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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  • Site-wide: 6,888

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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Mapping genetic effects on cellular phenotypes with "cell villages"

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  • Site-wide: 7,272
  • In genetics: 345
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Protein-coding repeat polymorphisms strongly shape diverse human phenotypes

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  • In genetics: 395
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Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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  • Site-wide: 9,539
  • In genomics: 1,048
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Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses

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  • In genetics: 758
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The Genetic Landscape of Diamond-Blackfan Anemia

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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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Insights into dispersed duplications and complex structural mutations from whole genome sequencing 706 families

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  • Site-wide: 55,490
  • In genomics: 4,207
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  • Site-wide: 50,991
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  • Site-wide: 67,520

Biological insights from the whole genome analysis of human embryonic stem cells

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  • In genomics: 4,899
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