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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 57,524 bioRxiv papers from 264,866 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: 23,754 (rank: 793 (tie) out of 264,866)
  • Categories:
    • genetics: 18,101 (rank: 351 out of 25,229)
    • genomics: 5,653 (rank: 1,970 out of 30,302)

Downloads per author, site-wide

Preprints

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

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  • Downloaded 8,665 times
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    • In genetics: 11 out of 3,296
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    • Site-wide: 1,938 out of 57,524
  • Since beginning of last month:
    • Site-wide: 8,709 out of 57,524

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

genetics more details view paper
  • Downloaded 4,218 times
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    • Site-wide: 512 out of 57,524
    • In genetics: 60 out of 3,296
  • Year to date:
    • Site-wide: 26,020 out of 57,524
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    • Site-wide: 20,306 out of 57,524

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

genetics more details view paper
  • Downloaded 2,170 times
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    • Site-wide: 1,766 out of 57,524
    • In genetics: 175 out of 3,296
  • Year to date:
    • Site-wide: 39,874 out of 57,524
  • Since beginning of last month:
    • Site-wide: 34,917 out of 57,524

Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia

genomics more details view paper
  • Downloaded 1,742 times
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    • In genomics: 531 out of 4,030
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    • Site-wide: 33,636 out of 57,524
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    • Site-wide: 48,843 out of 57,524

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

genetics more details view paper
  • Downloaded 1,588 times
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    • Site-wide: 3,034 out of 57,524
    • In genetics: 275 out of 3,296
  • Year to date:
    • Site-wide: 42,184 out of 57,524
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    • Site-wide: 37,735 out of 57,524

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
  • Downloaded 1,260 times
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    • Site-wide: 4,434 out of 57,524
    • In genomics: 795 out of 4,030
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  • Since beginning of last month:
    • Site-wide: 32,296 out of 57,524

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 1,143 times
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    • Site-wide: 5,192 out of 57,524
    • In genetics: 426 out of 3,296
  • Year to date:
    • Site-wide: 33,985 out of 57,524
  • Since beginning of last month:
    • Site-wide: 32,312 out of 57,524

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

genomics more details view paper
  • Downloaded 1,111 times
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    • Site-wide: 5,446 out of 57,524
    • In genomics: 930 out of 4,030
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    • Site-wide: 19,758 out of 57,524
  • Since beginning of last month:
    • Site-wide: 6,390 out of 57,524

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

genomics more details view paper
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    • In genomics: 1,217 out of 4,030
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    • Site-wide: 36,715 out of 57,524
  • Since beginning of last month:
    • Site-wide: 39,030 out of 57,524

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 472 times
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    • Site-wide: 18,786 out of 57,524
    • In genomics: 2,216 out of 4,030
  • Year to date:
    • Site-wide: 18,433 out of 57,524
  • Since beginning of last month:
    • Site-wide: 21,933 out of 57,524

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

genetics more details view paper
  • Downloaded 317 times
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    • Site-wide: 28,418 out of 57,524
    • In genetics: 1,837 out of 3,296
  • Year to date:
    • Site-wide: 25,949 out of 57,524
  • Since beginning of last month:
    • Site-wide: 39,432 out of 57,524

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

genomics more details view paper
  • Downloaded 178 times
  • Download rankings, all-time:
    • Site-wide: 42,703 out of 57,524
    • In genomics: 3,522 out of 4,030
  • Year to date:
    • Site-wide: 44,729 out of 57,524
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    • Site-wide: 46,925 out of 57,524

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