Author: Robert E Handsaker

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Preprints

Multi-platform discovery of haplotype-resolved structural variation in human genomes

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The GTEx Consortium atlas of genetic regulatory effects across human tissues

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Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses

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The Genetic Landscape of Diamond-Blackfan Anemia

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Mapping genetic effects on cellular phenotypes with "cell villages"

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

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The Genetic Architecture of DNA Replication Timing in Human Pluripotent Stem Cells

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