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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 67,221 bioRxiv papers from 295,976 authors.

Author: Claire Churchhouse

Rankings

  • All-time downloads: 27,228 (rank: 768 out of 295,454)
  • Categories:
    • bioinformatics: 312 (rank: 18,758 (tie) out of 25,779)
    • genetics: 25,969 (rank: 167 out of 29,470)
    • genomics: 947 (rank: 14,001 (tie) out of 33,659)

Downloads per author, site-wide

Preprints

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

genetics more details view paper
  • Downloaded 9,111 times
  • Download rankings, all-time:
    • Site-wide: 145 out of 67,145
    • In genetics: 12 out of 3,776
  • Year to date:
    • Site-wide: 582 out of 67,145
  • Since beginning of last month:
    • Site-wide: 1,995 out of 67,145

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
  • Downloaded 6,349 times
  • Download rankings, all-time:
    • Site-wide: 286 out of 67,145
    • In genetics: 34 out of 3,776
  • Year to date:
    • Site-wide: 317 out of 67,145
  • Since beginning of last month:
    • Site-wide: 2,069 out of 67,145

Common risk variants identified in autism spectrum disorder

genetics more details view paper
  • Downloaded 6,044 times
  • Download rankings, all-time:
    • Site-wide: 317 out of 67,145
    • In genetics: 36 out of 3,776
  • Year to date:
    • Site-wide: 906 out of 67,145
  • Since beginning of last month:
    • Site-wide: 4,910 out of 67,145

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: 2,718 out of 67,145
    • In genetics: 247 out of 3,776
  • Year to date:
    • Site-wide: 30,879 out of 67,145
  • Since beginning of last month:
    • Site-wide: 54,988 out of 67,145

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

genetics more details view paper
  • Downloaded 1,529 times
  • Download rankings, all-time:
    • Site-wide: 3,826 out of 67,145
    • In genetics: 332 out of 3,776
  • Year to date:
    • Site-wide: 891 out of 67,145
  • Since beginning of last month:
    • Site-wide: 5,741 out of 67,145

Enrichment of rare protein truncating variants in amyotrophic lateral sclerosis patients

genomics more details view paper
  • Downloaded 947 times
  • Download rankings, all-time:
    • Site-wide: 8,460 out of 67,145
    • In genomics: 1,314 out of 4,562
  • Year to date:
    • Site-wide: 8,978 out of 67,145
  • Since beginning of last month:
    • Site-wide: 9,038 out of 67,145

Schizophrenia risk conferred by protein-coding de novo mutations

genetics more details view paper
  • Downloaded 620 times
  • Download rankings, all-time:
    • Site-wide: 15,869 out of 67,145
    • In genetics: 1,086 out of 3,776
  • Year to date:
    • Site-wide: 9,021 out of 67,145
  • Since beginning of last month:
    • Site-wide: 22,725 out of 67,145

Genetic predisposition to myeloproliferative neoplasms implicates hematopoietic stem cell biology

genetics more details view paper
  • Downloaded 447 times
  • Download rankings, all-time:
    • Site-wide: 24,158 out of 67,145
    • In genetics: 1,592 out of 3,776
  • Year to date:
    • Site-wide: 7,756 out of 67,145
  • Since beginning of last month:
    • Site-wide: 4,555 out of 67,145

PAIRUP-MS: Pathway Analysis and Imputation to Relate Unknowns in Profiles from Mass Spectrometry-based metabolite data

bioinformatics more details view paper
  • Downloaded 312 times
  • Download rankings, all-time:
    • Site-wide: 35,065 out of 67,145
    • In bioinformatics: 4,364 out of 6,625
  • Year to date:
    • Site-wide: 59,254 out of 67,145
  • Since beginning of last month:
    • Site-wide: 65,159 out of 67,145

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