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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 66,889 bioRxiv papers from 294,492 authors.

Author: Jukka S. Moilanen

  • Most recently observed institution: Department of Clinical Genetics, Oulu University Hospital, Oulu, Finland

Rankings

  • All-time downloads: 3,257 (rank: 19,521 (tie) out of 294,492)
  • Categories:
    • genetics: 2,345 (rank: 5,402 (tie) out of 29,418)
    • genomics: 912 (rank: 14,560 (tie) out of 33,523)

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: 2,705 out of 66,889
    • In genetics: 246 out of 3,766
  • Year to date:
    • Site-wide: 30,482 out of 66,889
  • Since beginning of last month:
    • Site-wide: 49,492 out of 66,889

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

genomics more details view paper
  • Downloaded 912 times
  • Download rankings, all-time:
    • Site-wide: 8,923 out of 66,889
    • In genomics: 1,366 out of 4,549
  • Year to date:
    • Site-wide: 45,923 out of 66,889
  • Since beginning of last month:
    • Site-wide: 51,744 out of 66,889

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 476 times
  • Download rankings, all-time:
    • Site-wide: 22,225 out of 66,889
    • In genetics: 1,485 out of 3,766
  • Year to date:
    • Site-wide: 49,526 out of 66,889
  • Since beginning of last month:
    • Site-wide: 53,289 out of 66,889

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