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Author: Daniel P Howrigan

  • Most recently observed institution: Broad Institute

Rankings

  • All-time downloads: 30,041 (rank: 1,590 out of 404,161)
  • Categories:
    • bioinformatics: 2,302 (rank: 4,755 (tie) out of 34,272)
    • genetics: 26,621 (rank: 206 out of 36,792)
    • genomics: 1,118 (rank: 16,531 (tie) out of 42,763)

Downloads per author, site-wide

Preprints

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

genetics more details view paper
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    • In genetics: 16 out of 4,824
  • Year to date:
    • Site-wide: 1,652 out of 94,912
  • Since beginning of last month:
    • Site-wide: 4,211 out of 94,912

Common risk variants identified in autism spectrum disorder

genetics more details view paper
  • Downloaded 6,698 times
  • Download rankings, all-time:
    • Site-wide: 493 out of 94,912
    • In genetics: 41 out of 4,824
  • Year to date:
    • Site-wide: 4,246 out of 94,912
  • Since beginning of last month:
    • Site-wide: 3,678 out of 94,912

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

bioinformatics more details view paper
  • Downloaded 2,302 times
  • Download rankings, all-time:
    • Site-wide: 3,085 out of 94,912
    • In bioinformatics: 540 out of 8,837
  • Year to date:
    • Site-wide: 41,890 out of 94,912
  • Since beginning of last month:
    • Site-wide: 17,544 out of 94,912

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

genetics more details view paper
  • Downloaded 2,255 times
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    • Site-wide: 3,183 out of 94,912
    • In genetics: 240 out of 4,824
  • Year to date:
    • Site-wide: 79,810 out of 94,912
  • Since beginning of last month:
    • Site-wide: 68,970 out of 94,912

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

genetics more details view paper
  • Downloaded 1,868 times
  • Download rankings, all-time:
    • Site-wide: 4,352 out of 94,912
    • In genetics: 316 out of 4,824
  • Year to date:
    • Site-wide: 12,423 out of 94,912
  • Since beginning of last month:
    • Site-wide: 20,819 out of 94,912

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
  • Downloaded 1,692 times
  • Download rankings, all-time:
    • Site-wide: 5,118 out of 94,912
    • In genetics: 371 out of 4,824
  • Year to date:
    • Site-wide: 66,732 out of 94,912
  • Since beginning of last month:
    • Site-wide: 61,113 out of 94,912

Refining the role of de novo protein truncating variants in neurodevelopmental disorders using population reference samples

genetics more details view paper
  • Downloaded 1,388 times
  • Download rankings, all-time:
    • Site-wide: 7,122 out of 94,912
    • In genetics: 504 out of 4,824
  • Year to date:
    • Site-wide: 65,945 out of 94,912
  • Since beginning of last month:
    • Site-wide: 64,715 out of 94,912

Enrichment of rare protein truncating variants in amyotrophic lateral sclerosis patients

genomics more details view paper
  • Downloaded 1,118 times
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    • Site-wide: 10,251 out of 94,912
    • In genomics: 1,472 out of 5,955
  • Year to date:
    • Site-wide: 29,799 out of 94,912
  • Since beginning of last month:
    • Site-wide: 37,897 out of 94,912

Paternal-age-related de novo mutations and risk for five disorders

genetics more details view paper
  • Downloaded 829 times
  • Download rankings, all-time:
    • Site-wide: 16,475 out of 94,912
    • In genetics: 1,043 out of 4,824
  • Year to date:
    • Site-wide: 59,745 out of 94,912
  • Since beginning of last month:
    • Site-wide: 64,444 out of 94,912

Schizophrenia risk conferred by protein-coding de novo mutations

genetics more details view paper
  • Downloaded 775 times
  • Download rankings, all-time:
    • Site-wide: 18,297 out of 94,912
    • In genetics: 1,154 out of 4,824
  • Year to date:
    • Site-wide: 34,571 out of 94,912
  • Since beginning of last month:
    • Site-wide: 48,319 out of 94,912

Evaluation of copy number burden in specific epilepsy types from a genome-wide study of 18,564 subjects

genetics more details view paper
  • Downloaded 491 times
  • Download rankings, all-time:
    • Site-wide: 34,187 out of 94,912
    • In genetics: 2,001 out of 4,824
  • Year to date:
    • Site-wide: 29,825 out of 94,912
  • Since beginning of last month:
    • Site-wide: 31,719 out of 94,912

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

genetics more details view paper
  • Downloaded 308 times
  • Download rankings, all-time:
    • Site-wide: 55,266 out of 94,912
    • In genetics: 3,086 out of 4,824
  • Year to date:
    • Site-wide: 86,259 out of 94,912
  • Since beginning of last month:
    • Site-wide: 77,511 out of 94,912

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