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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 62,745 bioRxiv papers from 278,406 authors.

Author: Nicholas L Smith

  • Most recently observed institution: University of Washington

Rankings

  • All-time downloads: 14,537 (rank: 2,164 (tie) out of 278,406)
  • Categories:
    • genetics: 9,191 (rank: 980 out of 27,728)
    • genomics: 5,346 (rank: 2,238 out of 31,951)

Downloads per author, site-wide

Preprints

Recovery of trait heritability from whole genome sequence data

genetics more details view paper
  • Downloaded 7,755 times
  • Download rankings, all-time:
    • Site-wide: 173 out of 62,745
    • In genetics: 19 out of 3,562
  • Year to date:
    • Site-wide: 28 out of 62,745
  • Since beginning of last month:
    • Site-wide: 385 out of 62,745

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

genomics more details view paper
  • Downloaded 3,670 times
  • Download rankings, all-time:
    • Site-wide: 744 out of 62,745
    • In genomics: 191 out of 4,316
  • Year to date:
    • Site-wide: 122 out of 62,745
  • Since beginning of last month:
    • Site-wide: 340 out of 62,745

Genome-wide Meta-analysis of 158,000 Individuals of European Ancestry Identifies Three Loci Associated with Chronic Back Pain

genomics more details view paper
  • Downloaded 813 times
  • Download rankings, all-time:
    • Site-wide: 9,817 out of 62,745
    • In genomics: 1,446 out of 4,316
  • Year to date:
    • Site-wide: 29,765 out of 62,745
  • Since beginning of last month:
    • Site-wide: 45,131 out of 62,745

Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

genetics more details view paper
  • Downloaded 808 times
  • Download rankings, all-time:
    • Site-wide: 9,897 out of 62,745
    • In genetics: 729 out of 3,562
  • Year to date:
    • Site-wide: 2,138 out of 62,745
  • Since beginning of last month:
    • Site-wide: 2,929 out of 62,745

Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies

genetics more details view paper
  • Downloaded 628 times
  • Download rankings, all-time:
    • Site-wide: 14,204 out of 62,745
    • In genetics: 994 out of 3,562
  • Year to date:
    • Site-wide: 10,664 out of 62,745
  • Since beginning of last month:
    • Site-wide: 38,891 out of 62,745

Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

genomics more details view paper
  • Downloaded 526 times
  • Download rankings, all-time:
    • Site-wide: 18,008 out of 62,745
    • In genomics: 2,170 out of 4,316
  • Year to date:
    • Site-wide: 4,501 out of 62,745
  • Since beginning of last month:
    • Site-wide: 164 out of 62,745

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

genomics more details view paper
  • Downloaded 337 times
  • Download rankings, all-time:
    • Site-wide: 29,541 out of 62,745
    • In genomics: 2,932 out of 4,316
  • Year to date:
    • Site-wide: 9,400 out of 62,745
  • Since beginning of last month:
    • Site-wide: 7,088 out of 62,745

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