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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 70,903 bioRxiv papers from 309,378 authors.

Author: Daniel P Howrigan

  • Most recently observed institution: Broad Institute

Rankings

  • All-time downloads: 27,346 (rank: 857 out of 309,294)
  • Categories:
    • bioinformatics: 2,190 (rank: 3,751 (tie) out of 26,873)
    • genetics: 24,185 (rank: 193 out of 30,603)
    • genomics: 971 (rank: 14,645 (tie) out of 34,888)

Downloads per author, site-wide

Preprints

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

genetics more details view paper
  • Downloaded 9,270 times
  • Download rankings, all-time:
    • Site-wide: 150 out of 70,881
    • In genetics: 12 out of 3,928
  • Year to date:
    • Site-wide: 2,238 out of 70,881
  • Since beginning of last month:
    • Site-wide: 1,996 out of 70,881

Common risk variants identified in autism spectrum disorder

genetics more details view paper
  • Downloaded 6,141 times
  • Download rankings, all-time:
    • Site-wide: 323 out of 70,881
    • In genetics: 36 out of 3,928
  • Year to date:
    • Site-wide: 6,117 out of 70,881
  • Since beginning of last month:
    • Site-wide: 3,746 out of 70,881

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

genetics more details view paper
  • Downloaded 2,207 times
  • Download rankings, all-time:
    • Site-wide: 2,177 out of 70,881
    • In genetics: 201 out of 3,928
  • Year to date:
    • Site-wide: 35,106 out of 70,881
  • Since beginning of last month:
    • Site-wide: 61,718 out of 70,881

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

bioinformatics more details view paper
  • Downloaded 2,190 times
  • Download rankings, all-time:
    • Site-wide: 2,215 out of 70,881
    • In bioinformatics: 445 out of 6,940
  • Year to date:
    • Site-wide: 50,301 out of 70,881
  • Since beginning of last month:
    • Site-wide: 24,294 out of 70,881

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
  • Downloaded 1,628 times
  • Download rankings, all-time:
    • Site-wide: 3,668 out of 70,881
    • In genetics: 310 out of 3,928
  • Year to date:
    • Site-wide: 38,053 out of 70,881
  • Since beginning of last month:
    • Site-wide: 39,343 out of 70,881

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

genetics more details view paper
  • Downloaded 1,601 times
  • Download rankings, all-time:
    • Site-wide: 3,775 out of 70,881
    • In genetics: 318 out of 3,928
  • Year to date:
    • Site-wide: 8,031 out of 70,881
  • Since beginning of last month:
    • Site-wide: 6,052 out of 70,881

Refining the role of de novo protein truncating variants in neurodevelopmental disorders using population reference samples

genetics more details view paper
  • Downloaded 1,324 times
  • Download rankings, all-time:
    • Site-wide: 5,210 out of 70,881
    • In genetics: 419 out of 3,928
  • Year to date:
    • Site-wide: 32,050 out of 70,881
  • Since beginning of last month:
    • Site-wide: 65,597 out of 70,881

Enrichment of rare protein truncating variants in amyotrophic lateral sclerosis patients

genomics more details view paper
  • Downloaded 971 times
  • Download rankings, all-time:
    • Site-wide: 8,707 out of 70,881
    • In genomics: 1,339 out of 4,728
  • Year to date:
    • Site-wide: 32,913 out of 70,881
  • Since beginning of last month:
    • Site-wide: 21,351 out of 70,881

Paternal-age-related de novo mutations and risk for five disorders

genetics more details view paper
  • Downloaded 756 times
  • Download rankings, all-time:
    • Site-wide: 12,856 out of 70,881
    • In genetics: 879 out of 3,928
  • Year to date:
    • Site-wide: 32,544 out of 70,881
  • Since beginning of last month:
    • Site-wide: 61,375 out of 70,881

Schizophrenia risk conferred by protein-coding de novo mutations

genetics more details view paper
  • Downloaded 645 times
  • Download rankings, all-time:
    • Site-wide: 16,161 out of 70,881
    • In genetics: 1,101 out of 3,928
  • Year to date:
    • Site-wide: 34,185 out of 70,881
  • Since beginning of last month:
    • Site-wide: 24,406 out of 70,881

Evaluation of copy number burden in specific epilepsy types from a genome-wide study of 18,564 subjects

genetics more details view paper
  • Downloaded 349 times
  • Download rankings, all-time:
    • Site-wide: 34,015 out of 70,881
    • In genetics: 2,123 out of 3,928
  • Year to date:
    • Site-wide: 17,448 out of 70,881
  • Since beginning of last month:
    • Site-wide: 15,265 out of 70,881

Heterogeneous Contribution of Microdeletions in the Development of Common Generalized and Focal epilepsies

genetics more details view paper
  • Downloaded 264 times
  • Download rankings, all-time:
    • Site-wide: 43,353 out of 70,881
    • In genetics: 2,611 out of 3,928
  • Year to date:
    • Site-wide: 58,779 out of 70,881
  • Since beginning of last month:
    • Site-wide: 66,463 out of 70,881

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