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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 62,502 bioRxiv papers from 277,505 authors.

Author: Patricia A Peyser

  • Most recently observed institution: Michigan State University

Rankings

  • All-time downloads: 10,182 (rank: 3,769 (tie) out of 277,505)
  • Categories:
    • genetics: 2,282 (rank: 5,261 out of 27,685)
    • genomics: 7,900 (rank: 1,346 out of 31,917)

Downloads per author, site-wide

Preprints

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: 743 out of 62,502
    • In genomics: 190 out of 4,300
  • Year to date:
    • Site-wide: 122 out of 62,502
  • Since beginning of last month:
    • Site-wide: 316 out of 62,502

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

genomics more details view paper
  • Downloaded 2,968 times
  • Download rankings, all-time:
    • Site-wide: 1,095 out of 62,502
    • In genomics: 261 out of 4,300
  • Year to date:
    • Site-wide: 10,633 out of 62,502
  • Since beginning of last month:
    • Site-wide: 13,028 out of 62,502

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

genetics more details view paper
  • Downloaded 1,654 times
  • Download rankings, all-time:
    • Site-wide: 3,082 out of 62,502
    • In genetics: 270 out of 3,551
  • Year to date:
    • Site-wide: 22,949 out of 62,502
  • Since beginning of last month:
    • Site-wide: 41,508 out of 62,502

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: 14,161 out of 62,502
    • In genetics: 988 out of 3,551
  • Year to date:
    • Site-wide: 10,536 out of 62,502
  • Since beginning of last month:
    • Site-wide: 36,060 out of 62,502

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: 17,943 out of 62,502
    • In genomics: 2,164 out of 4,300
  • Year to date:
    • Site-wide: 4,455 out of 62,502
  • Since beginning of last month:
    • Site-wide: 151 out of 62,502

Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

genomics more details view paper
  • Downloaded 399 times
  • Download rankings, all-time:
    • Site-wide: 24,762 out of 62,502
    • In genomics: 2,643 out of 4,300
  • Year to date:
    • Site-wide: 7,017 out of 62,502
  • Since beginning of last month:
    • Site-wide: 12,598 out of 62,502

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: 29,418 out of 62,502
    • In genomics: 2,923 out of 4,300
  • Year to date:
    • Site-wide: 9,305 out of 62,502
  • Since beginning of last month:
    • Site-wide: 6,543 out of 62,502

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