major depression and antidepressant response in Mexican-Americans.
score: 0.8753484, Molecular psychiatry, 2009, Dong, C; Wong, M-L; Licinio, J

More aroused, less fatigued: fatty acid amide hydrolase gene polymorphisms influence acute response to amphetamine.
score: 0.87502287, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2010, Dlugos, Andrea M et. al.

Reconsidering Association Testing Methods Using Single-Variant Test Statistics as Alternatives to Pooling Tests for Sequence Data with Rare Variants
score: 0.87491633, PLoS ONE, 2012, Kinnamon, Daniel D.; Hershberger, Ray E.; Martin, Eden R.

Analyses and Comparison of Accuracy of Different Genotype Imputation Methods
score: 0.87457001, PLoS ONE, 2008, Pei, Yu-Fang et. al.

Genetic Modification of the Association between Peripubertal Dioxin Exposure and Pubertal Onset in a Cohort of Russian Boys
score: 0.87359433, Environmental Health Perspectives, 2012, Humblet, Olivier et. al.

Evidence for a possible association of neurotrophin receptor ( NTRK-3) gene polymorphisms with hippocampal function and schizophrenia
score: 0.87185944, Neurobiology of Disease, 2009, Otnæss, Mona K. et. al.

Variation in MSRA Modifies Risk of Neonatal Intestinal Obstruction in Cystic Fibrosis
score: 0.87175794, PLoS Genetics, 2012, Henderson, Lindsay B. et. al.

Identification of a Mutation Associated with Fatal Foal Immunodeficiency Syndrome in the Fell and Dales Pony
score: 0.87124583, PLoS Genetics, 2011, Fox-Clipsham, Laura Y. et. al.

Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia
score: 0.87096508, Journal of the American College of Cardiology, 2012, Jamshidi, Yalda et. al.

Identification of non-synonymous polymorphisms in the WDSOF1 gene as novel susceptibility markers for low bone mineral density in Japanese postmenopausal women
score: 0.87094863, Bone, 2010, Urano, Tomohiko et. al.

Histone deacetylase gene variants predict brain volume changes in multiple sclerosis
score: 0.86993487, Neurobiology of Aging, 2013, Inkster, Becky et. al.

Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?
score: 0.86973868, Molecular psychiatry, 2009, Le Hellard, S et. al.

The galanin receptor 1 gene associates with tobacco craving in smokers seeking cessation treatment.
score: 0.86972848, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Lori, Adriana et. al.

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.
score: 0.86782997, Nature genetics, 2008, Helgadottir, Anna et. al.

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap.
score: 0.8670845, Bioinformatics (Oxford, England), 2008, Johnson, Andrew D et. al.

Impact of the AHI1 Gene on the Vulnerability to Schizophrenia: A Case-Control Association Study
score: 0.86652014, PLoS ONE, 2010, Rivero, Olga et. al.

A 3' UTR transition within DEFB1 is associated with chronic and aggressive periodontitis.
score: 0.8654072, Genes and immunity, 2010, Schaefer, A S et. al.

Psychiatric genetics: progress amid controversy.
score: 0.86512147, Nature reviews. Genetics, 2008, Burmeister, Margit; McInnis, Melvin G; Zöllner, Sebastian

Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing
score: 0.86421721, Genes and immunity, 2009, Douglas, Katherine B. et. al.

A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis
score: 0.86406754, Genes and immunity, 2010, Ban, Maria et. al.

Postural Changes in Blood Pressure Associated with Interactions between Candidate Genes for Chronic Respiratory Diseases and Exposure to Particulate Matter
score: 0.86233935, Environmental Health Perspectives, 2009, Wilker, Elissa et. al.

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes.
score: 0.86127954, Nature genetics, 2012, Bonnefond, Amélie et. al.

Bivariate genome-wide linkage analysis of femoral bone traits and leg lean mass: Framingham study.
score: 0.85955524, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2009, Karasik, David et. al.

Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: A Danish national birth cohort-based study
score: 0.85799519, Schizophrenia Research, 2012, Agerbo, Esben et. al.

Genomewide Linkage Scan for Nicotine Dependence: Identification of a Chromosome 5 Risk Locus
score: 0.85726537, Biological Psychiatry, 2007, Gelernter, Joel et. al.

Association of BANK1 and TNFSF4 with systemic lupus erythematosus in Hong Kong Chinese
score: 0.85670626, Genes and Immunity, 2009, Chang, Y K et. al.

Epidemiological, genetic and epigenetic aspects of the research on healthy ageing and longevity
score: 0.85468486, Immunity & Ageing : I & A, 2012, Montesanto, Alberto et. al.

A genome-wide association scan for rheumatoid arthritis data by Hotelling's T 2 tests
score: 0.85393107, BMC Proceedings, 2009, Chen, Lianfu et. al.

Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients.
score: 0.85297016, Proceedings of the National Academy of Sciences of the United States of America, 2010, Traynor, Bryan J et. al.

A Permutation Procedure to Correct for Confounders in Case-Control Studies, Including Tests of Rare Variation
score: 0.85272722, The American Journal of Human Genetics, 2012, Epstein, Michael P. et. al.

Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thickness
score: 0.85261885, Molecular Vision, 2010, Desronvil, T. et. al.

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.
score: 0.84928211, Nature genetics, 2011, Elia, Josephine et. al.

Genetic variants associated with Von Willebrand factor levels in healthy men and women identified using the HumanCVD BeadChip.
score: 0.84893729, Annals of human genetics, 2011, Zabaneh, Delilah et. al.

Associations of Variants in CHRNA5/A3/B4 Gene Cluster with Smoking Behaviors in a Korean Population
score: 0.84774339, PLoS ONE, 2010, Li, Ming D. et. al.

Systematic Testing of Literature Reported Genetic Variation Associated with Coronary Restenosis: Results of the GENDER Study
score: 0.84628782, PLoS ONE, 2012, Verschuren, Jeffrey J. W. et. al.

A genome-wide scan of 10 000 gene-centric variants and colorectal cancer risk.
score: 0.84613858, European journal of human genetics : EJHG, 2009, Webb, Emily et. al.

CD39/Adenosine Pathway Is Involved in AIDS Progression
score: 0.84612588, PLoS Pathogens, 2011, Nikolova, Maria et. al.

Meta-analysis and Imputation Identifies a 109 kb Risk Haplotype Spanning TNFAIP3 Associated with Lupus Nephritis and Hematologic Manifestations
score: 0.84612185, Genes and immunity, 2009, Bates, Jared S. et. al.

Genetic variability in the NMDA-dependent AMPA trafficking cascade is associated with alcohol dependence.
score: 0.84575753, Addiction biology, 2012, Karpyak, Victor M et. al.

Alterations in KLRB1 gene expression and a Scandinavian multiple sclerosis association study of the KLRB1 SNP rs4763655.
score: 0.844943, European journal of human genetics : EJHG, 2011, Søndergaard, Helle Bach et. al.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
score: 0.84412754, Nature genetics, 2007, Autism Genome Project Consortium, et. al.

Comparison of Genome Wide Variation between Malawians and African Ancestry HapMap Populations
score: 0.84383841, Journal of human genetics, 2010, Joubert, Bonnie R. et. al.

Tissue-Specific Genetic Control of Splicing: Implications for the Study of Complex Traits
score: 0.84247122, PLoS Biology, 2008, Heinzen, Erin L et. al.

Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain
score: 0.8422593, PLoS Genetics, 2010, Gibbs, J. Raphael et. al.

A 17q12 allele is associated with altered NK cell subsets and function.
score: 0.84187003, Journal of immunology (Baltimore, Md. : 1950), 2012, Xia, Zongqi et. al.

Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome
score: 0.83883069, Lancet, 2012, Charchar, Fadi J et. al.

Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome
score: 0.83883069, The Lancet, 2012, Charchar, Fadi J et. al.

Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
score: 0.83863446, British Journal of Cancer, 2011, Osorio, A et. al.

Genetic Investigation into the Endophenotypic Status of Central Corneal Thickness and Optic Disc Parameters in Relation to Open-Angle Glaucoma
score: 0.83822041, American Journal of Ophthalmology, 2012, Dimasi, David P. et. al.

Melatonin receptor 1 B polymorphisms associated with the risk of gestational diabetes mellitus
score: 0.83815551, BMC Medical Genetics, 2011, Kim, Jason Y et. al.

Allowing for sex differences increases power in a GWAS of multiplex Autism families.
score: 0.83775367, Molecular psychiatry, 2012, Lu, A T-H; Cantor, R M

The obesity gene, TMEM18, is of ancient origin, found in majority of neuronal cells in all major brain regions and associated with obesity in severely obese children
score: 0.83734222, BMC Medical Genetics, 2010, Almén, Markus Sällman et. al.

Multiethnic Genetic Association Studies Improve Power for Locus Discovery
score: 0.8372929, PLoS ONE, 2010, Pulit, Sara L.; Voight, Benjamin F.; de Bakker, Paul I. W.

A New Methodology to Associate SNPs with Human Diseases According to Their Pathway Related Context
score: 0.83717698, PLoS ONE, 2011, Bakir-Gungor, Burcu; Sezerman, Osman Ugur

Genome-Wide Association Study Identifies Loci for Body Composition and Structural Soundness Traits in Pigs
score: 0.83579883, PLoS ONE, 2011, Fan, Bin et. al.

A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.
score: 0.83573437, Proceedings of the National Academy of Sciences of the United States of America, 2010, Abitbol, Marie et. al.

Candidate-Gene Screening and Association Analysis at the Autism-Susceptibility Locus on Chromosome 16p: Evidence of Association at GRIN2A and ABAT
score: 0.83545714, The American Journal of Human Genetics, 2005, Barnby, Gabrielle et. al.

A genome-wide association study for quantitative trait loci of show-jumping in Hanoverian warmblood horses.
score: 0.83483317, Animal genetics, 2012, Schröder, W; Klostermann, A; Stock, K F; Distl, O

Fidelity of SNP Array Genotyping Using Epstein Barr Virus-Transformed B-Lymphocyte Cell Lines: Implications for Genome-Wide Association Studies
score: 0.83337599, PLoS ONE, 2009, Herbeck, Joshua T. et. al.

Genetic Analysis of Variation in Human Meiotic Recombination
score: 0.83313384, PLoS Genetics, 2009, Chowdhury, Reshmi et. al.

Common variants in FLNB / CRTAP , not ARHGEF3 at 3p, are associated with osteoporosis in southern Chinese women
score: 0.83298064, Osteoporosis International, 2009, Li, G. H. Y.; Kung, A. W. C.; Huang, Q.-Y.

New common variants affecting susceptibility to basal cell carcinoma.
score: 0.83157972, Nature genetics, 2009, Stacey, Simon N et. al.

Evaluating the association of common PBX1 variants with type 2 diabetes
score: 0.83145736, BMC Medical Genetics, 2008, Duesing, Konsta et. al.

Pharmacogenomic discovery using cell-based models.
score: 0.83011118, Pharmacological reviews, 2009, Welsh, Marleen et. al.

Detectable clonal mosaicism from birth to old age and its relationship to cancer
score: 0.82972298, Nature genetics, 2012, Laurie, Cathy C. et. al.

Two-Dimensional Genome Scan Identifies Multiple Genetic Interactions in Bipolar Affective Disorder
score: 0.82954329, Biological Psychiatry, 2010, Fullerton, Janice M. et. al.

The Rotterdam Study: 2012 objectives and design update
score: 0.82917144, European Journal of Epidemiology, 2011, Hofman, Albert et. al.

A gene variant of 11β-hydroxysteroid dehydrogenase type 1 is associated with obesity in children.
score: 0.82888095, International journal of obesity (2005), 2012, Olza, J et. al.

Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
score: 0.82837495, The American Journal of Human Genetics, 2008, Antoniou, Antonis C. et. al.

ITGAM is associated with disease susceptibility and renal nephritis of systemic lupus erythematosus in Hong Kong Chinese and Thai
score: 0.82746691, Human Molecular Genetics, 2009, Yang, Wanling et. al.

Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.
score: 0.82632683, Genes and immunity, 2009, Howson, J M M et. al.

Evaluation of LOXL1 polymorphisms in exfoliation syndrome in a Chinese population
score: 0.82623839, Molecular Vision, 2009, Chen, Ling et. al.

The ESR1 (6q25) Locus Is Associated with Calcaneal Ultrasound Parameters and Radial Volumetric Bone Mineral Density in European Men
score: 0.82595289, PLoS ONE, 2011, Holliday, Kate L. et. al.

TNFAIP3 gene polymorphisms are associated with response to TNF blockade in psoriasis.
score: 0.82559619, The Journal of investigative dermatology, 2012, Tejasvi, Trilokraj et. al.

Analysis of epistasis for diabetic nephropathy among type 2 diabetic patients.
score: 0.82444607, Human molecular genetics, 2006, Hsieh, Chang-Hsun et. al.

Genome-wide association analysis reveals a SOD1 mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis.
score: 0.82262939, Proceedings of the National Academy of Sciences of the United States of America, 2009, Awano, Tomoyuki et. al.

Dense mapping of IL18 shows no association in SLE
score: 0.82250557, Human Molecular Genetics, 2010, Guerra, Sandra G. et. al.

Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease
score: 0.82167906, Heart Rhythm, 2009, Tseng, Zian H. et. al.

Phenotype Restricted Genome-Wide Association Study Using a Gene-Centric Approach Identifies Three Low-Risk Neuroblastoma Susceptibility Loci
score: 0.82054117, PLoS Genetics, 2011, Nguyễn, Lễ B. et. al.

Dual-specificity phosphatase 1 as a pharmacogenetic modifier of inhaled steroid response among asthmatic patients
score: 0.82028597, The Journal of Allergy and Clinical Immunology, 2010, Jin, Ying et. al.

Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples.
score: 0.82013486, The pharmacogenomics journal, 2010, Hong, H et. al.

Common Variants in the Type 2 Diabetes KCNQ1 Gene Are Associated with Impairments in Insulin Secretion During Hyperglycaemic Glucose Clamp
score: 0.81972753, PLoS ONE, 2012, van Vliet-Ostaptchouk, Jana V. et. al.

Mapping of the IRF8 Gene Identifies a 3'UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma Subtypes.
score: 0.81955838, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2013, Slager, Susan L et. al.

Detailed Investigation of the Role of Common and Low-Frequency WFS1 Variants in Type 2 Diabetes Risk
score: 0.818861, Diabetes, 2009, Fawcett, Katherine A. et. al.

Bayesian Variable Selection in Searching for Additive and Dominant Effects in Genome-Wide Data
score: 0.81799108, PLoS ONE, 2012, Peltola, Tomi et. al.

OpenADAM: an open source genome-wide association data management system for Affymetrix SNP arrays
score: 0.81774699, BMC Genomics, 2008, Yeung, J MY; Sham, P C; Chan, A SW; Cherny, S S

A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia.
score: 0.81769164, Molecular psychiatry, 2010, Datta, S R et. al.

Exploring genetic determinants of plasma total cholesterol levels and their predictive value in a longitudinal study
score: 0.81756178, Atherosclerosis, 2010, Lu, Yingchang et. al.

Genetic predictors of increase in suicidal ideation during antidepressant treatment in the GENDEP project.
score: 0.81704337, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Perroud, Nader et. al.

Genetics of Human Cardiovascular Disease
score: 0.81662947, Cell, 2012, Kathiresan, Sekar; Srivastava, Deepak

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians.
score: 0.81621863, Genes and immunity, 2008, Rubio, J P et. al.

Analysis of genome-wide association data by large-scale Bayesian logistic regression
score: 0.81492843, BMC Proceedings, 2009, Wang, Yuanjia; Sha, Nanshi; Fang, Yixin

Multiple Independent Loci at Chromosome 15q25.1 Affect Smoking Quantity: a Meta-Analysis and Comparison with Lung Cancer and COPD
score: 0.8146668, PLoS Genetics, 2010, Saccone, Nancy L. et. al.

Genes of the interleukin-18 pathway are associated with susceptibility to Barrett's esophagus and esophageal adenocarcinoma.
score: 0.81422106, The American journal of gastroenterology, 2012, Babar, Mahwash et. al.

APOE and Alzheimer disease: a major gene with semi-dominant inheritance.
score: 0.81416605, Molecular psychiatry, 2011, Genin, E et. al.

Dissecting the genetic make-up of North-East Sardinia using a large set of haploid and autosomal markers.
score: 0.81364725, European journal of human genetics : EJHG, 2012, Pardo, Luba M et. al.

No evidence of association of the rare nsSNP rs35667974 in IFIH1 with multiple sclerosis
score: 0.81352382, Journal of Neuroimmunology, 2010, Bergamaschi, Laura et. al.

Variation in the ATP-binding cassette transporter 2 gene is a separate risk factor for systemic lupus erythematosus within the MHC.
score: 0.8129356, Genes and immunity, 2009, Ramos, P S et. al.

Novel genes for QTc interval. How much heritability is explained, and how much is left to find?
score: 0.8117249, Genome Medicine, 2010, Jamshidi, Yalda et. al.

Follow-Up Association Study of Linkage Regions Reveals Multiple Candidate Genes for Carotid Plaque in Dominicans
score: 0.81092111, Atherosclerosis, 2012, Dong, Chuanhui et. al.

Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15
score: 0.81016113, Human Molecular Genetics, 2010, Nelson, George W. et. al.

Comparative Linkage Meta-Analysis Reveals Regionally-Distinct, Disparate Genetic Architectures: Application to Bipolar Disorder and Schizophrenia
score: 0.80915122, PLoS ONE, 2011, Tang, Brady; Thornton-Wells, Tricia; Askland, Kathleen D.

Polymorphisms of chitinases are not associated with asthma
score: 0.80882195, The Journal of Allergy and Clinical Immunology, 2010, Wu, Ann Chen et. al.

Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability.
score: 0.80830909, Nature reviews. Genetics, 2007, Beckmann, Jacques S et. al.

The Impact of Divergence Time on the Nature of Population Structure: An Example from Iceland
score: 0.80813101, PLoS Genetics, 2009, Price, Alkes L. et. al.

Genome Wide Association for Addiction: Replicated Results and Comparisons of Two Analytic Approaches
score: 0.80683397, PLoS ONE, 2010, Drgon, Tomas et. al.

Preliminary evidence of association between EFHC2, a gene implicated in fear recognition, and harm avoidance
score: 0.80661936, Neuroscience Letters, 2009, Blaya, Carolina et. al.

Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations.
score: 0.80513112, Molecular psychiatry, 2005, Li, T et. al.

Heroin addiction in African Americans: a hypothesis-driven association study.
score: 0.8051111, Genes, brain, and behavior, 2009, Levran, O et. al.

Genetic variation at CHRNA5-CHRNA3-CHRNB4 interacts with smoking status to influence body mass index
score: 0.8050452, International Journal of Epidemiology, 2011, Freathy, Rachel M et. al.

Replication of prostate cancer risk loci on 8q24, 11q13, 17q12, 19q33, and Xp11 in African Americans.
score: 0.80494965, The Prostate, 2010, Hooker, Stanley et. al.

Polygenic susceptibility to prostate and breast cancer: implications for personalised screening
score: 0.80481238, British Journal of Cancer, 2011, Pashayan, N et. al.

The utility of genome-wide association studies in hepatology.
score: 0.8041498, Hepatology (Baltimore, Md.), 2010, Karlsen, Tom H; Melum, Espen; Franke, Andre

ECR 2011 Book of Abstracts - B - Scientific Sessions
score: 0.80398132, Insights into Imaging, 2011,

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia.
score: 0.80291978, Molecular psychiatry, 2012, Lips, E S et. al.

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data
score: 0.80259689, BMC Genomics, 2010, Polašek, Ozren et. al.

Genetics of subcortical vascular dementia
score: 0.80201267, Experimental Gerontology, 2012, Schmidt, Helena et. al.

An interactive effect of batch size and composition contributes to discordant results in GWAS with the CHIAMO genotyping algorithm.
score: 0.80171821, The pharmacogenomics journal, 2010, Chierici, M; Miclaus, K; Vega, S; Furlanello, C

Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population.
score: 0.80134153, Journal of human genetics, 2010, Matsushita, Tomonaga et. al.

Brain Expressed microRNAs Implicated in Schizophrenia Etiology
score: 0.80109114, PLoS ONE, 2007, Hansen, Thomas et. al.

Variants in the human potassium channel gene ( KCNN3 ) are associated with migraine in a high risk genetic isolate
score: 0.8006007, The Journal of Headache and Pain, 2011, Cox, Hannah C. et. al.

Genomewide Linkage Analysis for Internal Carotid Artery Intimal Medial Thickness: Evidence for Linkage to Chromosome 12
score: 0.80029923, The American Journal of Human Genetics, 2004, Fox, Caroline S. et. al.

Identification of loci associated with tolerance to Johne's disease in Holstein cattle.
score: 0.80011658, Animal genetics, 2011, Zanella, R et. al.

Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence.
score: 0.80005977, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2010, Wessel, Jennifer et. al.

Role of PTPN22 in type 1 diabetes and other autoimmune diseases
score: 0.79916848, Seminars in Immunology, 2006, Bottini, Nunzio et. al.

Polymorphism in the GALNT1 gene and epithelial ovarian cancer in non-Hispanic white women: the Ovarian Cancer Association Consortium.
score: 0.79837411, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Phelan, Catherine M et. al.

Functional annotations of diabetes nephropathy susceptibility loci through analysis of genome-wide renal gene expression in rat models of diabetes mellitus
score: 0.79747329, BMC Medical Genomics, 2009, Hu, Yaomin et. al.

PAX6 Haplotypes Are Associated with High Myopia in Han Chinese
score: 0.79625252, PLoS ONE, 2011, Jiang, Bo et. al.

Recapitulation of genome-wide association studies on body mass index in the Korean population.
score: 0.79439594, International journal of obesity (2005), 2012, Hong, K W; Oh, B

Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease
score: 0.79437739, Genome Medicine, 2009, Silander, Kaisa et. al.

NCI60 Cancer Cell Line Panel Data and RNAi Analysis Help Identify EAF2 as a Modulator of Simvastatin and Lovastatin Response in HCT-116 Cells
score: 0.79427814, PLoS ONE, 2011, Savas, Sevtap et. al.

Ubiquitin-mediated proteasomal degradation of ABC transporters: a new aspect of genetic polymorphisms and clinical impacts.
score: 0.79358443, Journal of pharmaceutical sciences, 2011, Nakagawa, Hiroshi et. al.

Evaluating diagnostic accuracy of genetic profiles in affected offspring families.
score: 0.79342296, Statistics in medicine, 2010, Carayol, Jerome et. al.

Genetic Risk Factors for Hepatopulmonary Syndrome in Patients With Advanced Liver Disease
score: 0.79279538, Gastroenterology, 2010, Roberts, Kari E. et. al.

Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing
score: 0.79235405, Human Molecular Genetics, 2009, Heap, Graham A. et. al.

Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.
score: 0.79221403, Birth defects research. Part A, Clinical and molecular teratology, 2010, Nikopensius, Tiit et. al.

Large-Scale Candidate Gene Analysis of HDL Particle Features
score: 0.79209939, PLoS ONE, 2011, Kaess, Bernhard M. et. al.

An Investigation of Genome-Wide Studies Reported Susceptibility Loci for Ulcerative Colitis Shows Limited Replication in North Indians
score: 0.79132698, PLoS ONE, 2011, Juyal, Garima et. al.

Association at SYNE1 in both bipolar disorder and recurrent major depression.
score: 0.79013264, Molecular psychiatry, 2012, Green, E K et. al.

The C11orf30-LRRC32 region is associated with total serum IgE levels in asthmatic patients
score: 0.789715, The Journal of Allergy and Clinical Immunology, 2012, Li, Xingnan et. al.

An exploratory analysis on gene-environment interactions for Parkinson disease
score: 0.78891196, Neurobiology of Aging, 2012, Gao, Jianjun et. al.

The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants.
score: 0.78813416, Molecular psychiatry, 2013, Mowry, B J; Gratten, J

A LASSO-based approach to analyzing rare variants in genetic association studies
score: 0.78760116, BMC Proceedings, 2011, Brennan, Jennifer S et. al.

A genome-wide set of SNPs detects population substructure and long range linkage disequilibrium in wild sheep.
score: 0.78744592, Molecular ecology resources, 2011, Miller, J M et. al.

Neurobiology of attention deficit/hyperactivity disorder.
score: 0.78636628, Pediatric research, 2011, Purper-Ouakil, Diane et. al.

Variants in estrogen-related genes and risk of Parkinson's disease.
score: 0.78606583, Movement disorders : official journal of the Movement Disorder Society, 2011, Chung, Sun Ju et. al.

Recombination and linkage disequilibrium in Arabidopsis thaliana.
score: 0.78415697, Nature genetics, 2007, Kim, Sung et. al.

Association of the AFF3 gene and IL2/IL21 gene region with juvenile idiopathic arthritis
score: 0.78351868, Genes and Immunity, 2010, Hinks, A et. al.

Smoking Related Cancers and Loci at Chromosomes 15q25, 5p15, 6p22.1 and 6p21.33 in the Polish Population
score: 0.78315287, PLoS ONE, 2011, Jaworowska, Ewa et. al.

Extended IL10 haplotypes and their association with HIV progression to AIDS.
score: 0.782635, Genes and immunity, 2009, Oleksyk, T K et. al.

Identification and Functional Validation of the Novel Antimalarial Resistance Locus PF10_0355 in Plasmodium falciparum
score: 0.78223797, PLoS Genetics, 2011, Van Tyne, Daria et. al.

Using Canonical Correlation Analysis to Discover Genetic Regulatory Variants
score: 0.7818527, PLoS ONE, 2010, Naylor, Melissa G. et. al.

Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
score: 0.78105412, Movement disorders : official journal of the Movement Disorder Society, 2009, Rakovic, Aleksandar et. al.

Validation of pooled genotyping on the Affymetrix 500 k and SNP6.0 genotyping platforms using the polynomial-based probe-specific correction
score: 0.77772368, BMC Genetics, 2009, Anantharaman, Ramani; Chew, Fook Tim

A high-density single-nucleotide polymorphism screen of 23 candidate genes in attention deficit hyperactivity disorder: suggesting multiple susceptibility genes among Chinese Han population.
score: 0.77772082, Molecular psychiatry, 2009, Guan, L et. al.

Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene-environment study.
score: 0.77677512, Molecular psychiatry, 2010, Brezo, J et. al.

FAM5C Contributes to Aggressive Periodontitis
score: 0.77675106, PLoS ONE, 2010, Carvalho, Flavia M. et. al.

Associations of Six Single Nucleotide Polymorphisms in Obesity-Related Genes With BMI and Risk of Obesity in Chinese Children
score: 0.77436293, Diabetes, 2010, Wu, Lijun et. al.

A model-based approach for analysis of spatial structure in genetic data.
score: 0.77434236, Nature genetics, 2012, Yang, Wen-Yun et. al.

Genetic variations in ATP2B1, CSK, ARSG and CSMD1 loci are related to blood pressure and/or hypertension in two Korean cohorts.
score: 0.77335739, Journal of human hypertension, 2010, Hong, K-W et. al.

Association of genetic polymorphisms with chronic obstructive pulmonary disease in the Chinese Han population: a case–control study
score: 0.77333092, BMC Medical Genomics, 2012, Guo, Yi et. al.

A Genome Wide Survey of SNP Variation Reveals the Genetic Structure of Sheep Breeds
score: 0.77155709, PLoS ONE, 2009, Kijas, James W. et. al.

Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease
score: 0.7712665, The American Journal of Human Genetics, 2012, Soemedi, Rachel et. al.

Detecting rare variant associations: methods for testing haplotypes and multiallelic genotypes.
score: 0.77119558, Genetic epidemiology, 2011, Cantor, Rita M; Wilcox, Marsha

Evaluating outlier loci and their effect on the identification of pedigree errors
score: 0.77103265, BMC Genetics, 2005, Wang, Ke-Sheng; Liu, Michelle; Paterson, Andrew D

Genetics of type 1 diabetes mellitus.
score: 0.77012169, Genes and immunity, 2002, Pociot, F; McDermott, M F

Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 Children
score: 0.76964596, PLoS Medicine, 2011, Kilpeläinen, Tuomas O. et. al.

A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction
score: 0.76846752, PLoS Genetics, 2008, Weiss, Robert B. et. al.

Pathway-Based Analysis of a Melanoma Genome-Wide Association Study: Analysis of Genes Related to Tumour-Immunosuppression
score: 0.76760531, PLoS ONE, 2011, Schoof, Nils et. al.

Association of BANK1 and TNFSF4 with systemic lupus erythematosus in Hong Kong Chinese.
score: 0.76479326, Genes and immunity, 2009, Chang, Y K et. al.

Plasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugs
score: 0.76453266, Nature genetics, 2010, Mu, Jianbing et. al.

Tests for Genetic Interactions in Type 1 Diabetes
score: 0.76365175, Diabetes, 2011, Morahan, Grant et. al.

Revisiting the T-cell receptor alpha/delta locus and possible associations with multiple sclerosis.
score: 0.76350999, Genes and immunity, 2011, Watson, C T et. al.

Correlated genotypes in friendship networks.
score: 0.76237174, Proceedings of the National Academy of Sciences of the United States of America, 2011, Fowler, James H; Settle, Jaime E; Christakis, Nicholas A

A Variant near the Interleukin-6 Gene Is Associated with Fat Mass in Caucasian Men
score: 0.76216214, International journal of obesity (2005), 2010, Andersson, Niklas et. al.

No association of multiple type 2 diabetes loci with type 1 diabetes
score: 0.76213511, Diabetologia, 2009, Raj, S. M. et. al.

Genetic variants and prostate cancer risk: candidate replication and exploration of viral restriction genes.
score: 0.76100215, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, Breyer, Joan P et. al.

Heritability of Cardiovascular and Personality Traits in 6,148 Sardinians
score: 0.75971785, PLoS Genetics, 2006, Pilia, Giuseppe et. al.

Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates
score: 0.75912671, BMC Proceedings, 2011, Faye, Laura L; Bull, Shelley B

Ancestral susceptibility to colorectal cancer.
score: 0.75885285, Mutagenesis, 2012, Huhn, Stefanie et. al.

Genetic variation at the 8q24 locus confers risk to multiple myeloma.
score: 0.75620509, British journal of haematology, 2012, Tewari, Prerna et. al.

NYD-SP18 is associated with obesity in the NHLBI Family Heart Study.
score: 0.75541078, International journal of obesity (2005), 2008, Wilk, J B et. al.

Genetic admixture, social-behavioural factors and body composition are associated with blood pressure differently by racial-ethnic group among children.
score: 0.75505592, Journal of human hypertension, 2012, Klimentidis, Y C et. al.

Global similarity with local differences in linkage disequilibrium between the Dutch and HapMap-CEU populations.
score: 0.75433146, European journal of human genetics : EJHG, 2009, Pardo, Luba et. al.

Genetic architecture of prostate cancer in the Ashkenazi Jewish population
score: 0.75351218, British Journal of Cancer, 2011, Vijai, J et. al.

Epigenetic mechanisms in migraine: a promising avenue?
score: 0.75226851, BMC Medicine, 2013, Eising, Else et. al.

The Identification of Pathway Markers in Intracranial Aneurysm Using Genome-Wide Association Data from Two Different Populations
score: 0.75192884, PLoS ONE, 2013, Bakir-Gungor, Burcu; Sezerman, Osman Ugur

Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G x E) interaction.
score: 0.75188372, International journal of obesity (2005), 2009, Cornes, B K et. al.

A genome-wide CNV association study on panic disorder in a Japanese population.
score: 0.75060619, Journal of human genetics, 2011, Kawamura, Yoshiya et. al.

Loci From a Genome-Wide Analysis of Bilirubin Levels Are Associated With Gallstone Risk and Composition
score: 0.75053104, Gastroenterology, 2010, Buch, Stephan et. al.

Quantitative Genetics in the Era of Molecular Genetics: Learning Abilities and Disabilities as an Example
score: 0.75045685, Journal of the American Academy of Child & Adolescent Psychiatry, 2010, Haworth, Claire M.A.; Plomin, Robert

A functional haplotype implicated in vulnerability to develop cocaine dependence is associated with reduced PDYN expression in human brain.
score: 0.75038548, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Yuferov, Vadim et. al.

Gene expression profiling in monocytes and SNP association suggest the importance of the STAT1 gene for osteoporosis in both Chinese and Caucasians.
score: 0.75031648, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2010, Chen, Xiang-Ding et. al.

Genetic Variants of TSLP and Asthma in an Admixed Urban Population
score: 0.7502532, PLoS ONE, 2011, Liu, Mengling et. al.

Non-synonymous variants in the AMACR gene are associated with schizophrenia
score: 0.75009841, Schizophrenia Research, 2010, Bespalova, Irina N. et. al.

Common obesity-related genetic variants and papillary thyroid cancer risk.
score: 0.74931992, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Kitahara, Cari M et. al.

Univariate/Multivariate Genome-Wide Association Scans Using Data from Families and Unrelated Samples
score: 0.74702652, PLoS ONE, 2009, Zhang, Lei et. al.

Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral density.
score: 0.74556279, Human molecular genetics, 2012, Xiao, Su-Mei et. al.

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
score: 0.74314448, Molecular psychiatry, 2007, Ma, D Q et. al.

Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia
score: 0.74285108, Schizophrenia Research, 2012, Mattheisen, Manuel et. al.

Comparison of multimarker logistic regression models, with application to a genomewide scan of schizophrenia
score: 0.74221224, BMC Genetics, 2010, Wason, James MS; Dudbridge, Frank

Variants in ST8SIA1 do not play a major role in susceptibility to multiple sclerosis in Canadian families
score: 0.74214679, Journal of Neuroimmunology, 2009, Ramagopalan, Sreeram V. et. al.

Dopamine genes and nicotine dependence in treatment-seeking and community smokers.
score: 0.74105817, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Bergen, Andrew W et. al.

Common Variation in the Fat Mass and Obesity-Associated ( FTO ) Gene Confers Risk of Obesity and Modulates BMI in the Chinese Population
score: 0.740952, Diabetes, 2008, Chang, Yi-Cheng et. al.

Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy
score: 0.74056069, PLoS Genetics, 2010, Stark, Klaus et. al.

Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes
score: 0.73994855, Diabetes, 2008, Gaulton, Kyle J. et. al.

An Exploratory Study on CLU, CR1 and PICALM and Parkinson Disease
score: 0.73983696, PLoS ONE, 2011, Gao, Jianjun et. al.

Minor physical anomalies in autism: a meta-analysis.
score: 0.73959507, Molecular psychiatry, 2010, Ozgen, H M; Hop, J W; Hox, J J; Beemer, F A; van Engeland, H

High-Density SNP Mapping of the HLA Region Identifies Multiple Independent Susceptibility Loci Associated with Selective IgA Deficiency
score: 0.73853128, PLoS Genetics, 2012, Ferreira, Ricardo C. et. al.

