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Author: Olli Pietiläinen

  • Most recently observed institution: Department of Stem Cell and Regenerative Biology, University of Harvard

Rankings

  • All-time downloads: 6,065 (rank: 38,874 (tie) )
  • Categories:
    • genetics: 5,016 (rank: 3,872 (tie) )
    • genomics: 1,049 (rank: 23,032 (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: 5,993
    • In genetics: 256
  • Year to date:
    • Site-wide: 23,380
  • Since beginning of last month:
    • Site-wide: None

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
  • Downloaded 1,830 times
  • Download rankings, all-time:
    • Site-wide: 9,959
    • In genetics: 444
  • Year to date:
    • Site-wide: 67,320
  • Since beginning of last month:
    • Site-wide: 31,537

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: 22,778
    • In genomics: 2,161
  • Year to date:
    • Site-wide: 106,995
  • Since beginning of last month:
    • Site-wide: 59,818

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 604 times
  • Download rankings, all-time:
    • Site-wide: 48,548
    • In genetics: 2,162
  • Year to date:
    • Site-wide: 123,313
  • Since beginning of last month:
    • Site-wide: 23,119

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