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Author: Elmo Saarentaus

  • Most recently observed institution: Institute for Molecular Medicine Finland (FIMM)

Rankings

  • All-time downloads: 4,546 (rank: 52,588 (tie) )
  • Categories:
    • genetics: 4,546 (rank: 4,160 (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: 5,998
    • In genetics: 256
  • Year to date:
    • Site-wide: 23,573
  • Since beginning of last month:
    • Site-wide: None

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 610 times
  • Download rankings, all-time:
    • Site-wide: 48,121
    • In genetics: 2,144
  • Year to date:
    • Site-wide: 116,306
  • Since beginning of last month:
    • Site-wide: 16,255

Evaluation of copy number burden in specific epilepsy types from a genome-wide study of 18,564 subjects

genetics more details view paper
  • Downloaded 590 times
  • Download rankings, all-time:
    • Site-wide: 50,182
    • In genetics: 2,230
  • Year to date:
    • Site-wide: 104,525
  • Since beginning of last month:
    • Site-wide: None

Duplications at 19q13.33 in patients with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 407 times
  • Download rankings, all-time:
    • Site-wide: 75,906
    • In genetics: 3,312
  • Year to date:
    • Site-wide: 144,290
  • Since beginning of last month:
    • Site-wide: None

Heterogeneous Contribution of Microdeletions in the Development of Common Generalized and Focal epilepsies

genetics more details view paper
  • Downloaded 357 times
  • Download rankings, all-time:
    • Site-wide: 85,413
    • In genetics: 3,726
  • Year to date:
    • Site-wide: 131,234
  • Since beginning of last month:
    • Site-wide: None

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