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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 70,308 bioRxiv papers from 307,086 authors.

Author: Christian Gilissen

  • Most recently observed institution: Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center

Rankings

  • All-time downloads: 5,340 (rank: 11,467 (tie) out of 307,048)
  • Categories:
    • bioinformatics: 363 (rank: 18,211 (tie) out of 26,783)
    • genetics: 1,582 (rank: 8,057 (tie) out of 30,487)
    • genomics: 3,395 (rank: 4,583 out of 34,755)

Downloads per author, site-wide

Preprints

Population sequencing data reveal a compendium of mutational processes in human germline

genetics more details view paper

No bioRxiv download data for this paper yet.

Integrating healthcare and research genetic data empowers the discovery of 49 novel developmental disorders

genomics more details view paper
  • Downloaded 1,417 times
  • Download rankings, all-time:
    • Site-wide: 4,614 out of 70,317
    • In genomics: 822 out of 4,705
  • Year to date:
    • Site-wide: 3,974 out of 70,317
  • Since beginning of last month:
    • Site-wide: 436 out of 70,317

Germline De Novo Mutation Clusters Arise During Oocyte Aging In Genomic Regions With Increased Double-Strand Break Incidence

genomics more details view paper
  • Downloaded 1,081 times
  • Download rankings, all-time:
    • Site-wide: 7,256 out of 70,317
    • In genomics: 1,160 out of 4,705
  • Year to date:
    • Site-wide: 11,242 out of 70,317
  • Since beginning of last month:
    • Site-wide: 33,715 out of 70,317

Meta-analysis of 2,104 trios provides support for 10 novel candidate genes for intellectual disability

genetics more details view paper
  • Downloaded 955 times
  • Download rankings, all-time:
    • Site-wide: 8,882 out of 70,317
    • In genetics: 665 out of 3,900
  • Year to date:
    • Site-wide: 50,884 out of 70,317
  • Since beginning of last month:
    • Site-wide: 55,784 out of 70,317

Integrating healthcare and research genetic data empowers the discovery of 49 novel developmental disorders

genomics more details view paper
  • Downloaded 897 times
  • Download rankings, all-time:
    • Site-wide: 9,789 out of 70,317
    • In genomics: 1,458 out of 4,705
  • Year to date:
    • Site-wide: 51,762 out of 70,317
  • Since beginning of last month:
    • Site-wide: 3,614 out of 70,317

Resolving the dark matter of ABCA4 for 1,054 Stargardt disease probands through integrated genomics and transcriptomics

genetics more details view paper
  • Downloaded 470 times
  • Download rankings, all-time:
    • Site-wide: 24,334 out of 70,317
    • In genetics: 1,596 out of 3,900
  • Year to date:
    • Site-wide: 1,255 out of 70,317
  • Since beginning of last month:
    • Site-wide: 5,061 out of 70,317

MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains

bioinformatics more details view paper
  • Downloaded 363 times
  • Download rankings, all-time:
    • Site-wide: 32,319 out of 70,317
    • In bioinformatics: 4,111 out of 6,889
  • Year to date:
    • Site-wide: 65,717 out of 70,317
  • Since beginning of last month:
    • Site-wide: 43,782 out of 70,317

Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome.

genetics more details view paper
  • Downloaded 157 times
  • Download rankings, all-time:
    • Site-wide: 57,794 out of 70,317
    • In genetics: 3,366 out of 3,900
  • Year to date:
    • Site-wide: 3,137 out of 70,317
  • Since beginning of last month:
    • Site-wide: 1,587 out of 70,317

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