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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 70,281 bioRxiv papers from 306,896 authors.

Author: Christina Hultman

Rankings

  • All-time downloads: 13,924 (rank: 2,847 out of 306,896)
  • Categories:
    • genetics: 10,573 (rank: 922 out of 30,454)
    • genomics: 3,351 (rank: 4,629 out of 34,696)

Downloads per author, site-wide

Preprints

Common risk variants identified in autism spectrum disorder

genetics more details view paper
  • Downloaded 6,141 times
  • Download rankings, all-time:
    • Site-wide: 321 out of 70,281
    • In genetics: 36 out of 3,900
  • Year to date:
    • Site-wide: 2,937 out of 70,281
  • Since beginning of last month:
    • Site-wide: 3,745 out of 70,281

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

genetics more details view paper
  • Downloaded 2,202 times
  • Download rankings, all-time:
    • Site-wide: 2,164 out of 70,281
    • In genetics: 200 out of 3,900
  • Year to date:
    • Site-wide: 42,801 out of 70,281
  • Since beginning of last month:
    • Site-wide: 62,482 out of 70,281

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: 2,808 out of 70,281
    • In genetics: 252 out of 3,900
  • Year to date:
    • Site-wide: 31,600 out of 70,281
  • Since beginning of last month:
    • Site-wide: 32,166 out of 70,281

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 1,480 times
  • Download rankings, all-time:
    • Site-wide: 4,280 out of 70,281
    • In genomics: 777 out of 4,705
  • Year to date:
    • Site-wide: 4,544 out of 70,281
  • Since beginning of last month:
    • Site-wide: 4,687 out of 70,281

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

genomics more details view paper
  • Downloaded 1,267 times
  • Download rankings, all-time:
    • Site-wide: 5,520 out of 70,281
    • In genomics: 941 out of 4,705
  • Year to date:
    • Site-wide: 13,608 out of 70,281
  • Since beginning of last month:
    • Site-wide: 31,785 out of 70,281

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

genomics more details view paper
  • Downloaded 604 times
  • Download rankings, all-time:
    • Site-wide: 17,500 out of 70,281
    • In genomics: 2,145 out of 4,705
  • Year to date:
    • Site-wide: 51,543 out of 70,281
  • Since beginning of last month:
    • Site-wide: 40,462 out of 70,281

Characterization of single gene copy number variants in schizophrenia

genetics more details view paper
  • Downloaded 343 times
  • Download rankings, all-time:
    • Site-wide: 34,173 out of 70,281
    • In genetics: 2,132 out of 3,900
  • Year to date:
    • Site-wide: 32,964 out of 70,281
  • Since beginning of last month:
    • Site-wide: 26,757 out of 70,281

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