Rxivist logo

Author: Mandy Johnstone

  • Most recently observed institution: University of Edinburgh

Rankings

  • All-time downloads: 4,450 (rank: 17,184 (tie) out of 335,900)
  • Categories:
    • genetics: 2,884 (rank: 4,998 out of 32,494)
    • genomics: 944 (rank: 16,006 (tie) out of 36,915)
    • neuroscience: 622 (rank: 21,522 (tie) out of 56,763)

Downloads per author, site-wide

Preprints

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

genetics more details view paper
  • Downloaded 1,740 times
  • Download rankings, all-time:
    • Site-wide: 3,718 out of 77,477
    • In genetics: 295 out of 4,179
  • Year to date:
    • Site-wide: 6,415 out of 77,477
  • Since beginning of last month:
    • Site-wide: 9,219 out of 77,477

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
  • Downloaded 944 times
  • Download rankings, all-time:
    • Site-wide: 10,328 out of 77,477
    • In genomics: 1,503 out of 5,081
  • Year to date:
    • Site-wide: 61,751 out of 77,477
  • Since beginning of last month:
    • Site-wide: 75,203 out of 77,477

Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 865 times
  • Download rankings, all-time:
    • Site-wide: 11,849 out of 77,477
    • In genetics: 827 out of 4,179
  • Year to date:
    • Site-wide: 61,154 out of 77,477
  • Since beginning of last month:
    • Site-wide: 50,845 out of 77,477

DISC1 regulates N-Methyl-D-Aspartate receptor dynamics: Abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness

neuroscience more details view paper
  • Downloaded 311 times
  • Download rankings, all-time:
    • Site-wide: 42,855 out of 77,477
    • In neuroscience: 7,535 out of 13,873
  • Year to date:
    • Site-wide: 54,077 out of 77,477
  • Since beginning of last month:
    • Site-wide: 50,562 out of 77,477

Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunction

neuroscience more details view paper
  • Downloaded 311 times
  • Download rankings, all-time:
    • Site-wide: 42,929 out of 77,477
    • In neuroscience: 7,533 out of 13,873
  • Year to date:
    • Site-wide: 63,801 out of 77,477
  • Since beginning of last month:
    • Site-wide: 48,285 out of 77,477

Association of whole-genome and NETRIN1 signaling pathway-derived polygenic risk scores for Major Depressive Disorder and thalamic radiation white matter microstructure in UK Biobank

genetics more details view paper
  • Downloaded 279 times
  • Download rankings, all-time:
    • Site-wide: 47,000 out of 77,477
    • In genetics: 2,767 out of 4,179
  • Year to date:
    • Site-wide: 72,217 out of 77,477
  • Since beginning of last month:
    • Site-wide: 68,217 out of 77,477

PanLingua

Sign up for the Rxivist weekly newsletter! (Click here for more details.)


News