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Author: Jarmo Körkkö

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

Rankings

  • All-time downloads: 4,241 (rank: 56,928 (tie) )
  • Categories:
    • genetics: 3,192 (rank: 6,200 (tie) )
    • genomics: 1,049 (rank: 23,293 (tie) )

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 2,582 times
  • Download rankings, all-time:
    • Site-wide: 6,065
    • In genetics: 256
  • Year to date:
    • Site-wide: 24,838
  • Since beginning of last month:
    • Site-wide: None

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

genomics more details view paper
  • Downloaded 1,049 times
  • Download rankings, all-time:
    • Site-wide: 23,050
    • In genomics: 2,181
  • Year to date:
    • Site-wide: 112,636
  • Since beginning of last month:
    • Site-wide: 94,316

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 610 times
  • Download rankings, all-time:
    • Site-wide: 48,681
    • In genetics: 2,165
  • Year to date:
    • Site-wide: 120,354
  • Since beginning of last month:
    • Site-wide: 39,109

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