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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 73,307 bioRxiv papers from 319,075 authors.

Author: Ingileif Jonsdottir

  • Most recently observed institution: deCODE Genetics, Amgen inc., Reykjavik, Iceland

Rankings

  • All-time downloads: 4,409 (rank: 15,765 (tie) out of 319,075)
  • Categories:
    • bioinformatics: 1,373 (rank: 6,547 (tie) out of 27,654)
    • genetics: 1,225 (rank: 9,878 (tie) out of 31,247)
    • genomics: 1,811 (rank: 8,685 (tie) out of 35,528)

Downloads per author, site-wide

Preprints

Recurrence of de novo mutations in families

genomics more details view paper
  • Downloaded 1,811 times
  • Download rankings, all-time:
    • Site-wide: 3,202 out of 73,307
    • In genomics: 615 out of 4,869
  • Year to date:
    • Site-wide: 29,813 out of 73,307
  • Since beginning of last month:
    • Site-wide: 29,813 out of 73,307

Graphtyper: Population-scale genotyping using pangenome graphs

bioinformatics more details view paper
  • Downloaded 1,373 times
  • Download rankings, all-time:
    • Site-wide: 5,122 out of 73,307
    • In bioinformatics: 970 out of 7,149
  • Year to date:
    • Site-wide: 41,348 out of 73,307
  • Since beginning of last month:
    • Site-wide: 41,348 out of 73,307

Genome-wide analysis yields new loci associating with aortic valve stenosis

genetics more details view paper
  • Downloaded 448 times
  • Download rankings, all-time:
    • Site-wide: 27,247 out of 73,307
    • In genetics: 1,748 out of 4,027
  • Year to date:
    • Site-wide: 49,832 out of 73,307
  • Since beginning of last month:
    • Site-wide: 49,832 out of 73,307

A rare missense mutation in MYH6 confers high risk of coarctation of the aorta

genetics more details view paper
  • Downloaded 418 times
  • Download rankings, all-time:
    • Site-wide: 29,442 out of 73,307
    • In genetics: 1,862 out of 4,027
  • Year to date:
    • Site-wide: 66,026 out of 73,307
  • Since beginning of last month:
    • Site-wide: 66,026 out of 73,307

Mutations in RPL3L and MYZAP increase risk of atrial fibrillation

genetics more details view paper
  • Downloaded 359 times
  • Download rankings, all-time:
    • Site-wide: 34,588 out of 73,307
    • In genetics: 2,135 out of 4,027
  • Year to date:
    • Site-wide: 63,567 out of 73,307
  • Since beginning of last month:
    • Site-wide: 63,567 out of 73,307

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