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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: 3,571 (rank: 27,662 (tie) out of 379,082)
  • Categories:
    • genetics: 2,610 (rank: 5,825 (tie) out of 35,032)
    • genomics: 961 (rank: 17,820 (tie) out of 40,497)

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 2,077 times
  • Download rankings, all-time:
    • Site-wide: 3,389 out of 88,402
    • In genetics: 261 out of 4,590
  • Year to date:
    • Site-wide: 15,860 out of 88,402
  • Since beginning of last month:
    • Site-wide: 7,785 out of 88,402

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

genomics more details view paper
  • Downloaded 961 times
  • Download rankings, all-time:
    • Site-wide: 12,091 out of 88,402
    • In genomics: 1,675 out of 5,641
  • Year to date:
    • Site-wide: 80,480 out of 88,402
  • Since beginning of last month:
    • Site-wide: 82,242 out of 88,402

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 533 times
  • Download rankings, all-time:
    • Site-wide: 28,563 out of 88,402
    • In genetics: 1,742 out of 4,590
  • Year to date:
    • Site-wide: 78,827 out of 88,402
  • Since beginning of last month:
    • Site-wide: 69,288 out of 88,402

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