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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 66,819 bioRxiv papers from 294,207 authors.

Author: James T. R. Walters

  • Most recently observed institution: Analytic and Translational Genetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; 2Program in Medical and Population Genetics, Broad Institute of MIT and Harvard

Rankings

  • All-time downloads: 6,469 (rank: 8,453 (tie) out of 294,207)
  • Categories:
    • genetics: 1,885 (rank: 6,585 (tie) out of 29,327)
    • genomics: 4,276 (rank: 3,272 (tie) out of 33,464)
    • neuroscience: 308 (rank: 30,254 (tie) out of 49,287)

Downloads per author, site-wide

Preprints

Genetic Identification Of Brain Cell Types Underlying Schizophrenia

genomics more details view paper
  • Downloaded 3,364 times
  • Download rankings, all-time:
    • Site-wide: 940 out of 66,819
    • In genomics: 238 out of 4,549
  • Year to date:
    • Site-wide: 6,038 out of 66,819
  • Since beginning of last month:
    • Site-wide: 22,947 out of 66,819

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

genomics more details view paper
  • Downloaded 912 times
  • Download rankings, all-time:
    • Site-wide: 8,921 out of 66,819
    • In genomics: 1,366 out of 4,549
  • Year to date:
    • Site-wide: 45,809 out of 66,819
  • Since beginning of last month:
    • Site-wide: 51,350 out of 66,819

Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 835 times
  • Download rankings, all-time:
    • Site-wide: 10,203 out of 66,819
    • In genetics: 749 out of 3,766
  • Year to date:
    • Site-wide: 48,346 out of 66,819
  • Since beginning of last month:
    • Site-wide: 44,754 out of 66,819

Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels

genetics more details view paper
  • Downloaded 563 times
  • Download rankings, all-time:
    • Site-wide: 17,991 out of 66,819
    • In genetics: 1,206 out of 3,766
  • Year to date:
    • Site-wide: 37,296 out of 66,819
  • Since beginning of last month:
    • Site-wide: 39,153 out of 66,819

Analyses of rare and common alleles in parent-proband trios implicate rare missense variants in SLC6A1 in schizophrenia and confirm the involvement of loss of function intolerant and neurodevelopmental disorder genes.

genetics more details view paper
  • Downloaded 346 times
  • Download rankings, all-time:
    • Site-wide: 31,465 out of 66,819
    • In genetics: 1,998 out of 3,766
  • Year to date:
    • Site-wide: 11,550 out of 66,819
  • Since beginning of last month:
    • Site-wide: 13,590 out of 66,819

The role of rare copy number variants in depression

neuroscience more details view paper
  • Downloaded 308 times
  • Download rankings, all-time:
    • Site-wide: 35,123 out of 66,819
    • In neuroscience: 6,109 out of 11,969
  • Year to date:
    • Site-wide: 30,368 out of 66,819
  • Since beginning of last month:
    • Site-wide: 42,205 out of 66,819

Meta-analysis of Scandinavian Schizophrenia Exomes

genetics more details view paper
  • Downloaded 141 times
  • Download rankings, all-time:
    • Site-wide: 56,206 out of 66,819
    • In genetics: 3,283 out of 3,766
  • Year to date:
    • Site-wide: 36,040 out of 66,819
  • Since beginning of last month:
    • Site-wide: 1,238 out of 66,819

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