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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 67,354 bioRxiv papers from 296,792 authors.

Author: Christina Hultman

Rankings

  • All-time downloads: 13,671 (rank: 2,723 out of 296,881)
  • Categories:
    • genetics: 10,440 (rank: 905 out of 29,547)
    • genomics: 3,231 (rank: 4,532 (tie) out of 33,725)

Downloads per author, site-wide

Preprints

Common risk variants identified in autism spectrum disorder

genetics more details view paper
  • Downloaded 6,044 times
  • Download rankings, all-time:
    • Site-wide: 318 out of 67,403
    • In genetics: 36 out of 3,786
  • Year to date:
    • Site-wide: 917 out of 67,403
  • Since beginning of last month:
    • Site-wide: 5,507 out of 67,403

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

genetics more details view paper
  • Downloaded 2,195 times
  • Download rankings, all-time:
    • Site-wide: 2,076 out of 67,403
    • In genetics: 197 out of 3,786
  • Year to date:
    • Site-wide: 48,802 out of 67,403
  • Since beginning of last month:
    • Site-wide: 60,671 out of 67,403

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 67,403
    • In genetics: 249 out of 3,786
  • Year to date:
    • Site-wide: 31,266 out of 67,403
  • Since beginning of last month:
    • Site-wide: 57,680 out of 67,403

Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease

genomics more details view paper
  • Downloaded 1,395 times
  • Download rankings, all-time:
    • Site-wide: 4,505 out of 67,403
    • In genomics: 804 out of 4,574
  • Year to date:
    • Site-wide: 1,089 out of 67,403
  • Since beginning of last month:
    • Site-wide: 6,517 out of 67,403

Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders

genomics more details view paper
  • Downloaded 1,244 times
  • Download rankings, all-time:
    • Site-wide: 5,430 out of 67,403
    • In genomics: 928 out of 4,574
  • Year to date:
    • Site-wide: 15,236 out of 67,403
  • Since beginning of last month:
    • Site-wide: 15,332 out of 67,403

Evolutionary and functional data power search for obsessive-compulsive disorder genes

genomics more details view paper
  • Downloaded 592 times
  • Download rankings, all-time:
    • Site-wide: 17,006 out of 67,403
    • In genomics: 2,095 out of 4,574
  • Year to date:
    • Site-wide: 39,316 out of 67,403
  • Since beginning of last month:
    • Site-wide: 51,054 out of 67,403

Characterization of single gene copy number variants in schizophrenia

genetics more details view paper
  • Downloaded 332 times
  • Download rankings, all-time:
    • Site-wide: 33,240 out of 67,403
    • In genetics: 2,080 out of 3,786
  • Year to date:
    • Site-wide: 12,766 out of 67,403
  • Since beginning of last month:
    • Site-wide: 19,676 out of 67,403

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