An Analysis Pipeline for Genome-wide Association Studies
score: 0.73815701, Cancer Informatics, 2008, Stefanov, Stefan; Lautenberger, James; Gold, Bert

Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart disease.
score: 0.73799076, European journal of human genetics : EJHG, 2010, Kangas-Kontio, Tiia et. al.

Fine-mapping and candidate gene investigation within the PARK10 locus.
score: 0.73752403, European journal of human genetics : EJHG, 2009, Haugarvoll, Kristoffer et. al.

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study
score: 0.73720997, Lancet Neurology, 2006, Elbaz, Alexis et. al.

Population structure and genome-wide patterns of variation in Ireland and Britain.
score: 0.73679779, European journal of human genetics : EJHG, 2010, O'Dushlaine, Colm T et. al.

Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms.
score: 0.73602342, Molecular psychiatry, 2005, Butcher, L M et. al.

A −436C>A Polymorphism in the Human FAS Gene Promoter Associated with Severe Childhood Malaria
score: 0.73472082, PLoS Genetics, 2011, Schuldt, Kathrin et. al.

Association of CARD8 with inflammatory bowel disease in Koreans.
score: 0.73420162, Journal of human genetics, 2011, Yang, Suk-Kyun et. al.

Chromosome 15q25 ( CHRNA3-CHRNA5 ) Variation Impacts Indirectly on Lung Cancer Risk
score: 0.7337132, PLoS ONE, 2011, Wang, Yufei et. al.

Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.
score: 0.73341407, Nature genetics, 2011, Shea, Jessica et. al.

Reassessment of the type I diabetes association of the OAS1 locus.
score: 0.73214884, Genes and immunity, 2009, Qu, H-Q et. al.

Genetic Analysis of Cortical Thickness and Fractional Anisotropy of Water Diffusion in the Brain
score: 0.7321284, Frontiers in Neuroscience, 2011, Kochunov, Peter et. al.

Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations.
score: 0.73147325, International journal of obesity (2005), 2013, Yang, T-L et. al.

Recent advances in association studies of osteoarthritis susceptibility genes.
score: 0.73067871, Journal of human genetics, 2010, Dai, Jin; Ikegawa, Shiro

IFITM3 restricts the morbidity and mortality associated with influenza.
score: 0.72901219, Nature, 2012, Everitt, Aaron R et. al.

Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR).
score: 0.72891174, Molecular psychiatry, 2010, Strug, L J et. al.

Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci
score: 0.72744749, Molecular Autism, 2012, Hedges, Dale J et. al.

Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cells.
score: 0.72712893, Journal of immunology (Baltimore, Md. : 1950), 2011, Bezzerri, Valentino et. al.

Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids
score: 0.72498583, The American Journal of Human Genetics, 2012, Ameur, Adam et. al.

Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids
score: 0.72498583, The American Journal of Human Genetics, 2012, Ameur, Adam et. al.

A variant of the myosin light chain kinase gene is associated with severe asthma in African Americans.
score: 0.72485673, Genetic epidemiology, 2007, Flores, Carlos et. al.

Prevalence of Loss-of-Function FTO Mutations in Lean and Obese Individuals
score: 0.72445328, Diabetes, 2009, Meyre, David et. al.

Global variation in copy number in the human genome.
score: 0.72310562, Nature, 2006, Redon, Richard et. al.

Highly interconnected genes in disease-specific networks are enriched for disease-associated polymorphisms
score: 0.72291215, Genome Biology, 2012, Barrenäs, Fredrik et. al.

Understanding cardiovascular disease through the lens of genome-wide association studies
score: 0.7227316, Trends in Genetics, 2009, Arking, Dan E.; Chakravarti, Aravinda

Cleft lip and palate: understanding genetic and environmental influences.
score: 0.72249161, Nature reviews. Genetics, 2011, Dixon, Michael J et. al.

CRY2 Is Associated with Rapid Cycling in Bipolar Disorder Patients
score: 0.72222919, PLoS ONE, 2010, Sjöholm, Louise K. et. al.

The Genetics of Alzheimer Disease: Back to the Future
score: 0.72204544, Neuron, 2010, Bertram, Lars; Lill, Christina M.; Tanzi, Rudolph E.

Association of DISC1 with autism and Asperger syndrome.
score: 0.72124079, Molecular psychiatry, 2008, Kilpinen, H et. al.

Meta-analysis of genetic association studies under heterogeneity.
score: 0.72048075, European journal of human genetics : EJHG, 2012, Neupane, Binod; Loeb, Mark; Anand, Sonia S; Beyene, Joseph

Gene-Based Analysis of Regionally Enriched Cortical Genes in GWAS Data Sets of Cognitive Traits and Psychiatric Disorders
score: 0.7201884, PLoS ONE, 2012, Ersland, Kari M. et. al.

Genome-Wide Association Study SNPs in the Human Genome Diversity Project Populations: Does Selection Affect Unlinked SNPs with Shared Trait Associations?
score: 0.7195968, PLoS Genetics, 2011, Casto, Amanda M.; Feldman, Marcus W.

Mitochondrial Variants in Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
score: 0.71881789, PLoS ONE, 2009, Rollins, Brandi et. al.

Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development
score: 0.71840898, BMC Medical Genetics, 2011, Brisbin, Abra G et. al.

Gene-wide association study between the aromatase gene (CYP19A1) and female pattern hair loss.
score: 0.71802492, The British journal of dermatology, 2009, Yip, L et. al.

Interleukin 3 and schizophrenia: the impact of sex and family history.
score: 0.71780813, Molecular psychiatry, 2007, Chen, X et. al.

Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays.
score: 0.71777867, Cancer research, 2007, Stark, Mitchell; Hayward, Nicholas

Identification of multiple rare variants associated with a disease
score: 0.71728028, BMC Proceedings, 2011, Jung, Jeesun; Dantzer, Jessica; Liu, Yunlong

Polymorphisms in Predicted miRNA Binding Sites and Osteoporosis
score: 0.7170373, Journal of Bone and Mineral Research, 2010, Lei, Shu-Feng; Papasian, Christopher J; Deng, Hong-Wen

The Complement Component 5 Gene and Age-Related Macular Degeneration
score: 0.71644248, Ophthalmology, 2010, Baas, Dominique C. et. al.

The discovery of human genetic variations and their use as disease markers: past, present and future.
score: 0.71637241, Journal of human genetics, 2010, Ku, Chee Seng et. al.

Tracing Sub-Structure in the European American Population with PCA-Informative Markers
score: 0.71522218, PLoS Genetics, 2008, Paschou, Peristera et. al.

CRY2 Is Associated with Depression
score: 0.71497541, PLoS ONE, 2010, Lavebratt, Catharina et. al.

Detecting autozygosity through runs of homozygosity: A comparison of three autozygosity detection algorithms
score: 0.71466704, BMC Genomics, 2011, Howrigan, Daniel P; Simonson, Matthew A; Keller, Matthew C

A Functional Variant in MicroRNA-146a Promoter Modulates Its Expression and Confers Disease Risk for Systemic Lupus Erythematosus
score: 0.71453323, PLoS Genetics, 2011, Luo, Xiaobing et. al.

X Chromosomal Variation Is Associated with Slow Progression to AIDS in HIV-1-Infected Women
score: 0.71402725, The American Journal of Human Genetics, 2009, Siddiqui, Roman A. et. al.

Is Mate Choice in Humans MHC-Dependent?
score: 0.71268145, PLoS Genetics, 2008, Chaix, Raphaëlle; Cao, Chen; Donnelly, Peter

Variants of the RELA Gene are Associated with Schizophrenia and their Startle Responses
score: 0.71238308, Neuropsychopharmacology, 2011, Hashimoto, Ryota et. al.

New findings in the genetics of major psychoses
score: 0.71226153, Dialogues in Clinical Neuroscience, 2010, Nöthen, Markus M

Systematic association analysis of microRNA machinery genes with schizophrenia informs further study
score: 0.71223564, Neuroscience Letters, 2012, Zhang, Fuquan et. al.

Systematic association analysis of microRNA machinery genes with schizophrenia informs further study
score: 0.71223564, Neuroscience Letters, 2012, Zhang, Fuquan et. al.

Systematic Association Analysis of MicroRNA Machinery Genes With Schizophrenia Informs Further Study
score: 0.71223564, Neuroscience Letters, 2012, Zhang, Fuquan et. al.

Systematic association analysis of microRNA machinery genes with schizophrenia informs further study
score: 0.71223564, Neuroscience Letters, 2012, Zhang, Fuquan et. al.

Candidate genes for respiratory disease associated with markers of inflammation and endothelial dysfunction in elderly men
score: 0.71184171, Atherosclerosis, 2009, Wilker, Elissa H. et. al.

Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study
score: 0.7117043, BMC Medical Genetics, 2013, Pechlivanis, Sonali et. al.

Variation at the ANP32A gene is associated with risk of hip osteoarthritis in women.
score: 0.71153673, Arthritis and rheumatism, 2009, Valdes, Ana M et. al.

Genetic Variation in Base Excision Repair Pathway Genes, Pesticide Exposure, and Prostate Cancer Risk
score: 0.71149866, Environmental Health Perspectives, 2011, Barry, Kathryn Hughes et. al.

Differential association of circadian genes with mood disorders: CRY1 and NPAS2 are associated with unipolar major depression and CLOCK and VIP with bipolar disorder.
score: 0.71113815, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2010, Soria, Virginia et. al.

The NEI/NCBI dbGAP database: Genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration
score: 0.71079225, BMC Medical Genetics, 2008, Zhang, Hong et. al.

LINGO1 gene analysis in Parkinson's disease phenotypes.
score: 0.71040913, Movement disorders : official journal of the Movement Disorder Society, 2011, Lorenzo-Betancor, Oswaldo et. al.

What is complex about complex disorders?
score: 0.70960693, Genome Biology, 2012, Mitchell, Kevin J

Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk
score: 0.70932261, British Journal of Cancer, 2011, Stevens, K N et. al.

Identity by descent and association analysis of dichotomous traits based on large pedigrees
score: 0.70925419, BMC Proceedings, 2011, Liu, Tian; Thalamuthu, Anbupalam

Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility
score: 0.70821226, PLoS ONE, 2010, Zeller, Tanja et. al.

Assessment of the functionality of genome-wide canine SNP arrays and implications for canine disease association studies.
score: 0.70813994, Animal genetics, 2010, Ke, X et. al.

Coding Variant I62V in the Complement Factor H Gene Is Strongly Associated with Polypoidal Choroidal Vasculopathy
score: 0.70777424, Ophthalmology, 2009, Kondo, Naoshi; Honda, Shigeru; Kuno, Shin-ichi; Negi, Akira

Human Liver Methionine Cycle: MAT1A and GNMT Gene Resequencing, Functional Genomics, and Hepatic Genotype-Phenotype Correlation.
score: 0.70740301, Drug metabolism and disposition: the biological fate of chemicals, 2012, Ji, Yuan et. al.

Comprehensive analysis of CRP, CFH Y402H and environmental risk factors on risk of neovascular age-related macular degeneration
score: 0.70668894, Molecular Vision, 2008, Kim, Ivana K. et. al.

Systematic Analysis of Circadian Genes in a Population-Based Sample Reveals Association of TIMELESS with Depression and Sleep Disturbance
score: 0.70601333, PLoS ONE, 2010, Utge, Siddheshwar J. et. al.

Gender-specific association of TSNAX/DISC1 locus for schizophrenia and bipolar affective disorder in South Indian population.
score: 0.70599972, Journal of human genetics, 2012, Ram Murthy, Anjanappa et. al.

Genetic architecture of prostate cancer in the Ashkenazi Jewish population.
score: 0.70547277, British journal of cancer, 2011, Vijai, J et. al.

SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population
score: 0.70531607, Parkinsonism & Related Disorders, 2012, Trotta, Luca et. al.

Association of ERAP1, but not IL23R, with ankylosing spondylitis in a Han Chinese population.
score: 0.70529472, Arthritis and rheumatism, 2009, Davidson, Stuart I et. al.

An Immune Response Network Associated with Blood Lipid Levels
score: 0.70528095, PLoS Genetics, 2010, Inouye, Michael et. al.

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
score: 0.7051846, PLoS Genetics, 2012, Leblond, Claire S. et. al.

Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci
score: 0.70506086, BMC Proceedings, 2007, Cordell, Heather J et. al.

Gene mapping study for constitutive skin color in an isolated Mongolian population
score: 0.70502616, Experimental & Molecular Medicine, 2011, Paik, Seung Hwan et. al.

A Powerful Test of Parent-of-Origin Effects for Quantitative Traits Using Haplotypes
score: 0.70469844, PLoS ONE, 2011, Feng, Rui et. al.

A case-control study of rheumatoid arthritis identifies an associated single nucleotide polymorphism in the NCF4 gene, supporting a role for the NADPH-oxidase complex in autoimmunity
score: 0.70469619, Arthritis Research & Therapy, 2007, Olsson, Lina M et. al.

Genetic Variations in Plasma Circulating DNA of HBV-Related Hepatocellular Carcinoma Patients Predict Recurrence after Liver Transplantation
score: 0.70451597, PLoS ONE, 2011, Hu, Jie et. al.

Association of single-nucleotide polymorphisms in CCR6, TAGAP, and TNFAIP3 with rheumatoid arthritis in African Americans.
score: 0.70389983, Arthritis and rheumatism, 2012, Perkins, Elizabeth A et. al.

Genetic Heterogeneity in Latent Autoimmune Diabetes Is Linked to Various Degrees of Autoimmune Activity
score: 0.70378357, Diabetes, 2009, Pettersen, Elin et. al.

Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort
score: 0.7027483, BMC Medical Genetics, 2010, Ernst, Florian D et. al.

Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth
score: 0.70183624, BMC Medical Genomics, 2010, Plunkett, Jevon et. al.

Imaging the genetics of brain structure and function
score: 0.70120585, Biological Psychology, 2008, de Geus, Eco et. al.

Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios
score: 0.70118292, The American Journal of Human Genetics, 2005, Fallin, M. Daniele et. al.

Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease
score: 0.70095349, PLoS ONE, 2010, Jones, Lesley et. al.

Application of Genome-Wide Single Nucleotide Polymorphism Typing: Simple Association and Beyond
score: 0.70062374, PLoS Genetics, 2006, Gibbs, J. Raphael; Singleton, Andrew

Association of HPC2/ELAC2 and RNASEL non-synonymous variants with prostate cancer risk in African American familial and sporadic cases.
score: 0.7000456, The Prostate, 2008, Robbins, Christiane M et. al.

Pharmacogenetic interactions and their potential effects on genetic analyses of blood pressure.
score: 0.69956708, Statistics in medicine, 2011, Masca, Nicholas; Sheehan, Nuala A; Tobin, Martin D

Individual and Cumulative Effects of GWAS Susceptibility Loci in Lung Cancer: Associations after Sub-Phenotyping for COPD
score: 0.6989431, PLoS ONE, 2011, Young, Robert P. et. al.

Remapping the type I diabetes association of the CTLA4 locus.
score: 0.69789815, Genes and immunity, 2009, Qu, H-Q et. al.

Copy Number Variation in Schizophrenia in the Japanese Population
score: 0.69763226, Biological Psychiatry, 2010, Ikeda, Masashi et. al.

Mutational Characterization of the Bile Acid Receptor TGR5 in Primary Sclerosing Cholangitis
score: 0.69685237, PLoS ONE, 2010, Hov, Johannes R. et. al.

Variants of the RELA gene are associated with schizophrenia and their startle responses.
score: 0.69632502, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Hashimoto, Ryota et. al.

Linkage disequilibrium across two different single-nucleotide polymorphism genome scans
score: 0.69493367, BMC Genetics, 2005, Peralta, Juan Manuel et. al.

Association of single-nucleotide polymorphisms in the suppressor of cytokine signaling 2 ( SOCS2) gene with type 2 diabetes in the Japanese
score: 0.69377718, Genomics, 2006, Kato, Hitoshi et. al.

A Genomewide Scan Identifies Two Novel Loci Involved in Specific Language Impairment * * Members of the consortium are listed in the Appendix.
score: 0.69362928, The American Journal of Human Genetics, 2002, Consortium, The SLI

Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
score: 0.69317649, PLoS Genetics, 2007, Estivill, Xavier; Armengol, Lluís

Association of Variants of the Interleukin-23 Receptor Gene With Susceptibility to Pediatric Crohn’s Disease
score: 0.69254615, Clinical Gastroenterology and Hepatology, 2007, Baldassano, Robert N. et. al.

Challenges in reproducibility of genetic association studies: lessons learned from the obesity field.
score: 0.69223917, International journal of obesity (2005), 2012, Li, A; Meyre, D

The role of genetic variation in the causation of mental illness: an evolution-informed framework.
score: 0.69217704, Molecular psychiatry, 2009, Uher, R

Identity-by-Descent-Based Phasing and Imputation in Founder Populations Using Graphical Models
score: 0.6916964, Genetic Epidemiology, 2011, Palin, Kimmo et. al.

Estimation of absolute risk for prostate cancer using genetic markers and family history.
score: 0.69168021, The Prostate, 2009, Xu, Jianfeng et. al.

Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families.
score: 0.69152594, Molecular psychiatry, 2008, Wedenoja, J et. al.

Investigation of 15 of the top candidate genes for late-onset Alzheimer’s disease
score: 0.69125454, Human Genetics, 2010, Belbin, Olivia et. al.

Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites.
score: 0.69065932, Molecular psychiatry, 2012, Brouwers, N et. al.

Studies of a genetic variant in HK1 in relation to quantitative metabolic traits and to the prevalence of type 2 diabetes
score: 0.69065468, BMC Medical Genetics, 2011, Gjesing, Anette P et. al.

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries.
score: 0.69008928, Nature genetics, 2010, Park, Ju-Hyun et. al.

Association of the rs738409 polymorphism in PNPLA3 with liver damage and the development of nonalcoholic fatty liver disease
score: 0.68989608, BMC Medical Genetics, 2010, Hotta, Kikuko et. al.

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
score: 0.68915746, PLoS Genetics, 2009, Howie, Bryan N.; Donnelly, Peter; Marchini, Jonathan

Variation in the ICAM1 gene is not associated with severe malaria phenotypes.
score: 0.68879305, Genes and immunity, 2008, Fry, A E et. al.

Urinary albumin excretion in families with type 2 diabetes is heritable and genetically correlated to blood pressure.
score: 0.68841351, Kidney international, 2000, Fogarty, D G et. al.

The PTPN22 Locus and Rheumatoid Arthritis: No Evidence for an Effect on Risk Independent of Arg620Trp
score: 0.68798739, PLoS ONE, 2010, Wan Taib, Wan R. et. al.

A Permutation Procedure to Correct for Confounders in Case-Control Studies, Including Tests of Rare Variation
score: 0.68737206, The American Journal of Human Genetics, 2012, Epstein, Michael P. et. al.

A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans.
score: 0.68731828, Nature genetics, 2002, Prokunina, Ludmila et. al.

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
score: 0.68720766, Nature, 2011, Bertolotto, Corine et. al.

Prostate cancer risk variants are not associated with disease progression.
score: 0.68678972, The Prostate, 2012, Szulkin, Robert et. al.

Ancestral Components of Admixed Genomes in a Mexican Cohort
score: 0.68660324, PLoS Genetics, 2011, Johnson, Nicholas A. et. al.

Genetics of migraine in the age of genome-wide association studies
score: 0.68640529, The Journal of Headache and Pain, 2011, Schürks, Markus

Bibliography of the current world literature
score: 0.68594909, Current Opinion in Genetics & Development, 1993,

Effect of sample stratification on dairy GWAS results
score: 0.68575631, BMC Genomics, 2012, Ma, Li et. al.

Genetic, personality, and environmental predictors of drug use in adolescents
score: 0.68425673, Journal of Substance Abuse Treatment, 2010, Conner, Bradley T. et. al.

CYP1B1 variants are associated with prostate cancer in non-Hispanic and Hispanic Caucasians
score: 0.68366557, Carcinogenesis, 2008, Beuten, Joke et. al.

Gene set analysis of survival following ovarian cancer implicates macrolide binding and intracellular signaling genes.
score: 0.68300165, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Fridley, Brooke L et. al.

Discovering the hidden sub-network component in a ranked list of genes or proteins derived from genomic experiments
score: 0.68233699, Nucleic Acids Research, 2012, García-Alonso, Luz et. al.

Discovering the hidden sub-network component in a ranked list of genes or proteins derived from genomic experiments.
score: 0.68233699, Nucleic acids research, 2012, García-Alonso, Luz et. al.

Genetic investigation of DNA-repair pathway genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1 in sporadic colon cancer.
score: 0.68214347, International journal of cancer. Journal international du cancer, 2007, Schafmayer, Clemens et. al.

A study of prostaglandin pathway genes and interactions with current nonsteroidal anti-inflammatory drug use in colorectal adenoma.
score: 0.68183776, Cancer prevention research (Philadelphia, Pa.), 2012, Edwards, Todd L et. al.

Association between dopamine beta hydroxylase rs5320 polymorphism and smoking behaviour in elderly Japanese.
score: 0.68152417, Journal of human genetics, 2012, Ella, Elakeche et. al.

Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record
score: 0.68126543, BMC Cardiovascular Disorders, 2011, Ding, Keyue; Bailey, Kent R; Kullo, Iftikhar J

Evidence for two independent associations with type 1 diabetes at the 12q13 locus
score: 0.68121291, Genes and Immunity, 2011, Keene, Keith L. et. al.

Analysis of heterogeneity and epistasis in physiological mixed populations by combined structural equation modelling and latent class analysis
score: 0.68081601, BMC Genetics, 2008, Fenger, Mogens et. al.

cn.FARMS: a latent variable model to detect copy number variations in microarray data with a low false discovery rate
score: 0.67963051, Nucleic Acids Research, 2011, Clevert, Djork-Arné et. al.

Genetic Variants in Major Histocompatibility Complex-Linked Genes Associate With Pediatric Liver Transplant Rejection
score: 0.67884161, Gastroenterology, 2008, Sindhi, Rakesh et. al.

Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative.
score: 0.67819226, Genetic epidemiology, 2012, Liu, Eric Yi et. al.

Common Variants in the Adiponectin Gene ( ADIPOQ ) Associated With Plasma Adiponectin Levels, Type 2 Diabetes, and Diabetes-Related Quantitative Traits
score: 0.67794753, Diabetes, 2008, Hivert, Marie-France et. al.

Copy Number Variation in Familial Parkinson Disease
score: 0.67762126, PLoS ONE, 2011, Pankratz, Nathan et. al.

The Genetic Analysis Workshop 16 Problem 3: simulation of heritable longitudinal cardiovascular phenotypes based on actual genome-wide single-nucleotide polymorphisms in the Framingham Heart Study
score: 0.67760772, BMC Proceedings, 2009, Kraja, Aldi T et. al.

Evaluation of Toll-like receptor and adaptor molecule polymorphisms for susceptibility to tuberculosis in a Colombian population.
score: 0.67731836, International journal of immunogenetics, 2012, Sánchez, D; Lefebvre, C; Rioux, J; García, L F; Barrera, L F

Glycine and a glycine dehydrogenase (GLDC) SNP as citalopram/escitalopram response biomarkers in depression: pharmacometabolomics-informed pharmacogenomics.
score: 0.67693128, Clinical pharmacology and therapeutics, 2011, Ji, Y et. al.

Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.
score: 0.67692632, Genetic epidemiology, 2010, Locke, Adam E et. al.

Estimating human mutation rate using autozygosity in a founder population
score: 0.67604199, Nature genetics, 2012, Campbell, Catarina D. et. al.

The landscape of recombination in African Americans.
score: 0.67592293, Nature, 2011, Hinch, Anjali G et. al.

A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1
score: 0.67559463, The American Journal of Human Genetics, 2010, Morange, Pierre-Emmanuel et. al.

Genome-wide analysis of haplotype interaction for the data from the North American Rheumatoid Arthritis Consortium
score: 0.67553901, BMC Proceedings, 2009, Park, Jungsun; Namkung, Junghyun; Jhun, Mina; Park, Taesung

Reconciling the analysis of IBD and IBS in complex trait studies.
score: 0.67442149, Nature reviews. Genetics, 2010, Powell, Joseph E; Visscher, Peter M; Goddard, Michael E

Human genetic variations: Beacons on the pathways to successful ageing
score: 0.67342027, Mechanisms of Ageing and Development, 2009, Cluett, Christie; Melzer, David

A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer.
score: 0.6727869, The Journal of investigative dermatology, 2012, Wheless, Lee et. al.

Single and multigenic analysis of the association between variants in 12 steroid hormone metabolism genes and risk of prostate cancer.
score: 0.67102078, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, Beuten, Joke et. al.

Footprints of genetic susceptibility to pulmonary tuberculosis: Cytokine gene variants in north Indians
score: 0.67023909, The Indian Journal of Medical Research, 2012, Abhimanyu, ; Bose, Mridula; Jha, Pankaj

Role of genetic variants in the CHRNA5-CHRNA3-CHRNB4 cluster in nicotine dependence risk: importance of gene-environment interplay.
score: 0.66899145, Molecular psychiatry, 2009, Greenbaum, L; Rigbi, A; Teltsh, O; Lerer, B

No association between TNFSF15 and IL23R with ulcerative colitis in Koreans.
score: 0.66891411, Journal of human genetics, 2011, Yang, Suk-Kyun et. al.

Large-scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand.
score: 0.66882749, Arthritis and rheumatism, 2009, Evangelou, Evangelos et. al.

Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase.
score: 0.66840953, Proceedings of the National Academy of Sciences of the United States of America, 2012, Jacob, Chaim O et. al.

Population differences in SLE susceptibility genes: STAT4 and BLK, but not PXK, are associated with systemic lupus erythematosus in Hong Kong Chinese.
score: 0.66824687, Genes and immunity, 2009, Yang, W et. al.

Replicated genetic evidence supports a role for HOMER2 in schizophrenia
score: 0.66704252, Neuroscience Letters, 2010, Gilks, William P. et. al.

Genetic variants in vitamin D metabolism-related genes and body mass index: analysis of genome-wide scan data of approximately 7000 Chinese women.
score: 0.66680144, International journal of obesity (2005), 2012, Dorjgochoo, T et. al.

A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.
score: 0.66679183, Molecular psychiatry, 2008, Asherson, P et. al.

BOOST: A Fast Approach to Detecting Gene-Gene Interactions in Genome-wide Case-Control Studies
score: 0.66672024, The American Journal of Human Genetics, 2010, Wan, Xiang et. al.

A Multi-SNP Locus-Association Method Reveals a Substantial Fraction of the Missing Heritability
score: 0.66619377, The American Journal of Human Genetics, 2012, Ehret, Georg B. et. al.

Association of the 15q25 and 5p15 lung cancer susceptibility regions with gene expression in lung tumor tissue.
score: 0.66616513, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Fehringer, Gord et. al.

PRKCA: A Positional Candidate Gene for Body Mass Index and Asthma
score: 0.66612918, The American Journal of Human Genetics, 2009, Murphy, Amy et. al.

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)
score: 0.66597845, British Journal of Cancer, 2009, Osorio, A et. al.

Assessment of hepatocyte growth factor in ovarian cancer mortality.
score: 0.66497226, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Goode, Ellen L et. al.

Geographic differences in allele frequencies of susceptibility SNPs for cardiovascular disease
score: 0.66469636, BMC Medical Genetics, 2011, Ding, Keyue; Kullo, Iftikhar J

Family-based association tests using genotype data with uncertainty.
score: 0.6640112, Biostatistics (Oxford, England), 2012, Yu, Zhaoxia

Admixture Mapping Provides Evidence of Association of the VNN1 Gene with Hypertension
score: 0.66390661, PLoS ONE, 2007, Zhu, Xiaofeng; Cooper, Richard S.

Nicotinic acetylcholine receptor β2 subunit gene implicated in a systems-based candidate gene study of smoking cessation
score: 0.66262125, Human Molecular Genetics, 2008, Conti, David V. et. al.

Common variants in FOXP1 are associated with generalized vitiligo
score: 0.66259677, Nature genetics, 2010, Jin, Ying et. al.

Principal-component-based population structure adjustment in the North American Rheumatoid Arthritis Consortium data: impact of single-nucleotide polymorphism set and analysis method
score: 0.6616916, BMC Proceedings, 2009, Peloso, Gina M; Timofeev, Nadia; Lunetta, Kathryn L

Metabolic and genetic predictors of circulating adipocyte fatty acid-binding protein.
score: 0.66128533, International journal of obesity (2005), 2012, Tönjes, A et. al.

SNPexp - A web tool for calculating and visualizing correlation between HapMap genotypes and gene expression levels
score: 0.66060086, BMC Bioinformatics, 2010, Holm, Kristian; Melum, Espen; Franke, Andre; Karlsen, Tom H

Elastic-net regularization approaches for genome-wide association studies of rheumatoid arthritis
score: 0.65989783, BMC Proceedings, 2009, Cho, Seoae et. al.

Identification of Type 1 Diabetes–Associated DNA Methylation Variable Positions That Precede Disease Diagnosis
score: 0.65978743, PLoS Genetics, 2011, Rakyan, Vardhman K. et. al.

Adiponectin and resistin gene polymorphisms in association with their respective adipokine levels.
score: 0.6597039, Annals of human genetics, 2011, Lau, Cia-Hin; Muniandy, Sekaran

The PLIN4 Variant rs8887 Modulates Obesity Related Phenotypes in Humans through Creation of a Novel miR-522 Seed Site
score: 0.65925635, PLoS ONE, 2011, Richardson, Kris et. al.

Meta-analysis of genome-wide linkage studies across autoimmune diseases.
score: 0.65920409, European journal of human genetics : EJHG, 2009, Forabosco, Paola et. al.

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
score: 0.65885592, Molecular Psychiatry, 2009, Elia, J et. al.

BR-squared: a practical solution to the winner’s curse in genome-wide scans
score: 0.65857167, Human Genetics, 2011, Sun, Lei et. al.

Evidence for two independent prostate cancer risk-associated loci in the HNF1B gene at 17q12.
score: 0.65854735, Nature genetics, 2008, Sun, Jielin et. al.

Quantitative trait loci, genes, and polymorphisms that regulate bone mineral density in mouse
score: 0.65820792, Genomics, 2009, Xiong, Qing et. al.

SparSNP: Fast and memory-efficient analysis of all SNPs for phenotype prediction
score: 0.65727325, BMC Bioinformatics, 2012, Abraham, Gad et. al.

Synopsis and meta-analysis of genetic association studies in osteoporosis for the focal adhesion family genes: the CUMAGAS-OSTEOporosis information system
score: 0.65704285, BMC Medicine, 2011, Zintzaras, Elias et. al.

Different WDR36 mutation pattern in Chinese patients with primary open-angle glaucoma
score: 0.65593927, Molecular Vision, 2009, Fan, Bao Jian et. al.

R-Gada: a fast and flexible pipeline for copy number analysis in association studies
score: 0.65545339, BMC Bioinformatics, 2010, Pique-Regi, Roger; Cáceres, Alejandro; González, Juan R

A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals.
score: 0.65519217, Journal of human genetics, 2011, Teo, Shu-Mei et. al.

A high-density SNP genome-wide linkage scan in a large autism extended pedigree.
score: 0.65434593, Molecular psychiatry, 2009, Allen-Brady, K et. al.

A Major Histocompatibility Class I Locus Contributes to Multiple Sclerosis Susceptibility Independently from HLA-DRB1*15:01
score: 0.65429893, PLoS ONE, 2010, Cree, Bruce A. C. et. al.

Pharmacogenetics in psychiatry: translating research into clinical practice.
score: 0.65204355, Molecular psychiatry, 2012, Malhotra, A K; Zhang, J-P; Lencz, T

Saliva-derived DNA performs well in large-scale, high-density single-nucleotide polymorphism microarray studies.
score: 0.65128267, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Bahlo, Melanie et. al.

Analysis of North American Rheumatoid Arthritis Consortium data using a penalized logistic regression approach
score: 0.65108278, BMC Proceedings, 2009, Croiseau, Pascal; Cordell, Heather J

Willows: a memory efficient tree and forest construction package
score: 0.6501891, BMC Bioinformatics, 2009, Zhang, Heping; Wang, Minghui; Chen, Xiang

Whole-genome amplification enables accurate genotyping for microarray-based high-density single nucleotide polymorphism array.
score: 0.64917577, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2008, Jasmine, Farzana et. al.

Designing pharmacogenetic projects in industry: practical design perspectives from the Industry Pharmacogenomics Working Group.
score: 0.64732491, The pharmacogenomics journal, 2009, Bromley, C M et. al.

SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population.
score: 0.64677921, Journal of human genetics, 2011, Kim, Jong-Min et. al.

Association Analysis in African Americans of European-Derived Type 2 Diabetes Single Nucleotide Polymorphisms From Whole-Genome Association Studies
score: 0.64595967, Diabetes, 2008, Lewis, Joshua P. et. al.

The ANO3/MUC15 locus is associated with eczema in families ascertained through asthma
score: 0.64456624, The Journal of Allergy and Clinical Immunology, 2012, Dizier, Marie-Hélène et. al.

A Genome-Wide Gene Expression Signature of Environmental Geography in Leukocytes of Moroccan Amazighs
score: 0.64423225, PLoS Genetics, 2008, Idaghdour, Youssef et. al.

Pathway-based analysis using reduced gene subsets in genome-wide association studies
score: 0.64358229, BMC Bioinformatics, 2011, Zhao, Jingyuan et. al.

Single nucleotide polymorphisms (SNPs) involved in insulin resistance, weight regulation, lipid metabolism and inflammation in relation to metabolic syndrome: an epidemiological study
score: 0.64315753, Cardiovascular Diabetology, 2012, Povel, Cécile M et. al.

Identification of improved IL28B SNPs and haplotypes for prediction of drug response in treatment of hepatitis C using massively parallel sequencing in a cross-sectional European cohort
score: 0.64239418, Genome Medicine, 2011, Smith, Katherine R et. al.

Involvement of the atrial natriuretic peptide transcription factor GATA4 in alcohol dependence, relapse risk and treatment response to acamprosate.
score: 0.64224534, The pharmacogenomics journal, 2011, Kiefer, F et. al.

Identification of correlated genetic variants jointly associated with rheumatoid arthritis using ridge regression
score: 0.64160054, BMC Proceedings, 2009, Sun, Yan V et. al.

Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives
score: 0.64117767, BMC Proceedings, 2011, Akula, Nirmala et. al.

Fine Mapping of Genetic Variants in BIN1 , CLU , CR1 and PICALM for Association with Cerebrospinal Fluid Biomarkers for Alzheimer's Disease
score: 0.64034618, PLoS ONE, 2011, Kauwe, John S. K. et. al.

Multiple Loci within the Major Histocompatibility Complex Confer Risk of Psoriasis
score: 0.64018951, PLoS Genetics, 2009, Feng, Bing-Jian et. al.

Consent for genetic research in the Framingham Heart Study.
score: 0.64016437, American journal of medical genetics. Part A, 2010, Levy, Daniel et. al.

SRD5A2 is associated with increased cortisol metabolism in schizophrenia spectrum disorders
score: 0.63909867, Progress in Neuropsychopharmacology & Biological Psychiatry, 2010, Steen, Nils Eiel et. al.

