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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

Rankings

  • All-time downloads: 33,472 (rank: 5,407 )
  • Categories:
    • genetic and genomic medicine: 5,333 (rank: 208 (tie) )
    • genetics: 27,090 (rank: 254 )
    • genomics: 1,049 (rank: 23,042 (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 10,415 times
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    • Site-wide: 909
    • In genetics: 23
  • Year to date:
    • Site-wide: 8,359
  • Since beginning of last month:
    • Site-wide: 34,181

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

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  • Downloaded 7,565 times
  • Download rankings, all-time:
    • Site-wide: 1,346
    • In genetics: 36
  • Year to date:
    • Site-wide: 31,057
  • Since beginning of last month:
    • Site-wide: 93,507

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

genetic and genomic medicine more details view paper
  • Downloaded 4,672 times
  • Download rankings, all-time:
    • Site-wide: 2,589
    • In genetic and genomic medicine: 11
  • Year to date:
    • Site-wide: 955
  • Since beginning of last month:
    • Site-wide: 8,882

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

genetics more details view paper
  • Downloaded 2,070 times
  • Download rankings, all-time:
    • Site-wide: 8,289
    • In genetics: 362
  • Year to date:
    • Site-wide: 60,521
  • Since beginning of last month:
    • Site-wide: None

De novo Variants In Neurodevelopmental Disorders With Epilepsy

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  • Downloaded 2,014 times
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    • Site-wide: 8,638
    • In genetics: 375
  • Year to date:
    • Site-wide: 51,332
  • Since beginning of last month:
    • Site-wide: None

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

genetics more details view paper
  • Downloaded 1,818 times
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    • Site-wide: 10,079
    • In genetics: 448
  • Year to date:
    • Site-wide: 42,230
  • Since beginning of last month:
    • Site-wide: 61,011

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

genomics more details view paper
  • Downloaded 1,049 times
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    • Site-wide: 22,780
    • In genomics: 2,164
  • Year to date:
    • Site-wide: 106,578
  • Since beginning of last month:
    • Site-wide: 60,909

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

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  • Downloaded 1,042 times
  • Download rankings, all-time:
    • Site-wide: 23,023
    • In genetics: 1,055
  • Year to date:
    • Site-wide: 91,915
  • Since beginning of last month:
    • Site-wide: 93,678

Schizophrenia risk conferred by protein-coding de novo mutations

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  • Downloaded 874 times
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    • Site-wide: 29,590
    • In genetics: 1,359
  • Year to date:
    • Site-wide: 95,286
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    • Site-wide: 93,158

Contribution of Retrotransposition to Developmental Disorders

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  • Downloaded 800 times
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    • In genetics: 1,536
  • Year to date:
    • Site-wide: 142,351
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    • Site-wide: None

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

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  • Downloaded 661 times
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    • Site-wide: 43,402
    • In genetic and genomic medicine: 171
  • Year to date:
    • Site-wide: 5,703
  • Since beginning of last month:
    • Site-wide: 19,937

Meta-analysis of Scandinavian Schizophrenia Exomes

genetics more details view paper
  • Downloaded 492 times
  • Download rankings, all-time:
    • Site-wide: 62,206
    • In genetics: 2,749
  • Year to date:
    • Site-wide: 72,596
  • Since beginning of last month:
    • Site-wide: 82,294

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