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Author: Tarjinder Singh

  • ORCiD: http://orcid.org/0000-0003-0601-6815
  • Most recently observed institution: Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard; Analytic and Translational Genetics Unit, Massachusetts General Hospital

Rankings

  • All-time downloads: 44,828 (rank: 5,746 )
  • Categories:
    • genetic and genomic medicine: 12,194 (rank: 111 )
    • genetics: 28,860 (rank: 296 )
    • genomics: 1,128 (rank: 27,343 (tie) )
    • neuroscience: 793 (rank: 46,660 (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
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    • In genetics: 24
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    • Site-wide: 13,878
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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

genetic and genomic medicine more details view paper
  • Downloaded 9,041 times
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    • Site-wide: 1,540
    • In genetic and genomic medicine: 9
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    • Site-wide: 662
  • Since beginning of last month:
    • Site-wide: 509

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

genetics more details view paper
  • Downloaded 7,854 times
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    • Site-wide: 1,844
    • In genetics: 40
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    • Site-wide: 49,317
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    • Site-wide: 33,677

De novo Variants In Neurodevelopmental Disorders With Epilepsy

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  • Downloaded 2,275 times
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    • Site-wide: 10,718
    • In genetics: 414
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Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

genetics more details view paper
  • Downloaded 2,261 times
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    • In genetics: 402
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ASD and ADHD have a similar burden of rare protein-truncating variants

genetics more details view paper
  • Downloaded 2,073 times
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    • Site-wide: 12,330
    • In genetics: 455
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Exome sequencing in bipolar disorder reveals shared risk gene AKAP11 with schizophrenia

genetic and genomic medicine more details view paper
  • Downloaded 1,640 times
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    • In genetic and genomic medicine: 105
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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 1,167 times
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    • In genetics: 1,204
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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
  • Downloaded 1,146 times
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    • In genomics: 2,528
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Schizophrenia risk conferred by protein-coding de novo mutations

genetics more details view paper
  • Downloaded 990 times
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    • In genetics: 1,536
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The impact of rare protein coding genetic variation on adult cognitive function

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  • Downloaded 975 times
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    • Site-wide: 39,935
    • In genetic and genomic medicine: 296
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Using brain cell-type-specific protein interactomes to interpret genetic data in schizophrenia

genetic and genomic medicine more details view paper
  • Downloaded 954 times
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    • Site-wide: 41,290
    • In genetic and genomic medicine: 268
  • Year to date:
    • Site-wide: 13,129
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    • Site-wide: 16,553

Contribution of Retrotransposition to Developmental Disorders

genetics more details view paper
  • Downloaded 901 times
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    • In genetics: 1,770
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    • Site-wide: 149,508
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Rare schizophrenia risk variant burden is conserved in diverse human populations

genetic and genomic medicine more details view paper
  • Downloaded 890 times
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    • In genetic and genomic medicine: 315
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The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

neuroscience more details view paper
  • Downloaded 868 times
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    • Site-wide: 47,651
    • In neuroscience: 6,881
  • Year to date:
    • Site-wide: 22,056
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    • Site-wide: 138,380

Meta-analysis of Scandinavian Schizophrenia Exomes

genetics more details view paper
  • Downloaded 749 times
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    • Site-wide: 59,353
    • In genetics: 2,364
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    • Site-wide: 81,032
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