Associations of insulin-like growth factor binding protein-3 gene polymorphisms with IGF-I activity and lipid parameters in adolescents.
score: 0.63796289, International journal of obesity (2005), 2009, Mong, J L Y et. al.

Genome-wide association analysis of rheumatoid arthritis data via haplotype sharing
score: 0.63738901, BMC Proceedings, 2009, Allen, Andrew S; Satten, Glen A

High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene.
score: 0.63684695, Molecular psychiatry, 2010, Strom, S P et. al.

Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma.
score: 0.6367992, Nature genetics, 2012, Guichard, Cécile et. al.

Common variants in P2RY11 are associated with narcolepsy
score: 0.63671962, Nature genetics, 2010, Kornum, Birgitte R et. al.

Association of CFH , LOC387715 , and HTRA1 polymorphisms with exudative age-related macular degeneration in a northern Chinese population
score: 0.63618735, Molecular Vision, 2008, Xu, Yule et. al.

Future Use of Genomics in Coronary Artery Disease
score: 0.63605006, Journal of the American College of Cardiology, 2007, Damani, Samir B.; Topol, Eric J.

Association study of genetic polymorphism in ABCC4 with cyclophosphamide-induced adverse drug reactions in breast cancer patients.
score: 0.63569725, Journal of human genetics, 2009, Low, Siew-Kee et. al.

Replication of Putative Susceptibility Loci from Genome-Wide Association Studies Associated with Coronary Atherosclerosis in Chinese Han Population
score: 0.63551203, PLoS ONE, 2011, Xie, Fang et. al.

Genomic determinants of the efficiency of internal ribosomal entry sites of viral and cellular origin
score: 0.63443514, Nucleic Acids Research, 2008, Kazadi, Kayole et. al.

Association between the SERPING1 Gene and Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy in Japanese
score: 0.63441676, PLoS ONE, 2011, Nakata, Isao et. al.

Development and Characterization of a High Density SNP Genotyping Assay for Cattle
score: 0.63336253, PLoS ONE, 2009, Matukumalli, Lakshmi K. et. al.

Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis.
score: 0.63290174, Genes and immunity, 2005, Zhang, Z et. al.

Neurobeachin, a Regulator of Synaptic Protein Targeting, Is Associated with Body Fat Mass and Feeding Behavior in Mice and Body-Mass Index in Humans
score: 0.63241225, PLoS Genetics, 2012, Olszewski, Pawel K. et. al.

Comparison of two-phase analyses for case-control genetic association studies.
score: 0.63210855, Statistics in medicine, 2008, Zheng, Gang; Meyer, Mark; Li, Wentian; Yang, Yaning

Genome-wide analysis of extended pedigrees confirms IL2-IL21 linkage and shows additional regions of interest potentially influencing coeliac disease risk.
score: 0.6295389, Tissue antigens, 2011, Einarsdottir, E et. al.

FTO variant rs9939609 is associated with body mass index and waist circumference, but not with energy intake or physical activity in European- and African-American youth
score: 0.62887091, BMC Medical Genetics, 2010, Liu, Gaifen et. al.

A pathway-based association analysis model using common and rare variants
score: 0.62829241, BMC Proceedings, 2011, Cheng, Lu et. al.

Stroke genetics: prospects for personalized medicine
score: 0.62823227, BMC Medicine, 2012, Markus, Hugh S

Impact of cytokine and cytokine receptor gene polymorphisms on cellular immunity after smallpox vaccination
score: 0.62756558, Gene, 2012, Ovsyannikova, Inna G. et. al.

An African Ancestry-Specific Allele of CTLA4 Confers Protection against Rheumatoid Arthritis in African Americans
score: 0.62732158, PLoS Genetics, 2009, Kelley, James M. et. al.

The CHRNA5-A3-B4 gene cluster in nicotine addiction.
score: 0.62711668, Molecular psychiatry, 2012, Berrettini, W H; Doyle, G A

Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms.
score: 0.62669719, Molecular psychiatry, 2009, Holmans, P A et. al.

Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels
score: 0.62637313, Human Genomics, 2004, Hinds, David A et. al.

Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey – A Meta-Analysis of Three Independent Studies
score: 0.62624166, PLoS ONE, 2012, Hernesniemi, Jussi A. et. al.

From monogenic to polygenic obesity: recent advances
score: 0.62577428, European Child & Adolescent Psychiatry, 2010, Hinney, Anke; Vogel, Carla I. G.; Hebebrand, Johannes

A common coding variant in CASP8 is associated with breast cancer risk.
score: 0.6243356, Nature genetics, 2007, Cox, Angela et. al.

Association of candidate genes with antisocial drug dependence in adolescents
score: 0.62371645, Drug and Alcohol Dependence, 2008, Corley, Robin P. et. al.

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
score: 0.62350514, Molecular psychiatry, 2010, Elia, J et. al.

Crohn's Disease Loci Are Common Targets of Protozoa-Driven Selection.
score: 0.62309536, Molecular biology and evolution, 2013, Cagliani, Rachele et. al.

Detectable clonal mosaicism and its relationship to aging and cancer.
score: 0.62293227, Nature genetics, 2012, Jacobs, Kevin B et. al.

Visualization of Shared Genomic Regions and Meiotic Recombination in High-Density SNP Data
score: 0.62282541, PLoS ONE, 2009, Roberson, Elisha D. O.; Pevsner, Jonathan

STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis -acting influences on gene expression
score: 0.62271393, BMC Medical Genetics, 2009, Cunnington, Michael S et. al.

Myocilin polymorphisms and high myopia in subjects of European origin
score: 0.62262023, Molecular Vision, 2009, Zayats, Tetyana et. al.

Resampling procedures to identify important SNPs using a consensus approach
score: 0.62259196, BMC Proceedings, 2011, Pardy, Christopher; Motyer, Allan; Wilson, Susan

Predicting genetic predisposition in humans: the promise of whole-genome markers.
score: 0.62242468, Nature reviews. Genetics, 2010, de los Campos, Gustavo; Gianola, Daniel; Allison, David B

Spontaneous preterm birth in African Americans is associated with infection and inflammatory response gene variants
score: 0.62206247, American Journal of Obstetrics and Gynecology, 2009, Velez, Digna R. et. al.

A High-Density Screen for Linkage in Multiple Sclerosis
score: 0.62101857, The American Journal of Human Genetics, 2005,

A genome wide association study between copy number variation (CNV) and human height in Chinese population
score: 0.62089666, Journal of Genetics and Genomics, 2010, Li, Xi et. al.

Current genetic methodologies in the identification of disaster victims and in forensic analysis
score: 0.61829355, Journal of Applied Genetics, 2011, Ziętkiewicz, Ewa et. al.

Estrogen receptor 1 gene (ESR1) is associated with restrictive anorexia nervosa.
score: 0.61770753, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2010, Versini, Audrey et. al.

Genetic variations and heterosexual HIV-1 infection: analysis of clustered genes encoding CC-motif chemokine ligands.
score: 0.6174288, Genes and immunity, 2012, Hu, L et. al.

Linkage analysis using principal components of gene expression data
score: 0.61613362, BMC Proceedings, 2007, Atkinson, Elizabeth J et. al.

Genetic analysis of typical wet-type age-related macular degeneration and polypoidal choroidal vasculopathy in Japanese population
score: 0.61533151, Journal of Ocular Biology, Diseases, and Informatics, 2009, Goto, Asako et. al.

A genome-wide study of preferential amplification/hybridization in microarray-based pooled DNA experiments
score: 0.61507389, Nucleic Acids Research, 2006, Yang, H.-C. et. al.

The ubiquitin ligase adaptor Ndfip1 regulates T cell-mediated gastrointestinal inflammation and inflammatory bowel disease susceptibility.
score: 0.61504878, Mucosal immunology, 2011, Ramon, H E et. al.

Pharmacogenetics of antipsychotic-induced weight gain: review and clinical implications.
score: 0.61448363, Molecular psychiatry, 2012, Lett, T A P et. al.

Asthma and genes encoding components of the vitamin D pathway
score: 0.61440537, Respiratory Research, 2009, Bossé, Yohan et. al.

Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.
score: 0.614271, Cancer research, 2011, Rafnar, Thorunn et. al.

Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 Regions Identifies Functional and Histology-Specific Lung Cancer Susceptibility Loci in African-Americans.
score: 0.61367305, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2013, Walsh, Kyle M et. al.

Simple strategies for haplotype analysis of the X chromosome with application to age-related macular degeneration.
score: 0.61331445, European journal of human genetics : EJHG, 2011, Jiang, Renfang et. al.

Whole-genome association mapping of gene expression in the human prefrontal cortex.
score: 0.61166389, Molecular psychiatry, 2010, Liu, C et. al.

Genomic Regions Identified by Overlapping Clusters of Nominally-Positive SNPs from Genome-Wide Studies of Alcohol and Illegal Substance Dependence
score: 0.6107687, PLoS ONE, 2011, Johnson, Catherine et. al.

Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG.
score: 0.61066624, The Prostate, 2012, Lu, Lingyi et. al.

Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism.
score: 0.61016234, Molecular psychiatry, 2006, Baghai, T C et. al.

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls
score: 0.60942756, Human Molecular Genetics, 2011, Soemedi, Rachel et. al.

Analysis of detailed phenotype profiles reveals CHRNA5-CHRNA3-CHRNB4 gene cluster association with several nicotine dependence traits.
score: 0.6090178, Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco, 2012, Broms, Ulla et. al.

Replication of neuroblastoma SNP association at the BARD1 locus in African-Americans.
score: 0.60886758, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Latorre, Valeria et. al.

Study of eight GWAS-identified common variants for association with obesity-related indices in Chinese children at puberty.
score: 0.60764944, International journal of obesity (2005), 2012, Wang, J et. al.

Analysis of the contribution of FTO , NPC1, ENPP1, NEGR1, GNPDA2 and MC4R genes to obesity in Mexican children
score: 0.60760253, BMC Medical Genetics, 2013, Mejía-Benítez, Aurora et. al.

Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis.
score: 0.60682933, European journal of human genetics : EJHG, 2012, Moskvina, Valentina et. al.

Local Ancestry Corrects for Population Structure in Saccharomyces cerevisiae Genome-Wide Association Studies.
score: 0.60561205, Genetics, 2012, Diao, Liyang; Chen, Kevin C

Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort.
score: 0.60548245, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, Middeldorp, Anneke et. al.

MEIS1 and BTBD9 : genetic association with restless leg syndrome in end stage renal disease
score: 0.60403661, Journal of Medical Genetics, 2011, Schormair, Barbara et. al.

Frequent Loss of Genome Gap Region in 4p16.3 Subtelomere in Early-Onset Type 2 Diabetes Mellitus
score: 0.60345567, Experimental Diabetes Research, 2011, Kudo, Hirohito et. al.

Association study of candidate genes for the prevalence and progression of knee osteoarthritis.
score: 0.60181575, Arthritis and rheumatism, 2004, Valdes, Ana M et. al.

European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus.
score: 0.60179809, Arthritis and rheumatism, 2009, Chung, Sharon A et. al.

Common genetic variants, acting additively, are a major source of risk for autism
score: 0.60169215, Molecular Autism, 2012, Klei, Lambertus et. al.

Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women
score: 0.60130666, Journal of Cancer Epidemiology, 2009, Van Dyke, Alison L. et. al.

Prevalence in the United States of Selected Candidate Gene Variants
score: 0.60060574, American Journal of Epidemiology, 2008, Chang, Man-huei et. al.

Genome-wide prediction of childhood asthma and related phenotypes in a longitudinal birth cohort
score: 0.59968399, The Journal of Allergy and Clinical Immunology, 2012, Spycher, Ben D. et. al.

Copy Number and Loss of Heterozygosity Detected by SNP Array of Formalin-Fixed Tissues Using Whole-Genome Amplification
score: 0.59904918, PLoS ONE, 2011, Stokes, Angela et. al.

The genetics of attention deficit/hyperactivity disorder in adults, a review.
score: 0.59880853, Molecular psychiatry, 2012, Franke, B et. al.

Genetic variation in the odorant receptors family 13 and the mhc loci influence mate selection in a multiple sclerosis dataset
score: 0.59869366, BMC Genomics, 2010, Khankhanian, Pouya et. al.

Admixture in Hispanic Americans: its impact on ITGAM association and implications for admixture mapping in SLE.
score: 0.59783592, Genes and immunity, 2009, Molineros, J E et. al.

Influence of variations across the MMP-1 and -3 genes on the serum levels of MMP-1 and -3 and disease activity in rheumatoid arthritis.
score: 0.59747829, Genes and immunity, 2012, Chen, Y; Nixon, N B; Dawes, P T; Mattey, D L

Epigenome-wide association studies for common human diseases.
score: 0.59741005, Nature reviews. Genetics, 2011, Rakyan, Vardhman K et. al.

Confirmation of novel type 1 diabetes risk loci in families
score: 0.59707699, Diabetologia, 2012, Cooper, J. D. et. al.

Identification of genes and haplotypes that predict rheumatoid arthritis using random forests
score: 0.59697926, BMC Proceedings, 2009, Tang, Rui et. al.

A Whole-Genome SNP Association Study of NCI60 Cell Line Panel Indicates a Role of Ca 2+ Signaling in Selenium Resistance
score: 0.5967788, PLoS ONE, 2010, Savas, Sevtap et. al.

Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
score: 0.5967283, BMC Medical Genetics, 2012, Huhn, Stefanie et. al.

Efficient Computation of Significance Levels for Multiple Associations in Large Studies of Correlated Data, Including Genomewide Association Studies
score: 0.59656872, The American Journal of Human Genetics, 2004, Dudbridge, Frank; Koeleman, Bobby P.C.

Whole-genome sequencing of multiple Arabidopsis thaliana populations.
score: 0.59606624, Nature genetics, 2011, Cao, Jun et. al.

Genome-Wide Association Study of Copy Number Variants Suggests LTBP1 and FGD4 Are Important for Alcohol Drinking
score: 0.59597643, PLoS ONE, 2012, Pei, Yu-Fang et. al.

Exploring the link between MORF4L1 and risk of breast cancer
score: 0.59554949, Breast Cancer Research : BCR, 2011, Martrat, Griselda et. al.

Neuropsychological Endophenotype Approach to Genome-wide Linkage Analysis Identifies Susceptibility Loci for ADHD on 2q21.1 and 13q12.11
score: 0.59374957, The American Journal of Human Genetics, 2008, Rommelse, Nanda N.J. et. al.

Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort
score: 0.59374956, Neurobiology of Aging, 2010, Lakatos, Anita et. al.

CLOCK Gene Variants Associate with Sleep Duration in Two Independent Populations
score: 0.5935263, Biological Psychiatry, 2010, Allebrandt, Karla V. et. al.

Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability.
score: 0.59318677, Genetic epidemiology, 2011, Kutalik, Zoltán et. al.

The novel and independent association between single-point SNP of NPHP4 gene and renal function in non-diabetic Japanese population: the Takahata study.
score: 0.59231799, Journal of human genetics, 2010, Konta, Tsuneo et. al.

Bioinformatics challenges for genome-wide association studies
score: 0.59085703, Bioinformatics, 2010, Moore, Jason H.; Asselbergs, Folkert W.; Williams, Scott M.

Refining genetic associations in multiple sclerosis
score: 0.59066129, Lancet Neurology, 2008,

Whole-exome sequencing of a pedigree segregating asthma
score: 0.59049995, BMC Medical Genetics, 2012, DeWan, Andrew T et. al.

Extending Rare-Variant Testing Strategies: Analysis of Noncoding Sequence and Imputed Genotypes
score: 0.58964071, The American Journal of Human Genetics, 2010, Zawistowski, Matthew et. al.

Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis
score: 0.58918581, The American Journal of Human Genetics, 2012, Jordan, Catherine T. et. al.

Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis
score: 0.58918581, The American Journal of Human Genetics, 2012, Jordan, Catherine T. et. al.

Cytokine and cytokine receptor single-nucleotide polymorphisms predict risk for non-small cell lung cancer among women.
score: 0.58741562, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, Van Dyke, Alison L et. al.

Gene- or region-based association study via kernel principal component analysis
score: 0.58734451, BMC Genetics, 2011, Gao, Qingsong et. al.

High-Resolution Detection of Identity by Descent in Unrelated Individuals
score: 0.58702167, The American Journal of Human Genetics, 2010, Browning, Sharon R.; Browning, Brian L.

Genome-wide linkage in Utah autism pedigrees.
score: 0.58695559, Molecular psychiatry, 2010, Allen-Brady, K et. al.

Haplotype Analysis Improved Evidence for Candidate Genes for Intramuscular Fat Percentage from a Genome Wide Association Study of Cattle
score: 0.58670255, PLoS ONE, 2011, Barendse, William

Migraine: a complex genetic disorder
score: 0.58639559, Lancet Neurology, 2007, Wessman, Maija et. al.

Meta-analysis indicates that common variants at the DISC1 locus are not associated with schizophrenia
score: 0.5860925, Molecular Psychiatry, 2011, Mathieson, I; Munafò, M R; Flint, J

High-throughput single-nucleotide polymorphism analysis of the IL1RN locus in patients with ankylosing spondylitis by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry.
score: 0.58586261, Arthritis and rheumatism, 2003, Maksymowych, Walter P et. al.

Host Genetic Risk Factors for West Nile Virus Infection and Disease Progression
score: 0.58525117, PLoS ONE, 2011, Bigham, Abigail W. et. al.

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.
score: 0.58502857, Nature genetics, 2009, Tuupanen, Sari et. al.

A Single Nucleotide Polymorphism within the Acetyl-Coenzyme A Carboxylase Beta Gene Is Associated with Proteinuria in Patients with Type 2 Diabetes
score: 0.58492819, PLoS Genetics, 2010, Maeda, Shiro et. al.

Anxiety and depression in children and adults: influence of serotonergic and neurotrophic genes?
score: 0.58467076, Genes, Brain, and Behavior, 2010, Middeldorp, C M et. al.

The association between cannabinoid receptor 1 gene (CNR1) and cannabis dependence symptoms in adolescents and young adults
score: 0.58398644, Drug and Alcohol Dependence, 2009, Hartman, Christie A. et. al.

Association of anti-cyclic citrullinated peptide antibody levels with PADI4 haplotypes in early rheumatoid arthritis and with shared epitope alleles in very late rheumatoid arthritis.
score: 0.58316739, Arthritis and rheumatism, 2007, Cha, Seongwon et. al.

A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease.
score: 0.58308721, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2012, Gianfrancesco, Fernando et. al.

Polymorphisms in predicted miRNA binding sites and osteoporosis.
score: 0.58215105, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2011, Lei, Shu-Feng; Papasian, Christopher J; Deng, Hong-Wen

DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines
score: 0.58139833, Genome Biology, 2011, Bell, Jordana T et. al.

Assessment of genotype imputation methods
score: 0.5804304, BMC Proceedings, 2009, Biernacka, Joanna M et. al.

Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11.
score: 0.57982211, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, Lu, Lingyi et. al.

A DNA resequencing array for genes involved in Parkinson’s disease
score: 0.57972634, Parkinsonism and Related Disorders, 2012, Wilkins, E.J. et. al.

Common variants conferring risk of schizophrenia: A pathway analysis of GWAS data
score: 0.57938591, Schizophrenia Research, 2010, Jia, Peilin et. al.

Association analysis of the chromosome 4p15-p16 candidate region for bipolar disorder and schizophrenia.
score: 0.57937014, Molecular psychiatry, 2007, Christoforou, A et. al.

Clear and independent associations of several HLA-DRB1 alleles with differential antibody responses to hepatitis B vaccination in youth
score: 0.57920246, Human Genetics, 2009, Li, Yufeng et. al.

IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients.
score: 0.57870285, European journal of human genetics : EJHG, 2009, Couturier, Nicolas et. al.

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations
score: 0.57866795, Bioinformatics, 2010, Denny, Joshua C. et. al.

PRKCA and Multiple Sclerosis: Association in Two Independent Populations
score: 0.57848517, PLoS Genetics, 2006, Saarela, Janna et. al.

Polymorphisms and haplotypes in the caspase-3, caspase-7, and caspase-8 genes and risk for endometrial cancer: a population-based, case-control study in a Chinese population.
score: 0.57776316, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, Xu, Hong-Li et. al.

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms
score: 0.57713155, Nucleic Acids Research, 2008, Diskin, Sharon J. et. al.

Efficient mapping of mendelian traits in dogs through genome-wide association.
score: 0.57649103, Nature genetics, 2007, Karlsson, Elinor K et. al.

Evidence for multiple loci from a genome scan of autism kindreds.
score: 0.57634199, Molecular psychiatry, 2006, Schellenberg, G D et. al.

Genome screen for a combined bone phenotype using principal component analysis: the Framingham study
score: 0.57598369, Bone, 2004, Karasik, D; Cupples, L.A; Hannan, M.T; Kiel, D.P

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects
score: 0.57572187, Behavior Genetics, 2010, Newbury, D. F. et. al.

The dystrobrevin binding protein 1 ( DTNBP1) gene is associated with schizophrenia in the Irish Case Control Study of Schizophrenia (ICCSS) sample
score: 0.57545345, Schizophrenia Research, 2009, Riley, Brien et. al.

Strong Signature of Natural Selection within an FHIT Intron Implicated in Prostate Cancer Risk
score: 0.57502361, PLoS ONE, 2008, Ding, Yan et. al.

A reappraisal of the association between Dysbindin ( DTNBP1) and schizophrenia in a large combined case–control and family-based sample of German ancestry
score: 0.57387115, Schizophrenia Research, 2010, Strohmaier, Jana et. al.

Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure.
score: 0.57242617, Nature genetics, 2009, Newton-Cheh, Christopher et. al.

Admixture in Hispanic-Americans: Its impact on ITGAM association and implications for admixture mapping in SLE
score: 0.57220843, Genes and immunity, 2009, Molineros, Julio E. et. al.

Association of common polymorphisms in known susceptibility genes with rheumatoid arthritis in a Slovak population using osteoarthritis patients as controls
score: 0.5719444, Arthritis Research & Therapy, 2009, Stark, Klaus et. al.

Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1-Interacting Genes.
score: 0.57174653, Cancer research, 2011, Rebbeck, Timothy R et. al.

Obesity and diabetes genes are associated with being born small for gestational age: Results from the Auckland Birthweight Collaborative study
score: 0.57143155, BMC Medical Genetics, 2010, Morgan, Angharad R et. al.

HNF1B and Endometrial Cancer Risk: Results from the PAGE study
score: 0.57121002, PLoS ONE, 2012, Setiawan, Veronica Wendy et. al.

Chemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait loci.
score: 0.57094625, Proceedings of the National Academy of Sciences of the United States of America, 2010, Gamazon, Eric R et. al.

Identification of KCNJ15 as a Susceptibility Gene in Asian Patients with Type 2 Diabetes Mellitus
score: 0.57060142, The American Journal of Human Genetics, 2010, Okamoto, Koji et. al.

Gender-stratified gene and gene-treatment interactions in smoking cessation.
score: 0.57056591, The pharmacogenomics journal, 2012, Lee, W et. al.

Identification of IRAK1 as a risk gene with critical role in the pathogenesis of systemic lupus erythematosus.
score: 0.57030353, Proceedings of the National Academy of Sciences of the United States of America, 2009, Jacob, Chaim O et. al.

Identification of the oxidative stress-related gene MSRA as a rheumatoid arthritis susceptibility locus by genome-wide pathway analysis.
score: 0.5693647, Arthritis and rheumatism, 2010, Martín, Jose-Ezequiel et. al.

Neuregulin 3 (NRG3) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition.
score: 0.56886882, Molecular psychiatry, 2011, Morar, B et. al.

Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children.
score: 0.56847042, Molecular psychiatry, 2008, Meaburn, E L et. al.

Single Nucleotide Polymorphisms in the Wnt and BMP Pathways and Colorectal Cancer Risk in a Spanish Cohort
score: 0.56820852, PLoS ONE, 2010, Fernández-Rozadilla, Ceres et. al.

Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset
score: 0.56604269, Human Genetics, 2012, Ramos, Eliana Marisa et. al.

Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms
score: 0.56498656, Molecular psychiatry, 2008, Holmans, PA et. al.

A Phenomics-Based Strategy Identifies Loci on APOC1 , BRAP , and PLCG1 Associated with Metabolic Syndrome Phenotype Domains
score: 0.5632993, PLoS Genetics, 2011, Avery, Christy L. et. al.

Thyroid Stimulating Hormone Receptor (TSHR) Intron 1 Variants Are Major Risk Factors for Graves' Disease in Three European Caucasian Cohorts
score: 0.56273679, PLoS ONE, 2010, Płoski, Rafał et. al.

IL-22RA2 associates with multiple sclerosis and macrophage effector mechanisms in experimental neuroinflammation.
score: 0.5617807, Journal of immunology (Baltimore, Md. : 1950), 2010, Beyeen, Amennai D et. al.

Disparity of innate immunity-related gene effects on asthma and allergy on Karelia.
score: 0.56150183, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2011, Zhang, Guicheng et. al.

Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.
score: 0.56108725, Annals of neurology, 2011, Elbaz, Alexis et. al.

Genetic associations of common deletion polymorphisms in families with Avellino corneal dystrophy
score: 0.56083355, Biochemical and Biophysical Research Communications, 2009, Park, Miey et. al.

Optimizing the Power of Genome-Wide Association Studies by Using Publicly Available Reference Samples to Expand the Control Group
score: 0.56076448, Genetic Epidemiology, 2010, Zhuang, Joanna J et. al.

The genetic basis of alcoholism: multiple phenotypes, many genes, complex networks
score: 0.56047906, Genome Biology, 2012, Morozova, Tatiana V et. al.

An Evolutionary Genomic Approach to Identify Genes Involved in Human Birth Timing
score: 0.56036279, PLoS Genetics, 2011, Plunkett, Jevon et. al.

Opportunities and Challenges in the Genetics of COPD 2010: An International COPD Genetics Conference Report
score: 0.55953337, COPD, 2011, Silverman, Edwin K et. al.

Allelic association of G72/G30 with schizophrenia and bipolar disorder: A comprehensive meta-analysis
score: 0.55906516, Schizophrenia Research, 2008, Shi, Jiajun et. al.

Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene
score: 0.55900366, Human Molecular Genetics, 2011, Davison, Lucy J. et. al.

The choice of null distributions for detecting gene-gene interactions in genome-wide association studies
score: 0.55893541, BMC Bioinformatics, 2011, Yang, Can et. al.

Association Analysis of Canonical Wnt Signalling Genes in Diabetic Nephropathy
score: 0.55821695, PLoS ONE, 2011, Kavanagh, David H. et. al.

Comparison of Microsatellites Versus Single-Nucleotide Polymorphisms in a Genome Linkage Screen for Prostate Cancer–Susceptibility Loci
score: 0.55605624, The American Journal of Human Genetics, 2004, Schaid, Daniel J. et. al.

Transforming Growth Factor Beta 2 and Heme Oxygenase 1 Genes Are Risk Factors for the Cerebral Malaria Syndrome in Angolan Children
score: 0.55502795, PLoS ONE, 2010, Sambo, Maria Rosário et. al.

Phosphodiesterase 4D polymorphisms and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study.
score: 0.5547226, Human molecular genetics, 2006, Song, Qing et. al.

Association between an 8q24 locus and the risk of colorectal cancer in Japanese
score: 0.55459048, BMC Cancer, 2009, Matsuo, Keitaro et. al.

Novel genetic markers improve measures of atrial fibrillation risk prediction.
score: 0.55377339, European heart journal, 2013, Everett, Brendan M et. al.

Genetic variants of the DDR1 gene are associated with vitiligo in two independent Brazilian population samples.
score: 0.5535964, The Journal of investigative dermatology, 2010, Silva de Castro, Caio Cesar et. al.

Association of Neurexin 3 polymorphisms with smoking behavior.
score: 0.55239655, Genes, brain, and behavior, 2012, Docampo, E et. al.

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia.
score: 0.552244, Molecular psychiatry, 2010, Rodríguez-Santiago, B et. al.

Single-nucleotide polymorphisms at five loci are associated with C-reactive protein levels in a cohort of Filipino young adults.
score: 0.55135377, Journal of human genetics, 2011, Curocichin, Ghenadie et. al.

Association of Common Variants in NPPA and NPPB with Circulating Natriuretic Peptides and Blood Pressure
score: 0.55125025, Nature genetics, 2009, Newton-Cheh, Christopher et. al.

The signatures of autozygosity among patients with colorectal cancer.
score: 0.54984757, Cancer research, 2008, Bacolod, Manny D et. al.

Mutation analysis of the MSMB gene in familial prostate cancer
score: 0.54950761, British Journal of Cancer, 2009, Kote-Jarai, Z et. al.

Pathway-Based Approaches for Analysis of Genomewide Association Studies
score: 0.54880482, The American Journal of Human Genetics, 2007, Wang, Kai; Li, Mingyao; Bucan, Maja

Confirmation of a positive association between prostate cancer risk and a locus at chromosome 8q24.
score: 0.54807812, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2007, Suuriniemi, Miia et. al.

Association of New Loci Identified in European Genome-Wide Association Studies with Susceptibility to Type 2 Diabetes in the Japanese
score: 0.54794835, PLoS ONE, 2011, Ohshige, Toshihiko et. al.

Genome-wide prediction of childhood asthma and related phenotypes in a longitudinal birth cohort
score: 0.54775167, The Journal of Allergy and Clinical Immunology, 2012, Spycher, Ben D. et. al.

Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma
score: 0.54750027, Molecular Vision, 2008, Aragon-Martin, Jose A. et. al.

Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome.
score: 0.54729588, Journal of human genetics, 2009, Kuniba, Hideo et. al.

The German multi-centre study on smoking-related behavior-description of a population-based case-control study.
score: 0.54680553, Addiction biology, 2011, Lindenberg, Annette et. al.

Quantitative Founder-Effect Analysis of French Canadian Families Identifies Specific Loci Contributing to Metabolic Phenotypes of Hypertension
score: 0.54672501, The American Journal of Human Genetics, 2005, Hamet, P. et. al.

Replication of genetic association studies in asthma and related phenotypes.
score: 0.54660764, Journal of human genetics, 2010, Undarmaa, Siizkhuu et. al.

SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population
score: 0.54601044, Parkinsonism and Related Disorders, 2012, Trotta, Luca et. al.

Genetic variation in CYP3A43 explains racial difference in olanzapine clearance.
score: 0.54559491, Molecular psychiatry, 2011, Bigos, K L et. al.

Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping.
score: 0.54506271, Genetic epidemiology, 2006, Ellis, Nathan A et. al.

Analysis of an extended chromosome locus 2p14–21 for replication of the 2p16.3 association with glaucoma susceptibility
score: 0.54501205, Molecular Vision, 2011, Kim, Kyunglan et. al.

Mutational load analysis of unrelated individuals
score: 0.54485707, BMC Proceedings, 2011, Howrigan, Daniel P et. al.

New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
score: 0.54480343, Nature genetics, 2007, GAIN Collaborative Research Group, et. al.

Genome-wide scans using archived neonatal dried blood spot samples
score: 0.54415622, BMC Genomics, 2009, Hollegaard, Mads V et. al.

Catechol O-methyltransferase variants and cognitive performance in schizophrenia and bipolar disorder versus controls
score: 0.54243497, Schizophrenia Research, 2010, Wirgenes, Katrine V. et. al.

The neuropeptide galanin and variants in the GalR1 gene are associated with nicotine dependence.
score: 0.54225802, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Jackson, Kia J et. al.

A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss
score: 0.54205443, The American Journal of Human Genetics, 2010, Sırmacı, Aslı et. al.

Identification of Genomic Regions Associated with Phenotypic Variation between Dog Breeds using Selection Mapping
score: 0.54168119, PLoS Genetics, 2011, Vaysse, Amaury et. al.

A two-stage association study identifies methyl-CpG-binding domain protein 2 gene polymorphisms as candidates for breast cancer susceptibility.
score: 0.54109072, European journal of human genetics : EJHG, 2012, Sapkota, Yadav et. al.

Lack of association between genetic polymorphisms within DUSP12 - ATF6 locus and glucose metabolism related traits in a Chinese population
score: 0.54076797, BMC Medical Genetics, 2011, Hu, Cheng et. al.

Assessment of the value of a genetic risk score in improving the estimation of coronary risk
score: 0.54066146, Atherosclerosis, 2012, Lluis-Ganella, Carla et. al.

Assessment of the value of a genetic risk score in improving the estimation of coronary risk
score: 0.54066146, Atherosclerosis, 2012, Lluis-Ganella, Carla et. al.

Assessment of the value of a genetic risk score in improving the estimation of coronary risk
score: 0.54066146, Atherosclerosis, 2012, Lluis-Ganella, Carla et. al.

CLOCK is suggested to associate with comorbid alcohol use and depressive disorders
score: 0.54049386, Journal of Circadian Rhythms, 2010, Sjöholm, Louise K et. al.

Genome-wide association study identifies two major loci affecting calving ease and growth-related traits in cattle.
score: 0.54006204, Genetics, 2011, Pausch, Hubert et. al.

The autoimmune disease-associated IL2RA locus is involved in the clinical manifestations of systemic sclerosis.
score: 0.53981758, Genes and immunity, 2012, Martin, J-E et. al.

Robust Estimation of Experimentwise P Values Applied to a Genome Scan of Multiple Asthma Traits Identifies a New Region of Significant Linkage on Chromosome 20q13
score: 0.53958876, The American Journal of Human Genetics, 2005, Ferreira, Manuel A.R. et. al.

The role of genetic markers in hepatitis C virus therapy: a major step for individualized care.
score: 0.53931319, Liver international : official journal of the International Association for the Study of the Liver, 2011, McHutchison, John G

Multivariate association analysis of the components of metabolic syndrome from the Framingham Heart Study
score: 0.53925127, BMC Proceedings, 2009, Baker, Allison R et. al.

Mapping the Genetic Architecture of Gene Expression in Human Liver
score: 0.5390168, PLoS Biology, 2008, Schadt, Eric E et. al.

A tutorial on statistical methods for population association studies.
score: 0.53876754, Nature reviews. Genetics, 2006, Balding, David J

Variants of Arachidonate 5-Lipoxygenase-activating Protein ( ALOX5AP) Gene and Risk of Coronary Heart Disease: A Meta-analysis
score: 0.53811013, Archives of Medical Research, 2010, Huang, Hao; Zeng, Zhi; Li, Jing; Zhang, Li; Chen, Yucheng

Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study.
score: 0.53767667, European journal of human genetics : EJHG, 2011, Wineinger, Nathan E et. al.

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.
score: 0.53756332, Nature genetics, 2008, Korn, Joshua M et. al.

Matrix metalloproteinase 1 (MMP1) is associated with early-onset lung cancer.
score: 0.53715524, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2008, Sauter, Wiebke et. al.

Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder
score: 0.53665207, Molecular psychiatry, 2008, Schulze, TG et. al.

