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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: 15,119 (rank: 4,674 out of 397,991)
  • Categories:
    • genetics: 11,458 (rank: 1,121 out of 36,549)
    • genomics: 3,661 (rank: 5,505 (tie) out of 42,257)

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Preprints

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

genetics more details view paper
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    • Site-wide: 82,595 out of 93,254
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    • Site-wide: 81,021 out of 93,254

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

genomics more details view paper
  • Downloaded 1,378 times
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    • Site-wide: 7,086 out of 93,254
    • In genomics: 1,099 out of 5,873
  • Year to date:
    • Site-wide: 50,437 out of 93,254
  • Since beginning of last month:
    • Site-wide: 52,715 out of 93,254

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

genomics more details view paper
  • Downloaded 1,267 times
  • Download rankings, all-time:
    • Site-wide: 8,159 out of 93,254
    • In genomics: 1,233 out of 5,873
  • Year to date:
    • Site-wide: 18,370 out of 93,254
  • Since beginning of last month:
    • Site-wide: 16,463 out of 93,254

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

genomics more details view paper
  • Downloaded 1,016 times
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    • Site-wide: 11,769 out of 93,254
    • In genomics: 1,626 out of 5,873
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    • Site-wide: 6,211 out of 93,254
  • Since beginning of last month:
    • Site-wide: 6,513 out of 93,254

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

genetics more details view paper
  • Downloaded 808 times
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    • Site-wide: 16,804 out of 93,254
    • In genetics: 1,069 out of 4,770
  • Year to date:
    • Site-wide: 25,342 out of 93,254
  • Since beginning of last month:
    • Site-wide: 32,097 out of 93,254

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

genetics more details view paper
  • Downloaded 799 times
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    • Site-wide: 17,103 out of 93,254
    • In genetics: 1,095 out of 4,770
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    • Site-wide: 61,846 out of 93,254
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    • Site-wide: 74,187 out of 93,254

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

genetics more details view paper
  • Downloaded 661 times
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    • In genetics: 1,424 out of 4,770
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  • Since beginning of last month:
    • Site-wide: 11,790 out of 93,254

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
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    • Site-wide: 36,943 out of 93,254
    • In genetics: 2,163 out of 4,770
  • Year to date:
    • Site-wide: 57,811 out of 93,254
  • Since beginning of last month:
    • Site-wide: 53,654 out of 93,254

Common breast cancer risk loci predispose to distinct tumor subtypes

genetics more details view paper
  • Downloaded 318 times
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    • Site-wide: 52,851 out of 93,254
    • In genetics: 2,974 out of 4,770
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    • Site-wide: 29,551 out of 93,254
  • Since beginning of last month:
    • Site-wide: 31,697 out of 93,254

Modelling the developmental spliceosomal craniofacial disorder Burn-McKeown syndrome using induced pluripotent stem cells

genetics more details view paper
  • Downloaded 129 times
  • Download rankings, all-time:
    • Site-wide: 83,152 out of 93,254
    • In genetics: 4,380 out of 4,770
  • Year to date:
    • Site-wide: 35,061 out of 93,254
  • Since beginning of last month:
    • Site-wide: 26,972 out of 93,254

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