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PLINK: a tool set for whole-genome association and population-based linkage analyses.

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Analysis of protein-coding genetic variation in 60,706 humans

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Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

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An atlas of genetic correlations across human diseases and traits

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Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence

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Mapping genomic loci implicates genes and synaptic biology in schizophrenia

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Clinical use of current polygenic risk scores may exacerbate health disparities

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Current clinical use of polygenic scores will risk exacerbating health disparities

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Synaptic, transcriptional and chromatin genes disrupted in autism

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Partitioning heritability by functional annotation using genome-wide association summary statistics

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Identification of common genetic risk variants for autism spectrum disorder

Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium, Grove, J., BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 23andMe Research Team, Ripke, S., Als, T. D., Mattheisen, M., Walters, R. K., Won, H., et al. (2019) · Nature Genetics

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Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

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Analysis of shared heritability in common disorders of the brain

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

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A genomic mutational constraint map using variation in 76,156 human genomes

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The mutational constraint spectrum quantified from variation in 141,456 humans

Karczewski, K. J., Francioli, L. C., Tiao, G., Cummings, B. B., Alföldi, J., Wang, Q., Collins, R. L., Laricchia, K. M., Ganna, A., Birnbaum, D. P., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory)

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Genome-wide association study identifies 30 loci associated with bipolar disorder

eQTLGen Consortium, Stahl, E. A., BIOS Consortium, the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Breen, G., Forstner, A. J., McQuillin, A., Ripke, S., Trubetskoy, V., Mattheisen, M., et al. (2019) · Nature Genetics

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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

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Efficient Bayesian mixed-model analysis increases association power in large cohorts

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Genome-wide association analysis identifies 13 new risk loci for schizophrenia

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Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations

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