about
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPsGenome-wide association analysis identifies 13 new risk loci for schizophreniaCommon variants associated with plasma triglycerides and risk for coronary artery diseaseGenome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureThe genetic architecture of type 2 diabetesPartitioning heritability by functional annotation using genome-wide association summary statistics.Discovery of rare variants for complex phenotypes.Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection.Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders.Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases.Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.Deep-coverage whole genome sequences and blood lipids among 16,324 individualsFunctional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projectsGenetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran ProgramWhole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulationComparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traitsTranscriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insightsLarge-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteriaDiscovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorderTransancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disordersAttention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causalityA genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopmentIdentification of common genetic risk variants for autism spectrum disorderGenome-wide de novo risk score implicates promoter variation in autism spectrum disorderLarge-scale GWAS reveals insights into the genetic architecture of same-sex sexual behaviorPublisher Correction: Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseasesAuthor Correction: A global overview of pleiotropy and genetic architecture in complex traitsGWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample sizeInternational meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk lociPublisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestriesCorrection: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationExome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock proteinAutism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variantsAuthor Correction: Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selectionPolygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancersRecent advances in understanding of attention deficit hyperactivity disorder (ADHD): how genetics are shaping our conceptualization of this disorderPublisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein
P50
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P50
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