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Author: Tianyun Wang

  • ORCiD: http://orcid.org/0000-0002-5179-087X
  • Most recently observed institution: Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA

Rankings

  • All-time downloads: 11,357 (rank: 26,419 (tie) )
  • Categories:
    • genetic and genomic medicine: 806 (rank: 6,331 (tie) )
    • genetics: 5,164 (rank: 4,218 )
    • genomics: 3,220 (rank: 9,065 (tie) )
    • neurology: 1,546 (rank: 1,294 (tie) )

Downloads per author, site-wide

Preprints

Targeted long-read sequencing resolves complex structural variants and identifies missing disease-causing variants

genomics more details view paper
  • Downloaded 3,303 times
  • Download rankings, all-time:
    • Site-wide: 5,537
    • In genomics: 524
  • Year to date:
    • Site-wide: 16,488
  • Since beginning of last month:
    • Site-wide: 20,547

Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes

genetics more details view paper
  • Downloaded 2,856 times
  • Download rankings, all-time:
    • Site-wide: 6,832
    • In genetics: 255
  • Year to date:
    • Site-wide: 60,674
  • Since beginning of last month:
    • Site-wide: 38,078

Pathogenic SPTBN1 variants cause a novel autosomal dominant neurodevelopmental syndrome

neurology more details view paper
  • Downloaded 1,420 times
  • Download rankings, all-time:
    • Site-wide: 19,305
    • In neurology: 48
  • Year to date:
    • Site-wide: 36,994
  • Since beginning of last month:
    • Site-wide: 24,735

Recent ultra-rare inherited mutations identify novel autism candidate risk genes

genetics more details view paper
  • Downloaded 1,307 times
  • Download rankings, all-time:
    • Site-wide: 21,915
    • In genetics: 910
  • Year to date:
    • Site-wide: 60,151
  • Since beginning of last month:
    • Site-wide: 65,043

Integrated gene analyses of de novo mutations from 46,612 trios with autism and developmental disorders

genetics more details view paper
  • Downloaded 1,228 times
  • Download rankings, all-time:
    • Site-wide: 24,203
    • In genetics: 1,207
  • Year to date:
    • Site-wide: 6,182
  • Since beginning of last month:
    • Site-wide: 6,162

Integrating de novo and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes

genetic and genomic medicine more details view paper
  • Downloaded 993 times
  • Download rankings, all-time:
    • Site-wide: 33,302
    • In genetic and genomic medicine: 225
  • Year to date:
    • Site-wide: 6,754
  • Since beginning of last month:
    • Site-wide: 5,780

De novo variants in the PSMC3 proteasome AAA-ATPase subunit gene cause neurodevelopmental disorders associated with type I interferonopathies.

neurology more details view paper
  • Downloaded 250 times
  • Download rankings, all-time:
    • Site-wide: 148,445
    • In neurology: 953
  • Year to date:
    • Site-wide: 26,052
  • Since beginning of last month:
    • Site-wide: 23,829

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