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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 66,879 bioRxiv papers from 294,441 authors.

Author: Shaun M. Purcell

  • Most recently observed institution: Sleep Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Rankings

  • All-time downloads: 52,312 (rank: 264 out of 294,441)
  • Categories:
    • genetics: 24,803 (rank: 182 out of 29,418)
    • genomics: 27,509 (rank: 213 out of 33,523)

Downloads per author, site-wide

Preprints

Analysis of protein-coding genetic variation in 60,706 humans

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  • Downloaded 21,535 times
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    • In genomics: 7 out of 4,549
  • Year to date:
    • Site-wide: 3,374 out of 66,879
  • Since beginning of last month:
    • Site-wide: 6,964 out of 66,879

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

genetics more details view paper
  • Downloaded 8,828 times
  • Download rankings, all-time:
    • Site-wide: 152 out of 66,879
    • In genetics: 14 out of 3,766
  • Year to date:
    • Site-wide: 2,386 out of 66,879
  • Since beginning of last month:
    • Site-wide: 4,350 out of 66,879

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: 282 out of 66,879
    • In genetics: 33 out of 3,766
  • Year to date:
    • Site-wide: 314 out of 66,879
  • Since beginning of last month:
    • Site-wide: 1,705 out of 66,879

Regulatory variants explain much more heritability than coding variants across 11 common diseases

genetics more details view paper
  • Downloaded 4,280 times
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    • Site-wide: 599 out of 66,879
    • In genetics: 60 out of 3,766
  • Year to date:
    • Site-wide: 26,819 out of 66,879
  • Since beginning of last month:
    • Site-wide: 20,830 out of 66,879

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

genetics more details view paper
  • Downloaded 2,195 times
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    • Site-wide: 2,056 out of 66,879
    • In genetics: 197 out of 3,766
  • Year to date:
    • Site-wide: 47,670 out of 66,879
  • Since beginning of last month:
    • Site-wide: 53,573 out of 66,879

Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia

genomics more details view paper
  • Downloaded 1,782 times
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    • Site-wide: 2,940 out of 66,879
    • In genomics: 583 out of 4,549
  • Year to date:
    • Site-wide: 37,881 out of 66,879
  • Since beginning of last month:
    • Site-wide: 47,257 out of 66,879

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

genetics more details view paper
  • Downloaded 1,609 times
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    • Site-wide: 3,482 out of 66,879
    • In genetics: 299 out of 3,766
  • Year to date:
    • Site-wide: 51,291 out of 66,879
  • Since beginning of last month:
    • Site-wide: 54,620 out of 66,879

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
  • Downloaded 1,298 times
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    • Site-wide: 4,996 out of 66,879
    • In genomics: 881 out of 4,549
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  • Since beginning of last month:
    • Site-wide: 41,060 out of 66,879

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
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    • In genomics: 928 out of 4,549
  • Year to date:
    • Site-wide: 14,762 out of 66,879
  • Since beginning of last month:
    • Site-wide: 11,021 out of 66,879

Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits

genetics more details view paper
  • Downloaded 1,182 times
  • Download rankings, all-time:
    • Site-wide: 5,852 out of 66,879
    • In genetics: 467 out of 3,766
  • Year to date:
    • Site-wide: 38,348 out of 66,879
  • Since beginning of last month:
    • Site-wide: 20,510 out of 66,879

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

genomics more details view paper
  • Downloaded 912 times
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    • Site-wide: 8,924 out of 66,879
    • In genomics: 1,366 out of 4,549
  • Year to date:
    • Site-wide: 45,930 out of 66,879
  • Since beginning of last month:
    • Site-wide: 51,744 out of 66,879

Integrative analysis of rare variants and pathway information shows convergent results between immune pathways, drug targets and epilepsy genes

genomics more details view paper
  • Downloaded 540 times
  • Download rankings, all-time:
    • Site-wide: 18,953 out of 66,879
    • In genomics: 2,264 out of 4,549
  • Year to date:
    • Site-wide: 19,795 out of 66,879
  • Since beginning of last month:
    • Site-wide: 22,330 out of 66,879

Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

genetics more details view paper
  • Downloaded 360 times
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    • Site-wide: 30,257 out of 66,879
    • In genetics: 1,920 out of 3,766
  • Year to date:
    • Site-wide: 30,161 out of 66,879
  • Since beginning of last month:
    • Site-wide: 37,539 out of 66,879

mTADA: a framework for analyzing de novo mutations in multiple traits

genomics more details view paper
  • Downloaded 198 times
  • Download rankings, all-time:
    • Site-wide: 48,272 out of 66,879
    • In genomics: 3,899 out of 4,549
  • Year to date:
    • Site-wide: 54,226 out of 66,879
  • Since beginning of last month:
    • Site-wide: 52,742 out of 66,879

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