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Author: Jarmo Körkkö

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

Rankings

  • All-time downloads: 3,684 (rank: 29,159 (tie) out of 404,161)
  • Categories:
    • genetics: 2,711 (rank: 5,905 (tie) out of 36,792)
    • genomics: 973 (rank: 18,581 (tie) out of 42,763)

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 2,168 times
  • Download rankings, all-time:
    • Site-wide: 3,420 out of 94,912
    • In genetics: 254 out of 4,824
  • Year to date:
    • Site-wide: 12,789 out of 94,912
  • Since beginning of last month:
    • Site-wide: 8,515 out of 94,912

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

genomics more details view paper
  • Downloaded 973 times
  • Download rankings, all-time:
    • Site-wide: 12,812 out of 94,912
    • In genomics: 1,740 out of 5,955
  • Year to date:
    • Site-wide: 82,870 out of 94,912
  • Since beginning of last month:
    • Site-wide: 67,771 out of 94,912

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 543 times
  • Download rankings, all-time:
    • Site-wide: 30,082 out of 94,912
    • In genetics: 1,798 out of 4,824
  • Year to date:
    • Site-wide: 82,954 out of 94,912
  • Since beginning of last month:
    • Site-wide: 68,140 out of 94,912

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