Rxivist logo

Author: Tarjinder Singh

  • ORCiD: http://orcid.org/0000-0003-0601-6815
  • Most recently observed institution: Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA

Rankings

  • All-time downloads: 31,261 (rank: 4,860 )
  • Categories:
    • genetic and genomic medicine: 3,748 (rank: 215 (tie) )
    • genetics: 26,490 (rank: 247 )
    • genomics: 1,023 (rank: 21,624 (tie) )

Downloads per author, site-wide

Preprints

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

genetics more details view paper
  • Downloaded 10,216 times
  • Download rankings, all-time:
    • Site-wide: 779
    • In genetics: 22
  • Year to date:
    • Site-wide: 5,901
  • Since beginning of last month:
    • Site-wide: 11,300

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation

genetics more details view paper
  • Downloaded 7,482 times
  • Download rankings, all-time:
    • Site-wide: 1,160
    • In genetics: 36
  • Year to date:
    • Site-wide: 22,676
  • Since beginning of last month:
    • Site-wide: 33,377

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

genetic and genomic medicine more details view paper
  • Downloaded 3,367 times
  • Download rankings, all-time:
    • Site-wide: 3,508
    • In genetic and genomic medicine: 11
  • Year to date:
    • Site-wide: 972
  • Since beginning of last month:
    • Site-wide: 1,017

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

genetics more details view paper
  • Downloaded 2,021 times
  • Download rankings, all-time:
    • Site-wide: 7,337
    • In genetics: 347
  • Year to date:
    • Site-wide: 46,579
  • Since beginning of last month:
    • Site-wide: 59,235

De novo Variants In Neurodevelopmental Disorders With Epilepsy

genetics more details view paper
  • Downloaded 1,957 times
  • Download rankings, all-time:
    • Site-wide: 7,707
    • In genetics: 360
  • Year to date:
    • Site-wide: 38,777
  • Since beginning of last month:
    • Site-wide: 50,979

ASD and ADHD have a similar burden of rare protein-truncating variants

genetics more details view paper
  • Downloaded 1,744 times
  • Download rankings, all-time:
    • Site-wide: 9,184
    • In genetics: 438
  • Year to date:
    • Site-wide: 34,398
  • Since beginning of last month:
    • Site-wide: 58,488

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

genomics more details view paper
  • Downloaded 1,023 times
  • Download rankings, all-time:
    • Site-wide: 20,303
    • In genomics: 2,033
  • Year to date:
    • Site-wide: 89,513
  • Since beginning of last month:
    • Site-wide: 83,605

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

genetics more details view paper
  • Downloaded 999 times
  • Download rankings, all-time:
    • Site-wide: 20,989
    • In genetics: 1,006
  • Year to date:
    • Site-wide: 101,651
  • Since beginning of last month:
    • Site-wide: 81,631

Schizophrenia risk conferred by protein-coding de novo mutations

genetics more details view paper
  • Downloaded 837 times
  • Download rankings, all-time:
    • Site-wide: 27,035
    • In genetics: 1,309
  • Year to date:
    • Site-wide: 93,072
  • Since beginning of last month:
    • Site-wide: 90,859

Contribution of Retrotransposition to Developmental Disorders

genetics more details view paper
  • Downloaded 787 times
  • Download rankings, all-time:
    • Site-wide: 29,471
    • In genetics: 1,434
  • Year to date:
    • Site-wide: 122,844
  • Since beginning of last month:
    • Site-wide: 124,123

Meta-analysis of Scandinavian Schizophrenia Exomes

genetics more details view paper
  • Downloaded 447 times
  • Download rankings, all-time:
    • Site-wide: 59,710
    • In genetics: 2,769
  • Year to date:
    • Site-wide: 60,339
  • Since beginning of last month:
    • Site-wide: 78,897

Exome sequencing in bipolar disorder reveals shared risk gene AKAP11 with schizophrenia

genetic and genomic medicine more details view paper
  • Downloaded 381 times
  • Download rankings, all-time:
    • Site-wide: 69,870
    • In genetic and genomic medicine: 231
  • Year to date:
    • Site-wide: 4,317
  • Since beginning of last month:
    • Site-wide: 1,234

PanLingua

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


News