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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,660 bioRxiv papers from 278,042 authors.

Author: Daniel P Howrigan

  • Most recently observed institution: Broad Institute

Rankings

  • All-time downloads: 26,151 (rank: 738 out of 278,042)
  • Categories:
    • bioinformatics: 2,143 (rank: 3,379 (tie) out of 24,398)
    • genetics: 23,127 (rank: 189 out of 27,703)
    • genomics: 881 (rank: 13,903 (tie) out of 31,942)

Downloads per author, site-wide

Preprints

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

genetics more details view paper
  • Downloaded 8,867 times
  • Download rankings, all-time:
    • Site-wide: 134 out of 62,660
    • In genetics: 11 out of 3,561
  • Year to date:
    • Site-wide: 560 out of 62,660
  • Since beginning of last month:
    • Site-wide: 1,707 out of 62,660

Common risk variants identified in autism spectrum disorder

genetics more details view paper
  • Downloaded 5,933 times
  • Download rankings, all-time:
    • Site-wide: 303 out of 62,660
    • In genetics: 37 out of 3,561
  • Year to date:
    • Site-wide: 780 out of 62,660
  • Since beginning of last month:
    • Site-wide: 2,885 out of 62,660

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

genetics more details view paper
  • Downloaded 2,180 times
  • Download rankings, all-time:
    • Site-wide: 1,904 out of 62,660
    • In genetics: 183 out of 3,561
  • Year to date:
    • Site-wide: 44,492 out of 62,660
  • Since beginning of last month:
    • Site-wide: 52,792 out of 62,660

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

bioinformatics more details view paper
  • Downloaded 2,143 times
  • Download rankings, all-time:
    • Site-wide: 1,973 out of 62,660
    • In bioinformatics: 405 out of 6,242
  • Year to date:
    • Site-wide: 11,318 out of 62,660
  • Since beginning of last month:
    • Site-wide: 22,574 out of 62,660

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

genetics more details view paper
  • Downloaded 1,601 times
  • Download rankings, all-time:
    • Site-wide: 3,249 out of 62,660
    • In genetics: 286 out of 3,561
  • Year to date:
    • Site-wide: 45,724 out of 62,660
  • Since beginning of last month:
    • Site-wide: 46,547 out of 62,660

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

genetics more details view paper
  • Downloaded 1,414 times
  • Download rankings, all-time:
    • Site-wide: 4,022 out of 62,660
    • In genetics: 349 out of 3,561
  • Year to date:
    • Site-wide: 776 out of 62,660
  • Since beginning of last month:
    • Site-wide: 6,575 out of 62,660

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

genetics more details view paper
  • Downloaded 1,301 times
  • Download rankings, all-time:
    • Site-wide: 4,586 out of 62,660
    • In genetics: 383 out of 3,561
  • Year to date:
    • Site-wide: 38,326 out of 62,660
  • Since beginning of last month:
    • Site-wide: 55,541 out of 62,660

Enrichment of rare protein truncating variants in amyotrophic lateral sclerosis patients

genomics more details view paper
  • Downloaded 881 times
  • Download rankings, all-time:
    • Site-wide: 8,656 out of 62,660
    • In genomics: 1,321 out of 4,312
  • Year to date:
    • Site-wide: 9,094 out of 62,660
  • Since beginning of last month:
    • Site-wide: 9,256 out of 62,660

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

genetics more details view paper
  • Downloaded 725 times
  • Download rankings, all-time:
    • Site-wide: 11,570 out of 62,660
    • In genetics: 818 out of 3,561
  • Year to date:
    • Site-wide: 31,877 out of 62,660
  • Since beginning of last month:
    • Site-wide: 34,837 out of 62,660

Schizophrenia risk conferred by protein-coding de novo mutations

genetics more details view paper
  • Downloaded 573 times
  • Download rankings, all-time:
    • Site-wide: 16,036 out of 62,660
    • In genetics: 1,098 out of 3,561
  • Year to date:
    • Site-wide: 8,319 out of 62,660
  • Since beginning of last month:
    • Site-wide: 19,526 out of 62,660

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

genetics more details view paper
  • Downloaded 283 times
  • Download rankings, all-time:
    • Site-wide: 34,439 out of 62,660
    • In genetics: 2,154 out of 3,561
  • Year to date:
    • Site-wide: 12,293 out of 62,660
  • Since beginning of last month:
    • Site-wide: 19,563 out of 62,660

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

genetics more details view paper
  • Downloaded 250 times
  • Download rankings, all-time:
    • Site-wide: 37,934 out of 62,660
    • In genetics: 2,330 out of 3,561
  • Year to date:
    • Site-wide: 57,751 out of 62,660
  • Since beginning of last month:
    • Site-wide: 40,257 out of 62,660

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