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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: 5,270 (rank: 17,681 (tie) out of 380,926)
  • Categories:
    • genetics: 4,307 (rank: 3,659 out of 35,213)
    • genomics: 963 (rank: 17,827 (tie) out of 40,647)

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 2,093 times
  • Download rankings, all-time:
    • Site-wide: 3,364 out of 88,847
    • In genetics: 260 out of 4,602
  • Year to date:
    • Site-wide: 14,477 out of 88,847
  • Since beginning of last month:
    • Site-wide: 8,419 out of 88,847

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

genetics more details view paper
  • Downloaded 1,681 times
  • Download rankings, all-time:
    • Site-wide: 4,814 out of 88,847
    • In genetics: 360 out of 4,602
  • Year to date:
    • Site-wide: 61,834 out of 88,847
  • Since beginning of last month:
    • Site-wide: 79,196 out of 88,847

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

genomics more details view paper
  • Downloaded 963 times
  • Download rankings, all-time:
    • Site-wide: 12,100 out of 88,847
    • In genomics: 1,672 out of 5,668
  • Year to date:
    • Site-wide: 79,302 out of 88,847
  • Since beginning of last month:
    • Site-wide: 76,904 out of 88,847

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: 28,659 out of 88,847
    • In genetics: 1,747 out of 4,602
  • Year to date:
    • Site-wide: 79,424 out of 88,847
  • Since beginning of last month:
    • Site-wide: 86,255 out of 88,847

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