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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 70,836 bioRxiv papers from 309,140 authors.

Author: Jarmo Körkkö

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

Rankings

  • All-time downloads: 3,310 (rank: 21,020 (tie) out of 309,140)
  • Categories:
    • genetics: 2,381 (rank: 5,591 (tie) out of 30,603)
    • genomics: 929 (rank: 15,195 (tie) out of 34,886)

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

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

genomics more details view paper
  • Downloaded 929 times
  • Download rankings, all-time:
    • Site-wide: 9,372 out of 70,836
    • In genomics: 1,414 out of 4,726
  • Year to date:
    • Site-wide: 32,135 out of 70,836
  • Since beginning of last month:
    • Site-wide: 49,548 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

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