Genetic analysis of albuminuria in aging mice and concordance with loci for human diabetic nephropathy found in a genome-wide association scan.
score: 0.53611796, Kidney international, 2010, Tsaih, Shirng-Wern et. al.

Systematic evaluation of bladder cancer risk-associated single-nucleotide polymorphisms in a Chinese population.
score: 0.53568509, Molecular carcinogenesis, 2012, Ma, Zhicheng et. al.

Susceptibility Variants for Waist Size in Relation to Abdominal, Visceral and Hepatic Adiposity in Postmenopausal Women
score: 0.535123, Journal of the Academy of Nutrition and Dietetics, 2012, Lim, Unhee et. al.

Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples
score: 0.53473893, Biomarker Insights, 2010, Loomis, Stephanie J. et. al.

Nicotinic receptor gene variants influence susceptibility to heavy smoking.
score: 0.53423582, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2008, Stevens, Victoria L et. al.

Intermediate Phenotypes Identify Divergent Pathways to Alzheimer's Disease
score: 0.53416902, PLoS ONE, 2010, Shulman, Joshua M. et. al.

Association of nicotinic acetylcholine receptor subunit alpha 4 polymorphisms with nicotine dependence in 5500 Germans.
score: 0.53394498, The pharmacogenomics journal, 2009, Breitling, L P et. al.

DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.
score: 0.53365343, Proceedings of the National Academy of Sciences of the United States of America, 2008, Lettre, Guillaume et. al.

Exposed: The Genetic Underpinnings of Ulcerative Colitis Relative to Crohn's Disease
score: 0.53301105, Gastroenterology, 2009, Brant, Steven R.

Knobbed acrosome defect is associated with a region containing the genes STK17b and HECW2 on porcine chromosome 15
score: 0.53142547, BMC Genomics, 2010, Sironen, Anu et. al.

Identification of an aggressive prostate cancer predisposing variant at 11q13.
score: 0.53003544, International journal of cancer. Journal international du cancer, 2011, Nurminen, Riikka et. al.

Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis.
score: 0.52995193, Inflammatory bowel diseases, 2011, Diaz-Gallo, Lina-Marcela et. al.

Sex differences and genomics in autoimmune diseases
score: 0.52902692, Journal of Autoimmunity, 2012, Amur, Shashi; Parekh, Ameeta; Mummaneni, Padmaja

No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls
score: 0.52826598, Annals of the Rheumatic Diseases, 2012, Hudson, Gavin et. al.

A three-stage approach for genome-wide association studies with family data for quantitative traits
score: 0.52772446, BMC Genetics, 2010, Chen, Ming-Huei et. al.

Meta-analysis and imputation identifies a 109 kb risk haplotype spanning TNFAIP3 associated with lupus nephritis and hematologic manifestations.
score: 0.52719763, Genes and immunity, 2009, Bates, J S et. al.

Mammalian gene studies
score: 0.52652736, Current Opinion in Biotechnology, 1994,

Evaluating the Role of LPIN1 Variation in Insulin Resistance, Body Weight, and Human Lipodystrophy in U.K. Populations
score: 0.52614121, Diabetes, 2008, Fawcett, Katherine A. et. al.

Novel human genetic variants associated with extrapulmonary tuberculosis: a pilot genome wide association study
score: 0.52592707, BMC Research Notes, 2011, Oki, Noffisat O et. al.

PKNOX2 gene is significantly associated with substance dependence in European-origin women.
score: 0.52557924, Proceedings of the National Academy of Sciences of the United States of America, 2009, Chen, Xiang; Cho, Kelly; Singer, Burton H; Zhang, Heping

Epistatic study reveals two genetic interactions in blood pressure regulation
score: 0.5254018, BMC Medical Genetics, 2013, Ndiaye, Ndeye Coumba et. al.

Genetics of Recurrent Vertigo and Vestibular Disorders
score: 0.52454247, Current Genomics, 2011, Gazquez, Irene; Lopez-Escamez, Jose A

A Functional Variant in ERAP1 Predisposes to Multiple Sclerosis
score: 0.5239374, PLoS ONE, 2012, Guerini, Franca Rosa et. al.

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon.
score: 0.52382218, Human molecular genetics, 2008, Zalloua, Pierre A et. al.

Evaluation of A2BP1 as an Obesity Gene
score: 0.52347234, Diabetes, 2010, Ma, Lijun et. al.

The ANO3/MUC15 locus is associated with eczema in families ascertained through asthma
score: 0.52326146, The Journal of Allergy and Clinical Immunology, 2012, Dizier, Marie-Hélène et. al.

The Genetics of Obesity
score: 0.52300172, Current Diabetes Reports, 2010, Herrera, Blanca M.; Lindgren, Cecilia M.

From expression pattern to genetic association in asthma and asthma-related phenotypes
score: 0.52295057, BMC Research Notes, 2012, Vaillancourt, Vanessa T et. al.

Independent replication analysis of genetic loci with previous evidence of association with juvenile idiopathic arthritis
score: 0.52238215, Pediatric Rheumatology Online Journal, 2013, Ellis, Justine A et. al.

Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.
score: 0.52006072, Journal of human genetics, 2010, Wang, Ying et. al.

Common genetic variants in the vitamin D pathway including genome-wide associated variants are not associated with breast cancer risk among Chinese women.
score: 0.51921625, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Dorjgochoo, Tsogzolmaa et. al.

A genome-wide linkage scan for genes controlling variation in urinary albumin excretion in type II diabetes.
score: 0.51911578, Kidney international, 2006, Krolewski, A S et. al.

Comparison of buccal and blood-derived canine DNA, either native or whole genome amplified, for array-based genome-wide association studies
score: 0.51877705, BMC Research Notes, 2011, Rincon, Gonzalo et. al.

Inferences from genomic models in stratified populations.
score: 0.51804779, Genetics, 2012, Janss, Luc et. al.

Case–control association analysis of polymorphisms in the delta-opioid receptor, OPRD1, with cocaine and opioid addicted populations
score: 0.51778848, Drug and Alcohol Dependence, 2013, Crist, R.C. et. al.

Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates
score: 0.51708032, PLoS ONE, 2011, Wei, Wenhua et. al.

Current software for genotype imputation
score: 0.51679596, Human Genomics, 2009, Ellinghaus, David et. al.

CNstream: A method for the identification and genotyping of copy number polymorphisms using Illumina microarrays
score: 0.51664137, BMC Bioinformatics, 2010, Alonso, Arnald et. al.

Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis
score: 0.51618843, Annals of the Rheumatic Diseases, 2010, Hinks, Anne et. al.

The role of polymorphisms in ADAM33, a disintegrin and metalloprotease 33, in childhood asthma and lung function in two German populations
score: 0.51578262, Respiratory Research, 2006, Schedel, Michaela et. al.

Type 2 diabetes: new genes, new understanding
score: 0.51572732, Trends in Genetics, 2008, Prokopenko, Inga; McCarthy, Mark I.; Lindgren, Cecilia M.

Association between arachidonate 5-lipoxygenase-activating protein (ALOX5AP) and lung function in a Korean population.
score: 0.51565093, Scandinavian journal of immunology, 2012, Ro, M et. al.

Association of the histidine-triad nucleotide-binding protein-1 (HINT1) gene variants with nicotine dependence.
score: 0.51529973, The pharmacogenomics journal, 2011, Jackson, K J et. al.

Genome-Wide Linkage Scan for Primary Open Angle Glaucoma: Influences of Ancestry and Age at Diagnosis
score: 0.51522942, PLoS ONE, 2011, Crooks, Kristy R. et. al.

13th Meeting of the Irish Society of Human Genetics
score: 0.51512129, The Ulster Medical Journal, 2010,

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies
score: 0.51501715, The American Journal of Human Genetics, 2010, Price, Alkes L. et. al.

Bayesian analysis of genetic interactions in case-control studies, with application to adiponectin genes and colorectal cancer risk.
score: 0.5148806, Annals of human genetics, 2011, Yi, Nengjun; Kaklamani, Virginia G; Pasche, Boris

Leukocyte DNA Methylation Signature Differentiates Pancreatic Cancer Patients from Healthy Controls
score: 0.5146444, PLoS ONE, 2011, Pedersen, Katrina S. et. al.

Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures
score: 0.51408056, Biological Psychiatry, 2009, Wray, Naomi R. et. al.

Allelic variation in ApoC3, ApoA5 and LPL genes and first and second generation antipsychotic effects on serum lipids in patients with schizophrenia.
score: 0.51383511, The pharmacogenomics journal, 2008, Smith, R C et. al.

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays
score: 0.51355532, Nucleic Acids Research, 2010, Dellinger, Andrew E. et. al.

Common breast cancer susceptibility loci are associated with triple-negative breast cancer.
score: 0.51350447, Cancer research, 2011, Stevens, Kristen N et. al.

Identification and Replication of Three Novel Myopia Common Susceptibility Gene Loci on Chromosome 3q26 using Linkage and Linkage Disequilibrium Mapping
score: 0.51315114, PLoS Genetics, 2008, Andrew, Toby et. al.

Consistently Replicating Locus Linked to Migraine on 10q22-q23
score: 0.51197482, The American Journal of Human Genetics, 2008, Anttila, Verneri et. al.

Genome-wide association study (GWAS)-identified disease risk alleles do not compromise human longevity.
score: 0.51147912, Proceedings of the National Academy of Sciences of the United States of America, 2010, Beekman, Marian et. al.

Genome-wide linkage scan for nicotine dependence in European Americans and its converging results with African Americans in the Mid-South Tobacco Family sample.
score: 0.51075273, Molecular psychiatry, 2008, Li, M D et. al.

Constructing gene association networks for rheumatoid arthritis using the backward genotype-trait association (BGTA) algorithm
score: 0.51031501, BMC Proceedings, 2007, Ding, Yuejing et. al.

Computational and statistical approaches to analyzing variants identified by exome sequencing
score: 0.51006556, Genome Biology, 2011, Stitziel, Nathan O; Kiezun, Adam; Sunyaev, Shamil

Common Functional Genetic Variants in Catecholamine Storage Vesicle Protein Promoter Motifs Interact to Trigger Systemic Hypertension
score: 0.50897787, Journal of the American College of Cardiology, 2010, Zhang, Kuixing et. al.

No evidence of IL21 association with multiple sclerosis in a Swedish population.
score: 0.50848346, Tissue antigens, 2011, Lindén, M et. al.

Association of CD40 with rheumatoid arthritis confirmed in a large UK case-control study
score: 0.50784367, Annals of the Rheumatic Diseases, 2009, Orozco, Gisela et. al.

A Latent Model for Prioritization of SNPs for Functional Studies
score: 0.50779145, PLoS ONE, 2011, Fridley, Brooke L. et. al.

Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study.
score: 0.50706132, European journal of human genetics : EJHG, 2009, Ehret, Georg B et. al.

Hunter-gatherer genomic diversity suggests a southern African origin for modern humans.
score: 0.50686438, Proceedings of the National Academy of Sciences of the United States of America, 2011, Henn, Brenna M et. al.

Two-stage case-control association study of polymorphisms in rheumatoid arthritis susceptibility genes with schizophrenia.
score: 0.50655718, Journal of human genetics, 2009, Watanabe, Yuichiro et. al.

Association study of common variants in the sFRP1 gene region and parameters of bone strength and body composition in two independent healthy Caucasian male cohorts
score: 0.50627967, Molecular Genetics and Metabolism, 2012, Boudin, Eveline et. al.

Genome-wide association studies using an adaptive two-stage analysis for a case-control design
score: 0.50622117, BMC Proceedings, 2007, Song, Kijoung et. al.

Fine mapping the TAGAP risk locus in rheumatoid arthritis
score: 0.50539465, Genes and Immunity, 2011, Chen, R et. al.

Difference between age-related macular degeneration and polypoidal choroidal vasculopathy in the hereditary contribution of the A69S variant of the age-related maculopathy susceptibility 2 gene ( ARMS2 )
score: 0.50498462, Molecular Vision, 2011, Yanagisawa, Suiho et. al.

Dopamine transporter genotype predicts behavioural and neural measures of response inhibition.
score: 0.50475184, Molecular psychiatry, 2012, Cummins, T D R et. al.

Combined Functional and Positional Gene Information for the Identification of Susceptibility Variants in Celiac Disease
score: 0.50440626, Gastroenterology, 2008, Castellanos–Rubio, Ainara et. al.

Neuropeptide Y Gene Polymorphisms Confer Risk of Early-Onset Atherosclerosis
score: 0.50421042, PLoS Genetics, 2009, Shah, Svati H. et. al.

Cell adhesion molecules contribute to Alzheimer's disease: multiple pathway analyses of two genome-wide association studies.
score: 0.50408352, Journal of neurochemistry, 2012, Liu, Guiyou et. al.

A statistical method for region-based meta-analysis of genome-wide association studies in genetically diverse populations
score: 0.50334444, European Journal of Human Genetics, 2011, Wang, Xu et. al.

The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample.
score: 0.50326649, Alcoholism, clinical and experimental research, 2008, Lind, Penelope A et. al.

PRESTO: Rapid calculation of order statistic distributions and multiple-testing adjusted P-values via permutation for one and two-stage genetic association studies
score: 0.50314714, BMC Bioinformatics, 2008, Browning, Brian L

The success of pharmacogenomics in moving genetic association studies from bench to bedside: study design and implementation of precision medicine in the post-GWAS era
score: 0.50262035, Human Genetics, 2012, Ritchie, Marylyn D.

Genotype and Ancestry Modulate Brain's DAT Availability in Healthy Humans
score: 0.50211386, PLoS ONE, 2011, Shumay, Elena et. al.

Conditional Random Fields for Fast, Large-Scale Genome-Wide Association Studies
score: 0.50209263, PLoS ONE, 2011, Huang, Jim C. et. al.

Association of IL6 and CCL2 gene polymorphisms with the outcome of allogeneic haematopoietic stem cell transplantation.
score: 0.50208236, Bone marrow transplantation, 2009, Ambruzova, Z et. al.

LIN28B , LIN28A , KISS1 , and KISS1R in idiopathic central precocious puberty
score: 0.50202153, BMC Research Notes, 2011, Tommiska, Johanna et. al.

Sequencing of TNFAIP3 and association of variants with multiple autoimmune diseases.
score: 0.50175728, Genes and immunity, 2011, Musone, S L et. al.

Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
score: 0.50121626, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Engel, Christoph et. al.

Polymorphisms in IL12A and cockroach allergy in children with asthma
score: 0.50011163, Clinical and molecular allergy : CMA, 2008, Pistiner, Michael et. al.

Quality control issues and the identification of rare functional variants with next-generation sequencing data.
score: 0.49977135, Genetic epidemiology, 2011, Hemmelmann, Claudia; Daw, E Warwick; Wilson, Alexander F

Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits
score: 0.49930171, PLoS Genetics, 2010, Segrè, Ayellet V. et. al.

Ancestry-informative markers on chromosomes 2, 8 and 15 are associated with insulin-related traits in a racially diverse sample of children
score: 0.4988564, Human Genomics, 2011, Klimentidis, Yann C et. al.

Genetic variation in cholinergic muscarinic-2 receptor gene modulates M2 receptor binding in vivo and accounts for reduced binding in bipolar disorder.
score: 0.49875084, Molecular psychiatry, 2011, Cannon, D M et. al.

Risk of Type 2 Diabetes and Obesity Is Differentially Associated with Variation in FTO in Whites and African-Americans in the ARIC Study
score: 0.49874568, PLoS ONE, 2010, Bressler, Jan et. al.

Prediction of lung cancer risk in a Chinese population using a multifactorial genetic model
score: 0.49871203, BMC Medical Genetics, 2012, Li, Huan et. al.

Fine-Mapping Chromosome 20 in 230 Systemic Lupus Erythematosus Sib Pair and Multiplex Families: Evidence for Genetic Epistasis with Chromosome 16q12
score: 0.49805161, The American Journal of Human Genetics, 2006, Gaffney, Patrick M. et. al.

A comprehensive candidate gene approach identifies genetic variation associated with osteosarcoma
score: 0.49763457, BMC Cancer, 2011, Mirabello, Lisa et. al.

Causal graph-based analysis of genome-wide association data in rheumatoid arthritis
score: 0.49719962, Biology Direct, 2011, Alekseyenko, Alexander V et. al.

A powerful hybrid approach to select top single-nucleotide polymorphisms for genome-wide association study
score: 0.49670786, BMC Genetics, 2011, Wang, Jian; Shete, Sanjay

Combined Effect of Inflammatory Gene Polymorphisms and the Risk of Ischemic Stroke in a Prospective Cohort of Subjects With Type 2 Diabetes: A Go-DARTS Study
score: 0.49649753, Diabetes, 2010, Palmer, Colin N.A. et. al.

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits.
score: 0.49499393, Nature genetics, 2012, Yang, Jian et. al.

Association study of polymorphisms in cholecystokinin gene and its receptors with antipsychotic induced weight gain in schizophrenia patients
score: 0.49467974, Progress in Neuropsychopharmacology & Biological Psychiatry, 2010, Tiwari, Arun K. et. al.

Use of Genome-Wide Expression Data to Mine the “Gray Zone” of GWA Studies Leads to Novel Candidate Obesity Genes
score: 0.49414727, PLoS Genetics, 2010, Naukkarinen, Jussi et. al.

Dopamine genes and nicotine dependence in treatment seeking and community smokers
score: 0.4932061, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Bergen, Andrew W. et. al.

Plasma lipoproteins: genetic influences and clinical implications.
score: 0.49281116, Nature reviews. Genetics, 2009, Hegele, Robert A

Genome-wide association study for empirically derived metabolic phenotypes in the Framingham Heart Study offspring cohort
score: 0.49224595, BMC Proceedings, 2009, Wilcox, Marsha et. al.

DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders.
score: 0.49216084, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Reif, Andreas et. al.

Interaction of SLC6A4 and DRD2 polymorphisms is associated with a history of delirium tremens.
score: 0.49167871, Addiction biology, 2010, Karpyak, Victor M et. al.

The ITGAV rs3738919 variant and susceptibility to rheumatoid arthritis in four Caucasian sample sets
score: 0.49114545, Arthritis Research & Therapy, 2009, Hollis-Moffatt, Jade E et. al.

The Type 2 Diabetes Associated Minor Allele of rs2237895 KCNQ1 Associates with Reduced Insulin Release Following an Oral Glucose Load
score: 0.49109007, PLoS ONE, 2009, Holmkvist, Johan et. al.

Copy number variations (CNVs) identified in Korean individuals
score: 0.49087743, BMC Genomics, 2008, Kang, Tae-Wook et. al.

Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles
score: 0.49074672, The American Journal of Human Genetics, 2008, Bruder, Carl E.G. et. al.

Genome-wide scan revealed genetic loci for energy metabolism in Hispanic children and adolescents.
score: 0.49036147, International journal of obesity (2005), 2008, Cai, G; Cole, S A; Butte, N F; Voruganti, V S; Comuzzie, A G

Variation in CHI3LI in Relation to Type 2 Diabetes and Related Quantitative Traits
score: 0.4899484, PLoS ONE, 2009, Rathcke, Camilla Noelle et. al.

Bias due to two-stage residual-outcome regression analysis in genetic association studies.
score: 0.48908074, Genetic epidemiology, 2011, Demissie, Serkalem; Cupples, L Adrienne

phenosim - A software to simulate phenotypes for testing in genome-wide association studies
score: 0.48866271, BMC Bioinformatics, 2011, Günther, Torsten; Gawenda, Inka; Schmid, Karl J

Growth mixture modelling in families of the Framingham Heart Study
score: 0.48821739, BMC Proceedings, 2009, Kerner, Berit; Muthén, Bengt O

MCP1 SNPs and Pulmonary Tuberculosis in Cohorts from West Africa, the USA and Argentina: Lack of Association or Epistasis with IL12B Polymorphisms
score: 0.48736445, PLoS ONE, 2012, Velez Edwards, Digna R. et. al.

Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease.
score: 0.48726455, Movement disorders : official journal of the Movement Disorder Society, 2011, Mata, Ignacio F et. al.

Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese population.
score: 0.48719209, Journal of human genetics, 2010, Hotta, Kikuko et. al.

Analysis of the association between CD40 and CD40 ligand polymorphisms and systemic sclerosis
score: 0.48714855, Arthritis Research & Therapy, 2012, Teruel, María et. al.

Genetics of hypertension: From experimental animals to humans
score: 0.48545904, Biochimica et Biophysica Acta, 2010, Delles, Christian et. al.

Genetics of hypertension: From experimental animals to humans
score: 0.48545904, BBA - Molecular Basis of Disease, 2010, Delles, Christian et. al.

Common Polymorphisms Influencing Serum Uric Acid Levels Contribute to Susceptibility to Gout, but Not to Coronary Artery Disease
score: 0.48543104, PLoS ONE, 2009, Stark, Klaus et. al.

SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels
score: 0.48507478, BMC Genomics, 2008, Sanders, Mathijs A et. al.

Using a higher criticism statistic to detect modest effects in a genome-wide study of rheumatoid arthritis
score: 0.48477475, BMC Proceedings, 2009, Parkhomenko, Elena et. al.

A putative functional variant within the UBAC2 gene is associated with increased risk of Behçet's disease.
score: 0.48468198, Arthritis and rheumatism, 2011, Sawalha, Amr H et. al.

Using maximal segmental score in genome-wide association studies.
score: 0.48442176, Genetic epidemiology, 2012, Lin, Ying-Chao et. al.

Genetic variants at CD28 , PRDM1 , and CD2/CD58 are associated with rheumatoid arthritis risk
score: 0.48419584, Nature genetics, 2009, Raychaudhuri, Soumya et. al.

Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele.
score: 0.48354332, Birth defects research. Part A, Clinical and molecular teratology, 2010, O'Byrne, Michelle R et. al.

A functional EXO1 promoter variant is associated with prolonged life expectancy in centenarians
score: 0.48245426, Mechanisms of Ageing and Development, 2009, Nebel, Almut et. al.

Type 2 Diabetes Risk Alleles Are Associated With Reduced Size at Birth
score: 0.48145811, Diabetes, 2009, Freathy, Rachel M. et. al.

Abstracts of the XXV Congress of the International Academy of Pathology. October 10-15, 2004. Queensland, Australia.
score: 0.48014317, Pathology international, 2004,

Genome-Wide Linkage Scan to Identify Loci Associated with Type 2 Diabetes and Blood Lipid Phenotypes in the Sikh Diabetes Study
score: 0.47929029, PLoS ONE, 2011, Sanghera, Dharambir K. et. al.

Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis
score: 0.47926317, PLoS Genetics, 2008, Fernando, Michelle M. A. et. al.

MicroRNA processing and binding site polymorphisms are not replicated in the Ovarian Cancer Association Consortium.
score: 0.47909549, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Permuth-Wey, Jennifer et. al.

Statistical Genetic Approaches for Mapping Ophthalmic Trait and Disease Genes
score: 0.47883226, American Journal of Ophthalmology, 2009, Sinsheimer, Janet

Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients
score: 0.4784094, Human Immunology, 2012, Fourati, Hajer et. al.

Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients
score: 0.4784094, Human Immunology, 2012, Fourati, Hajer et. al.

Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients
score: 0.4784094, Human Immunology, 2012, Fourati, Hajer et. al.

Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients
score: 0.4784094, Human Immunology, 2012, Fourati, Hajer et. al.

Data mining of high density genomic variant data for prediction of Alzheimer's disease risk
score: 0.47818984, BMC Medical Genetics, 2012, Briones, Natalia; Dinu, Valentin

Genetic determinants of the ankle-brachial index: A meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium
score: 0.47808968, Atherosclerosis, 2012, Wassel, Christina L. et. al.

Aryl hydrocarbon receptor nuclear translocator (ARNT) gene as a positional and functional candidate for type 2 diabetes and prediabetic intermediate traits: Mutation detection, case-control studies, and gene expression analysis
score: 0.47766416, BMC Medical Genetics, 2008, Das, Swapan K et. al.

Replication and meta-analysis of TMEM132D gene variants in panic disorder
score: 0.47722034, Translational Psychiatry, 2012, Erhardt, A et. al.

Assessing sources of inconsistencies in genotypes and their effects on genome-wide association studies with HapMap samples
score: 0.47719222, The Pharmacogenomics Journal, 2010, Hong, H et. al.

P-selectin genotype is associated with the development of cancer cachexia
score: 0.47690128, EMBO Molecular Medicine, 2012, Tan, Benjamin H L et. al.

A community-based study of nucleotide excision repair polymorphisms in relation to risk of non-melanoma skin cancer
score: 0.47498277, The Journal of Investigative Dermatology, 2012, Wheless, Lee et. al.

A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes.
score: 0.47470489, Genes and immunity, 2009, Magitta, N F et. al.

ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry
score: 0.47461605, Molecular Psychiatry, 2011, Bierut, Laura Jean et. al.

Association of an NKG2D gene variant with systemic lupus erythematosus in two populations
score: 0.47432083, Human Immunology, 2010, Kabalak, Gamze et. al.

Whole-genome variance components linkage analysis using single-nucleotide polymorphisms versus microsatellites on quantitative traits of derived phenotypes from factor analysis of electroencephalogram waves
score: 0.47413312, BMC Genetics, 2005, Yu, Yi et. al.

Comparative analysis of methods for detecting interacting loci
score: 0.47316507, BMC Genomics, 2011, Chen, Li et. al.

Chromosomal variation in lymphoblastoid cell lines.
score: 0.47311691, Human mutation, 2012, Shirley, Matthew D et. al.

Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes.
score: 0.4730624, European journal of human genetics : EJHG, 2012, de Jong, Simone et. al.

Two common chromosome 8q24 variants are associated with increased risk for prostate cancer.
score: 0.47270603, Cancer research, 2007, Wang, Liang et. al.

Presymptomatic Risk Assessment for Chronic Non-Communicable Diseases
score: 0.47257953, PLoS ONE, 2010, Padhukasahasram, Badri et. al.

Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women
score: 0.47218753, Journal of Psychiatric Research, 2010, Costas, Javier et. al.

Dietary fat intake and polymorphisms at the PPARG locus modulate BMI and type 2 diabetes risk in the D.E.S.I.R. prospective study.
score: 0.47214193, International journal of obesity (2005), 2012, Lamri, A et. al.

Analysis of the IL28RA locus as genetic risk factor for multiple sclerosis
score: 0.47143356, Journal of Neuroimmunology, 2012, Lopez de Lapuente, A. et. al.

GALC Deletions Increase the Risk of Primary Open-Angle Glaucoma: The Role of Mendelian Variants in Complex Disease
score: 0.4713718, PLoS ONE, 2011, Liu, Yutao et. al.

Identification of single nucleotide polymorphisms in the bovine solute carrier family 11 member 1 (SLC11A1) gene and their association with infection by Mycobacterium avium subspecies paratuberculosis
score: 0.47119902, Journal of Dairy Science, 2010, Ruiz-Larrañaga, O. et. al.

Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites
score: 0.47094856, Molecular Psychiatry, 2011, Brouwers, N et. al.

Variability in the Heritability of Body Mass Index: A Systematic Review and Meta-Regression
score: 0.47073201, Frontiers in Endocrinology, 2012, Elks, Cathy E. et. al.

Screening of DNA-variants in the properdin gene ( CFP) in age-related macular degeneration (AMD)
score: 0.47064743, Molecular Immunology, 2010, Seitsonen, Sanna et. al.

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.
score: 0.47020719, Nature genetics, 2008, Kopp, Jeffrey B et. al.

Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness
score: 0.46986348, Molecular Vision, 2010, Dimasi, David P. et. al.

A Comparison of Approaches to Estimate the Inbreeding Coefficient and Pairwise Relatedness Using Genomic and Pedigree Data in a Sheep Population
score: 0.46972402, PLoS ONE, 2011, Li, Meng-Hua et. al.

Diverse Genome-wide Association Studies Associate the IL12/IL23 Pathway with Crohn Disease
score: 0.46942887, The American Journal of Human Genetics, 2009, Wang, Kai et. al.

Is the thrifty genotype hypothesis supported by evidence based on confirmed type 2 diabetes- and obesity-susceptibility variants?
score: 0.46832188, Diabetologia, 2009, Southam, L. et. al.

A Kinship-Based Modification of the Armitage Trend Test to Address Hidden Population Structure and Small Differential Genotyping Errors
score: 0.46774332, PLoS ONE, 2009, Rakovski, Cyril S.; Stram, Daniel O.

Confirmation of association between multiple sclerosis and CYP27B1.
score: 0.46752494, European journal of human genetics : EJHG, 2010, Sundqvist, Emilie et. al.

Copy number variation and cytidine analogue cytotoxicity: A genome-wide association approach
score: 0.4671509, BMC Genomics, 2010, Kalari, Krishna R et. al.

Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.
score: 0.46670093, Journal of human genetics, 2010, Bae, Joon Seol et. al.

Polymorphisms in the myosin light chain kinase gene that confer risk of severe sepsis are associated with a lower risk of asthma
score: 0.46667468, The Journal of Allergy and Clinical Immunology, 2007, Gao, Li et. al.

A Human Type 1 Diabetes Susceptibility Locus Maps to Chromosome 21q22.3
score: 0.46654927, Diabetes, 2008, Concannon, Patrick et. al.

Genetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritis.
score: 0.46646794, Genes and immunity, 2010, Ockinger, J et. al.

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
score: 0.46602847, Nature Genetics, 2011, Trynka, Gosia et. al.

Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
score: 0.46597221, Nature Genetics, 2011, Rivas, Manuel A. et. al.

Circulating 25-hydroxyvitamin D and risk of non-hodgkin lymphoma: Cohort Consortium Vitamin D Pooling Project of Rarer Cancers.
score: 0.46539619, American journal of epidemiology, 2010, Purdue, Mark P et. al.

A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color
score: 0.46518689, The American Journal of Human Genetics, 2008, Sturm, Richard A. et. al.

Discovering joint associations between disease and gene pairs with a novel similarity test
score: 0.46512905, BMC Genetics, 2010, Lin, Wan-Yu; Lee, Wen-Chung

Genetic epidemiology: the use of old and new tools for multiple sclerosis
score: 0.4648697, Trends in Neurosciences, 2008, Ramagopalan, Sreeram V.; Dyment, David A.; Ebers, George C.

DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder.
score: 0.46486047, Molecular psychiatry, 2009, Hennah, W et. al.

Gene-Environment Interaction in the Etiology of Mathematical Ability Using SNP Sets
score: 0.46479265, Behavior Genetics, 2010, Docherty, Sophia J.; Kovas, Yulia; Plomin, Robert

Application of a novel hybrid study design to explore gene-environment interactions in orofacial clefts.
score: 0.46405728, Annals of human genetics, 2012, Skare, Oivind et. al.

Two common nonsynonymous paraoxonase 1 ( PON1 ) gene polymorphisms and brain astrocytoma and meningioma
score: 0.46401697, BMC Neurology, 2010, Martínez, Carmen et. al.

Comparison of identical single nucleotide polymorphisms genotyped by the GeneChip Targeted Genotyping 25K, Affymetrix 500K and Illumina 550K platforms
score: 0.46386473, Genomics, 2009, Kim, Ka-Kyung et. al.

Promise and pitfalls of the Immunochip
score: 0.46376884, Arthritis Research & Therapy, 2011, Cortes, Adrian; Brown, Matthew A

The association of variants in the FTO gene with longitudinal body mass index profiles in non-Hispanic white children and adolescents.
score: 0.46339191, International journal of obesity (2005), 2012, Hallman, D M et. al.

Association analysis of susceptibility candidate region on chromosome 5q31 for tuberculosis.
score: 0.46276917, Genes and immunity, 2010, Ridruechai, C et. al.

Gene expression profiling in whole blood identifies distinct biological pathways associated with obesity
score: 0.46251143, BMC Medical Genomics, 2010, Ghosh, Sujoy et. al.

Same or different? Insights into the etiology of phonological awareness and rapid naming
score: 0.4624305, Biological Psychology, 2009, Naples, Adam J. et. al.

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL
score: 0.46203618, Journal of Neuroimmunology, 2009, Sulonen, Anna-Maija et. al.

The HLA genomic loci map: expression, interaction, diversity and disease.
score: 0.46115933, Journal of human genetics, 2009, Shiina, Takashi et. al.

Determination of the obesity-associated gene variants within the entire FTO gene by ultra-deep targeted sequencing in obese and lean children
score: 0.46014922, International Journal of Obesity (2005), 2012, Sällman Almén, M et. al.

Genetic variations in the sonic hedgehog pathway affect clinical outcomes in non-muscle-invasive bladder cancer.
score: 0.45988577, Cancer prevention research (Philadelphia, Pa.), 2010, Chen, Meng et. al.

Linkage and candidate gene studies of autism spectrum disorders in European populations.
score: 0.45985701, European journal of human genetics : EJHG, 2010, Holt, Richard et. al.

Novel Susceptibility Locus at 22q11 for Diabetic Nephropathy in Type 1 Diabetes
score: 0.45962679, PLoS ONE, 2011, Wessman, Maija et. al.

An autoimmune-associated variant in PTPN2 reveals an impairment of IL-2R signaling in CD4 + T cells
score: 0.45814049, Genes and immunity, 2010, Long, S Alice et. al.

Genomic landscape of positive natural selection in Northern European populations.
score: 0.45807935, European journal of human genetics : EJHG, 2010, Lappalainen, Tuuli et. al.

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies.
score: 0.45805138, Nature genetics, 2012, Pasaniuc, Bogdan et. al.

The association of genetic variants of type 2 diabetes with kidney function.
score: 0.4572318, Kidney international, 2012, Franceschini, Nora et. al.

The Role of Genetics in the Etiology of Schizophrenia
score: 0.45562527, Psychiatric Clinics of North America, 2010, Gejman, Pablo V.; Sanders, Alan R.; Duan, Jubao

Heritability of prevalent vertebral fracture and volumetric bone mineral density and geometry at the lumbar spine in three generations of the Framingham study.
score: 0.45508562, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2012, Liu, Ching-Ti et. al.

Pathway analysis following association study
score: 0.45497127, BMC Proceedings, 2011, Ngwa, Julius S et. al.

Association between a SLC23A2 gene variation, plasma vitamin C levels, and risk of glaucoma in a Mediterranean population
score: 0.45488013, Molecular Vision, 2011, Zanon-Moreno, Vicente et. al.

Oxidative risk for atherothrombotic cardiovascular disease
score: 0.45465097, Free Radical Biology and Medicine, 2009, Leopold, Jane A.; Loscalzo, Joseph

Genome-Wide Association Studies, Field Synopses, and the Development of the Knowledge Base on Genetic Variation and Human Diseases
score: 0.45418365, American Journal of Epidemiology, 2009, Khoury, Muin J. et. al.

AVPR1A and SLC6A4 Polymorphisms in Choral Singers and Non-Musicians: A Gene Association Study
score: 0.45390073, PLoS ONE, 2012, Morley, Andrew P. et. al.

Replication study of SNP associations for colorectal cancer in Hong Kong Chinese
score: 0.45365526, British Journal of Cancer, 2010, Ho, J W et. al.

Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS).
score: 0.45293052, Genetic epidemiology, 2011, Feng, Tao; Elston, Robert C; Zhu, Xiaofeng

IL10 Haplotype Associated with Tuberculin Skin Test Response but Not with Pulmonary TB
score: 0.45209998, PLoS ONE, 2009, Thye, Thorsten et. al.

Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population
score: 0.45182664, PLoS ONE, 2011, Moens, Lotte N. et. al.

Pathway Analysis of GWAS Provides New Insights into Genetic Susceptibility to 3 Inflammatory Diseases
score: 0.45146088, PLoS ONE, 2009, Eleftherohorinou, Hariklia et. al.

The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency.
score: 0.45109627, Genes and immunity, 2009, Haimila, K et. al.

Nucleotide polymorphism of the TNF gene cluster in six Chinese populations.
score: 0.45065857, Journal of human genetics, 2010, Zhang, Yongbiao et. al.

8q24 risk alleles in West African and Caribbean men.
score: 0.45020903, The Prostate, 2012, Murphy, Adam B et. al.

Prostate cancer susceptibility polymorphism rs2660753 is not associated with invasive ovarian cancer.
score: 0.45009081, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Amankwah, Ernest K et. al.

Detection for gene-gene co-association via kernel canonical correlation analysis
score: 0.45001006, BMC Genetics, 2012, Yuan, Zhongshang et. al.

Multiple Sclerosis Risk Variant HLA-DRB1*1501 Associates with High Expression of DRB1 Gene in Different Human Populations
score: 0.44976033, PLoS ONE, 2012, Alcina, Antonio et. al.

Integrated Genetic and Epigenetic Analysis Identifies Haplotype-Specific Methylation in the FTO Type 2 Diabetes and Obesity Susceptibility Locus
score: 0.44974876, PLoS ONE, 2010, Bell, Christopher G. et. al.

Application of Homozygosity Haplotype Analysis to Genetic Mapping with High-Density SNP Genotype Data
score: 0.44940159, PLoS ONE, 2009, Jiang, Haiyan et. al.

Genome-wide association studies provide new insights into type 2 diabetes aetiology.
score: 0.44897523, Nature reviews. Genetics, 2007, Frayling, Timothy M

NO role of NOS2A susceptibility polymorphisms in rheumatoid arthritis
score: 0.44893875, Nitric Oxide, 2009, Varadé, Jezabel et. al.

The Empirical Power of Rare Variant Association Methods: Results from Sanger Sequencing in 1,998 Individuals
score: 0.44892674, PLoS Genetics, 2012, Ladouceur, Martin et. al.

Genetic Variation in the Proximal Promoter of ABC and SLC Superfamilies: Liver and Kidney Specific Expression and Promoter Activity Predict Variation
score: 0.4484079, PLoS ONE, 2009, Hesselson, Stephanie E. et. al.

NordicDB: a Nordic pool and portal for genome-wide control data.
score: 0.44769449, European journal of human genetics : EJHG, 2010, Leu, Monica et. al.

PADI4 genotype is not associated with rheumatoid arthritis in a large UK Caucasian population
score: 0.4476107, Annals of the Rheumatic Diseases, 2010, Burr, Marian L et. al.

A multicenter study confirms CD226 gene association with systemic sclerosis-related pulmonary fibrosis
score: 0.447559, Arthritis Research & Therapy, 2012, Bossini-Castillo, Lara et. al.

Discovering genetic associations with high-dimensional neuroimaging phenotypes: A sparse reduced-rank regression approach
score: 0.44754865, Neuroimage, 2010, Vounou, Maria; Nichols, Thomas E.; Montana, Giovanni

Breaking barriers in the genomics and pharmacogenetics of drug addiction.
score: 0.44722396, Clinical pharmacology and therapeutics, 2010, Ho, M K et. al.

Genetic influences on craving for alcohol
score: 0.4470643, Addictive Behaviors, 2013, Agrawal, Arpana et. al.

Genetic and functional evaluation of the role of CXCR1 and CXCR2 in susceptibility to visceral leishmaniasis in north-east India
score: 0.44706099, BMC Medical Genetics, 2011, Mehrotra, Sanjana et. al.

Population structure, differential bias and genomic control in a large-scale, case-control association study.
score: 0.4458054, Nature genetics, 2005, Clayton, David G et. al.

Genotype×age interaction in human transcriptional ageing
score: 0.44542394, Mechanisms of Ageing and Development, 2012, Kent, Jack W. et. al.

Common and specific liability to addiction: Approaches to association studies of opioid addiction
score: 0.44515388, Drug and Alcohol Dependence, 2012, Nielsen, David A.; Kreek, Mary Jeanne

Common and specific liability to addiction: Approaches to association studies of opioid addiction
score: 0.44515388, Drug and Alcohol Dependence, 2012, Nielsen, David A.; Kreek, Mary Jeanne

Common and specific liability to addiction: Approaches to association studies of opioid addiction
score: 0.44515388, Drug and Alcohol Dependence, 2012, Nielsen, David A.; Kreek, Mary Jeanne

Association between polymorphisms in the adiponectin gene and cardiovascular disease: a meta-analysis
score: 0.4444286, BMC Medical Genetics, 2012, Zhang, Huan; Mo, Xingbo; Hao, Yongchen; Gu, Dongfeng

Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility to multiple autoimmune diseases.
score: 0.44341254, Rheumatology (Oxford, England), 2010, Maiti, Amit K et. al.

Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24
score: 0.44256464, The American Journal of Human Genetics, 2000, Vionnet, Nathalie et. al.

Human eye colour and HERC2, OCA2 and MATP
score: 0.44193984, Forensic Science International: Genetics, 2010, Mengel-From, Jonas et. al.

Principal components ancestry adjustment for Genetic Analysis Workshop 17 data
score: 0.44175676, BMC Proceedings, 2011, Jin, Jing et. al.

Association of DISC1 and TSNAX genes and affective disorders in the depression case-control (DeCC) and bipolar affective case-control (BACCS) studies.
score: 0.44147761, Molecular psychiatry, 2010, Schosser, A et. al.

Lack of association of CFD polymorphisms with advanced age-related macular degeneration
score: 0.44094523, Molecular Vision, 2010, Zeng, Jiexi et. al.

Evidences on three relevant obesogenes: MC4R, FTO and PPARγ. Approaches for personalized nutrition.
score: 0.44072589, Molecular nutrition & food research, 2011, Razquin, Cristina; Marti, Amelia; Martinez, Jose Alfredo

IL28B genetic variations are associated with high sustained virological response (SVR) of interferon-α plus ribavirin therapy in Taiwanese chronic HCV infection.
score: 0.44071656, Genes and immunity, 2011, Chen, J-Y et. al.

Fractalkine Is a Novel Human Adipochemokine Associated With Type 2 Diabetes
score: 0.44029845, Diabetes, 2011, Shah, Rachana et. al.

A genome-wide analysis of loss of heterozygosity and chromosomal copy number variation in Proteus syndrome using high-density SNP microarrays.
score: 0.43937354, Journal of human genetics, 2010, Yilmaz, Ahmet et. al.

World collaborative report on in vitro fertilization, 2000
score: 0.43864245, Fertility and Sterility, 2006, Adamson, G. David et. al.

Pathway Analysis Using Information from Allele-Specific Gene Methylation in Genome-Wide Association Studies for Bipolar Disorder
score: 0.43852096, PLoS ONE, 2013, Chuang, Li-Chung et. al.

Is laminin gamma-1 a candidate gene for advanced pelvic organ prolapse?
score: 0.43833814, American Journal of Obstetrics and Gynecology, 2010, Chen, Chen et. al.

Genome mapping in intensively studied wild vertebrate populations
score: 0.43798207, Trends in Genetics, 2010, Slate, Jon et. al.

A genome-wide SNP scan reveals two loci associated with the chicken resistance to Marek's disease.
score: 0.43754784, Animal genetics, 2012, Li, D F et. al.

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
score: 0.43746884, Brain, 2011, van der Zee, Julie et. al.

Correction of Population Stratification in Large Multi-Ethnic Association Studies
score: 0.43730042, PLoS ONE, 2008, Serre, David et. al.

Copy number loss of (src homology 2 domain containing)-transforming protein 2 ( SHC2 ) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy
score: 0.43708801, Molecular Brain, 2011, Sasaki, Hidenao et. al.

Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
score: 0.43689912, Human Molecular Genetics, 2011, Dempster, Emma L. et. al.

Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia
score: 0.43670385, BMC Medical Genetics, 2010, Wang, Li-San et. al.

Multifaceted genomic risk for brain function in schizophrenia
score: 0.43657046, Neuroimage, 2012, Chen, Jiayu et. al.

Multifaceted genomic risk for brain function in schizophrenia
score: 0.43657046, Neuroimage, 2012, Chen, Jiayu et. al.

Multifaceted genomic risk for brain function in schizophrenia
score: 0.43657046, Neuroimage, 2012, Chen, Jiayu et. al.

Multifaceted genomic risk for brain function in schizophrenia
score: 0.43657046, Neuroimage, 2012, Chen, Jiayu et. al.

Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14.
score: 0.43640043, Molecular psychiatry, 2006, Etain, B et. al.

ARMS2 ( LOC387715) Variants in Japanese Patients with Exudative Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy
score: 0.43565644, American Journal of Ophthalmology, 2009, Gotoh, Norimoto et. al.

A High-Resolution Linkage-Disequilibrium Map of the Human Major Histocompatibility Complex and First Generation of Tag Single-Nucleotide Polymorphisms
score: 0.43537351, The American Journal of Human Genetics, 2005, Miretti, Marcos M. et. al.

Assessment of gene-covariate interactions by incorporating covariates into association mapping
score: 0.43442275, BMC Proceedings, 2009, Chiu, Yen-Feng et. al.

A Third-Pass Genome Scan in Panic Disorder: Evidence for Multiple Susceptibility Loci
score: 0.43415163, Biological Psychiatry, 2006, Fyer, Abby J. et. al.

Genome-wide linkage analysis of QTL for growth and body composition employing the PorcineSNP60 BeadChip
score: 0.43328078, BMC Genetics, 2012, Fernández, Ana I et. al.

Follow-up investigation of 12 proposed linkage regions in multiple sclerosis.
score: 0.43317958, Genes and immunity, 2006, Herrera, B M et. al.

Challenges of molecular nutrition research 6: the nutritional phenotype database to store, share and evaluate nutritional systems biology studies
score: 0.43288266, Genes & Nutrition, 2010, van Ommen, Ben et. al.

Identifying Host Genetic Risk Factors in the Context of Public Health Surveillance for Invasive Pneumococcal Disease
score: 0.43229451, PLoS ONE, 2011, Lingappa, Jairam R. et. al.

Scan-Statistic Approach Identifies Clusters of Rare Disease Variants in LRP2, a Gene Linked and Associated with Autism Spectrum Disorders, in Three Datasets
score: 0.43220005, The American Journal of Human Genetics, 2012, Ionita-Laza, Iuliana; Makarov, Vlad; Buxbaum, Joseph D.

Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans
score: 0.43182442, Nucleic Acids Research, 2006, Meaburn, Emma et. al.

Multiple autoimmune diseases syndrome in Italian Greyhounds: Preliminary studies of genome–wide diversity and possible associations within the dog leukocyte antigen (DLA) complex
score: 0.43122103, Veterinary Immunology and Immunopathology, 2012, Pedersen, Niels C. et. al.

Is Replication the Gold Standard for Validating Genome-Wide Association Findings?
score: 0.43048128, PLoS ONE, 2008, Liu, Yong-Jun et. al.

Comparison of the power between microsatellite and single-nucleotide polymorphism markers for linkage and linkage disequilibrium mapping of an electrophysiological phenotype
score: 0.43033076, BMC Genetics, 2005, Lin, Hsiu-Fen; Juo, Suh-Hang Hank; Cheng, Rong

Pharmacogenetics of deoxycytidine kinase: identification and characterization of novel genetic variants.
score: 0.42998288, The Journal of pharmacology and experimental therapeutics, 2007, Lamba, Jatinder K et. al.

Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder
score: 0.42936633, PLoS ONE, 2010, Glessner, Joseph T. et. al.

ERCC4 associated with breast cancer risk: a two-stage case-control study using high-throughput genotyping.
score: 0.42932515, Cancer research, 2006, Milne, Roger Laughlin et. al.

Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes
score: 0.42917339, PLoS ONE, 2011, Li, Li et. al.

Investigating the Pathogenic Role of PADI4 in Oesophageal Cancer
score: 0.42913841, International Journal of Biological Sciences, 2011, Chang, Xiaotian et. al.

Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population.
score: 0.429073, Journal of human genetics, 2012, Tabassum, Rubina et. al.

Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies
score: 0.42817197, Molecular Vision, 2011, Wang, Qin et. al.

Association analysis of COMT polymorphisms with schizophrenia and smooth pursuit eye movement abnormality.
score: 0.42775536, Journal of human genetics, 2009, Park, Byung Lae et. al.

Custom genotyping for substance addiction susceptibility genes in Jordanians of Arab descent
score: 0.4273689, BMC Research Notes, 2012, AL-Eitan, Laith N et. al.

Platelet genomics and the risk of atherothrombosis.
score: 0.42626763, Journal of thrombosis and haemostasis : JTH, 2007, Ouwehand, W H et. al.

Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder.
score: 0.42587382, Molecular psychiatry, 2009, Schulze, T G et. al.

Neuronal calcium sensor-1 and cocaine addiction: A genetic association study in African-Americans and European Americans
score: 0.4251101, Neuroscience Letters, 2012, Multani, Pushpinder K. et. al.

Neuronal calcium sensor-1 and cocaine addiction: A genetic association study in African-Americans and European Americans
score: 0.4251101, Neuroscience Letters, 2012, Multani, Pushpinder K. et. al.

Neuronal calcium sensor-1 and cocaine addiction: A genetic association study in African-Americans and European Americans
score: 0.4251101, Neuroscience Letters, 2012, Multani, Pushpinder K. et. al.

Orofacial Cleft Risk Is Increased with Maternal Smoking and Specific Detoxification-Gene Variants
score: 0.42402358, The American Journal of Human Genetics, 2007, Shi, Min et. al.

Genome-wide association study for T lymphocyte subpopulations in swine
score: 0.42325176, BMC Genomics, 2012, Lu, Xin et. al.

The influence of polygenic risk for bipolar disorder on neural activation assessed using fMRI
score: 0.42291746, Translational Psychiatry, 2012, Whalley, H C et. al.

Effect of BDNF val66met polymorphism on declarative memory and its neural substrate: A meta-analysis
score: 0.4223347, Neuroscience and Biobehavioral Reviews, 2012, Kambeitz, Joseph P. et. al.

Predicting multiallelic genes using unphased and flanking single nucleotide polymorphisms.
score: 0.42190136, Genetic epidemiology, 2011, Li, Shuying S et. al.

Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement
score: 0.42161743, European Journal of Epidemiology, 2009, Little, Julian et. al.

Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1
score: 0.42139764, Genomics, 2008, Bento, J.L. et. al.

Haplotypes of DNMT1 and DNMT3B are associated with mutagen sensitivity induced by benzo[a]pyrene diol epoxide among smokers.
score: 0.42082454, Carcinogenesis, 2008, Leng, Shuguang et. al.

Genetic Variants in Interferon Regulatory Factor 2 ( IRF2 ) are Associated with Atopic Dermatitis and Eczema Herpeticum
score: 0.42022013, The Journal of Investigative Dermatology, 2011, Gao, Pei-Song et. al.

Association analysis of positional obesity candidate genes based on integrated data from transcriptomics and linkage analysis.
score: 0.41989446, International journal of obesity (2005), 2008, Jiao, H et. al.

Softwares and methods for estimating genetic ancestry in human populations
score: 0.41900479, Human Genomics, 2013, Liu, Yushi et. al.

Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs.
score: 0.41891955, The Journal of pharmacology and experimental therapeutics, 2009, Rana, Brinda K et. al.

New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?
score: 0.41877167, Frontiers in Behavioral Neuroscience, 2010, Nieratschker, Vanessa et. al.

Predicting inhaled corticosteroid response in asthma with two associated SNPs.
score: 0.41873068, The pharmacogenomics journal, 2012, McGeachie, M J et. al.

A genome-wide association screen identifies regions on chromosomes 1q25 and 7p21 as risk loci for sporadic prostate cancer.
score: 0.41845611, Prostate cancer and prostatic diseases, 2008, Nam, R K et. al.

Identifying rare disease variants in the Genetic Analysis Workshop 17 simulated data: a comparison of several statistical approaches
score: 0.41844537, BMC Proceedings, 2011, Fan, Ruixue et. al.

Comprehensive analysis of the ATM , CHEK2 and ERBB2 genes in relation to breast tumour characteristics and survival: a population-based case-control and follow-up study
score: 0.41838931, Breast Cancer Research, 2006, Einarsdóttir, Kristjana et. al.

A simple method for assessing the strength of evidence for association at the level of the whole gene
score: 0.41791636, Advances and applications in bioinformatics and chemistry : AABC, 2008, Curtis, David; Vine, Anna E; Knight, Jo

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma
score: 0.41706164, Lancet Oncology, 2010, Bayley, Jean-Pierre et. al.

The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection, and main outcome.
score: 0.41703996, Genes and immunity, 2009, Julier, C et. al.

Multilocus Association Testing of Quantitative Traits Based on Partial Least-Squares Analysis
score: 0.41700447, PLoS ONE, 2011, Zhang, Feng; Guo, Xiong; Deng, Hong-Wen

Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies.
score: 0.41609116, Human molecular genetics, 2012, Abnet, Christian C et. al.

Catechol O-methyltransferase pharmacogenomics and selective serotonin reuptake inhibitor response.
score: 0.41608095, The pharmacogenomics journal, 2012, Ji, Y et. al.

The 2nd Schizophrenia International Research Society Conference, 10–14 April 2010, Florence, Italy: Summaries of oral sessions
score: 0.41581352, Schizophrenia Research, 2010, Baharnoori, Moogeh et. al.

Cholesteryl Ester Transfer Protein ( CETP ) Polymorphisms Affect mRNA Splicing, HDL Levels, and Sex-Dependent Cardiovascular Risk
score: 0.41499016, PLoS ONE, 2012, Papp, Audrey C. et. al.

Evidence That HLA Class I and II Associations With Type 1 Diabetes, Autoantibodies to GAD and Autoantibodies to IA-2, Are Distinct
score: 0.41479636, Diabetes, 2011, Howson, Joanna M.M. et. al.

Genetic polymorphisms of innate immunity-related inflammatory pathways and their association with factors related to type 2 diabetes
score: 0.41424336, BMC Medical Genetics, 2011, Arora, Paul et. al.

TRAF1 polymorphisms associated with rheumatoid arthritis susceptibility in Asians and in Caucasians.
score: 0.4140891, Arthritis and rheumatism, 2009, Han, Tae-Un; Bang, So-Young; Kang, Changwon; Bae, Sang-Cheol

PTPN22 and myasthenia gravis: Replication in an Italian population and meta-analysis of literature data
score: 0.41398948, Neuromuscular Disorders, 2012, Provenzano, Carlo et. al.

Variants in the gene encoding C3 are associated with asthma and related phenotypes among African Caribbean families.
score: 0.4134375, Genes and immunity, 2006, Barnes, K C et. al.

Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26.
score: 0.41303171, Molecular psychiatry, 2007, Vazza, G et. al.

Comparison of similarity-based tests and pooling strategies for rare variants
score: 0.41291835, BMC Genomics, 2013, Zakharov, Sergii; Salim, Agus; Thalamuthu, Anbupalam

Transcriptome analysis and molecular signature of human retinal pigment epithelium
score: 0.41289175, Human Molecular Genetics, 2010, Strunnikova, N.V. et. al.

Common variants in FOXP1 are associated with generalized vitiligo.
score: 0.41283254, Nature genetics, 2010, Jin, Ying et. al.

Two independent prostate cancer risk-associated Loci at 11q13.
score: 0.41164002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, Zheng, S Lilly et. al.

Copy number variation of the APC gene is associated with regulation of bone mineral density
score: 0.41158714, Bone, 2012, Chew, Shelby et. al.

Characterization of the 10q26-orthologue in rhesus monkeys corroborates a functional connection between ARMS2 and HTRA1
score: 0.41129305, Experimental Eye Research, 2012, Pahl, Lisa et. al.

Characterization of the 10q26-orthologue in rhesus monkeys corroborates a functional connection between ARMS2 and HTRA1
score: 0.41129305, Experimental Eye Research, 2012, Pahl, Lisa et. al.

Characterization of the 10q26-orthologue in rhesus monkeys corroborates a functional connection between ARMS2 and HTRA1
score: 0.41129305, Experimental Eye Research, 2012, Pahl, Lisa et. al.

Characterization of the 10q26-orthologue in rhesus monkeys corroborates a functional connection between ARMS2 and HTRA1
score: 0.41129305, Experimental Eye Research, 2012, Pahl, Lisa et. al.

Clustering and commonalities among autoimmune diseases
score: 0.41104126, Journal of Autoimmunity, 2009, Mackay, Ian R.

Simple and Efficient Analysis of Disease Association with Missing Genotype Data
score: 0.4107575, The American Journal of Human Genetics, 2008, Lin, D.Y.; Hu, Y.; Huang, B.E.

A single nucleotide polymorphism in APOA5 determines triglyceride levels in Hong Kong and Guangzhou Chinese.
score: 0.41068004, European journal of human genetics : EJHG, 2010, Jiang, Chao Qiang et. al.

Small Deletion Variants Have Stable Breakpoints Commonly Associated with Alu Elements
score: 0.41028172, PLoS ONE, 2008, de Smith, Adam J. et. al.

Classification of rheumatoid arthritis status with candidate gene and genome-wide single-nucleotide polymorphisms using random forests
score: 0.41013676, BMC Proceedings, 2007, Sun, Yan V et. al.

Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population.
score: 0.40993878, Journal of human genetics, 2009, Sha, Bao-Yong et. al.

ROADTRIPS: Case-Control Association Testing with Partially or Completely Unknown Population and Pedigree Structure
score: 0.40928043, The American Journal of Human Genetics, 2010, Thornton, Timothy; McPeek, Mary Sara

Family-Based Bivariate Association Tests for Quantitative Traits
score: 0.40908571, PLoS ONE, 2009, Zhang, Lei et. al.

Genome-Wide Association Studies: Progress in Identifying Genetic Biomarkers in Common, Complex Diseases
score: 0.40899833, Biomarker Insights, 2007, Kingsmore, Stephen F. et. al.

CYP2B6 variants and plasma efavirenz concentrations during antiretroviral therapy in Port-au-Prince, Haiti.
score: 0.40825768, The Journal of infectious diseases, 2009, Leger, Paul et. al.

Joint identification of multiple genetic variants via elastic-net variable selection in a genome-wide association analysis.
score: 0.4082288, Annals of human genetics, 2010, Cho, Seoae et. al.

Variant ABO blood group alleles, secretor status, and risk of pancreatic cancer: results from the pancreatic cancer cohort consortium.
score: 0.4079041, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Wolpin, Brian M et. al.

Abnormal melatonin synthesis in autism spectrum disorders.
score: 0.40789751, Molecular psychiatry, 2008, Melke, J et. al.

Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines
score: 0.40726394, BMC Medical Genomics, 2011, Eng, Lawson et. al.

Nonmetric multidimensional scaling corrects for population structure in association mapping with different sample types.
score: 0.4070025, Genetics, 2009, Zhu, Chengsong; Yu, Jianming

Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.
score: 0.40687462, Annals of human genetics, 2008, Wang, L et. al.

Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome.
score: 0.40686296, Nature genetics, 2011, Guernsey, Duane L et. al.

Association between KCNJ6 ( GIRK2 ) Gene Polymorphisms and Postoperative Analgesic Requirements after Major Abdominal Surgery
score: 0.40662684, PLoS ONE, 2009, Nishizawa, Daisuke et. al.

PADI4 gene polymorphism is not associated with ankylosing spondylitis in Chinese Han population.
score: 0.40637313, Scandinavian journal of immunology, 2010, Chen, R et. al.

A Genome-Wide Linkage Scan for Distinct Subsets of Schizophrenia Characterized by Age at Onset and Neurocognitive Deficits
score: 0.40636945, PLoS ONE, 2011, Lien, Yin-Ju et. al.

The PhenX Toolkit: Get the Most From Your Measures
score: 0.40618258, American Journal of Epidemiology, 2011, Hamilton, Carol M. et. al.

Genetic variation in H2AFX contributes to risk of non-Hodgkin lymphoma.
score: 0.40545899, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2007, Novik, Karen L et. al.

Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2 , KCNQ1 , and WFS1 in Type 2 Diabetes in a Chinese population
score: 0.40468198, BMC Medical Genetics, 2010, Han, Xueyao et. al.

A novel analytical method, Birth Date Selection Mapping, detects response of the Angus ( Bos taurus ) genome to selection on complex traits
score: 0.4044871, BMC Genomics, 2012, Decker, Jared E et. al.

Sex-specific findings from a genome-wide linkage analysis of human fatness in non-Hispanic whites and African Americans: the HyperGEN study.
score: 0.40376436, International journal of obesity (2005), 2005, Lewis, C E et. al.

pHCR: a parallel haplotype configuration reduction algorithm for haplotype interaction analysis.
score: 0.40354374, Journal of human genetics, 2009, Makarasara, Wattanan et. al.

Absence of association of a single-nucleotide polymorphism in the TERT-CLPTM1L locus with age-related phenotypes in a large multicohort study: the HALCyon programme.
score: 0.40348108, Aging cell, 2011, Alfred, Tamuno et. al.

Genetic Biomarkers of Hypertension and Future Challenges Integrating Epigenomics
score: 0.4032564, Clinica Chimica Acta, 2012, El Shamieh, Said; Visvikis-Siest, Sophie

Genetic biomarkers of hypertension and future challenges integrating epigenomics
score: 0.4032564, Clinica Chimica Acta, 2012, El Shamieh, Said; Visvikis-Siest, Sophie

Genetic biomarkers of hypertension and future challenges integrating epigenomics
score: 0.4032564, Clinica Chimica Acta, 2012, El Shamieh, Said; Visvikis-Siest, Sophie

Genetic biomarkers of hypertension and future challenges integrating epigenomics
score: 0.4032564, Clinica Chimica Acta, 2012, El Shamieh, Said; Visvikis-Siest, Sophie

Genetic determinants of juvenile stroke
score: 0.40305342, Thrombosis Research, 2012, Pezzini, Alessandro

Phasing of Many Thousands of Genotyped Samples
score: 0.40287725, The American Journal of Human Genetics, 2012, Williams, Amy L. et. al.

A2BP1 as a novel susceptible gene for primary biliary cirrhosis in Japanese patients
score: 0.40265146, Human Immunology, 2010, Joshita, Satoru et. al.

A Genome Wide Association Scan of Bovine Tuberculosis Susceptibility in Holstein-Friesian Dairy Cattle
score: 0.40252626, PLoS ONE, 2012, Finlay, Emma K. et. al.

Polymorphisms within the C-Reactive Protein (CRP) Promoter Region Are Associated with Plasma CRP Levels
score: 0.40109096, The American Journal of Human Genetics, 2005, Carlson, Christopher S. et. al.

Cigarette experimentation in Mexican origin youth: psychosocial and genetic determinants.
score: 0.40098317, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Wilkinson, Anna V et. al.

Genetic variations in the CYP17A1 and NT5C2 genes are associated with a reduction in visceral and subcutaneous fat areas in Japanese women.
score: 0.40090738, Journal of human genetics, 2012, Hotta, Kikuko et. al.

Investigating the relationship between UMODL1 gene polymorphisms and high myopia: a case–control study in Chinese
score: 0.39940874, BMC Medical Genetics, 2012, Zhu, Miao-miao et. al.

Association between arterial stiffness and variations in oestrogen-related genes.
score: 0.39899149, Journal of human hypertension, 2009, Peter, I et. al.

Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour
score: 0.39843246, Human Molecular Genetics, 2011, Peden, John F.; Farrall, Martin

Genetic variants in the HLA-G region are associated with Kawasaki disease
score: 0.3980606, Human Immunology, 2008, Kim, Jae-Jung et. al.

Performance of random forest when SNPs are in linkage disequilibrium
score: 0.39797577, BMC Bioinformatics, 2009, Meng, Yan A et. al.

Evidence of the contribution of the X chromosome to systemic sclerosis susceptibility: association with the functional IRAK1 196Phe/532Ser haplotype.
score: 0.39781491, Arthritis and rheumatism, 2011, Dieudé, P et. al.

Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.
score: 0.39773423, Molecular psychiatry, 2011, Lesch, K-P et. al.

Systems Genetics Analysis of Gene-by-Environment Interactions in Human Cells
score: 0.39671336, The American Journal of Human Genetics, 2010, Romanoski, Casey E. et. al.

Inherited Variation in Vitamin D Genes Is Associated With Predisposition to Autoimmune Disease Type 1 Diabetes
score: 0.39580476, Diabetes, 2011, Cooper, Jason D. et. al.

Gene hunting of the Genetic Analysis Workshop 16 rheumatoid arthritis data using rough set theory
score: 0.3954269, BMC Proceedings, 2009, Aporntewan, Chatchawit et. al.

From HLA association to function.
score: 0.39502488, Nature genetics, 2012, Barrett, Jeffrey C

Analysis of genomic diversity in Mexican Mestizo populations to develop genomic medicine in Mexico.
score: 0.39453288, Proceedings of the National Academy of Sciences of the United States of America, 2009, Silva-Zolezzi, Irma et. al.

Determination of the obesity-associated gene variants within the entire FTO gene by ultra-deep targeted sequencing in obese and lean children.
score: 0.39376131, International journal of obesity (2005), 2012, Sällman Almén, M et. al.

Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task.
score: 0.39365001, Molecular psychiatry, 2011, Walter, H et. al.

Genetic variation in the Sorbs of eastern Germany in the context of broader European genetic diversity.
score: 0.39312307, European journal of human genetics : EJHG, 2011, Veeramah, Krishna R et. al.

Does genetic regulation of IgE begin in utero? Evidence from T H1/T H2 gene polymorphisms and cord blood total IgE
score: 0.39259276, The Journal of Allergy and Clinical Immunology, 2010, Hong, Xiumei et. al.

Interaction between smoking and functional polymorphism in the TGFB1 gene is associated with ischaemic heart disease and myocardial infarction in patients with rheumatoid arthritis: a cross-sectional study
score: 0.39204723, Arthritis Research & Therapy, 2012, Chen, Ying; Dawes, Peter T; Packham, Jon C; Mattey, Derek L

Genetic Architecture of Plasma Adiponectin Overlaps With the Genetics of Metabolic Syndrome–Related Traits
score: 0.39177964, Diabetes Care, 2010, Henneman, Peter et. al.

The effect of genome-wide association scan quality control on imputation outcome for common variants
score: 0.39135571, European Journal of Human Genetics, 2011, Southam, Lorraine et. al.

Association of Estimated Glomerular Filtration Rate and Urinary Uromodulin Concentrations with Rare Variants Identified by UMOD Gene Region Sequencing
score: 0.39133161, PLoS ONE, 2012, Köttgen, Anna et. al.

Common and specific liability to addiction: approaches to association studies of opioid addiction
score: 0.39081672, Drug and Alcohol Dependence, 2012, Nielsen, David A.; Kreek, Mary Jeanne

Absence of association of a single-nucleotide polymorphism in the TERT-CLPTM1L locus with age-related phenotypes in a large multicohort study: the HALCyon programme
score: 0.39059944, Aging Cell, 2011, Alfred, Tamuno et. al.

Replication Study for the Association Between Four Loci Identified by a Genome-Wide Association Study on European American Subjects With Type 1 Diabetes and Susceptibility to Diabetic Nephropathy in Japanese Subjects With Type 2 Diabetes
score: 0.38995162, Diabetes, 2010, Maeda, Shiro et. al.

Enhanced Statistical Tests for GWAS in Admixed Populations: Assessment using African Americans from CARe and a Breast Cancer Consortium
score: 0.38956192, PLoS Genetics, 2011, Pasaniuc, Bogdan et. al.

Interleukin 4, interleukin 4 receptor-α and interleukin 10 gene polymorphisms in Chagas disease.
score: 0.3894602, Parasite immunology, 2011, Flórez, O; Martín, J; González, C I

Identification of a Role for the ARHGEF3 Gene in Postmenopausal Osteoporosis
score: 0.3888704, The American Journal of Human Genetics, 2008, Mullin, Ben H. et. al.

Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome.
score: 0.38857822, Genes and immunity, 2011, Nordmark, G et. al.

C-reactive protein as a predictor of hypertension in the Hong Kong Cardiovascular Risk Factor Prevalence Study (CRISPS) cohort.
score: 0.38784182, Journal of human hypertension, 2012, Cheung, B M Y et. al.

Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study
score: 0.38669915, BMC Medical Genetics, 2009, Wolf, Christiane et. al.

Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function
score: 0.38657779, PLoS Genetics, 2010, Raychaudhuri, Soumya et. al.

Heritability in the Efficiency of Nonsense-Mediated mRNA Decay in Humans
score: 0.38638439, PLoS ONE, 2010, Seoighe, Cathal; Gehring, Chris

Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q.
score: 0.38555968, Molecular psychiatry, 2003, Wijsman, E M et. al.

Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families
score: 0.38538037, BMC Medical Genetics, 2012, Bailey-Wilson, Joan E et. al.

12th Annual Scientific Meeting of the Irish Society of Human Genetics, Friday 18th September 2009
score: 0.38523187, The Ulster Medical Journal, 2010,

Replicated associations of TNFAIP3 , TNIP1 and ETS1 with systemic lupus erythematosus in a southwestern Chinese population
score: 0.38517032, Arthritis Research & Therapy, 2011, Zhong, Hua et. al.

Phase I Metabolic Genes and Risk of Lung Cancer: Multiple Polymorphisms and mRNA Expression
score: 0.38394808, PLoS ONE, 2009, Rotunno, Melissa et. al.

FTO , Type 2 Diabetes, and Weight Gain Throughout Adult Life
score: 0.38393964, Diabetes, 2011, Hertel, Jens K. et. al.

Evidence for HTR1A and LHPP as interacting genetic risk factors in major depression.
score: 0.38384393, Molecular psychiatry, 2009, Neff, C D et. al.

Defining Alzheimer as a common age-related neurodegenerative process not inevitably leading to dementia
score: 0.38361776, Progress in Neurobiology, 2012, Ferrer, Isidro

Defining Alzheimer as a common age-related neurodegenerative process not inevitably leading to dementia
score: 0.38361776, Progress in Neurobiology, 2012, Ferrer, Isidro

Defining Alzheimer as a common age-related neurodegenerative process not inevitably leading to dementia
score: 0.38361776, Progress in Neurobiology, 2012, Ferrer, Isidro

Defining Alzheimer as a common age-related neurodegenerative process not inevitably leading to dementia
score: 0.38361776, Progress in Neurobiology, 2012, Ferrer, Isidro

Candidate gene analysis of spontaneous preterm delivery: New insights from re-analysis of a case-control study using case-parent triads and control-mother dyads
score: 0.38277672, BMC Medical Genetics, 2011, Myking, Solveig et. al.

Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data.
score: 0.38247743, Biostatistics (Oxford, England), 2007, Carvalho, Benilton et. al.

Common variants in genes that mediate immunity and risk of multiple myeloma.
score: 0.38184597, International journal of cancer. Journal international du cancer, 2007, Brown, Elizabeth E et. al.

Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence.
score: 0.38138679, The FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2010, Torri, Federica et. al.

Nature and nurture in neuropsychiatric genetics: where do we stand?
score: 0.38070768, Dialogues in Clinical Neuroscience, 2010, Dick, Danielle M.

Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent
score: 0.38068282, International Journal of Pediatric Otorhinolaryngology, 2009, Reutter, Heiko et. al.

Genetic variation in DLG5 is associated with inflammatory bowel disease.
score: 0.38059869, Nature genetics, 2004, Stoll, Monika et. al.

Tracking footprints of artificial selection in the dog genome.
score: 0.37956487, Proceedings of the National Academy of Sciences of the United States of America, 2010, Akey, Joshua M et. al.

Genetic mapping of habitual substance use, obesity-related traits, responses to mental and physical stress, and heart rate and blood pressure measurements reveals shared genes that are overrepresented in the neural synapse.
score: 0.37947485, Hypertension research : official journal of the Japanese Society of Hypertension, 2012, Nikpay, Majid et. al.

A Frameshift Mutation within LAMC2 Is Responsible for Herlitz Type Junctional Epidermolysis Bullosa (HJEB) in Black Headed Mutton Sheep
score: 0.37946697, PLoS ONE, 2011, Mömke, Stefanie et. al.

Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates
score: 0.37934518, Nucleic Acids Research, 2006, Macgregor, Stuart; Visscher, Peter M.; Montgomery, Grant

Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD.
score: 0.37893283, European journal of human genetics : EJHG, 2011, Saint-Pierre, Aude et. al.

Identification of MICA as a susceptibility gene for pulmonary Mycobacterium avium complex infection.
score: 0.37860858, The Journal of infectious diseases, 2009, Shojima, Junko et. al.

Variations in chromosomes 9 and 6p21.3 with risk of non-Hodgkin lymphoma.
score: 0.37755954, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Wang, Sophia S et. al.

Identifying association under a previous linkage peak on chromosome 16 for body mass index using cross-sectional and longitudinal data of the Framingham Heart Study
score: 0.37745849, BMC Proceedings, 2009, Li, Xiaohui et. al.

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration.
score: 0.37642865, Nature genetics, 2006, Maller, Julian et. al.

Identification of Alzheimer disease-associated variants in genes that regulate retromer function
score: 0.37589096, Neurobiology of Aging, 2012, Vardarajan, Badri N. et. al.

Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.
score: 0.37515218, Molecular psychiatry, 2007, Addington, A M et. al.

The expanding genetic overlap between multiple sclerosis and type I diabetes.
score: 0.37508743, Genes and immunity, 2009, International Multiple Sclerosis Genetics Consortium (IMSGC), et. al.

IndOR: a new statistical procedure to test for SNP-SNP epistasis in genome-wide association studies.
score: 0.37457366, Statistics in medicine, 2012, Emily, M

Genotype × Adiposity Interaction Linkage Analyses Reveal a Locus on Chromosome 1 for Lipoprotein-Associated Phospholipase A 2, a Marker of Inflammation and Oxidative Stress
score: 0.37454726, The American Journal of Human Genetics, 2007, Diego, Vincent P. et. al.

Lack of association between genetic variation in G-protein-coupled receptor for asthma susceptibility and childhood asthma and atopy.
score: 0.37394172, Genes and immunity, 2008, Wu, H et. al.

Investigation of lymphotoxin α genetic variants in migraine
score: 0.37342431, Gene, 2013, Oikari, Lotta E. et. al.

Evidence for associations between the purinergic receptor P2X(7) (P2RX7) and toxoplasmosis.
score: 0.37329758, Genes and immunity, 2010, Jamieson, S E et. al.

Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process.
score: 0.373094, European journal of human genetics : EJHG, 2012, Kuot, Abraham et. al.

Association and linkage of allelic variants of the dopamine transporter gene in ADHD.
score: 0.37283441, Molecular psychiatry, 2007, Friedel, S et. al.

Common variation in genes related to innate immunity and risk of adult glioma.
score: 0.37277505, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, Rajaraman, Preetha et. al.

Genetics of autoimmune neuroinflammation
score: 0.3727468, Current Opinion in Immunology, 2006, Olsson, Tomas et. al.

Further evidence for the association of genetic variants of ZNF804A with schizophrenia and a meta-analysis for genome-wide significance variant rs1344706
score: 0.37231931, Schizophrenia Research, 2012, Zhang, Rui et. al.

Triglyceride-rich lipoproteins and high-density lipoprotein cholesterol in patients at high risk of cardiovascular disease: evidence and guidance for management
score: 0.37033546, European Heart Journal, 2011, Chapman, M. John et. al.

Pathway and network-based analysis of genome-wide association studies in multiple sclerosis
score: 0.37027373, Human Molecular Genetics, 2009, Baranzini, Sergio E. et. al.

Identification of Genetic Variants Contributing to Cisplatin-Induced Cytotoxicity by Use of a Genomewide Approach
score: 0.37023508, The American Journal of Human Genetics, 2007, Huang, R. Stephanie et. al.

Importin-13 genetic variation is associated with improved airway responsiveness in childhood asthma
score: 0.37013875, Respiratory Research, 2009, Raby, Benjamin A et. al.

Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer.
score: 0.36891966, Cancer research, 2013, Wang, Li-E et. al.

SNCA variants are associated with increased risk for multiple system atrophy.
score: 0.3685067, Annals of neurology, 2009, Scholz, Sonja W et. al.

Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances
score: 0.3681216, Nucleic Acids Research, 2009, LaFramboise, Thomas

The effect of genetic variation in angiotensinogen on serum levels and blood pressure: a comparison of Nigerians and US blacks.
score: 0.36678957, Journal of human hypertension, 2006, Fejerman, L et. al.

ARNTL ( BMAL1 ) and NPAS2 Gene Variants Contribute to Fertility and Seasonality
score: 0.36593056, PLoS ONE, 2010, Kovanen, Leena et. al.

Copy Number Variation of KIR Genes Influences HIV-1 Control
score: 0.36430549, PLoS Biology, 2011, Pelak, Kimberly et. al.

Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism
score: 0.36369215, Neurogenetics, 2011, van Daalen, Emma et. al.

Human leukocyte antigen polymorphisms in Italian primary biliary cirrhosis: a multicenter study of 664 patients and 1992 healthy controls.
score: 0.36360567, Hepatology (Baltimore, Md.), 2008, Invernizzi, Pietro et. al.

Possible association of different G72/G30 SNPs with mood episodes and persecutory delusions in bipolar I Romanian patients
score: 0.36297643, Progress in Neuropsychopharmacology & Biological Psychiatry, 2010, Grigoroiu-Serbanescu, Maria et. al.

Mutations in genes encoding complement inhibitors CD46 and CFH affect the age at nephritis onset in patients with systemic lupus erythematosus
score: 0.36163403, Arthritis Research & Therapy, 2011, Jönsen, Andreas et. al.

Common Variants of the Liver Fatty Acid Binding Protein Gene Influence the Risk of Type 2 Diabetes and Insulin Resistance in Spanish Population
score: 0.36142553, PLoS ONE, 2012, Mansego, Maria Luisa et. al.

Adiponectin receptor 1 gene (ADIPOR1) variant is associated with advanced age-related macular degeneration in Finnish population
score: 0.36093085, Neuroscience Letters, 2012, Kaarniranta, Kai et. al.

Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.
score: 0.36084774, Molecular psychiatry, 2005, Petryshen, T L et. al.

Common genetic variants in the microRNA biogenesis pathway are not associated with breast cancer risk in Asian women.
score: 0.3608129, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012, Sung, Hyuna et. al.

Exploring case–control genetic association tests using phase diagrams
score: 0.36027468, Computational Biology and Chemistry, 2008, Li, Wentian; Suh, Young Ju; Yang, Yaning

The heritability and genetics of complement C3 expression in UK SLE families.
score: 0.36014798, Genes and immunity, 2009, Rhodes, B et. al.

Genetic Covariance Between γ-Glutamyl Transpeptidase and Fatty Liver Risk Factors: Role of β 2 -Adrenergic Receptor Genetic Variation in Twins
score: 0.35979644, Gastroenterology, 2010, Loomba, Rohit et. al.

Complement factor B polymorphism 32W protects against age-related macular degeneration
score: 0.35931484, Molecular Vision, 2011, Hughes, Anne E.; Mullan, Gemma M.; Bradley, Declan T.

Replication study of SNP associations for colorectal cancer in Hong Kong Chinese.
score: 0.35889414, British journal of cancer, 2011, Ho, J W et. al.

Abstracts of Melanoma 2010 Congress, the 7th International Melanoma Research Congress and the 4th Melanoma & Skin Cancer Centres Meeting. November 4-7, 2010. Sydney, Australia.
score: 0.35841243, Pigment cell & melanoma research, 2010,

Performance of random forests and logic regression methods using mini-exome sequence data
score: 0.35817738, BMC Proceedings, 2011, Kim, Yoonhee et. al.

Plasma CD93 concentration is a potential novel biomarker for coronary artery disease.
score: 0.35753204, Journal of internal medicine, 2011, Mälarstig, A et. al.

A systematic method for mapping multiple loci: An application to construct a genetic network for rheumatoid arthritis
score: 0.35719617, Gene, 2008, Li, Chuanxing et. al.

Genetic association of the human corticotropin releasing hormone receptor 1 (CRHR1) with binge drinking and alcohol intake patterns in two independent samples.
score: 0.35707252, Molecular psychiatry, 2006, Treutlein, J et. al.

Multiple independent genetic variants in the 8q24 region are associated with prostate cancer risk.
score: 0.35685425, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2008, Salinas, Claudia A et. al.

Polymorphisms of the BDNF gene show neither association with multiple sclerosis susceptibility nor clinical course
score: 0.35647358, Journal of Neuroimmunology, 2012, Mero, Inger-Lise et. al.

The heritability of risk and age at onset of Parkinson's disease after accounting for known genetic risk factors.
score: 0.35575979, Journal of human genetics, 2010, Hamza, Taye H; Payami, Haydeh

Evaluation of association tests for rare variants using simulated data sets in the Genetic Analysis Workshop 17 data
score: 0.35561233, BMC Proceedings, 2011, Chen, Wenan et. al.

Mexican-American Admixture Mapping Analyses for Diabetic Nephropathy in Type 2 Diabetes Mellitus
score: 0.35346151, Seminars in Nephrology, 2010, Adler, Sharon et. al.

Chapter 2 Genetics of the Framingham Heart Study Population
score: 0.35326994, Advances in Genetics, 2008, Govindaraju, Diddahally R. et. al.

Chapter 2 Genetics of the Framingham Heart Study Population
score: 0.35326994, Advances in Genetics, 2008, Govindaraju, Diddahally R. et. al.

Genetic associations of LYN with systemic lupus erythematosus.
score: 0.3527112, Genes and immunity, 2009, Lu, R et. al.

Abstract
score: 0.35262778, Pathology - Research and Practice, 2000,

Genetic adaptation of the fatty acid metabolism: A human-specific haplotype increasing the biosynthesis of long chain omega-3 and omega-6 fatty acids
score: 0.35242442, The American Journal of Human Genetics, 2012, Ameur, Adam et. al.

The future of model organisms in human disease research.
score: 0.35187416, Nature reviews. Genetics, 2011, Aitman, Timothy J et. al.

Association of SNPs and haplotypes in APOL1, 2 and 4 with schizophrenia
score: 0.35107245, Schizophrenia Research, 2008, Takahashi, Sakae et. al.

GWAS reveals new recessive loci associated with non-syndromic facial clefting
score: 0.35103045, European Journal of Medical Genetics, 2012, Camargo, Mauricio et. al.

Investigation of Multiple Susceptibility Loci for Inflammatory Bowel Disease in an Italian Cohort of Patients
score: 0.35056454, PLoS ONE, 2011, Latiano, Anna et. al.

Genetic determinants of HSP70 gene expression following heat shock
score: 0.3496411, Human Molecular Genetics, 2010, Maugeri, Narelle et. al.

Look who is calling: a comparison of genotype calling algorithms
score: 0.34946456, BMC Proceedings, 2009, Vens, Maren et. al.

Common allelic variants of the farnesyl diphosphate synthase gene influence the response of osteoporotic women to bisphosphonates.
score: 0.34936304, The pharmacogenomics journal, 2012, Olmos, J M et. al.

Replication of signals from recent studies of Crohn's disease identifies previously unknown disease loci for ulcerative colitis.
score: 0.34915294, Nature genetics, 2008, Franke, Andre et. al.

A genome-wide association study on androstenone levels in pigs reveals a cluster of candidate genes on chromosome 6
score: 0.34841677, BMC Genetics, 2010, Duijvesteijn, Naomi et. al.

Genome-wide DNA methylation analysis for diabetic nephropathy in type 1 diabetes mellitus
score: 0.34823158, BMC Medical Genomics, 2010, Bell, Christopher G et. al.

Replication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based study.
score: 0.34783691, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, Camp, Nicola J et. al.

Genome-wide linkage and association analysis of rheumatoid arthritis in a Canadian population
score: 0.3478034, BMC Proceedings, 2007, Wei, Zhi; Li, Mingyao

Cyclin D1 rare variants in UK multiple adenoma and early-onset colorectal cancer patients.
score: 0.34759186, Journal of human genetics, 2011, Bonilla, Carolina et. al.

Accelerating Haplotype-Based Genome-Wide Association Study Using Perfect Phylogeny and Phase-Known Reference Data
score: 0.34757336, PLoS ONE, 2011, He, Yungang et. al.

Overview of the Rapid Response data.
score: 0.34751295, Genes and immunity, 2009, Brown, W M et. al.

Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism
score: 0.34685448, PLoS ONE, 2009, van der Zwaag, Bert et. al.

Heritability of Problem Drinking and the Genetic Overlap with Personality in a General Population Sample
score: 0.34653442, Frontiers in Genetics, 2011, de Moor, Marleen H. M. et. al.

The role of the CD58 locus in multiple sclerosis.
score: 0.34627565, Proceedings of the National Academy of Sciences of the United States of America, 2009, De Jager, Philip L et. al.

Host genetic susceptibility to pneumococcal and meningococcal disease: a systematic review and meta-analysis
score: 0.34619554, The Lancet Infectious Diseases, 2009, Brouwer, Matthijs C et. al.

Evaluation of genetic susceptibility to childhood allergy and asthma in an African American urban population
score: 0.3461704, BMC Medical Genetics, 2011, Joubert, Bonnie R et. al.

EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units.
score: 0.34596589, European journal of human genetics : EJHG, 2011, Kam-Thong, Tony et. al.

Population differentiation as an indicator of recent positive selection in humans: an empirical evaluation.
score: 0.34528896, Genetics, 2009, Xue, Yali et. al.

The role of genetic variants in human longevity
score: 0.34528388, Ageing Research Reviews, 2010, Chung, Wen-Hung et. al.

Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes
score: 0.34522433, BMC Genetics, 2008, Shen, Fan et. al.

Genetic Variants in TGF-β Pathway Are Associated with Ovarian Cancer Risk
score: 0.34519456, PLoS ONE, 2011, Yin, Jikai et. al.

Ethnic differences in asthma and associated phenotypes: Collaborative Study on the Genetics of Asthma
score: 0.34399053, The Journal of Allergy and Clinical Immunology, 2001, Lester, Lucille A. et. al.

Genomic Runs of Homozygosity Record Population History and Consanguinity
score: 0.34394533, PLoS ONE, 2010, Kirin, Mirna et. al.

GENETICS OF PSORIASIS AND PSORIATIC ARTHRITIS
score: 0.34319344, Indian Journal of Dermatology, 2010, Chandran, Vinod

Ordered subset analysis for case-control studies.
score: 0.34292539, Genetic epidemiology, 2010, Qin, Xuejun; Hauser, Elizabeth R; Schmidt, Silke

Genome-wide association studies: potential next steps on a genetic journey.
score: 0.342746, Human molecular genetics, 2008, McCarthy, Mark I; Hirschhorn, Joel N

The neurodevelopmental model of schizophrenia: update 2005.
score: 0.34264787, Molecular psychiatry, 2005, Rapoport, J L; Addington, A M; Frangou, S; Psych, M R C

What Can Genome-Wide Association Studies Tell Us about the Genetics of Common Disease
score: 0.3423603, PLoS Genetics, 2008, Iles, Mark M

Cholesteryl ester transfer protein gene polymorphisms increase the risk of fatty liver in females independent of adiposity.
score: 0.34231226, Journal of gastroenterology and hepatology, 2012, Adams, Leon A et. al.

European survey on clinical use of cord blood for hematopoietic and non-hematopoietic indications
score: 0.34202802, Transfusion and Apheresis Science, 2010, Gratwohl, Alois; Baldomero, Helen

Common variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/2), adiponectin concentrations, and diabetes incidence in the Diabetes Prevention Program.
score: 0.34095911, Diabetic medicine : a journal of the British Diabetic Association, 2012, Mather, K J et. al.

Analysis of Neuropeptide S Receptor Gene ( NPSR1 ) Polymorphism in Rheumatoid Arthritis
score: 0.34042827, PLoS ONE, 2010, D'Amato, Mauro et. al.

What makes a good genetic association study?
score: 0.33954605, The Lancet, 2005, Hattersley, Andrew T; McCarthy, Mark I

Predictive performance of prostate cancer risk in Chinese men using 33 reported prostate cancer risk-associated SNPs.
score: 0.33885336, The Prostate, 2012, Zheng, Jie et. al.

Aquaporin 5 Polymorphisms and Rate of Lung Function Decline in Chronic Obstructive Pulmonary Disease
score: 0.33849266, PLoS ONE, 2010, Hansel, Nadia N. et. al.

Overlap of disease susceptibility loci for rheumatoid arthritis and juvenile idiopathic arthritis
score: 0.33748322, Annals of the Rheumatic Diseases, 2010, Hinks, Anne et. al.

Impact of rs361072 in the Phosphoinositide 3-Kinase p110β Gene on Whole-Body Glucose Metabolism and Subunit Protein Expression in Skeletal Muscle
score: 0.33690186, Diabetes, 2010, Ribel-Madsen, Rasmus et. al.

Meta-analysis indicates that common variants at the DISC1 locus are not associated with schizophrenia.
score: 0.33673476, Molecular psychiatry, 2012, Mathieson, I; Munafò, M R; Flint, J

Cytokine SNPs: Comparison of allele frequencies by race and implications for future studies
score: 0.33613367, Cytokine, 2009, Van Dyke, Alison L. et. al.

CCL genes in multiple sclerosis and systemic lupus erythematosus
score: 0.33608929, Journal of Neuroimmunology, 2008, Vyshkina, Tamara et. al.

SNPs Array Karyotyping Reveals a Novel Recurrent 20p13 Amplification in Primary Myelofibrosis
score: 0.33539482, PLoS ONE, 2011, Visani, Giuseppe et. al.

Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years
score: 0.33529475, Canadian Journal of Cardiology, 2012, Olesen, Morten S. et. al.

Saturation of the Human Phenome
score: 0.33524201, Current Genomics, 2010, Samuels, Mark E.

Proton pump inhibitors and the risk of overanticoagulation during acenocoumarol maintenance treatment.
score: 0.33442819, British journal of haematology, 2011, Teichert, Martina et. al.

The Obesity-Associated Polymorphisms FTO rs9939609 and MC4R rs17782313 and Endometrial Cancer Risk in Non-Hispanic White Women
score: 0.33434383, PLoS ONE, 2011, Lurie, Galina et. al.

Bioinformatics-Driven Identification and Examination of Candidate Genes for Non-Alcoholic Fatty Liver Disease
score: 0.33373879, PLoS ONE, 2011, Banasik, Karina et. al.

The role of patient mobilization after embryo transfer in in vitro fertilization programs
score: 0.33329244, American Journal of Obstetrics and Gynecology, 1995, Ben-Rafael, Zion; Orvieto, Raoul; Ashkenazi, Jacob

rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype.
score: 0.33327221, Genes and immunity, 2009, Steck, A K et. al.

Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays.
score: 0.33274357, Cancer research, 2008, Nancarrow, Derek J et. al.

No Association of nineteen COX-2 gene variants to preclinical markers of atherosclerosis The Cardiovascular Risk in Young Finns Study
score: 0.33262219, BMC Medical Genetics, 2012, Lähteelä, Kati et. al.

Can we identify genes for alcohol consumption in samples ascertained for heterogeneous purposes?
score: 0.33223675, Alcoholism, clinical and experimental research, 2009, Hansell, Narelle K et. al.

Large recurrent microdeletions associated with schizophrenia.
score: 0.33190325, Nature, 2008, Stefansson, Hreinn et. al.

ATRIUM: Testing Untyped SNPs in Case-Control Association Studies with Related Individuals
score: 0.33162498, The American Journal of Human Genetics, 2009, Wang, Zuoheng; McPeek, Mary Sara

SNP discovery, expression and cis-regulatory variation in the UGT2B genes.
score: 0.33107997, The pharmacogenomics journal, 2012, Sun, C et. al.

Genetic Variants at 6p21.1 and 7p15.3 Are Associated with Risk of Multiple Cancers in Han Chinese
score: 0.3306239, The American Journal of Human Genetics, 2012, Jin, Guangfu et. al.

Genetic Variants at 6p21.1 and 7p15.3 Are Associated with Risk of Multiple Cancers in Han Chinese
score: 0.3306239, The American Journal of Human Genetics, 2012, Jin, Guangfu et. al.

Association of PTPN22 1858 single-nucleotide polymorphism with rheumatoid arthritis in a German cohort: higher frequency of the risk allele in male compared to female patients
score: 0.33061632, Arthritis Research & Therapy, 2006, Pierer, Matthias et. al.

Early onset lung cancer, cigarette smoking and the SNP309 of the murine double minute-2 ( MDM2 ) gene
score: 0.33048258, BMC Cancer, 2008, Mittelstrass, Kirstin et. al.

Transcriptome Atlases of Mouse Brain Reveals Differential Expression Across Brain Regions and Genetic Backgrounds
score: 0.3297809, G3: Genes|Genomes|Genetics, 2012, Sun, Wei et. al.

The landscape of recombination in African Americans
score: 0.32974889, Nature, 2011, Hinch, Anjali G. et. al.

Genomewide High-Density SNP Linkage Analysis of 236 Japanese Families Supports the Existence of Schizophrenia Susceptibility Loci on Chromosomes 1p, 14q, and 20p
score: 0.32909468, The American Journal of Human Genetics, 2005, Arinami, Tadao et. al.

Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans
score: 0.3289825, Neuroscience Letters, 2012, Brambilla, Paola et. al.

Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans
score: 0.3289825, Neuroscience Letters, 2012, Brambilla, Paola et. al.

Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans
score: 0.3289825, Neuroscience Letters, 2012, Brambilla, Paola et. al.

Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans
score: 0.3289825, Neuroscience Letters, 2012, Brambilla, Paola et. al.

Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression
score: 0.32789567, Nature Genetics, 2012, Schödel, Johannes et. al.

Genotyping HLA-DRB1 and HLA-DQB1 alleles in Japanese patients with normal tension glaucoma
score: 0.32778162, Molecular Vision, 2010, Suzuki, Misa et. al.

Comparing single-nucleotide polymorphism marker-based and microsatellite marker-based linkage analyses
score: 0.327258, BMC Genetics, 2005, Ulgen, Ayse; Li, Wentian

A single nucleotide polymorphism rs9468925 of MHC region is associated with clinical features of generalized vitiligo in Chinese Han population.
score: 0.32724881, Journal of the European Academy of Dermatology and Venereology : JEADV, 2012, Liu, Jianlan et. al.

Whole Genome Distribution and Ethnic Differentiation of Copy Number Variation in Caucasian and Asian Populations
score: 0.32660519, PLoS ONE, 2009, Li, Jian et. al.

Microarray analysis of copy number variation in single cells.
score: 0.32631703, Nature protocols, 2012, Konings, Peter et. al.

Two common genetic variants near nuclear-encoded OXPHOS genes are associated with insulin secretion in vivo
score: 0.32612828, European Journal of Endocrinology, 2011, Olsson, Anders H et. al.

An autoimmune-associated variant in PTPN2 reveals an impairment of IL-2R signaling in CD4(+) T cells.
score: 0.32612395, Genes and immunity, 2011, Long, S A et. al.

Common genetic polymorphisms of microRNA biogenesis pathway genes and breast cancer survival
score: 0.32609298, BMC Cancer, 2012, Sung, Hyuna et. al.

Comparison of Pathway Analysis Approaches Using Lung Cancer GWAS Data Sets
score: 0.325866, PLoS ONE, 2012, Fehringer, Gordon et. al.

COMT polymorphisms and anxiety-related personality traits.
score: 0.32548871, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2005, Stein, Murray B et. al.

Polymorphisms at the Microseminoprotein-beta locus associated with physiologic variation in beta-microseminoprotein and prostate-specific antigen levels.
score: 0.32526268, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Xu, Xing et. al.

The genetics of lupus: a functional perspective
score: 0.32515381, Arthritis Research & Therapy, 2012, Guerra, Sandra G et. al.

Saliva samples are a viable alternative to blood samples as a source of DNA for high throughput genotyping
score: 0.32477613, BMC Medical Genomics, 2012, Abraham, Jean E et. al.

An association analysis of Per2 with panic disorder in the Japanese population.
score: 0.32454485, Journal of human genetics, 2011, Otowa, Takeshi et. al.

A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals
score: 0.32415581, The American Journal of Human Genetics, 2009, Browning, Brian L.; Browning, Sharon R.

Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels
score: 0.32379733, PLoS Genetics, 2007, Eberle, Michael A et. al.

Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancer.
score: 0.32349137, Carcinogenesis, 2012, Li, Donghui et. al.

Genome Wide Association Studies for Milk Production Traits in Chinese Holstein Population
score: 0.32293208, PLoS ONE, 2010, Jiang, Li et. al.

Polymorphism in Maternal LRP8 Gene Is Associated with Fetal Growth
score: 0.32224986, The American Journal of Human Genetics, 2006, Wang, Lin et. al.

From SNPs to Genes: Disease Association at the Gene Level
score: 0.32215947, PLoS ONE, 2011, Lehne, Benjamin; Lewis, Cathryn M.; Schlitt, Thomas

Single nucleotide polymorphisms of 8 inflammation-related genes and their associations with smoking-related cancers.
score: 0.32212143, International journal of cancer. Journal international du cancer, 2010, Oh, Sam S et. al.

A Genomewide Exploration Suggests a New Candidate Gene at Chromosome 11q23 as the Major Determinant of Plasma Homocysteine Levels: Results from the GAIT Project
score: 0.32176036, The American Journal of Human Genetics, 2005, Souto, Juan Carlos et. al.

HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk.
score: 0.32131578, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2013, Laitinen, Virpi H et. al.

Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders.
score: 0.32092231, Molecular psychiatry, 2011, Kim, S; Webster, M J

Association between the 2-bp deletion polymorphism in the duplicated version of the alpha7 nicotinic receptor gene and P50 sensory gating.
score: 0.32071518, European journal of human genetics : EJHG, 2013, Flomen, Rachel H et. al.

Fine mapping the TAGAP risk locus in rheumatoid arthritis.
score: 0.31974937, Genes and immunity, 2011, Chen, R et. al.

Evolutionary conserved longevity genes and human cognitive abilities in elderly cohorts.
score: 0.31958301, European journal of human genetics : EJHG, 2012, Lopez, Lorna M et. al.

Association between cytotoxic T lymphocyte antigen-4 polymorphism and type 1 diabetes: A meta-analysis
score: 0.31953423, Gene, 2013, Chen, Zixian et. al.

Genetic relatedness analysis: modern data and new challenges.
score: 0.31952427, Nature reviews. Genetics, 2006, Weir, Bruce S; Anderson, Amy D; Hepler, Amanda B

Genes to Diseases (G2D) Computational Method to Identify Asthma Candidate Genes
score: 0.31904168, PLoS ONE, 2008, Tremblay, Karine et. al.

Obesity–insulin targeted genes in the 3p26-25 region in human studies and LG/J and SM/J mice
score: 0.31863742, Metabolism, 2012, Kraja, Aldi T. et. al.

Characterizing Associations and SNP-Environment Interactions for GWAS-Identified Prostate Cancer Risk Markers—Results from BPC3
score: 0.31852921, PLoS ONE, 2011, Lindstrom, Sara et. al.

Polymorphisms in genes of interleukin 12 and its receptors and their association with protection against severe malarial anaemia in children in western Kenya
score: 0.31715107, Malaria Journal, 2010, Zhang, Lyna et. al.

Cumulative association of eight susceptibility genes with systemic lupus erythematosus in a Japanese female population.
score: 0.31658991, Journal of human genetics, 2011, Koga, Minori et. al.

Pharmacogenetics of pain and analgesia.
score: 0.31629624, Clinical genetics, 2012, Smith, M T; Muralidharan, A

Association mapping: methodologies, strategies, and issues.
score: 0.31627081, Genetic epidemiology, 2005, Havill, Lorena M; Dyer, Thomas D

Nucleotide excision repair pathway polymorphisms and pancreatic cancer risk: evidence for role of MMS19L.
score: 0.31604947, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009, McWilliams, Robert R et. al.

Investigation of Adducin 2 (beta) DNA polymorphisms in genetic predisposition to diabetic nephropathy in Type 1 diabetes.
score: 0.31529852, Diabetic medicine : a journal of the British Diabetic Association, 2008, Currie, D et. al.

Implications of Central Obesity-Related Variants in LYPLAL1, NRXN3, MSRA, and TFAP2B on Quantitative Metabolic Traits in Adult Danes
score: 0.31520912, PLoS ONE, 2011, Bille, Dorthe S. et. al.

An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found.
score: 0.31498837, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2005, Hartikainen, Jaana M et. al.

Pharmacogenetic pathway analysis of docetaxel elimination.
score: 0.31476646, Clinical pharmacology and therapeutics, 2009, Baker, S D et. al.

Follow-up of 1715 SNPs from the Wellcome Trust Case Control Consortium genome-wide association study in type I diabetes families.
score: 0.31468394, Genes and immunity, 2009, Cooper, J D et. al.

Investigation of potential non-HLA rheumatoid arthritis susceptibility loci in a European cohort increases the evidence for nine markers
score: 0.31463857, Annals of the Rheumatic Diseases, 2010, Plant, Darren et. al.

Large-Scale Evaluation of Candidate Genes Identifies Associations between VEGF Polymorphisms and Bladder Cancer Risk
score: 0.31407427, PLoS Genetics, 2007, García-Closas, Montserrat et. al.

Further replication studies of the EVE Consortium meta-analysis identifies 2 asthma risk loci in European Americans
score: 0.31320933, The Journal of Allergy and Clinical Immunology, 2012, Myers, Rachel A. et. al.

Further replication studies of the EVE Consortium meta-analysis identifies 2 asthma risk loci in European Americans
score: 0.31320933, The Journal of Allergy and Clinical Immunology, 2012, Myers, Rachel A. et. al.

Genetic variations in ZFP36 and their possible relationship to autoimmune diseases
score: 0.31314522, Journal of Autoimmunity, 2006, Carrick, Danielle Mercatante et. al.

A functional alternative splicing mutation in human tryptophan hydroxylase-2.
score: 0.31218969, Molecular psychiatry, 2011, Zhang, X et. al.

Haplotypes spanning SPEC2, PDZ-GEF2 and ACSL6 genes are associated with schizophrenia.
score: 0.31184134, Human molecular genetics, 2006, Chen, Xiangning et. al.

Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis.
score: 0.31176104, Human molecular genetics, 2013, Smith, Katherine R et. al.

Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder
score: 0.31162653, European Child & Adolescent Psychiatry, 2010, Rommelse, Nanda N. J. et. al.

Regulation of major histocompatibility complex class II gene expression, genetic variation and disease.
score: 0.3107802, Genes and immunity, 2010, Handunnetthi, L; Ramagopalan, S V; Ebers, G C; Knight, J C

Haplotype association analysis of North American Rheumatoid Arthritis Consortium data using a generalized linear model with regularization
score: 0.31049656, BMC Proceedings, 2009, Guo, Wei; Liang, Chin-yuan; Lin, Shili

A method for detecting epistasis in genome-wide studies using case-control multi-locus association analysis
score: 0.31044122, BMC Genomics, 2008, Gayán, Javier et. al.

An Extreme-Sib-Pair Genome Scan for Genes Regulating Blood Pressure
score: 0.31018426, The American Journal of Human Genetics, 1999, Xu, Xiping et. al.

A comparison between screened NIMH and clinically interviewed control samples on neuroticism and extraversion.
score: 0.30944187, Molecular psychiatry, 2008, Talati, A; Fyer, A J; Weissman, M M

A Common Variant in DRD3 Receptor Is Associated with Autism Spectrum Disorder
score: 0.30924197, Biological Psychiatry, 2009, de Krom, Mariken et. al.

Genetic polymorphism and response to treatment in chronic hepatitis C: The future of personalized medicine
score: 0.3087242, Journal of Hepatology, 2010, Asselah, Tarik

Racial disparity in pathophysiologic pathways of preterm birth based on genetic variants
score: 0.30866398, Reproductive Biology and Endocrinology : RB&E, 2009, Menon, Ramkumar et. al.

Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity.
score: 0.30792081, Aging cell, 2009, Pawlikowska, Ludmila et. al.

Patterns of population structure and environmental associations to aridity across the range of loblolly pine (Pinus taeda L., Pinaceae).
score: 0.30787173, Genetics, 2010, Eckert, Andrew J et. al.

Whole Genome Association Study in a Homogenous Population in Shandong Peninsula of China Reveals JARID2 as a Susceptibility Gene for Schizophrenia
score: 0.30713874, Journal of Biomedicine and Biotechnology, 2009, Liu, Yang et. al.

Analysis of the RELN gene as a genetic risk factor for autism.
score: 0.30682521, Molecular psychiatry, 2005, Skaar, D A et. al.

Genetics of complex respiratory diseases: implications for pathophysiology and pharmacology studies.
score: 0.30625145, British journal of pharmacology, 2011, Obeidat, Ma'en; Hall, Ian P

Association of Specific Haplotypes of Neurotrophic Tyrosine Kinase Receptor 2 Gene ( NTRK2) with Vulnerability to Nicotine Dependence in African-Americans and European-Americans
score: 0.3056182, Biological Psychiatry, 2007, Beuten, Joke et. al.

Allelic Skewing of DNA Methylation Is Widespread across the Genome
score: 0.30521146, The American Journal of Human Genetics, 2010, Schalkwyk, Leonard C. et. al.

Genomic Research to Identify Novel Pathways in the Development of Abdominal Aortic Aneurysm
score: 0.30479255, Cardiology Research and Practice, 2012, Harrison, Seamus C. et. al.

