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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 Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA

Rankings

  • All-time downloads: 29,285 (rank: 4,473 )
  • Categories:
    • genetic and genomic medicine: 2,380 (rank: 305 (tie) )
    • genetics: 25,902 (rank: 244 )
    • genomics: 1,003 (rank: 20,508 (tie) )

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Preprints

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

genetics more details view paper
  • Downloaded 9,959 times
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    • Site-wide: 703
    • In genetics: 22
  • Year to date:
    • Site-wide: 3,953
  • Since beginning of last month:
    • Site-wide: 3,336

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

genetics more details view paper
  • Downloaded 7,391 times
  • Download rankings, all-time:
    • Site-wide: 1,035
    • In genetics: 36
  • Year to date:
    • Site-wide: 12,918
  • Since beginning of last month:
    • Site-wide: 25,218

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

genetic and genomic medicine more details view paper
  • Downloaded 2,380 times
  • Download rankings, all-time:
    • Site-wide: 5,081
    • In genetic and genomic medicine: 12
  • Year to date:
    • Site-wide: 1,093
  • Since beginning of last month:
    • Site-wide: 1,394

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

genetics more details view paper
  • Downloaded 1,979 times
  • Download rankings, all-time:
    • Site-wide: 6,629
    • In genetics: 334
  • Year to date:
    • Site-wide: 24,004
  • Since beginning of last month:
    • Site-wide: 37,768

De novo Variants In Neurodevelopmental Disorders With Epilepsy

genetics more details view paper
  • Downloaded 1,901 times
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    • Site-wide: 7,054
    • In genetics: 347
  • Year to date:
    • Site-wide: 27,351
  • Since beginning of last month:
    • Site-wide: 43,598

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

genetics more details view paper
  • Downloaded 1,685 times
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    • Site-wide: 8,463
    • In genetics: 431
  • Year to date:
    • Site-wide: 18,038
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    • Site-wide: 65,174

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

genomics more details view paper
  • Downloaded 1,003 times
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    • Site-wide: 18,483
    • In genomics: 1,931
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    • Site-wide: 74,501
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    • Site-wide: 91,371

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

genetics more details view paper
  • Downloaded 982 times
  • Download rankings, all-time:
    • Site-wide: 19,051
    • In genetics: 969
  • Year to date:
    • Site-wide: 95,212
  • Since beginning of last month:
    • Site-wide: 92,715

Schizophrenia risk conferred by protein-coding de novo mutations

genetics more details view paper
  • Downloaded 819 times
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    • Site-wide: 24,720
    • In genetics: 1,243
  • Year to date:
    • Site-wide: 67,996
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    • Site-wide: 71,474

Contribution of Retrotransposition to Developmental Disorders

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  • Downloaded 776 times
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    • Site-wide: 26,651
    • In genetics: 1,348
  • Year to date:
    • Site-wide: 116,879
  • Since beginning of last month:
    • Site-wide: 66,101

Meta-analysis of Scandinavian Schizophrenia Exomes

genetics more details view paper
  • Downloaded 410 times
  • Download rankings, all-time:
    • Site-wide: 58,383
    • In genetics: 2,801
  • Year to date:
    • Site-wide: 82,719
  • Since beginning of last month:
    • Site-wide: 94,942

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