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Author: Vanessa C Wheeler

  • Most recently observed institution: Department of Neurology, Harvard Medical School

Rankings

  • All-time downloads: 12,050 (rank: 21,030 (tie) )
  • Categories:
    • genetics: 4,480 (rank: 4,413 (tie) )
    • genomics: 5,305 (rank: 5,133 (tie) )
    • neuroscience: 1,390 (rank: 21,722 (tie) )
    • systems biology: 875 (rank: 6,177 (tie) )

Downloads per author, site-wide

Preprints

Amplification-free, CRISPR-Cas9 Targeted Enrichment and SMRT Sequencing of Repeat-Expansion Disease Causative Genomic Regions

genomics more details view paper
  • Downloaded 5,305 times
  • Download rankings, all-time:
    • Site-wide: 2,442
    • In genomics: 215
  • Year to date:
    • Site-wide: 11,960
  • Since beginning of last month:
    • Site-wide: 12,386

Huntington's disease onset is determined by length of uninterrupted CAG, not encoded polyglutamine, and is modified by DNA maintenance mechanisms

genetics more details view paper
  • Downloaded 3,117 times
  • Download rankings, all-time:
    • Site-wide: 5,176
    • In genetics: 199
  • Year to date:
    • Site-wide: 27,057
  • Since beginning of last month:
    • Site-wide: 51,769

Huntingtin lowering reduces somatic instability at CAG-expanded loci

neuroscience more details view paper
  • Downloaded 957 times
  • Download rankings, all-time:
    • Site-wide: 30,311
    • In neuroscience: 3,881
  • Year to date:
    • Site-wide: 16,731
  • Since beginning of last month:
    • Site-wide: 21,093

Genome-scale transcriptional regulatory network models for the mouse and human striatum predict roles for SMAD3 and other transcription factors in Huntington's disease

systems biology more details view paper
  • Downloaded 875 times
  • Download rankings, all-time:
    • Site-wide: 34,592
    • In systems biology: 702
  • Year to date:
    • Site-wide: 136,670
  • Since beginning of last month:
    • Site-wide: 123,422

Genetic risk underlying psychiatric and cognitive symptoms in Huntington’s Disease

genetics more details view paper
  • Downloaded 851 times
  • Download rankings, all-time:
    • Site-wide: 35,999
    • In genetics: 1,575
  • Year to date:
    • Site-wide: 115,199
  • Since beginning of last month:
    • Site-wide: 133,893

Somatic CAG expansion in Huntington's disease is dependent on the MLH3 endonuclease domain, which can be excluded via MLH3 splice redirection to suppress expansion

genetics more details view paper
  • Downloaded 512 times
  • Download rankings, all-time:
    • Site-wide: 70,903
    • In genetics: 3,017
  • Year to date:
    • Site-wide: 69,009
  • Since beginning of last month:
    • Site-wide: 101,746

Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's disease

neuroscience more details view paper
  • Downloaded 433 times
  • Download rankings, all-time:
    • Site-wide: 85,053
    • In neuroscience: 12,606
  • Year to date:
    • Site-wide: 160,852
  • Since beginning of last month:
    • Site-wide: 158,701

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