Reviewer acknowledgement 2012
score: 0.304782, BMC Microbiology, 2013, Harris, Philippa K

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment
score: 0.30467819, American Journal of Human Genetics, 2009, Newbury, Dianne F. et. al.

Variation in IL7R predisposes to sarcoid inflammation.
score: 0.30398187, Genes and immunity, 2009, Heron, M et. al.

Integrated genetic and genomic approach in the SingaporeTranslational and Clinical Research in Psychosis Study: an overview.
score: 0.30387988, Early intervention in psychiatry, 2011, Sim, Kang et. al.

Rare Copy Number Variants Disrupt Genes Regulating Vascular Smooth Muscle Cell Adhesion and Contractility in Sporadic Thoracic Aortic Aneurysms and Dissections
score: 0.30360711, The American Journal of Human Genetics, 2010, Prakash, Siddharth K. et. al.

The association of a single-nucleotide polymorphism of the IL-2 inducible T-cell Kinase gene with asthma.
score: 0.30358131, Annals of human genetics, 2011, Lee, Shin-Hwa et. al.

A Bayesian genome screening of maximum number of drinks as an alcoholism phenotype with the new Haseman-Elston method
score: 0.30350526, BMC Genetics, 2005, Oh, Cheongeun et. al.

Identification of Sialyltransferase 8B as a Generalized Susceptibility Gene for Psychotic and Mood Disorders on Chromosome 15q25-26
score: 0.30322972, PLoS ONE, 2012, McAuley, Erica Z. et. al.

Reproductive aging-associated common genetic variants and the risk of breast cancer
score: 0.30273225, Breast Cancer Research : BCR, 2012, He, Chunyan et. al.

Nonparametric longitudinal allele-sharing model
score: 0.30234424, BMC Genetics, 2003, Kulle, Bettina et. al.

Early onset prostate cancer has a significant genetic component.
score: 0.30204294, The Prostate, 2012, Lange, Ethan M et. al.

T2DM: Why Epigenetics?
score: 0.30199613, Journal of Nutrition and Metabolism, 2011, Fradin, Delphine; Bougnères, Pierre

Fast detection of de novo copy number variants from SNP arrays for case-parent trios
score: 0.30186373, BMC Bioinformatics, 2012, Scharpf, Robert B et. al.

Differential Genetic Regulation of Canine Hip Dysplasia and Osteoarthritis
score: 0.30140955, PLoS ONE, 2010, Zhou, Zhengkui et. al.

BDNF Contributes to the Genetic Variance of Milk Fat Yield in German Holstein Cattle
score: 0.30130769, Frontiers in Genetics, 2011, Zielke, Lea G. et. al.

The Role of Geography in Human Adaptation
score: 0.30121617, PLoS Genetics, 2009, Coop, Graham et. al.

Gene-based multiple trait analysis for exome sequencing data
score: 0.30038057, BMC Proceedings, 2011, Zhao, Jingyuan; Thalamuthu, Anbupalam

UPDG: U tilities package for data analysis of P ooled D NA G WAS
score: 0.3000739, BMC Genetics, 2012, Ho, Daniel WH; Yap, Maurice KH; Yip, Shea Ping

Family-based samples can play an important role in genetic association studies.
score: 0.29996862, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2008, Lange, Ethan M et. al.

Association of genetic variants in chromosome 17q21 and adult-onset asthma in a Chinese Han population
score: 0.29989995, BMC Medical Genetics, 2011, Fang, QiuRong et. al.

Genes Involved in the Metabolism of Poly-Unsaturated Fatty-Acids (PUFA) and Risk for Crohn's Disease in Children & Young Adults
score: 0.29976937, PLoS ONE, 2010, Costea, Irina et. al.

Interacting haplotypes at the NPAS3 locus alter risk of schizophrenia and bipolar disorder.
score: 0.29933267, Molecular psychiatry, 2009, Pickard, B S et. al.

Direct assessment of multiple testing correction in case-control association studies with related individuals.
score: 0.2978645, Genetic epidemiology, 2011, Wang, Zuoheng

Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis
score: 0.29767413, Molecular Immunology, 2008, Montes, Tamara et. al.

The Effect of Single Nucleotide Polymorphisms from Genome Wide Association Studies in Multiple Sclerosis on Gene Expression
score: 0.29740515, PLoS ONE, 2010, Handel, Adam E. et. al.

How genomics has informed our understanding of the pathogenesis of osteoporosis
score: 0.29736204, Genome Medicine, 2009, Johnson, Mark L; Lara, Nuria; Kamel, Mohamed A

Understanding type 1 diabetes through genetics: advances and prospects.
score: 0.29719833, Nature reviews. Genetics, 2011, Polychronakos, Constantin; Li, Quan

Family-based association study of cocaine- and amphetamine-regulated transcript (CARTPT) and protein interaction with C-kinase-1 (PICK1) genes in attention-deficit hyperactivity disorder
score: 0.2962295, Psychiatry Research, 2012, Hsu, Cheng-Dien et. al.

Structural Variation of Chromosomes in Autism Spectrum Disorder
score: 0.29603943, The American Journal of Human Genetics, 2008, Marshall, Christian R. et. al.

Association of Systemic Lupus Erythematosus Clinical Features with European Population Genetic Substructure
score: 0.29592602, PLoS ONE, 2011, Alonso-Perez, Elisa et. al.

UMOD as a susceptibility gene for end-stage renal disease
score: 0.29576748, BMC Medical Genetics, 2012, Reznichenko, Anna et. al.

PCA-based bootstrap confidence interval tests for gene-disease association involving multiple SNPs
score: 0.29531377, BMC Genetics, 2010, Peng, Qianqian; Zhao, Jinghua; Xue, Fuzhong

Common genetic variants on chromosome 9p21 predict perioperative myocardial injury after coronary artery bypass graft surgery
score: 0.29493498, The Journal of Thoracic and Cardiovascular Surgery, 2010, Liu, Kuang-Yu et. al.

The association between leukocyte telomere length and cigarette smoking, dietary and physical variables, and risk of prostate cancer.
score: 0.29459643, Aging cell, 2009, Mirabello, Lisa et. al.

Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs
score: 0.2944111, BMC Genetics, 2008, Hannelius, Ulf et. al.

RS-SNP: a random-set method for genome-wide association studies
score: 0.29429635, BMC Genomics, 2011, D'Addabbo, Annarita et. al.

Evolution, revolution and heresy in the genetics of infectious disease susceptibility
score: 0.29426062, Philosophical Transactions of the Royal Society B: Biological Sciences, 2012, Hill, Adrian V. S.

Impact of whole genome amplification on analysis of copy number variants
score: 0.29378193, Nucleic Acids Research, 2008, Pugh, T. J. et. al.

Large-scale association analysis of TNF / LTA gene region polymorphisms in type 2 diabetes
score: 0.29375299, BMC Medical Genetics, 2010, Boraska, Vesna et. al.

Association of PDE11A global haplotype with major depression and antidepressant drug response
score: 0.29350123, Neuropsychiatric Disease and Treatment, 2009, Luo, Huai-Rong et. al.

Methionine adenosyltransferase 2A/2B and methylation: gene sequence variation and functional genomics.
score: 0.2929917, Drug metabolism and disposition: the biological fate of chemicals, 2011, Nordgren, Kendra K S et. al.

A two-stage association study identifies methyl-CpG-binding domain protein 2 gene polymorphisms as candidates for breast cancer susceptibility
score: 0.29285757, European Journal of Human Genetics, 2012, Sapkota, Yadav et. al.

Cytokine genetic polymorphisms and prostate cancer aggressiveness.
score: 0.29261052, Carcinogenesis, 2009, Zabaleta, Jovanny et. al.

The molecular basis of human retinal and vitreoretinal diseases
score: 0.29246318, Progress in Retinal and Eye Research, 2010, Berger, Wolfgang et. al.

Non-replication study of a genome-wide association study for hypertension and blood pressure in African Americans
score: 0.29224783, BMC Medical Genetics, 2012, Kidambi, Srividya et. al.

ALOX12 polymorphisms are associated with fat mass but not peak bone mineral density in Chinese nuclear families.
score: 0.29191395, International journal of obesity (2005), 2011, Xiao, W-J et. al.

Studies of Metabolic Phenotypic Correlates of 15 Obesity Associated Gene Variants
score: 0.29170537, PLoS ONE, 2011, Sandholt, Camilla Helene et. al.

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe.
score: 0.29148626, Human mutation, 2012, Rubio, Justin P et. al.

Recessive LAMC3 mutations cause malformations of occipital cortical development.
score: 0.29129846, Nature genetics, 2011, Barak, Tanyeri et. al.

Association between a variation in LRCH1 and knee osteoarthritis: a genome-wide single-nucleotide polymorphism association study using DNA pooling.
score: 0.29071824, Arthritis and rheumatism, 2006, Spector, Tim D et. al.

Multiple sclerosis susceptibility alleles in African Americans.
score: 0.29046301, Genes and immunity, 2010, Johnson, B A et. al.

Genetic Variants of the α-Synuclein Gene SNCA Are Associated with Multiple System Atrophy
score: 0.2902431, PLoS ONE, 2009, Al-Chalabi, Ammar et. al.

Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1
score: 0.29017748, BMC Proceedings, 2007, Curtin, Karen et. al.

Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy
score: 0.28971111, BMC Medical Genetics, 2010, Leak, Tennille S et. al.

Genetic Association and Expression Studies Indicate a Role of Toll-Like Receptor 8 in Pulmonary Tuberculosis
score: 0.28928119, PLoS Genetics, 2008, Davila, Sonia et. al.

DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity
score: 0.28922146, BMC Medical Genetics, 2008, Fan, Bao Jian et. al.

The Emerging Importance of Genetics in Epidemiologic Research III. Bioinformatics and Statistical Genetic Methods
score: 0.28878367, Annals of Epidemiology, 1999, Ellsworth, Darrell L.; Manolio, Teri A.; Mhs,

BDNF Val66Met is associated with introversion and interacts with 5-HTTLPR to influence neuroticism.
score: 0.28844303, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2010, Terracciano, Antonio et. al.

Polymorphisms in the interleukin-22 receptor alpha-1 gene are associated with severe chronic rhinosinusitis
score: 0.28838975, Otolaryngology - Head and Neck Surgery, 2009, Endam, Leandra Mfuna et. al.

Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study
score: 0.28793704, BMC Medical Genetics, 2011, Lopez-Escamez, José A et. al.

A new era for Type 2 diabetes genetics.
score: 0.2874518, Diabetic medicine : a journal of the British Diabetic Association, 2007, Zeggini, E

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese
score: 0.28704436, Molecular Vision, 2009, Lee, Kelvin Y.C. et. al.

Buffy coat specimens remain viable as a DNA source for highly multiplexed genome-wide genetic tests after long term storage
score: 0.28681643, Journal of Translational Medicine, 2011, Mychaleckyj, Josyf C et. al.

A statistical method for region-based meta-analysis of genome-wide association studies in genetically diverse populations.
score: 0.28680874, European journal of human genetics : EJHG, 2012, Wang, Xu et. al.

CCRaVAT and QuTie - enabling analysis of rare variants in large-scale case control and quantitative trait association studies
score: 0.28680135, BMC Bioinformatics, 2010, Lawrence, Robert et. al.

Common variation in the BRCA1 gene and prostate cancer risk.
score: 0.28648739, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2007, Douglas, Julie A et. al.

Inherited destiny? Genetics and gestational diabetes mellitus
score: 0.28531702, Genome Medicine, 2011, Watanabe, Richard M

Development of a fingerprinting panel using medically relevant polymorphisms
score: 0.28497484, BMC Medical Genomics, 2009, Cross, Deanna S; Ivacic, Lynn C; McCarty, Catherine A

A genetic association study of DNA methylation levels in the DRD4 gene region finds associations with nearby SNPs
score: 0.28478116, Behavioral and Brain Functions : BBF, 2012, Docherty, Sophia J et. al.

Deciphering the genetics of hereditary non-syndromic colorectal cancer.
score: 0.28470495, European journal of human genetics : EJHG, 2008, Papaemmanuil, Eli et. al.

Consistency of HLA associations between two independent measles vaccine cohorts: A replication study
score: 0.28455354, Vaccine, 2012, Ovsyannikova, Inna G. et. al.

Genetic analysis of six SNPs in candidate genes associated with high cross-race risk of development of thoracic aortic aneurysms and dissections in Chinese Han population.
score: 0.28409322, Acta pharmacologica Sinica, 2010, Liu, Ou et. al.

Adult Rat Bones Maintain Distinct Regionalized Expression of Markers Associated with Their Development
score: 0.28373815, PLoS ONE, 2009, Rawlinson, Simon C. F. et. al.

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders.
score: 0.28352863, Human molecular genetics, 2008, Mercader, Josep Maria et. al.

Genetic variation in SH3-domain GRB2-like (endophilin)-interacting protein 1 has a major impact on fat mass.
score: 0.28271083, International journal of obesity (2005), 2012, Cummings, N et. al.

Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits
score: 0.28223722, PLoS Genetics, 2011, Paul, Dirk S. et. al.

IGF-1 gene polymorphisms in Polish families with high-grade myopia
score: 0.28183289, Molecular Vision, 2011, Rydzanicz, Malgorzata et. al.

Cell regulation
score: 0.28178807, Current Opinion in Cell Biology, 1996,

Association analysis of formyl peptide receptor 2 (FPR2) polymorphisms and aspirin exacerbated respiratory diseases.
score: 0.28035451, Journal of human genetics, 2012, Kim, Hee-Jeong et. al.

Differential contribution of genetic variation in multiple brain nicotinic cholinergic receptors to nicotine dependence: recent progress and emerging open questions.
score: 0.28025198, Molecular psychiatry, 2009, Greenbaum, L; Lerer, B

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene.
score: 0.27990231, European journal of human genetics : EJHG, 2009, Hilgert, Nele et. al.

Genetic association of CR1 with Alzheimer's disease: A tentative disease mechanism
score: 0.27974157, Neurobiology of Aging, 2012, Hazrati, Lili-Naz et. al.

Genetic Linkage to Chromosome 22q12 for a Heavy-Smoking Quantitative Trait in Two Independent Samples
score: 0.27969798, The American Journal of Human Genetics, 2007, Saccone, Scott F. et. al.

Confirmation that SNPs in the high mobility group-A2 gene (HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2.
score: 0.27969412, Electrophoresis, 2011, Takeshita, Haruo et. al.

A Randomized Trial Comparing Intravitreal Triamcinolone Acetonide and Focal/Grid Photocoagulation for Diabetic Macular Edema
score: 0.27913665, Ophthalmology, 2008,

Genetic variation in SIRT1 affects susceptibility of lung squamous cell carcinomas in former uranium miners from the Colorado plateau.
score: 0.27894028, Carcinogenesis, 2013, Leng, Shuguang et. al.

Genome-wide association studies using single-nucleotide polymorphisms versus haplotypes: an empirical comparison with data from the North American Rheumatoid Arthritis Consortium
score: 0.27885091, BMC Proceedings, 2009, Shim, Heejung et. al.

An application of Random Forests to a genome-wide association dataset: Methodological considerations & new findings
score: 0.27875649, BMC Genetics, 2010, Goldstein, Benjamin A et. al.

Genetic variation in Glutathione S-Transferase Omega-1, Arsenic Methyltransferase and Methylene-tetrahydrofolate Reductase, arsenic exposure and bladder cancer: a case–control study
score: 0.27838235, Environmental Health, 2012, Beebe-Dimmer, Jennifer L et. al.

Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation
score: 0.278302, PLoS Genetics, 2011, Lefeber, Dirk J. et. al.

A deletion mutation in bovine SLC4A2 is associated with osteopetrosis in Red Angus cattle
score: 0.27770747, BMC Genomics, 2010, Meyers, Stacey N et. al.

Gender Differences in Genetic Risk Profiles for Cardiovascular Disease
score: 0.2772748, PLoS ONE, 2008, Silander, Kaisa et. al.

Validation of IRF5 as multiple sclerosis risk gene: putative role in interferon beta therapy and human herpes virus-6 infection.
score: 0.27727248, Genes and immunity, 2011, Vandenbroeck, K et. al.

Para-inflammation in the aging retina
score: 0.27675857, Progress in Retinal and Eye Research, 2009, Xu, Heping; Chen, Mei; Forrester, John V.

Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.
score: 0.27646545, Molecular psychiatry, 2010, Palmieri, L et. al.

New Complexities in the Genetics of Stuttering: Significant Sex-Specific Linkage Signals
score: 0.27645478, The American Journal of Human Genetics, 2006, Suresh, Rathi et. al.

Outcomes of methotrexate therapy for psoriasis and relationship to genetic polymorphisms.
score: 0.27617548, The British journal of dermatology, 2009, Warren, R B et. al.

Association tests and software for copy number variant data
score: 0.27592134, Human Genomics, 2009, Plagnol, Vincent

Prevalence of common disease-associated variants in Asian Indians
score: 0.27577028, BMC Genetics, 2008, Pemberton, Trevor J et. al.

Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes.
score: 0.27551006, Journal of human genetics, 2012, Yamaguchi-Kabata, Yumi et. al.

Pharmacogenomics of the RNA world: structural RNA polymorphisms in drug therapy.
score: 0.2753394, Clinical pharmacology and therapeutics, 2011, Sadee, W et. al.

Haplotypes of intron 4 of the estrogen receptor alpha gene and hip fractures: a replication study in Caucasians
score: 0.27472931, BMC Medical Genetics, 2010, Velasco, Javier et. al.

Whole genome association studies in complex diseases: where do we stand?
score: 0.27454952, Dialogues in Clinical Neuroscience, 2010, Need, Anna C.

Variants of the interleukin-1 receptor antagonist gene are associated with fat mass in men.
score: 0.27452106, International journal of obesity (2005), 2009, Andersson, N et. al.

Two missense variants in UHRF1BP1 are independently associated with systemic lupus erythematosus in Hong Kong Chinese.
score: 0.27411242, Genes and immunity, 2011, Zhang, Y et. al.

So Many Correlated Tests, So Little Time! Rapid Adjustment of P Values for Multiple Correlated Tests
score: 0.27382737, The American Journal of Human Genetics, 2007, Conneely, Karen N.; Boehnke, Michael

PTPN22 1858C>T Polymorphism Distribution in Europe and Association with Rheumatoid Arthritis: Case-Control Study and Meta-Analysis
score: 0.27365838, PLoS ONE, 2011, Totaro, Michele Ciro et. al.

Genetic variants in the chemokines and chemokine receptors in Chagas disease
score: 0.27289563, Human Immunology, 2012, Flórez, Oscar; Martín, Javier; González, Clara Isabel

Genetic variants in the chemokines and chemokine receptors in Chagas disease
score: 0.27289563, Human Immunology, 2012, Flórez, Oscar; Martín, Javier; González, Clara Isabel

Genetic variants in the chemokines and chemokine receptors in Chagas disease
score: 0.27289563, Human Immunology, 2012, Flórez, Oscar; Martín, Javier; González, Clara Isabel

Current status of lupus genetics
score: 0.27277462, Arthritis Research & Therapy, 2007, Sestak, Andrea L et. al.

The SNAP-25 gene is associated with cognitive ability: evidence from a family-based study in two independent Dutch cohorts.
score: 0.27256518, Molecular psychiatry, 2006, Gosso, M F et. al.

An integrated expression phenotype mapping approach defines common variants in LEP, ALOX15 and CAPNS1 associated with induction of IL-6
score: 0.27202566, Human Molecular Genetics, 2009, Fairfax, Benjamin P. et. al.

A comparative study of three methods for detecting association of quantitative traits in samples of related subjects
score: 0.27200488, BMC Proceedings, 2009, Saint Pierre, Aude; Vitezica, Zulma; Martinez, Maria

The Rotterdam Study: objectives and design update
score: 0.27200339, European Journal of Epidemiology, 2007, Hofman, Albert et. al.

The use of common mitochondrial variants to detect and characterise population structure in the Australian population: implications for genome-wide association studies.
score: 0.27192432, European journal of human genetics : EJHG, 2008, Byrne, Enda M et. al.

MicroRNA target site polymorphisms and human disease
score: 0.27189535, Trends in Genetics, 2008, Sethupathy, Praveen; Collins, Francis S.

Variable selection in logistic regression for detecting SNP-SNP interactions: the rheumatoid arthritis example.
score: 0.27188477, European journal of human genetics : EJHG, 2008, Lin, Hui-Yi et. al.

Association of serotonin and dopamine gene pathways with behavioral subphenotypes in dementia
score: 0.27129439, Neurobiology of Aging, 2012, Proitsi, Petroula et. al.

Variation in Catechol- O-Methyltransferase Is Associated with Duloxetine Response in a Clinical Trial for Major Depressive Disorder
score: 0.27126665, Biological Psychiatry, 2009, Perlis, Roy H. et. al.

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
score: 0.27126462, Nature genetics, 2009, Khanna, Hemant et. al.

Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients
score: 0.26967188, Neurobiology of Aging, 2012, van Blitterswijk, Marka et. al.

Genetic Factors Predisposing to Systemic Lupus Erythematosus and Lupus Nephritis
score: 0.26914276, Seminars in Nephrology, 2010, Ramos, Paula S. et. al.

Finding disease candidate genes by liquid association
score: 0.26867423, Genome Biology, 2007, Li, Ker-Chau et. al.

Advances in molecular genetics of panic disorder.
score: 0.26824391, Molecular psychiatry, 2010, Maron, E; Hettema, J M; Shlik, J

The prostate cancer risk locus at 10q11 is associated with DNA repair capacity
score: 0.26792511, DNA Repair, 2012, Rinckleb, Antje E. et. al.

Imaging genetics of FOXP2 in dyslexia.
score: 0.26757252, European journal of human genetics : EJHG, 2012, Wilcke, Arndt et. al.

Genetic Variance in the Adiponutrin Gene Family and Childhood Obesity
score: 0.26714829, PLoS ONE, 2009, Johansson, Lovisa E. et. al.

Genetic Control of Obesity and Gut Microbiota Composition in Response to High-Fat, High-Sucrose Diet in Mice
score: 0.26637643, Cell Metabolism, 2013, Parks, Brian W. et. al.

Interrogating Type 2 Diabetes Genome-Wide Association Data Using a Biological Pathway-Based Approach
score: 0.26523128, Diabetes, 2009, Perry, John R.B. et. al.

Pancreatic cancer risk and ABO blood group alleles: results from the pancreatic cancer cohort consortium.
score: 0.26492557, Cancer research, 2010, Wolpin, Brian M et. al.

Genome-Wide Analysis of Copy Number Variation in Type 1 Diabetes
score: 0.26479627, PLoS ONE, 2010, Grayson, Britney L. et. al.

Risk-taking behavior in a gambling task associated with variations in the tryptophan hydroxylase 2 gene: relevance to psychiatric disorders.
score: 0.26449927, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2010, Juhasz, Gabriella et. al.

IL-4 receptor polymorphisms predict reduction in asthma exacerbations during response to an anti–IL-4 receptor α antagonist
score: 0.26439017, The Journal of Allergy and Clinical Immunology, 2012, Slager, Rebecca E. et. al.

IL-4 receptor polymorphisms predict reduction in asthma exacerbations during response to an anti–IL-4 receptor α antagonist
score: 0.26439017, The Journal of Allergy and Clinical Immunology, 2012, Slager, Rebecca E. et. al.

Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease.
score: 0.2635875, Movement disorders : official journal of the Movement Disorder Society, 2009, Sutherland, Greg T et. al.

Integrating Rare-Variant Testing, Function Prediction, and Gene Network in Composite Resequencing-Based Genome-Wide Association Studies (CR-GWAS)
score: 0.26357059, G3: Genes|Genomes|Genetics, 2011, Zhu, Chengsong; Li, Xianran; Yu, Jianming

Contributions of Dopamine-Related Genes and Environmental Factors to Highly Sensitive Personality: A Multi-Step Neuronal System-Level Approach
score: 0.26340561, PLoS ONE, 2011, Chen, Chunhui et. al.

Reprioritizing Genetic Associations in Hit Regions Using LASSO-Based Resample Model Averaging
score: 0.26302519, Genetic Epidemiology, 2012, Valdar, William et. al.

Analysis of MMP2 promoter polymorphisms in childhood obesity
score: 0.26285372, BMC Research Notes, 2011, Morgan, Angharad R et. al.

Type 2 diabetes mellitus and inflammation: Prospects for biomarkers of risk and nutritional intervention
score: 0.26260118, Diabetes, metabolic syndrome and obesity : targets and therapy, 2010, Badawi, Alaa et. al.

Two genome-wide linkage disequilibrium screens in Scandinavian multiple sclerosis patients
score: 0.26243549, Journal of Neuroimmunology, 2003, Harbo, Hanne F. et. al.

Haplotypic background of a private allele at high frequency in the Americas.
score: 0.2617003, Molecular biology and evolution, 2009, Schroeder, Kari B et. al.

Contribution of TMC6 and TMC8 (EVER1 and EVER2) variants to cervical cancer susceptibility.
score: 0.26154949, International journal of cancer. Journal international du cancer, 2012, Castro, Felipe A et. al.

Associations of vascular endothelial growth factor (VEGF) with adhesion and inflammation molecules in a healthy population
score: 0.26117936, Cytokine, 2013, Azimi-Nezhad, Mohsen et. al.

Leader of the pack: gene mapping in dogs and other model organisms.
score: 0.26107072, Nature reviews. Genetics, 2008, Karlsson, Elinor K; Lindblad-Toh, Kerstin

No evidence of association between functional polymorphisms located within IL6R and IL6ST genes and systemic sclerosis.
score: 0.26077512, Tissue antigens, 2012, Cénit, M C et. al.

Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study
score: 0.26055133, Lipids in Health and Disease, 2012, Lv, Xiaofei et. al.

CDH13 is associated with working memory performance in attention deficit/hyperactivity disorder.
score: 0.2601322, Genes, brain, and behavior, 2011, Arias-Vásquez, A et. al.

Haplotype structure of TNFRSF5-TNFSF5 (CD40-CD40L) and association analysis in systemic lupus erythematosus.
score: 0.25945459, European journal of human genetics : EJHG, 2005, Chadha, Sapna et. al.

An Autosomal Genomic Scan for Loci Linked to Type II Diabetes Mellitus and Body-Mass Index in Pima Indians
score: 0.25942312, The American Journal of Human Genetics, 1998, Hanson, Robert L. et. al.

Genome scan linkage analysis comparing microsatellites and single-nucleotide polymorphisms markers for two measures of alcoholism in chromosomes 1, 4, and 7
score: 0.25896634, BMC Genetics, 2005, Chen, Guanjie et. al.

The genetic basis of multiple sclerosis: a model for MS susceptibility
score: 0.25828069, BMC Neurology, 2010, Goodin, Douglas S

Recent human evolution has shaped geographical differences in susceptibility to disease
score: 0.25827222, BMC Genomics, 2011, Marigorta, Urko M et. al.

Interleukin-1 receptor antagonist haplotype associated with prostate cancer risk.
score: 0.25825947, British journal of cancer, 2005, Lindmark, F et. al.

Abstract
score: 0.25825857, Biological Psychiatry, 1999,

Major gender difference in association of FTO gene variant among severely obese children with obesity and obesity related phenotypes
score: 0.25780203, Biochemical and Biophysical Research Communications, 2008, Jacobsson, Josefin A. et. al.

Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human Genome
score: 0.25659741, The American Journal of Human Genetics, 2006, Locke, Devin P. et. al.

Avoiding mouse traps in schizophrenia genetics: lessons and promises from current and emerging mouse models
score: 0.25650867, Neuroscience, 2012, Kvajo, M.; McKellar, H.; Gogos, J.A.

To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests
score: 0.25453168, The American Journal of Human Genetics, 2010, Li, Yun; Byrnes, Andrea E.; Li, Mingyao

Whole-genome molecular haplotyping of single cells.
score: 0.25440126, Nature biotechnology, 2011, Fan, H Christina et. al.

The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility
score: 0.25397647, Molecular Pain, 2012, Holliday, Kate L et. al.

Systematic review of the evidence relating FEV 1 decline to giving up smoking
score: 0.25375049, BMC Medicine, 2010, Lee, Peter N; Fry, John S

Pooled analysis of phosphatidylinositol 3-kinase pathway variants and risk of prostate cancer.
score: 0.25335554, Cancer research, 2010, Koutros, Stella et. al.

Genome-wide linkage analysis of serum creatinine in three isolated European populations.
score: 0.25277049, Kidney international, 2009, Pattaro, Cristian et. al.

Copy Number Variants in Obesity-Related Syndromes: Review and Perspectives on Novel Molecular Approaches
score: 0.25276407, Journal of Obesity, 2012, D'Angelo, Carla Sustek; Koiffmann, Celia Priszkulnik

Human genetic susceptibility to infectious disease.
score: 0.25212167, Nature reviews. Genetics, 2012, Chapman, Stephen J; Hill, Adrian V S

Inflammation, Insulin Resistance, and Diabetes—Mendelian Randomization Using CRP Haplotypes Points Upstream
score: 0.25193318, PLoS Medicine, 2008, Brunner, Eric J et. al.

Familial associations of rheumatoid arthritis with autoimmune diseases and related conditions.
score: 0.25192679, Arthritis and rheumatism, 2009, Hemminki, Kari et. al.

Variation in the ATP-binding cassette transporter 2 gene is a separate risk factor for Systemic Lupus Erythematosus within the MHC
score: 0.25177287, Genes and immunity, 2009, Ramos, Paula S. et. al.

Large, rare chromosomal deletions associated with severe early-onset obesity.
score: 0.25144632, Nature, 2010, Bochukova, Elena G et. al.

An exonic insertion within Tex14 gene causes spermatogenic arrest in pigs
score: 0.25135963, BMC Genomics, 2011, Sironen, Anu et. al.

Meta-analyses of molecular association studies: Methodologic lessons for genetic epidemiology
score: 0.25083501, Journal of Clinical Epidemiology, 2003, Attia, John; Thakkinstian, Ammarin; D'Este, Catherine

Association of polymorphisms in C2, CFB and C3 with exudative age-related macular degeneration in a Korean population
score: 0.25062114, Experimental Eye Research, 2012, Kim, Suk Jin; Lee, Soo Jeong; Kim, Na Rae; Chin, Hee Seung

The genetics of Tourette syndrome: A review
score: 0.24996202, Journal of Psychosomatic Research, 2009, O'Rourke, Julia A. et. al.

Analysis of TNFAIP3 , a feedback inhibitor of nuclear factor-κB and the neighbor intergenic 6q23 region in rheumatoid arthritis susceptibility
score: 0.24992546, Arthritis Research & Therapy, 2009, Dieguez-Gonzalez, Rebeca et. al.

CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations.
score: 0.24988114, Genes and immunity, 2012, Eike, M C et. al.

ESR1/SYNE1 polymorphism and invasive epithelial ovarian cancer risk: an Ovarian Cancer Association Consortium study.
score: 0.24957326, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Doherty, Jennifer A et. al.

ITGA4 polymorphisms and susceptibility to multiple sclerosis
score: 0.24941149, Journal of Neuroimmunology, 2007, O'Doherty, Catherine et. al.

Genome-wide linkage analyses for age at diagnosis of hypertension and early-onset hypertension in the HyperGEN study
score: 0.24923749, American Journal of Hypertension, 2004, Wilk, Jemma B. et. al.

A Putative Alzheimer's Disease Risk Allele in PCK1 Influences Brain Atrophy in Multiple Sclerosis
score: 0.24911328, PLoS ONE, 2010, Xia, Zongqi et. al.

Body mass index and obesity- and diabetes-associated genotypes and risk for pancreatic cancer.
score: 0.24898613, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Tang, Hongwei et. al.

Phenotype forecasting with SNPs data through gene-based Bayesian networks
score: 0.24898555, BMC Bioinformatics, 2009, Malovini, Alberto et. al.

Efficiency robust statistics for genetic linkage and association studies under genetic model uncertainty.
score: 0.24837734, Statistics in medicine, 2010, Joo, Jungnam; Kwak, Minjung; Chen, Zehua; Zheng, Gang

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.
score: 0.2480919, Molecular psychiatry, 2011, Delahanty, R J et. al.

Genetic variants in the chemokines and chemokine receptors in Chagas disease
score: 0.24803435, Human Immunology, 2012, Flórez, Oscar; Martín, Javier; González, Clara Isabel

An Assessment of the Individual and Collective Effects of Variants on Height Using Twins and a Developmentally Informative Study Design
score: 0.2479436, PLoS Genetics, 2011, Vrieze, Scott I. et. al.

Interleukin-10 gene polymorphisms and chronic/aggressive periodontitis susceptibility: A meta-analysis based on 14 case-control studies
score: 0.24771471, Cytokine, 2012, Zhong, Qianfu; Ding, Cheng; Wang, Meilin; Sun, Ying; Xu, Yan

Interleukin-10 gene polymorphisms and chronic/aggressive periodontitis susceptibility: A meta-analysis based on 14 case-control studies
score: 0.24771471, Cytokine, 2012, Zhong, Qianfu; Ding, Cheng; Wang, Meilin; Sun, Ying; Xu, Yan

Associations between variants of the 8q24 chromosome and nine smoking-related cancer sites.
score: 0.24661657, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2008, Park, Sungshim Lani et. al.

IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma
score: 0.24584481, The American Journal of Human Genetics, 2007, Balaci, Lenuta et. al.

Genetic variation of genes involved in dihydrotestosterone metabolism and the risk of prostate cancer.
score: 0.24578108, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010, Setlur, Sunita R et. al.

Why do young women smoke? VII COMT as a risk modifying gene for Nicotine dependence - role of gene-gene interaction, personality, and environmental factors.
score: 0.24564894, Human psychopharmacology, 2010, Greenbaum, Lior et. al.

Pathway-based analysis of a genome-wide case-control association study of rheumatoid arthritis
score: 0.24547441, BMC Proceedings, 2009, Beyene, Joseph et. al.

Expression of concern re: Kulminski, A. 2011. Complex phenotypes and phenomenon of genome-wide inter-chromosomal linkage disequilibrium in the human genome. Experimental Gerontology. DOI: 10.1016/j.exger.2011.08.010
score: 0.24520029, Experimental Gerontology, 2012, Paterson, Andrew D.

Expression of concern re: Kulminski, A. 2011. Complex phenotypes and phenomenon of genome-wide inter-chromosomal linkage disequilibrium in the human genome. Experimental Gerontology. DOI: 10.1016/j.exger.2011.08.010
score: 0.24520029, Experimental Gerontology, 2012, Paterson, Andrew D.

Expression of concern re: Kulminski, A. 2011. Complex phenotypes and phenomenon of genome-wide inter-chromosomal linkage disequilibrium in the human genome. Experimental Gerontology. Doi: 10.1016/j.exger.2011.08.010
score: 0.24520029, Experimental Gerontology, 2012, Paterson, Andrew D.

Expression of concern re: Kulminski, A. 2011. Complex phenotypes and phenomenon of genome-wide inter-chromosomal linkage disequilibrium in the human genome. Experimental Gerontology. DOI: 10.1016/j.exger.2011.08.010
score: 0.24520029, Experimental Gerontology, 2012, Paterson, Andrew D.

