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Author: Jarmo Körkkö

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

Rankings

  • All-time downloads: 3,592 (rank: 27,812 (tie) out of 382,070)
  • Categories:
    • genetics: 2,629 (rank: 5,844 (tie) out of 35,241)
    • genomics: 963 (rank: 17,869 (tie) out of 40,702)

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 2,093 times
  • Download rankings, all-time:
    • Site-wide: 3,379 out of 89,140
    • In genetics: 260 out of 4,612
  • Year to date:
    • Site-wide: 14,741 out of 89,140
  • Since beginning of last month:
    • Site-wide: 9,472 out of 89,140

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

genomics more details view paper
  • Downloaded 963 times
  • Download rankings, all-time:
    • Site-wide: 12,150 out of 89,140
    • In genomics: 1,675 out of 5,693
  • Year to date:
    • Site-wide: 80,209 out of 89,140
  • Since beginning of last month:
    • Site-wide: 80,392 out of 89,140

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 536 times
  • Download rankings, all-time:
    • Site-wide: 28,567 out of 89,140
    • In genetics: 1,747 out of 4,612
  • Year to date:
    • Site-wide: 77,516 out of 89,140
  • Since beginning of last month:
    • Site-wide: 75,311 out of 89,140

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