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Author: Jukka S. Moilanen

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

Rankings

  • All-time downloads: 4,471 (rank: 61,912 (tie) )
  • Categories:
    • genetics: 3,366 (rank: 6,183 (tie) )
    • genomics: 1,105 (rank: 24,143 (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 2,711 times
  • Download rankings, all-time:
    • Site-wide: 6,367
    • In genetics: 257
  • Year to date:
    • Site-wide: 25,196
  • Since beginning of last month:
    • Site-wide: 36,766

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

genomics more details view paper
  • Downloaded 1,105 times
  • Download rankings, all-time:
    • Site-wide: 24,613
    • In genomics: 2,243
  • Year to date:
    • Site-wide: 109,873
  • Since beginning of last month:
    • Site-wide: 107,522

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 655 times
  • Download rankings, all-time:
    • Site-wide: 52,348
    • In genetics: 2,229
  • Year to date:
    • Site-wide: 124,354
  • Since beginning of last month:
    • Site-wide: 107,534

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