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Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis

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A genetic atlas of human admixture history

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Innate Immune Activity Conditions the Effect of Regulatory Variants upon Monocyte Gene Expression

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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

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Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

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Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

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Fine-mapping inflammatory bowel disease loci to single-variant resolution

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A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness

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Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: a soft clustering analysis

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Mapping DNA methylation across development, genotype and schizophrenia in the human frontal cortex

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Genetic Ancestry and Natural Selection Drive Population Differences in Immune Responses to Pathogens

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Genetic adaptation and Neandertal admixture shaped the immune system of human populations

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Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia

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Fast and accurate long-range phasing in a UK Biobank cohort

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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

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Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease

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The population history of northeastern Siberia since the Pleistocene

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Genome-Wide Inference of Ancestral Recombination Graphs

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The population genetics of structural variants in grapevine domestication

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Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

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A Functional Genomics Approach to Understand Variation in Cytokine Production in Humans

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Relatedness in the post-genomic era: is it still useful?

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Terminal Pleistocene Alaskan genome reveals first founding population of Native Americans

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Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

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Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease

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A direct test of the diathesis-stress model for depression

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Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci

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SumHer better estimates the SNP heritability of complex traits from summary statistics

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Genome-wide mapping of global-to-local genetic effects on human facial shape

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Quantifying the contribution of recessive coding variation to developmental disorders

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Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans

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Genomic insights into population history and biological adaptation in Oceania

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Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins

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Identification of 12 genetic loci associated with human healthspan

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Insights into the genetic architecture of the human face

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Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

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Genomic analysis of family data reveals additional genetic effects on intelligence and personality

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Signatures of Selection Reveal Candidate Genes Involved in Economic Traits and Cold Acclimation in Five Swedish Cattle Breeds

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Scans for Signatures of Selection in Russian Cattle Breed Genomes Reveal New Candidate Genes for Environmental Adaptation and Acclimation

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Polygenic risk score predicts prevalence of cardiovascular disease in patients with familial hypercholesterolemia

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Adaptive, convergent origins of the pygmy phenotype in African rainforest hunter-gatherers

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Massively parallel quantification of the regulatory effects of noncoding genetic variation in a human cohort

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Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

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Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development

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Genetic signature of natural selection in first Americans

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Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence

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Positive selection rather than relaxation of functional constraint drives the evolution of vision during chicken domestication

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Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

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Genome-wide Ancestry Patterns in Rapanui Suggest Pre-European Admixture with Native Americans

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Efficient cross-trait penalized regression increases prediction accuracy in large cohorts using secondary phenotypes

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Origin of the PSEN1 E280A mutation causing early‐onset Alzheimer's disease

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A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer’s Disease Brains

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Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population

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Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment

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Prediction model for pancreatic cancer risk in the general Japanese population

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Genome-wide association study and scan for signatures of selection point to candidate genes for body temperature maintenance under the cold stress in Siberian cattle populations

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Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior

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Genome-wide association study of blood lipids in Indians confirms universality of established variants

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meQTL and ncRNA functional analyses of 102 GWAS-SNPs associated with depression implicate HACE1 and SHANK2 genes

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DLX5/6 GABAergic Expression Affects Social Vocalization: Implications for Human Evolution

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