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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: 14,570 (rank: 4,191 out of 364,218)
  • Categories:
    • genetics: 11,157 (rank: 1,055 out of 34,077)
    • genomics: 3,413 (rank: 5,401 out of 39,230)

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
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    • Site-wide: 69,234 out of 84,643
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    • Site-wide: 67,818 out of 84,643

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

genomics more details view paper
  • Downloaded 1,358 times
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    • Site-wide: 6,504 out of 84,643
    • In genomics: 1,046 out of 5,463
  • Year to date:
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    • Site-wide: 30,892 out of 84,643

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

genomics more details view paper
  • Downloaded 1,200 times
  • Download rankings, all-time:
    • Site-wide: 7,985 out of 84,643
    • In genomics: 1,220 out of 5,463
  • Year to date:
    • Site-wide: 18,901 out of 84,643
  • Since beginning of last month:
    • Site-wide: 17,375 out of 84,643

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

genomics more details view paper
  • Downloaded 855 times
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    • Site-wide: 13,747 out of 84,643
    • In genomics: 1,829 out of 5,463
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    • Site-wide: 7,209 out of 84,643
  • Since beginning of last month:
    • Site-wide: 6,930 out of 84,643

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

genetics more details view paper
  • Downloaded 782 times
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    • Site-wide: 15,750 out of 84,643
    • In genetics: 1,029 out of 4,444
  • Year to date:
    • Site-wide: 54,197 out of 84,643
  • Since beginning of last month:
    • Site-wide: 49,889 out of 84,643

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

genetics more details view paper
  • Downloaded 771 times
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    • In genetics: 1,055 out of 4,444
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    • Site-wide: 21,457 out of 84,643
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    • Site-wide: 14,442 out of 84,643

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

genetics more details view paper
  • Downloaded 573 times
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    • In genetics: 1,563 out of 4,444
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    • Site-wide: 6,488 out of 84,643

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 437 times
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    • In genetics: 2,066 out of 4,444
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    • Site-wide: 51,672 out of 84,643

Common breast cancer risk loci predispose to distinct tumor subtypes

genetics more details view paper
  • Downloaded 230 times
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    • In genetics: 3,387 out of 4,444
  • Year to date:
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  • Since beginning of last month:
    • Site-wide: 67,462 out of 84,643

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

genetics more details view paper
  • Downloaded 81 times
  • Download rankings, all-time:
    • Site-wide: 80,744 out of 84,643
    • In genetics: 4,284 out of 4,444
  • Year to date:
    • Site-wide: 38,160 out of 84,643
  • Since beginning of last month:
    • Site-wide: 12,062 out of 84,643

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