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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 62,482 bioRxiv papers from 277,419 authors.

Author: Exome Aggregation Consortium

  • Most recently observed institution: Massachusetts General Hospital

Rankings

  • All-time downloads: 28,896 (rank: 619 out of 277,419)
  • Categories:
    • genetics: 4,364 (rank: 3,038 (tie) out of 27,685)
    • genomics: 24,532 (rank: 233 out of 31,917)

Downloads per author, site-wide

Preprints

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

genomics more details view paper
  • Downloaded 21,430 times
  • Download rankings, all-time:
    • Site-wide: 24 out of 62,482
    • In genomics: 6 out of 4,297
  • Year to date:
    • Site-wide: 3,393 out of 62,482
  • Since beginning of last month:
    • Site-wide: 4,837 out of 62,482

Efficient genotype compression and analysis of large genetic variation datasets

genomics more details view paper
  • Downloaded 3,102 times
  • Download rankings, all-time:
    • Site-wide: 1,009 out of 62,482
    • In genomics: 249 out of 4,297
  • Year to date:
    • Site-wide: 23,535 out of 62,482
  • Since beginning of last month:
    • Site-wide: 23,616 out of 62,482

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

genetics more details view paper
  • Downloaded 1,858 times
  • Download rankings, all-time:
    • Site-wide: 2,535 out of 62,482
    • In genetics: 235 out of 3,548
  • Year to date:
    • Site-wide: 50,582 out of 62,482
  • Since beginning of last month:
    • Site-wide: 58,085 out of 62,482

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

genetics more details view paper
  • Downloaded 1,558 times
  • Download rankings, all-time:
    • Site-wide: 3,387 out of 62,482
    • In genetics: 298 out of 3,548
  • Year to date:
    • Site-wide: 32,652 out of 62,482
  • Since beginning of last month:
    • Site-wide: 27,103 out of 62,482

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

genetics more details view paper
  • Downloaded 948 times
  • Download rankings, all-time:
    • Site-wide: 7,670 out of 62,482
    • In genetics: 595 out of 3,548
  • Year to date:
    • Site-wide: 24,020 out of 62,482
  • Since beginning of last month:
    • Site-wide: 22,378 out of 62,482

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