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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: 5,989 (rank: 36,746 (tie) )
  • Categories:
    • genetics: 4,949 (rank: 3,845 (tie) )
    • genomics: 1,040 (rank: 22,428 (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 2,542 times
  • Download rankings, all-time:
    • Site-wide: 5,768
    • In genetics: 252
  • Year to date:
    • Site-wide: 21,135
  • Since beginning of last month:
    • Site-wide: 41,086

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

genetics more details view paper
  • Downloaded 1,817 times
  • Download rankings, all-time:
    • Site-wide: 9,469
    • In genetics: 427
  • Year to date:
    • Site-wide: 58,018
  • Since beginning of last month:
    • Site-wide: 68,744

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

genomics more details view paper
  • Downloaded 1,040 times
  • Download rankings, all-time:
    • Site-wide: 21,667
    • In genomics: 2,107
  • Year to date:
    • Site-wide: 96,416
  • Since beginning of last month:
    • Site-wide: 75,258

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 590 times
  • Download rankings, all-time:
    • Site-wide: 47,112
    • In genetics: 2,146
  • Year to date:
    • Site-wide: 125,918
  • Since beginning of last month:
    • Site-wide: 101,964

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