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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 70,458 bioRxiv papers from 307,648 authors.

Author: Peter D. Stenson

  • Most recently observed institution: Cardiff University

Rankings

  • All-time downloads: 24,976 (rank: 963 out of 307,596)
  • Categories:
    • genetics: 2,957 (rank: 4,245 out of 30,486)
    • genomics: 22,019 (rank: 300 out of 34,771)

Downloads per author, site-wide

Preprints

Analysis of protein-coding genetic variation in 60,706 humans

genomics more details view paper
  • Downloaded 21,567 times
  • Download rankings, all-time:
    • Site-wide: 30 out of 70,446
    • In genomics: 7 out of 4,710
  • Year to date:
    • Site-wide: 34,584 out of 70,446
  • Since beginning of last month:
    • Site-wide: 18,451 out of 70,446

AMELIE accelerates Mendelian patient diagnosis directly from the primary literature

genetics more details view paper
  • Downloaded 1,802 times
  • Download rankings, all-time:
    • Site-wide: 3,066 out of 70,446
    • In genetics: 264 out of 3,906
  • Year to date:
    • Site-wide: 18,056 out of 70,446
  • Since beginning of last month:
    • Site-wide: 5,565 out of 70,446

Proteins linked to autosomal dominant and autosomal recessive disorders harbor characteristic rare missense mutation distribution patterns

genetics more details view paper
  • Downloaded 500 times
  • Download rankings, all-time:
    • Site-wide: 22,592 out of 70,446
    • In genetics: 1,506 out of 3,906
  • Year to date:
    • Site-wide: 57,999 out of 70,446
  • Since beginning of last month:
    • Site-wide: 61,000 out of 70,446

AVADA Enables Automated Genetic Variant Curation Directly from the Full Text Literature

genetics more details view paper
  • Downloaded 483 times
  • Download rankings, all-time:
    • Site-wide: 23,597 out of 70,446
    • In genetics: 1,556 out of 3,906
  • Year to date:
    • Site-wide: 15,997 out of 70,446
  • Since beginning of last month:
    • Site-wide: 28,594 out of 70,446

S-CAP extends clinical-grade pathogenicity prediction to genetic variants that affect RNA splicing

genomics more details view paper
  • Downloaded 452 times
  • Download rankings, all-time:
    • Site-wide: 25,505 out of 70,446
    • In genomics: 2,714 out of 4,710
  • Year to date:
    • Site-wide: 54,543 out of 70,446
  • Since beginning of last month:
    • Site-wide: 64,760 out of 70,446

AMELIE 2 speeds up Mendelian diagnosis by matching patient phenotype & genotype to primary literature

genetics more details view paper
  • Downloaded 172 times
  • Download rankings, all-time:
    • Site-wide: 55,683 out of 70,446
    • In genetics: 3,254 out of 3,906
  • Year to date:
    • Site-wide: 12,888 out of 70,446
  • Since beginning of last month:
    • Site-wide: 10,414 out of 70,446

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