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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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Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

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Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

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Influence of Child Abuse on Adult Depression: Moderation by the Corticotropin-Releasing Hormone Receptor Gene

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Identifying Signatures of Natural Selection in Tibetan and Andean Populations Using Dense Genome Scan Data

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A High-Density Whole-Genome Association Study Reveals That APOE Is the Major Susceptibility Gene for Sporadic Late-Onset Alzheimer's Disease

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Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

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A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

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Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1

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A Spectrum of PCSK9 Alleles Contributes to Plasma Levels of Low-Density Lipoprotein Cholesterol

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Abnormal melatonin synthesis in autism spectrum disorders

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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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A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration

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Genetic variation in human NPY expression affects stress response and emotion

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Three functional variants of IFN regulatory factor 5 ( IRF5 ) define risk and protective haplotypes for human lupus

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Population genomics reveal recent speciation and rapid evolutionary adaptation in polar bears

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Multiple Independent Loci at Chromosome 15q25.1 Affect Smoking Quantity: a Meta-Analysis and Comparison with Lung Cancer and COPD

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A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color

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Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease

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Implication of Genetic Variants Near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in Type 2 Diabetes and Obesity in 6,719 Asians

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Glutamate transporter gene SLC1A1 associated with obsessive-compulsive disorder

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Variation near complement factor I is associated with risk of advanced AMD

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Galectin-3, a novel endogenous TREM2 ligand, detrimentally regulates inflammatory response in Alzheimer’s disease

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Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition

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Definition And Clinical Importance Of Haplotypes.

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Cardiac Sodium Channel ( SCN5A ) Variants Associated with Atrial Fibrillation

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Cigarette Smoking Strongly Modifies the Association of LOC387715 and Age-Related Macular Degeneration

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Physical Activity and the Association of Common FTO Gene Variants With Body Mass Index and Obesity

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Whole-genome association study identifies STK39 as a hypertension susceptibility gene

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A High-Density Screen for Linkage in Multiple Sclerosis

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Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus

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Variation in the μ-opioid receptor gene ( OPRM1 ) is associated with dispositional and neural sensitivity to social rejection

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Interaction of childhood maltreatment with the corticotropin-releasing hormone receptor gene: effects on hypothalamic-pituitary-adrenal axis reactivity

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