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Author: Meriel McEntagart

  • Most recently observed institution: Department of Clinical Genetics, St Georges Hospital, London, UK

Rankings

  • All-time downloads: 9,456 (rank: 16,474 (tie) out of 514,095)
  • Categories:
    • genetics: 9,072 (rank: 1,830 out of 38,823)
    • genomics: 384 (rank: 35,609 (tie) out of 45,849)

Downloads per author, site-wide

Preprints

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation

genetics more details view paper
  • Downloaded 7,340 times
  • Download rankings, all-time:
    • Site-wide: 965 out of 119,234
    • In genetics: 35 out of 5,154
  • Year to date:
    • Site-wide: 21,382 out of 119,234
  • Since beginning of last month:
    • Site-wide: 21,443 out of 119,234

Pathogenicity and selective constraint on variation near splice sites

genetics more details view paper
  • Downloaded 1,469 times
  • Download rankings, all-time:
    • Site-wide: 9,643 out of 119,234
    • In genetics: 501 out of 5,154
  • Year to date:
    • Site-wide: 36,568 out of 119,234
  • Since beginning of last month:
    • Site-wide: 20,349 out of 119,234

Whole genome sequencing for diagnosis of neurological repeat expansion disorders

genomics more details view paper
  • Downloaded 384 times
  • Download rankings, all-time:
    • Site-wide: 58,092 out of 119,234
    • In genomics: 4,361 out of 6,459
  • Year to date:
    • Site-wide: 19,811 out of 119,234
  • Since beginning of last month:
    • Site-wide: 716 out of 119,234

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

genetics more details view paper
  • Downloaded 263 times
  • Download rankings, all-time:
    • Site-wide: 78,688 out of 119,234
    • In genetics: 3,754 out of 5,154
  • Year to date:
    • Site-wide: 78,260 out of 119,234
  • Since beginning of last month:
    • Site-wide: 111,735 out of 119,234

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