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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 71,071 bioRxiv papers from 310,086 authors.

Author: Exome Aggregation Consortium

  • Most recently observed institution: Massachusetts General Hospital

Rankings

  • All-time downloads: 29,230 (rank: 753 out of 310,116)
  • Categories:
    • genetics: 4,493 (rank: 3,202 out of 30,681)
    • genomics: 24,737 (rank: 257 out of 34,981)

Downloads per author, site-wide

Preprints

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

genomics more details view paper
  • Downloaded 21,578 times
  • Download rankings, all-time:
    • Site-wide: 31 out of 71,082
    • In genomics: 7 out of 4,740
  • Year to date:
    • Site-wide: 15,433 out of 71,082
  • Since beginning of last month:
    • Site-wide: 18,453 out of 71,082

Efficient genotype compression and analysis of large genetic variation datasets

genomics more details view paper
  • Downloaded 3,159 times
  • Download rankings, all-time:
    • Site-wide: 1,148 out of 71,082
    • In genomics: 268 out of 4,740
  • Year to date:
    • Site-wide: 44,710 out of 71,082
  • Since beginning of last month:
    • Site-wide: 23,594 out of 71,082

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples

genetics more details view paper
  • Downloaded 1,894 times
  • Download rankings, all-time:
    • Site-wide: 2,833 out of 71,082
    • In genetics: 252 out of 3,937
  • Year to date:
    • Site-wide: 29,035 out of 71,082
  • Since beginning of last month:
    • Site-wide: 50,799 out of 71,082

Quantifying the unobserved protein-coding variants in human populations provides a roadmap for large-scale sequencing projects

genetics more details view paper
  • Downloaded 1,599 times
  • Download rankings, all-time:
    • Site-wide: 3,791 out of 71,082
    • In genetics: 322 out of 3,937
  • Year to date:
    • Site-wide: 42,154 out of 71,082
  • Since beginning of last month:
    • Site-wide: 34,413 out of 71,082

Pathogenic ASXL1 somatic variants in reference databases complicate germline variant interpretation for Bohring-Opitz Syndrome

genetics more details view paper
  • Downloaded 1,000 times
  • Download rankings, all-time:
    • Site-wide: 8,318 out of 71,082
    • In genetics: 623 out of 3,937
  • Year to date:
    • Site-wide: 54,892 out of 71,082
  • Since beginning of last month:
    • Site-wide: 30,880 out of 71,082

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