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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 62,198 bioRxiv papers from 276,129 authors.

Author: Christine Søholm Hansen

  • Most recently observed institution: Center for Neonatal Screening, Department for Congenital Disorders, Statens Serum Institut

Rankings

  • All-time downloads: 15,178 (rank: 1,961 out of 276,129)
  • Categories:
    • genetics: 15,178 (rank: 573 out of 27,666)

Downloads per author, site-wide

Preprints

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

genetics more details view paper
  • Downloaded 8,726 times
  • Download rankings, all-time:
    • Site-wide: 137 out of 62,198
    • In genetics: 13 out of 3,537
  • Year to date:
    • Site-wide: 2,164 out of 62,198
  • Since beginning of last month:
    • Site-wide: 6,065 out of 62,198

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
  • Downloaded 5,966 times
  • Download rankings, all-time:
    • Site-wide: 294 out of 62,198
    • In genetics: 35 out of 3,537
  • Year to date:
    • Site-wide: 311 out of 62,198
  • Since beginning of last month:
    • Site-wide: 50,906 out of 62,198

Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

genetics more details view paper
  • Downloaded 486 times
  • Download rankings, all-time:
    • Site-wide: 19,490 out of 62,198
    • In genetics: 1,317 out of 3,537
  • Year to date:
    • Site-wide: 39,361 out of 62,198
  • Since beginning of last month:
    • Site-wide: 31,642 out of 62,198

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