Rxivist logo

Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 70,836 bioRxiv papers from 309,140 authors.

Author: Elmo Saarentaus

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

Rankings

  • All-time downloads: 3,304 (rank: 21,089 (tie) out of 309,140)
  • Categories:
    • genetics: 3,304 (rank: 3,917 out of 30,603)

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 1,887 times
  • Download rankings, all-time:
    • Site-wide: 2,837 out of 70,836
    • In genetics: 253 out of 3,925
  • Year to date:
    • Site-wide: 49,874 out of 70,836
  • Since beginning of last month:
    • Site-wide: 32,238 out of 70,836

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 494 times
  • Download rankings, all-time:
    • Site-wide: 23,079 out of 70,836
    • In genetics: 1,529 out of 3,925
  • Year to date:
    • Site-wide: 66,105 out of 70,836
  • Since beginning of last month:
    • Site-wide: 33,645 out of 70,836

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

genetics more details view paper
  • Downloaded 349 times
  • Download rankings, all-time:
    • Site-wide: 33,978 out of 70,836
    • In genetics: 2,121 out of 3,925
  • Year to date:
    • Site-wide: 16,609 out of 70,836
  • Since beginning of last month:
    • Site-wide: 15,268 out of 70,836

Duplications at 19q13.33 in patients with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 310 times
  • Download rankings, all-time:
    • Site-wide: 37,920 out of 70,836
    • In genetics: 2,334 out of 3,925
  • Year to date:
    • Site-wide: 65,112 out of 70,836
  • Since beginning of last month:
    • Site-wide: 53,045 out of 70,836

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

genetics more details view paper
  • Downloaded 264 times
  • Download rankings, all-time:
    • Site-wide: 43,339 out of 70,836
    • In genetics: 2,612 out of 3,925
  • Year to date:
    • Site-wide: 57,146 out of 70,836
  • Since beginning of last month:
    • Site-wide: 65,434 out of 70,836

PanLingua

Sign up for the Rxivist weekly newsletter! (Click here for more details.)


News