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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 62,745 bioRxiv papers from 278,406 authors.

Author: William G Newman

  • ORCiD: http://orcid.org/0000-0002-6382-4678
  • Most recently observed institution: Manchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester NIHR Biomedical Research Centre, Manchester University Hospitals NHS, Foundation Trust, Manchester Academic Health Science Centre

Rankings

  • All-time downloads: 12,731 (rank: 2,712 out of 278,406)
  • Categories:
    • genetics: 10,212 (rank: 864 (tie) out of 27,721)
    • genomics: 2,519 (rank: 5,422 (tie) out of 31,945)

Downloads per author, site-wide

Preprints

Exploring the genetic architecture of inflammatory bowel disease by whole genome sequencing identifies association at ADCY7

genetics more details view paper
  • Downloaded 8,223 times
  • Download rankings, all-time:
    • Site-wide: 153 out of 62,745
    • In genetics: 16 out of 3,562
  • Year to date:
    • Site-wide: 50,164 out of 62,745
  • Since beginning of last month:
    • Site-wide: 36,621 out of 62,745

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

genomics more details view paper
  • Downloaded 1,267 times
  • Download rankings, all-time:
    • Site-wide: 4,788 out of 62,745
    • In genomics: 844 out of 4,316
  • Year to date:
    • Site-wide: 46,420 out of 62,745
  • Since beginning of last month:
    • Site-wide: 34,802 out of 62,745

Whole genome sequencing enables definitive diagnosis of Cystic Fibrosis and Primary Ciliary Dyskinesia

genomics more details view paper
  • Downloaded 929 times
  • Download rankings, all-time:
    • Site-wide: 7,980 out of 62,745
    • In genomics: 1,242 out of 4,316
  • Year to date:
    • Site-wide: 3,680 out of 62,745
  • Since beginning of last month:
    • Site-wide: 4,466 out of 62,745

Inherited BRCA1 epimutation as a novel cause of breast and ovarian cancer

genetics more details view paper
  • Downloaded 705 times
  • Download rankings, all-time:
    • Site-wide: 12,050 out of 62,745
    • In genetics: 849 out of 3,562
  • Year to date:
    • Site-wide: 29,093 out of 62,745
  • Since beginning of last month:
    • Site-wide: 40,503 out of 62,745

Deleterious genetic variants in NOTCH1 are a major contributor to the incidence of non-syndromic Tetralogy of Fallot

genetics more details view paper
  • Downloaded 604 times
  • Download rankings, all-time:
    • Site-wide: 14,990 out of 62,745
    • In genetics: 1,042 out of 3,562
  • Year to date:
    • Site-wide: 20,048 out of 62,745
  • Since beginning of last month:
    • Site-wide: 25,016 out of 62,745

A homozygous variant in mitochondrial RNase P subunit PRORP is associated with Perrault syndrome characterized by hearing loss and primary ovarian insufficiency

genetics more details view paper
  • Downloaded 353 times
  • Download rankings, all-time:
    • Site-wide: 28,183 out of 62,745
    • In genetics: 1,810 out of 3,562
  • Year to date:
    • Site-wide: 43,453 out of 62,745
  • Since beginning of last month:
    • Site-wide: 22,774 out of 62,745

Functional and in-silico interrogation of rare genomic variants impacting RNA splicing for the diagnosis of genomic disorders

genomics more details view paper
  • Downloaded 323 times
  • Download rankings, all-time:
    • Site-wide: 30,757 out of 62,745
    • In genomics: 3,009 out of 4,316
  • Year to date:
    • Site-wide: 10,053 out of 62,745
  • Since beginning of last month:
    • Site-wide: 433 out of 62,745

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

genetics more details view paper
  • Downloaded 196 times
  • Download rankings, all-time:
    • Site-wide: 44,540 out of 62,745
    • In genetics: 2,701 out of 3,562
  • Year to date:
    • Site-wide: 20,514 out of 62,745
  • Since beginning of last month:
    • Site-wide: 1,105 out of 62,745

Common breast cancer risk loci predispose to distinct tumor subtypes

genetics more details view paper
  • Downloaded 131 times
  • Download rankings, all-time:
    • Site-wide: 53,243 out of 62,745
    • In genetics: 3,116 out of 3,562
  • Year to date:
    • Site-wide: 31,877 out of 62,745
  • Since beginning of last month:
    • Site-wide: 13,175 out of 62,745

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