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Statistical significance for genomewide studies

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The International HapMap Project

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The Structure of Haplotype Blocks in the Human Genome

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Haplotype tagging for the identification of common disease genes

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Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21

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A haplotype map of the human genome

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A second generation human haplotype map of over 3.1 million SNPs

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Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

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A new multipoint method for genome-wide association studies by imputation of genotypes

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Genome-wide association study identifies novel breast cancer susceptibility loci

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Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications

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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

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Carnitine—metabolism and functions

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Genetic Mapping in Human Disease

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Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1

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Genotype Imputation

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Integrated detection and population-genetic analysis of SNPs and copy number variation

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TRAF1–C5 as a Risk Locus for Rheumatoid Arthritis — A Genomewide Study

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Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

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A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC

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Common deletion polymorphisms in the human genome

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Multiple regions within 8q24 independently affect risk for prostate cancer

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Interleukin 7 receptor α chain ( IL7R ) shows allelic and functional association with multiple sclerosis

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Copy-number variation and association studies of human disease

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Progress and promise of genome-wide association studies for human complex trait genetics

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TXNIP regulates peripheral glucose metabolism in humans

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Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis

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No Significant Association of 14 Candidate Genes With Schizophrenia in a Large European Ancestry Sample: Implications for Psychiatric Genetics

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Common variants in 40 genes assessed for diabetes incidence and response to metformin and lifestyle intervention in the Diabetes Prevention Program

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A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

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Analysis of 94 Candidate Genes and 12 Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia

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A Powerful and Flexible Multilocus Association Test for Quantitative Traits

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Genetic Risk Factors for Post-Infectious Irritable Bowel Syndrome Following a Waterborne Outbreak of Gastroenteritis

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Genetic predictors of response to antidepressants in the GENDEP project

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An enzyme in the kynurenine pathway that governs vulnerability to suicidal behavior by regulating excitotoxicity and neuroinflammation

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Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: Current and developing technologies

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A Statistical Method for Predicting Classical HLA Alleles from SNP Data

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CLOCK genetic variation and metabolic syndrome risk: modulation by monounsaturated fatty acids

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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

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High-Density SNP Screening of the Major Histocompatibility Complex in Systemic Lupus Erythematosus Demonstrates Strong Evidence for Independent Susceptibility Regions

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Genetics of posttraumatic stress disorder: review and recommendations for future studies

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Mapping Trait Loci by Use of Inferred Ancestral Recombination Graphs

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PERIOD2 variants are associated with abdominal obesity, psycho-behavioral factors, and attrition in the dietary treatment of obesity

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Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene–environment study

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Genetic variants in human CLOCK associate with total energy intake and cytokine sleep factors in overweight subjects (GOLDN population)

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Association of NFKB1, which encodes a subunit of the transcription factor NF- B, with alcohol dependence

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Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene

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Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence

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Single nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studies

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Identification of Common Variants in the SHBG Gene Affecting Sex Hormone-Binding Globulin Levels and Breast Cancer Risk in Postmenopausal Women

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Gene‐Trait Similarity Regression for Multimarker‐Based Association Analysis

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Effects of the MAOA gene and levels of exposure to violence on antisocial outcomes

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Candidate Gene Analysis of the Human Natural Killer-1 Carbohydrate Pathway and Perineuronal Nets in Schizophrenia: B3GAT2 Is Associated with Disease Risk and Cortical Surface Area

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GABRR1 and GABRR2, encoding the GABA‐A receptor subunits ρ1 and ρ2, are associated with alcohol dependence

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Effects of NRG1 and DAOA genetic variation on transition to psychosis in individuals at ultra-high risk for psychosis

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Genetic variation in ATP5O is associated with skeletal muscle ATP50 mRNA expression and glucose uptake in young twins

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Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies

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Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene

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Serum 25-hydroxyvitamin D3 levels and vitamin D receptor variants in melanoma patients from the Mediterranean area of Barcelona

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Integration of Alzheimer’s disease genetics and myeloid genomics reveals novel disease risk mechanisms

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CYP4F2 affects phenotypic outcome in adrenoleukodystrophy by modulating the clearance of very long-chain fatty acids

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Evidence for the involvement of the glucocorticoid receptor gene in bipolar disorder in an isolated northern Swedish population

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Genetic Variants and Early Cigarette Smoking and Nicotine Dependence Phenotypes in Adolescents

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Variation in maturity-onset diabetes of the young genes influence response to interventions for diabetes prevention

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Sequence variants of the HTR3A gene contribute to the genetic prediction of postoperative nausea in Taiwan

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