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Author: Robert E Handsaker

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  • All-time downloads: 27,699 (rank: 4,344 out of 509,520)
  • Categories:
    • genetics: 13,642 (rank: 963 out of 38,578)
    • genomics: 14,057 (rank: 957 (tie) out of 45,500)

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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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Mapping genetic effects on cellular phenotypes with "cell villages"

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

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    • Site-wide: 84,173 out of 118,102

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

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    • Site-wide: 39,427 out of 118,102

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

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

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    • In genomics: 5,524 out of 6,432
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