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Author: Andrea Byrnes

  • Most recently observed institution: Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston MA, USA. Broad Institute of MIT and Harvard, Cambridge MA, USA

Rankings

  • All-time downloads: 12,931 (rank: 5,722 (tie) out of 396,015)
  • Categories:
    • genetics: 10,985 (rank: 1,170 out of 36,268)
    • genomics: 1,946 (rank: 9,932 (tie) out of 42,120)

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Preprints

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

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    • Site-wide: 14,185 out of 92,758
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    • Site-wide: 19,050 out of 92,758

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

genetics more details view paper
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    • In genetics: 240 out of 4,753
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    • Site-wide: 77,332 out of 92,758
  • Since beginning of last month:
    • Site-wide: 58,741 out of 92,758

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

genetics more details view paper
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    • Site-wide: 9,120 out of 92,758

Landscape of X chromosome inactivation across human tissues

genomics more details view paper
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    • In genomics: 696 out of 5,851
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Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

genetics more details view paper
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    • Site-wide: 4,329 out of 92,758
    • In genetics: 315 out of 4,753
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    • Site-wide: 12,135 out of 92,758
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    • Site-wide: 22,334 out of 92,758

Junction-skipping regulation in complex disease

genetics more details view paper
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    • In genetics: 2,947 out of 4,753
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    • Site-wide: 54,212 out of 92,758

Heterogeneous Contribution of Microdeletions in the Development of Common Generalized and Focal epilepsies

genetics more details view paper
  • Downloaded 305 times
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    • In genetics: 3,063 out of 4,753
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  • Since beginning of last month:
    • Site-wide: 77,136 out of 92,758

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