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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 73,182 bioRxiv papers from 318,593 authors.

Author: Christine Søholm Hansen

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

Rankings

  • All-time downloads: 16,021 (rank: 2,435 (tie) out of 318,721)
  • Categories:
    • genetics: 16,021 (rank: 604 out of 31,252)

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 8,908 times
  • Download rankings, all-time:
    • Site-wide: 180 out of 73,219
    • In genetics: 14 out of 4,019
  • Year to date:
    • Site-wide: 14,289 out of 73,219
  • Since beginning of last month:
    • Site-wide: 14,289 out of 73,219

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
  • Downloaded 6,593 times
  • Download rankings, all-time:
    • Site-wide: 304 out of 73,219
    • In genetics: 32 out of 4,019
  • Year to date:
    • Site-wide: 3,543 out of 73,219
  • Since beginning of last month:
    • Site-wide: 3,543 out of 73,219

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

genetics more details view paper
  • Downloaded 520 times
  • Download rankings, all-time:
    • Site-wide: 22,718 out of 73,219
    • In genetics: 1,503 out of 4,019
  • Year to date:
    • Site-wide: 39,382 out of 73,219
  • Since beginning of last month:
    • Site-wide: 39,382 out of 73,219

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