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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 60,239 bioRxiv papers from 267,831 authors.

Author: Nicholas L Smith

  • Most recently observed institution: University of Washington

Rankings

  • All-time downloads: 13,350 (rank: 2,415 out of 267,843)
  • Categories:
    • genetics: 8,864 (rank: 1,004 out of 27,094)
    • genomics: 4,486 (rank: 2,737 out of 31,259)

Downloads per author, site-wide

Preprints

Recovery of trait heritability from whole genome sequence data

genetics more details view paper
  • Downloaded 7,511 times
  • Download rankings, all-time:
    • Site-wide: 175 out of 60,240
    • In genetics: 19 out of 3,435
  • Year to date:
    • Site-wide: 27 out of 60,240
  • Since beginning of last month:
    • Site-wide: 397 out of 60,240

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

genomics more details view paper
  • Downloaded 3,401 times
  • Download rankings, all-time:
    • Site-wide: 829 out of 60,240
    • In genomics: 215 out of 4,181
  • Year to date:
    • Site-wide: 121 out of 60,240
  • Since beginning of last month:
    • Site-wide: 529 out of 60,240

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 807 times
  • Download rankings, all-time:
    • Site-wide: 9,572 out of 60,240
    • In genomics: 1,430 out of 4,181
  • Year to date:
    • Site-wide: 28,123 out of 60,240
  • Since beginning of last month:
    • Site-wide: 19,821 out of 60,240

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

genetics more details view paper
  • Downloaded 736 times
  • Download rankings, all-time:
    • Site-wide: 10,930 out of 60,240
    • In genetics: 787 out of 3,435
  • Year to date:
    • Site-wide: 2,216 out of 60,240
  • Since beginning of last month:
    • Site-wide: 1,251 out of 60,240

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 617 times
  • Download rankings, all-time:
    • Site-wide: 13,985 out of 60,240
    • In genetics: 988 out of 3,435
  • Year to date:
    • Site-wide: 10,007 out of 60,240
  • Since beginning of last month:
    • Site-wide: 31,995 out of 60,240

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 278 times
  • Download rankings, all-time:
    • Site-wide: 33,655 out of 60,240
    • In genomics: 3,140 out of 4,181
  • Year to date:
    • Site-wide: 11,262 out of 60,240
  • Since beginning of last month:
    • Site-wide: 4,769 out of 60,240

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