Association of galanin haplotypes with alcoholism and anxiety in two ethnically distinct populations.
score: 0.24516537, Molecular psychiatry, 2006, Belfer, I et. al.

Guidelines and Recommendations for Laboratory Analysis in the Diagnosis and Management of Diabetes Mellitus
score: 0.24347726, Diabetes Care, 2011, Sacks, David B. et. al.

Genetic Basis of Sjögren's Syndrome. How Strong is the Evidence?
score: 0.24324835, Clinical and Developmental Immunology, 2006, Anaya, Juan-Manuel et. al.

Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients
score: 0.24300662, Journal of Autoimmunity, 2009, Akkad, D.A. et. al.

Personalized medicine and atrial fibrillation: will it ever happen?
score: 0.24271835, BMC Medicine, 2012, Lubitz, Steven A; Ellinor, Patrick T

Incorporation of genetic model parameters for cost-effective designs of genetic association studies using DNA pooling
score: 0.24271728, BMC Genomics, 2007, Ji, Fei et. al.

Despite identifying some shared gene associations with human atopic dermatitis the use of multiple dog breeds from various locations limits detection of gene associations in canine atopic dermatitis
score: 0.24227769, Veterinary Immunology and Immunopathology, 2010, Wood, Shona H. et. al.

Genetics of pigmentation in skin cancer — A review
score: 0.24171279, Mutation Research-Reviews in Mutation Research, 2010, Scherer, Dominique; Kumar, Rajiv

On Sharing Quantitative Trait GWAS Results in an Era of Multiple-omics Data and the Limits of Genomic Privacy
score: 0.24166786, The American Journal of Human Genetics, 2012, Im, Hae Kyung et. al.

On Sharing Quantitative Trait GWAS Results in an Era of Multiple-omics Data and the Limits of Genomic Privacy
score: 0.24166786, The American Journal of Human Genetics, 2012, Im, Hae Kyung et. al.

A theoretical molecular network for dyslexia: integrating available genetic findings.
score: 0.24159452, Molecular psychiatry, 2011, Poelmans, G; Buitelaar, J K; Pauls, D L; Franke, B

LINGO1 Variants in the French-Canadian Population
score: 0.24073704, PLoS ONE, 2011, Bourassa, Cynthia V. et. al.

Incorporating prior knowledge to facilitate discoveries in a genome-wide association study on age-related macular degeneration
score: 0.24033314, BMC Research Notes, 2010, Lin, Wan-Yu; Lee, Wen-Chung

Meta-analysis supports association between serotonin transporter (5-HTT) and suicidal behavior.
score: 0.24029134, Molecular psychiatry, 2007, Li, D; He, L

A genome-wide approach identifies that the aspartate metabolism pathway contributes to asparaginase sensitivity.
score: 0.23984422, Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K, 2011, Chen, S-H et. al.

Genetic Adaptation of the Hypoxia-Inducible Factor Pathway to Oxygen Pressure among Eurasian Human Populations.
score: 0.23974798, Molecular biology and evolution, 2012, Ji, Lin-Dan et. al.

Genome-wide association in bipolar.
score: 0.23935785, Molecular psychiatry, 2008, Gershon, E S; Liu, C; Badner, J A

Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium
score: 0.23917133, Lancet Oncology, 2006, Rothman, Nathaniel et. al.

Cultural inheritance drives site fidelity and migratory connectivity in a long-distance migrant.
score: 0.23914008, Molecular ecology, 2010, Harrison, Xavier A et. al.

Whole-Genome association analysis of susceptibility to paratuberculosis in holstein cattle.
score: 0.2390863, Animal genetics, 2010, Kirkpatrick, B W; Shi, X; Shook, G E; Collins, M T

Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays
score: 0.23892313, Genome Biology, 2008, Staaf, Johan et. al.

FTO gene variation and measures of body mass in an African population
score: 0.2388431, BMC Medical Genetics, 2009, Hennig, Branwen J et. al.

17q12-21 Variants are associated with asthma and interact with active smoking in an adult population from the United Kingdom
score: 0.23857756, Annals of Allergy, Asthma & Immunology, 2012, Marinho, Susana et. al.

17q12-21 Variants are associated with asthma and interact with active smoking in an adult population from the United Kingdom
score: 0.23857756, Annals of Allergy, Asthma & Immunology, 2012, Marinho, Susana et. al.

17q12-21 Variants are associated with asthma and interact with active smoking in an adult population from the United Kingdom
score: 0.23857756, Annals of Allergy, Asthma & Immunology, 2012, Marinho, Susana et. al.

Microduplications of 16p11.2 are associated with schizophrenia.
score: 0.23781827, Nature genetics, 2009, McCarthy, Shane E et. al.

Genetic differentiation of Jewish populations.
score: 0.23776539, Tissue antigens, 2010, Klitz, W et. al.

Alzheimer culprits: Cellular crossroads and interplay
score: 0.23739234, Cellular Signalling, 2012, Claeysen, Sylvie et. al.

Alzheimer culprits: Cellular crossroads and interplay
score: 0.23739234, Cellular Signalling, 2012, Claeysen, Sylvie et. al.

Alzheimer culprits: Cellular crossroads and interplay
score: 0.23739234, Cellular Signalling, 2012, Claeysen, Sylvie et. al.

Complement factor H polymorphisms, renal phenotypes and age-related macular degeneration: the Blue Mountains Eye Study.
score: 0.23690286, Genes and immunity, 2008, Xing, C et. al.

Referee acknowledgement for 2011.
score: 0.23651551, British journal of cancer, 2012,

Neonatal diabetes mellitus: a disease linked to multiple mechanisms
score: 0.2353002, Orphanet Journal of Rare Diseases, 2007, Polak, Michel; Cavé, Hélène

Associations of polymorphisms in the apolipoprotein A1/C3/A4/A5 gene cluster with familial combined hyperlipidaemia in Hong Kong Chinese
score: 0.23510134, Atherosclerosis, 2010, Liu, Zhi-Kai et. al.

Chromosome-scale selective sweeps shape Caenorhabditis elegans genomic diversity.
score: 0.23480195, Nature genetics, 2012, Andersen, Erik C et. al.

High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians
score: 0.23437679, Genome Biology, 2009, Matsuzaki, Hajime et. al.

Uniparental disomy in cancer
score: 0.23428128, Trends in Molecular Medicine, 2009, Tuna, Musaffe; Knuutila, Sakari; Mills, Gordon B.

A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first.
score: 0.23403358, European journal of human genetics : EJHG, 2009, Gijsbers, Antoinet C J et. al.

Interrogating 11 fast-evolving genes for signatures of recent positive selection in worldwide human populations.
score: 0.23308052, Molecular biology and evolution, 2009, Moreno-Estrada, Andrés et. al.

Human genetics of osteoporosis
score: 0.23261567, Best Practice & Research Clinical Endocrinology & Metabolism, 2008, Ferrari, Serge

Genome-wide association study reveals five nucleotide sequence variants for carcass traits in beef cattle.
score: 0.23242219, Animal genetics, 2011, Kim, Y; Ryu, J; Woo, J; Kim, J B; Kim, C Y; Lee, C

Variant alleles of the Wnt antagonist FRZB are determinants of hip shape and modify the relationship between hip shape and osteoarthritis.
score: 0.23240558, Arthritis and rheumatism, 2012, Baker-Lepain, Julie C et. al.

Hierarchical Generalized Linear Models for Multiple Groups of Rare and Common Variants: Jointly Estimating Group and Individual-Variant Effects
score: 0.23235256, PLoS Genetics, 2011, Yi, Nengjun; Liu, Nianjun; Zhi, Degui; Li, Jun

Significant association of ANKK1 and detection of a functional polymorphism with nicotine dependence in an African-American sample.
score: 0.23234714, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Huang, Weihua et. al.

The SERPINE2 Gene Is Associated with Chronic Obstructive Pulmonary Disease
score: 0.23233865, The American Journal of Human Genetics, 2006, DeMeo, Dawn L. et. al.

An Interferon-Induced Helicase ( IFIH1 ) Gene Polymorphism Associates With Different Rates of Progression From Autoimmunity to Type 1 Diabetes
score: 0.23176918, Diabetes, 2011, Winkler, Christiane et. al.

Goldsurfer2 (Gs2): A comprehensive tool for the analysis and visualization of genome wide association studies
score: 0.23176891, BMC Bioinformatics, 2008, Pettersson, Fredrik et. al.

Differential confounding of rare and common variants in spatially structured populations
score: 0.23151499, Nature genetics, 2011, Mathieson, Iain; McVean, Gil

Insulin Storage and Glucose Homeostasis in Mice Null for the Granule Zinc Transporter ZnT8 and Studies of the Type 2 Diabetes–Associated Variants
score: 0.23110436, Diabetes, 2009, Nicolson, Tamara J. et. al.

Genetic determinants of common obesity and their value in prediction
score: 0.23094617, Best Practice & Research Clinical Endocrinology & Metabolism, 2012, Loos, Ruth J.F.

Evaluating linkage disequilibrium and recombination provides a haplotype-tagging SNP panel of the major histocompatibility complex in African Americans.
score: 0.23045137, Genes and immunity, 2008, Kelley, J M et. al.

Cross-species replication of a resistin mRNA QTL, but not QTLs for circulating levels of resistin, in human and baboon.
score: 0.23002307, Heredity, 2008, Tejero, M E et. al.

The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies
score: 0.22986263, BMC Medical Genomics, 2011, McCarty, Catherine A et. al.

Natural selection and the distribution of identity-by-descent in the human genome.
score: 0.22974132, Genetics, 2010, Albrechtsen, Anders; Moltke, Ida; Nielsen, Rasmus

Genome-Wide Linkage Analysis of Obsessive-Compulsive Disorder Implicates Chromosome 1p36
score: 0.229315, Biological Psychiatry, 2012, Mathews, Carol A. et. al.

Genome-wide Linkage Analysis of Obsessive-Compulsive Disorder Implicates Chromosome 1p36
score: 0.229315, Biological Psychiatry, 2012, Mathews, Carol A. et. al.

Mining the LIPG Allelic Spectrum Reveals the Contribution of Rare and Common Regulatory Variants to HDL Cholesterol
score: 0.22925165, PLoS Genetics, 2011, Khetarpal, Sumeet A. et. al.

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
score: 0.2289415, Neuron, 2010, Johnson, Janel O. et. al.

Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease.
score: 0.22858455, Nature genetics, 2008, Romeo, Stefano et. al.

Transmission-ratio distortion in the Framingham Heart Study
score: 0.22854539, BMC Proceedings, 2009, Paterson, Andrew D et. al.

Low-penetrance susceptibility to hematological malignancy
score: 0.22846499, Current Opinion in Genetics & Development, 2010, Houlston, Richard S

The Genetics of Alzheimer's Disease
score: 0.2279757, Progress in Molecular Biology and Translational Science, 2012, Bertram, Lars; Tanzi, Rudolph E.

Vitamin D and multiple sclerosis
score: 0.22761742, Lancet Neurology, 2010, Ascherio, Alberto; Munger, Kassandra L; Simon, K Claire

Genetic association of the CHRNA6 and CHRNB3 genes with tobacco dependence in a nationally representative sample.
score: 0.22739193, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Hoft, Nicole R et. al.

Gene Copy-Number Variation and Associated Polymorphisms of Complement Component C4 in Human Systemic Lupus Erythematosus (SLE): Low Copy Number Is a Risk Factor for and High Copy Number Is a Protective Factor against SLE Susceptibility in European Americans
score: 0.2273311, The American Journal of Human Genetics, 2007, Yang, Yan et. al.

Association of autoimmunity to peptidyl arginine deiminase type 4 with genotype and disease severity in rheumatoid arthritis.
score: 0.22707676, Arthritis and rheumatism, 2008, Harris, Michelle L et. al.

Investigating the genetic association between ERAP1 and ankylosing spondylitis
score: 0.22705204, Human Molecular Genetics, 2009, Harvey, David et. al.

A twin study of self-regulatory eating in early childhood: estimates of genetic and environmental influence, and measurement considerations.
score: 0.22701991, International journal of obesity (2005), 2012, Faith, M S et. al.

Nocturnal Enuresis: A Suggestive Endophenotype Marker for a Subgroup of Inattentive Attention-Deficit/Hyperactivity Disorder
score: 0.22566777, The Journal of Pediatrics, 2009, Elia, Josephine et. al.

Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy.
score: 0.22543892, Nature medicine, 2009, Hassel, David et. al.

High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density
score: 0.22515113, Bone, 2010, Giroux, Sylvie et. al.

A haplotype of the norepinephrine transporter (Net) gene Slc6a2 is associated with clinical response to atomoxetine in attention-deficit hyperactivity disorder (ADHD).
score: 0.22512388, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Ramoz, Nicolas et. al.

Deletion of LCE3C and LCE3B genes is associated with psoriasis in a northern Chinese population.
score: 0.2246552, The British journal of dermatology, 2011, Xu, L et. al.

Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis.
score: 0.22400162, Nature genetics, 2010, Hirschfield, Gideon M et. al.

Assessment of SNPs associated with the human glucocorticoid receptor in primary open-angle glaucoma and steroid responders
score: 0.22394575, Molecular Vision, 2010, Fingert, John H. et. al.

No association between the ERBB3 gene and schizophrenia in a Japanese population
score: 0.22389252, Neuroscience Research, 2007, Watanabe, Yuichiro et. al.

Efficient Replication of over 180 Genetic Associations with Self-Reported Medical Data
score: 0.22357679, PLoS ONE, 2011, Tung, Joyce Y. et. al.

Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden
score: 0.2222487, Human Molecular Genetics, 2009, Renström, Frida et. al.

Mechanisms of peripheral neuropathy associated with bortezomib and vincristine in patients with newly diagnosed multiple myeloma: a prospective analysis of data from the HOVON-65/GMMG-HD4 trial
score: 0.22208095, Lancet Oncology, 2010, Broyl, Annemiek et. al.

Contents
score: 0.22150437, Current Opinion in Biotechnology, 1996,

Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13.
score: 0.22074738, Nature genetics, 2008, Barton, Anne et. al.

GSTM1, GSTT1, GSTP1, GSTA1 and colorectal cancer risk: A comprehensive meta-analysis
score: 0.22060221, European Journal of Cancer, 2010, Economopoulos, Konstantinos P.; Sergentanis, Theodoros N.

A gene variant near ATM is significantly associated with metformin treatment response in type 2 diabetes: a replication and meta-analysis of five cohorts
score: 0.22030276, Diabetologia, 2012, van Leeuwen, N. et. al.

Genetic and non-genetic correlates of vitamins K and D.
score: 0.22011168, European journal of clinical nutrition, 2009, Shea, M K et. al.

Age- and gender-specific awareness, treatment, and control of cardiovascular risk factors and subclinical vascular lesions in a founder population: The SardiNIA Study
score: 0.21989481, Nutrition, Metabolism and Cardiovascular Diseases, 2009, Scuteri, A. et. al.

Mass Homozygotes Accumulation in the NCI-60 Cancer Cell Lines As Compared to HapMap Trios, and Relation to Fragile Site Location
score: 0.2189561, PLoS ONE, 2012, Ruan, Xiaoyang et. al.

Estimating the Total Number of Susceptibility Variants Underlying Complex Diseases from Genome-Wide Association Studies
score: 0.21825622, PLoS ONE, 2010, So, Hon-Cheong; Yip, Benjamin H. K.; Sham, Pak Chung

Singleton SNPs in the human genome and implications for genome-wide association studies.
score: 0.21772054, European journal of human genetics : EJHG, 2008, Ke, Xiayi; Taylor, Martin S; Cardon, Lon R

The CD6 multiple sclerosis susceptibility allele is associated with alterations in CD4+ T cell proliferation.
score: 0.21769426, Journal of immunology (Baltimore, Md. : 1950), 2011, Kofler, David M et. al.

Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations.
score: 0.21757656, Journal of human genetics, 2010, Numata, Sanae et. al.

Quantitative-Trait Loci Influencing Body-Mass Index Reside on Chromosomes 7 and 13: The National Heart, Lung, and Blood Institute Family Heart Study
score: 0.21752186, The American Journal of Human Genetics, 2002, Feitosa, Mary F. et. al.

Genetic Architecture of MicroRNA Expression: Implications for the Transcriptome and Complex Traits
score: 0.21726, The American Journal of Human Genetics, 2012, Gamazon, Eric R. et. al.

Genetic Architecture of MicroRNA Expression: Implications for the Transcriptome and Complex Traits
score: 0.21726, The American Journal of Human Genetics, 2012, Gamazon, Eric R. et. al.

Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample.
score: 0.21691187, Molecular psychiatry, 2010, Riley, B et. al.

Studies of CTNNBL1 and FDFT1 variants and measures of obesity: analyses of quantitative traits and case-control studies in 18,014 Danes
score: 0.21664629, BMC Medical Genetics, 2009, Andreasen, Camilla Helene et. al.

Single-nucleotide polymorphisms within the antioxidant defence system and associations with aggressive prostate cancer.
score: 0.2164025, BJU international, 2011, Abe, Miyako et. al.

Genetic association analysis of the interleukin 7 gene ( IL7) in multiple sclerosis
score: 0.216107, Journal of Neuroimmunology, 2007, Lundmark, Frida; Duvefelt, Kristina; Hillert, Jan

A common cortactin gene variation confers differential susceptibility to severe asthma.
score: 0.21466574, Genetic epidemiology, 2008, Ma, Shwu-Fan et. al.

Comprehensive pathway-based interrogation of genetic variations in the nucleotide excision DNA repair pathway and risk of bladder cancer.
score: 0.21452556, Cancer, 2012, Xing, Jinliang et. al.

Acronyms of clinical trials in cardiology—1994
score: 0.21450818, The American Journal of Cardiology, 1994, Cheng, Tsung O.

Evidence of association between GDF5 polymorphisms and congenital dislocation of the hip in a Caucasian population
score: 0.21450695, Osteoarthritis and Cartilage, 2010, Rouault, K. et. al.

Estimation of historical effective population size using linkage disequilibria with marker data.
score: 0.21447757, Journal of animal breeding and genetics = Zeitschrift für Tierzüchtung und Züchtungsbiologie, 2012, Corbin, L J; Liu, A Y H; Bishop, S C; Woolliams, J A

The prostate cancer risk locus at 10q11 is associated with DNA repair capacity
score: 0.2144509, DNA Repair, 2012, Rinckleb, Antje E. et. al.

The prostate cancer risk locus at 10q11 is associated with DNA repair capacity
score: 0.2144509, DNA Repair, 2012, Rinckleb, Antje E. et. al.

A new analysis tool for individual-level allele frequency for genomic studies
score: 0.21329353, BMC Genomics, 2010, Yang, Hsin-Chou et. al.

GAB2 is not associated with late-onset Alzheimer's disease in Japanese.
score: 0.21325516, European journal of human genetics : EJHG, 2009, Miyashita, Akinori et. al.

Data analysis issues for allele-specific expression using Illumina's GoldenGate assay
score: 0.21321686, BMC Bioinformatics, 2010, Ritchie, Matthew E et. al.

Associations between cytokine/cytokine receptor single nucleotide polymorphisms and humoral immunity to measles, mumps and rubella in a Somali population.
score: 0.21314954, Tissue antigens, 2008, Dhiman, N et. al.

Thioredoxin reductase 1 haplotypes modify familial amyotrophic lateral sclerosis onset
score: 0.21288231, Free Radical Biology and Medicine, 2009, Mitchell, John; Morris, Alex; de Belleroche, Jacqueline

Depletion of potential A2M risk haplotype for Alzheimer's disease in long-lived individuals.
score: 0.21266443, European journal of human genetics : EJHG, 2010, Flachsbart, Friederike et. al.

No association between the FXYD6 gene and schizophrenia in the Chinese Han population
score: 0.21250355, Journal of Psychiatric Research, 2010, Zhang, Jing et. al.

Survey of SSC12 Regions Affecting Fatty Acid Composition of Intramuscular Fat Using High-Density SNP Data
score: 0.21241151, Frontiers in Genetics, 2011, Muñoz, María et. al.

A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer
score: 0.2123476, PLoS ONE, 2012, Campa, Daniele et. al.

A second genetic variant on chromosome 15q24-25.1 associates with lung cancer.
score: 0.21232616, Cancer research, 2010, Liu, Pengyuan et. al.

Opposing effects of the HLA-DRB1*0301-DQB1*0201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel.
score: 0.21192526, Genes and immunity, 2010, Benedek, G et. al.

Influence of Candidate Genes on Attention Problems in Children: A Longitudinal Study
score: 0.21172913, Behavior Genetics, 2010, van Beijsterveldt, Catherina E. M. et. al.

Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation.
score: 0.2108328, Biometrics, 2012, Schwender, Holger et. al.

Investigation of Type 2 Diabetes Risk Alleles Support CDKN2A/B , CDKAL1 , and TCF7L2 As Susceptibility Genes in a Han Chinese Cohort
score: 0.21070047, PLoS ONE, 2010, Wen, Jie et. al.

Association of the CCR5 gene with juvenile idiopathic arthritis
score: 0.21048, Genes and Immunity, 2010, Hinks, A et. al.

Pharmaceutical biotechnology
score: 0.21038479, Current Opinion in Biotechnology, 1997,

The role of aldehyde dehydrogenase-1 ( ALDH1A1 ) polymorphisms in harmful alcohol consumption in a Finnish population
score: 0.20904216, Human Genomics, 2008, Lind, Penelope A; Eriksson, C J Peter; Wilhelmsen, Kirk C

Association between the NBS1 E185Q polymorphism and cancer risk: a meta-analysis
score: 0.20876998, BMC Cancer, 2009, Lu, Meixia et. al.

Enriching the Analysis of Genomewide Association Studies with Hierarchical Modeling
score: 0.20871812, The American Journal of Human Genetics, 2007, Chen, Gary K.; Witte, John S.

Further Replication Studies of the EVE Consortium Meta-Analysis Identifies Two Asthma Risk Loci in European Americans
score: 0.20830356, The Journal of Allergy and Clinical Immunology, 2012, Myers, Rachel A. et. al.

Haplotype block structure of the genomic region of the mu opioid receptor gene.
score: 0.20799986, Journal of human genetics, 2011, Levran, Orna et. al.

Association of P2X 7 receptor polymorphisms with bone mineral density and osteoporosis risk in a cohort of Dutch fracture patients
score: 0.20784566, Osteoporosis International, 2012, Wesselius, A. et. al.

Whole Genome Sequences of a Male and Female Supercentenarian, Ages Greater than 114 Years
score: 0.20779685, Frontiers in Genetics, 2011, Sebastiani, Paola et. al.

Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays
score: 0.20735339, PLoS Genetics, 2008, Homer, Nils et. al.

Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases
score: 0.2072205, Orphanet Journal of Rare Diseases, 2012, Audo, Isabelle et. al.

Polymorphisms of transforming growth factor-β signaling pathway and Kawasaki disease in the Taiwanese population.
score: 0.2071473, Journal of human genetics, 2011, Kuo, Ho-Chang et. al.

Relationship between DDAH gene variants and serum ADMA level in individuals with type 1 diabetes
score: 0.20688957, Journal of Diabetes and Its Complications, 2012, Fogarty, Rhys D. et. al.

Prostate Cancer Susceptibility Loci Identified on Chromosome 12 in African Americans
score: 0.20682469, PLoS ONE, 2011, Bonilla, Carolina et. al.

Genetic modifiers of Hb E/β 0 thalassemia identified by a two-stage genome-wide association study
score: 0.20680634, BMC Medical Genetics, 2010, Sherva, Richard et. al.

A common 5'-UTR variant in MATE2-K is associated with poor response to metformin.
score: 0.20666119, Clinical pharmacology and therapeutics, 2011, Choi, J H et. al.

A mixed two-stage method for detecting interactions in genomewide association studies
score: 0.20655419, Journal of Theoretical Biology, 2010, Zuo, Yijun; Kang, Guolian

Estrogen and progesterone-related gene variants and colorectal cancer risk in women
score: 0.2059832, BMC Medical Genetics, 2011, Lin, Jennifer H et. al.

Investigation of rheumatoid arthritis susceptibility loci in juvenile idiopathic arthritis confirms high degree of overlap
score: 0.20574751, Annals of the Rheumatic Diseases, 2012, Hinks, Anne et. al.

Further evidence for an association between the gamma-aminobutyric acid receptor A, subunit 4 genes on chromosome 4 and Fagerström Test for Nicotine Dependence.
score: 0.20556165, Addiction (Abingdon, England), 2009, Agrawal, Arpana et. al.

PCLO gene: Its role in vulnerability to major depressive disorder
score: 0.20548642, Journal of Affective Disorders, 2012, Minelli, Alessandra et. al.

Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster( CHRNA5–CHRNA3–CHRNB4 ) interacts with maternalself-reported smoking status during pregnancy to influence birth weight
score: 0.20503324, Human Molecular Genetics, 2012, Tyrrell, Jessica et. al.

Lack of association between GTF2H4 genetic variants and AERD development and FEV1 decline by aspirin provocation.
score: 0.20502739, International journal of immunogenetics, 2012, Kim, J Y et. al.

Testing gene-environment interactions in gene-based association studies
score: 0.20476881, BMC Proceedings, 2011, Wang, Xuefeng et. al.

Ecto-5'-nucleotidase and thiopurine cellular circulation: association with cytotoxicity.
score: 0.20420034, Drug metabolism and disposition: the biological fate of chemicals, 2010, Li, Fang et. al.

Genome-wide association studies of quantitative traits with related individuals: little (power) lost but much to be gained.
score: 0.20417341, European journal of human genetics : EJHG, 2008, Visscher, Peter M; Andrew, Toby; Nyholt, Dale R

Macrophage migration inhibitory factor gene: Influence on rheumatoid arthritis susceptibility
score: 0.20385649, Human Immunology, 2007, Martínez, Alfonso et. al.

Reconstruction of a Functional Human Gene Network, with an Application for Prioritizing Positional Candidate Genes
score: 0.20280582, The American Journal of Human Genetics, 2006, Franke, Lude et. al.

Glucocorticoid receptor mRNA and protein isoform alterations in the orbitofrontal cortex in schizophrenia and bipolar disorder
score: 0.2025707, BMC Psychiatry, 2012, Sinclair, Duncan et. al.

Interleukin-1 receptor antagonist haplotype associated with prostate cancer risk
score: 0.20238449, British Journal of Cancer, 2005, Lindmark, F et. al.

Genetic variation in small proline rich protein 2B as a predictor for asthma among children with eczema
score: 0.20234399, Annals of Allergy, Asthma & Immunology, 2012, Epstein, Tolly G. et. al.

SNPs Associated with Cerebrospinal Fluid Phospho-Tau Levels Influence Rate of Decline in Alzheimer's Disease
score: 0.2022928, PLoS Genetics, 2010, Cruchaga, Carlos et. al.

Epigenetic mechanisms in neurological diseases: genes, syndromes, and therapies
score: 0.20206727, Lancet Neurology, 2009, Urdinguio, Rocio G; Sanchez-Mut, Jose V; Esteller, Manel

Autosomal Genomic Scan for Loci Linked to Obesity and Energy Metabolism in Pima Indians
score: 0.20196761, The American Journal of Human Genetics, 1998, Norman, R.A. et. al.

Predictive modeling in case-control single-nucleotide polymorphism studies in the presence of population stratification: a case study using Genetic Analysis Workshop 16 Problem 1 dataset
score: 0.20166607, BMC Proceedings, 2009, Arshadi, Niloofar; Chang, Billy; Kustra, Rafal

Site-specific protein O-glycosylation modulates proprotein processing — Deciphering specific functions of the large polypeptide GalNAc-transferase gene family
score: 0.20138966, BBA - General Subjects, 2012, Schjoldager, Katrine T.-B.G.; Clausen, Henrik

Site-specific protein O-glycosylation modulates proprotein processing — Deciphering specific functions of the large polypeptide GalNAc-transferase gene family
score: 0.20138966, BBA - General Subjects, 2012, Schjoldager, Katrine T.-B.G.; Clausen, Henrik

Site-specific protein O-glycosylation modulates proprotein processing — Deciphering specific functions of the large polypeptide GalNAc-transferase gene family
score: 0.20138966, BBA - General Subjects, 2012, Schjoldager, Katrine T.-B.G.; Clausen, Henrik

Genetic Loci Involved in Antibody Response to Mycobacterium avium ssp. paratuberculosis in Cattle
score: 0.20117902, PLoS ONE, 2010, Minozzi, Giulietta et. al.

Genomics of ADME gene expression: mapping expression quantitative trait loci relevant for absorption, distribution, metabolism and excretion of drugs in human liver.
score: 0.20114064, The pharmacogenomics journal, 2013, Schröder, A et. al.

Association of variations in the FTO, SCG3 and MTMR9 genes with metabolic syndrome in a Japanese population.
score: 0.20097049, Journal of human genetics, 2011, Hotta, Kikuko et. al.

Genetic Variants in Nuclear-Encoded Mitochondrial Genes Influence AIDS Progression
score: 0.2009464, PLoS ONE, 2010, Hendrickson, Sher L. et. al.

Copy-number variants in neurodevelopmental disorders: promises and challenges
score: 0.20040287, Trends in Genetics, 2009, Merikangas, Alison K.; Corvin, Aiden P.; Gallagher, Louise

Etiology of Type 1 Diabetes
score: 0.19980595, Immunity, 2010, Todd, John A.

Risk and protective genetic variants in suicidal behaviour: association with SLC1A2, SLC1A3, 5-HTR1B & NTRK2 polymorphisms
score: 0.1992786, Behavioral and Brain Functions : BBF, 2011, Murphy, Therese M et. al.

Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2 : association with major depression and antidepressant response in Mexican-Americans
score: 0.19916986, Molecular Psychiatry, 2009, Dong, C; Wong, M-L; Licinio, J

Common genetic variation modulating cardiac ECG parameters and susceptibility to sudden cardiac death
score: 0.19862138, Journal of Molecular and Cellular Cardiology, 2012, Kolder, Iris C.R.M.; Tanck, Michael W.T.; Bezzina, Connie R.

Computing Power and Sample Size for Case-Control Association Studies with Copy Number Polymorphism: Application of Mixture-Based Likelihood Ratio Test
score: 0.19856823, PLoS ONE, 2008, Kim, Wonkuk et. al.

Rapid multiplex high resolution melting method to analyze inflammatory related SNPs in preterm birth
score: 0.1981846, BMC Research Notes, 2012, Pereyra, Silvana et. al.

Estimates of array and pool-construction variance for planning efficient DNA-pooling genome wide association studies
score: 0.19733323, BMC Medical Genomics, 2011, Earp, Madalene A et. al.

Possible association between the androgen receptor gene and autism spectrum disorder
score: 0.1972305, Psychoneuroendocrinology, 2009, Henningsson, Susanne et. al.

Genetic susceptibility to cancer
score: 0.19711909, Annals of the ICRP, 1998,

Genome-wide profiling of chromosomal alterations in renal cell carcinoma using high-density single nucleotide polymorphism arrays.
score: 0.1965766, International journal of cancer. Journal international du cancer, 2009, Chen, Meng et. al.

CTLA4 dimorphisms and the multiple sclerosis phenotype
score: 0.19635915, Journal of Neuroimmunology, 2002, Masterman, Thomas et. al.

Variations in five genes and the severity of age-related macular degeneration: results from the Muenster aging and retina study.
score: 0.19628327, Eye (London, England), 2009, Farwick, A et. al.

Association of the FTO rs9939609 polymorphism with obesity in Roma/Gypsy population.
score: 0.19564093, American journal of physical anthropology, 2012, Mačeková, Soňa et. al.

Abstracts of the 42nd Annual Meeting of the Society for Epidemiologic Research. June 23-26, 2009. Anaheim, California, USA.
score: 0.19540296, American journal of epidemiology, 2009,

Identification of osteosarcoma driver genes by integrative analysis of copy number and gene expression data.
score: 0.19481839, Genes, chromosomes & cancer, 2012, Kuijjer, Marieke L et. al.

Screening of genetic variations of SLC15A2, SLC22A1, SLC22A2 and SLC22A6 genes.
score: 0.19475499, Journal of human genetics, 2011, Cheong, Hyun Sub et. al.

SPOT: a web-based tool for using biological databases to prioritize SNPs after a genome-wide association study
score: 0.19468302, Nucleic Acids Research, 2010, Saccone, Scott F. et. al.

The Finland–United States Investigation of Non–Insulin-Dependent Diabetes Mellitus Genetics (FUSION) Study. I. An Autosomal Genome Scan for Genes That Predispose to Type 2 Diabetes
score: 0.19465342, The American Journal of Human Genetics, 2000, Ghosh, Soumitra et. al.

Polymorphisms in nucleotide excision repair genes and endometrial cancer risk.
score: 0.19457657, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2011, Doherty, Jennifer A et. al.

SNP haplotype tagging from DNA pools of two individuals
score: 0.19441665, BMC Bioinformatics, 2003, Hoh, Josephine et. al.

Two-stage joint selection method to identify candidate markers from genome-wide association studies
score: 0.19440664, BMC Proceedings, 2009, Wu, Zheyang et. al.

Susceptibility Variants for Waist Size in Relation to Abdominal, Visceral, and Hepatic Adiposity in Postmenopausal Women
score: 0.19414623, Journal of the Academy of Nutrition and Dietetics, 2012, Lim, Unhee et. al.

Susceptibility Variants for Waist Size in Relation to Abdominal, Visceral, and Hepatic Adiposity in Postmenopausal Women
score: 0.19414623, Journal of the Academy of Nutrition and Dietetics, 2012, Lim, Unhee et. al.

Prostate cancer genomics, biology, and risk assessment through genome-wide association studies.
score: 0.193955, Cancer science, 2012, Nakagawa, Hidewaki et. al.

Design and analysis of multiple diseases genome-wide association studies without controls
score: 0.19388983, Gene, 2012, Chen, Zhongxue; Huang, Hanwen; Ng, Hon Keung Tony

Confirmation of association of the REL locus with rheumatoid arthritis susceptibility in the UK population
score: 0.19376297, Annals of the Rheumatic Diseases, 2010, Eyre, Stephen et. al.

The PTPN22*C1858T functional polymorphism is associated with susceptibility to inflammatory polyarthritis but neither this nor other variants spanning the gene is associated with disease outcome
score: 0.19368535, Annals of the Rheumatic Diseases, 2008, Naseem, H et. al.

Evidence for the Thr79Met polymorphism of the ileal fatty acid binding protein (FABP6) to be associated with type 2 diabetes in obese individuals
score: 0.19305007, Molecular Genetics and Metabolism, 2009, Fisher, Eva et. al.

AAV-mediated gene therapy for retinal disorders in large animal models.
score: 0.19294101, ILAR journal / National Research Council, Institute of Laboratory Animal Resources, 2009, Stieger, Knut et. al.

Rare Variants Create Synthetic Genome-Wide Associations
score: 0.19190871, PLoS Biology, 2010, Dickson, Samuel P. et. al.