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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 67,588 bioRxiv papers from 298,004 authors.

Author: Elmo Saarentaus

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

Rankings

  • All-time downloads: 3,218 (rank: 20,453 (tie) out of 298,080)
  • Categories:
    • genetics: 3,218 (rank: 3,826 out of 29,753)

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 1,869 times
  • Download rankings, all-time:
    • Site-wide: 2,732 out of 67,590
    • In genetics: 249 out of 3,799
  • Year to date:
    • Site-wide: 31,673 out of 67,590
  • Since beginning of last month:
    • Site-wide: 58,848 out of 67,590

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 478 times
  • Download rankings, all-time:
    • Site-wide: 22,549 out of 67,590
    • In genetics: 1,500 out of 3,799
  • Year to date:
    • Site-wide: 50,367 out of 67,590
  • Since beginning of last month:
    • Site-wide: 57,242 out of 67,590

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

genetics more details view paper
  • Downloaded 315 times
  • Download rankings, all-time:
    • Site-wide: 35,051 out of 67,590
    • In genetics: 2,171 out of 3,799
  • Year to date:
    • Site-wide: 13,974 out of 67,590
  • Since beginning of last month:
    • Site-wide: 33,395 out of 67,590

Duplications at 19q13.33 in patients with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 299 times
  • Download rankings, all-time:
    • Site-wide: 36,733 out of 67,590
    • In genetics: 2,269 out of 3,799
  • Year to date:
    • Site-wide: 58,606 out of 67,590
  • Since beginning of last month:
    • Site-wide: 63,701 out of 67,590

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

genetics more details view paper
  • Downloaded 257 times
  • Download rankings, all-time:
    • Site-wide: 41,448 out of 67,590
    • In genetics: 2,510 out of 3,799
  • Year to date:
    • Site-wide: 63,925 out of 67,590
  • Since beginning of last month:
    • Site-wide: 56,555 out of 67,590

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