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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 67,655 bioRxiv papers from 298,465 authors.

Author: Jarmo Körkkö

  • Most recently observed institution: Department of Clinical Genetics, Oulu University Hospital

Rankings

  • All-time downloads: 3,259 (rank: 20,204 (tie) out of 298,465)
  • Categories:
    • genetics: 2,347 (rank: 5,486 (tie) out of 29,895)
    • genomics: 912 (rank: 14,859 (tie) out of 34,054)

Downloads per author, site-wide

Preprints

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

genetics more details view paper
  • Downloaded 1,869 times
  • Download rankings, all-time:
    • Site-wide: 2,745 out of 67,655
    • In genetics: 251 out of 3,799
  • Year to date:
    • Site-wide: 31,765 out of 67,655
  • Since beginning of last month:
    • Site-wide: 61,654 out of 67,655

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
  • Downloaded 912 times
  • Download rankings, all-time:
    • Site-wide: 9,125 out of 67,655
    • In genomics: 1,389 out of 4,581
  • Year to date:
    • Site-wide: 47,859 out of 67,655
  • Since beginning of last month:
    • Site-wide: 61,396 out of 67,655

Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

genetics more details view paper
  • Downloaded 478 times
  • Download rankings, all-time:
    • Site-wide: 22,622 out of 67,655
    • In genetics: 1,504 out of 3,799
  • Year to date:
    • Site-wide: 50,879 out of 67,655
  • Since beginning of last month:
    • Site-wide: 58,408 out of 67,655

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