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Author: Tarjinder Singh

  • ORCiD: http://orcid.org/0000-0003-0601-6815
  • Most recently observed institution: Analytic and Translational Genetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; 2Program in Medical and Population Genetics, Broad Institute of MIT and Harvard

Rankings

  • All-time downloads: 23,183 (rank: 1,237 out of 318,750)
  • Categories:
    • genetics: 22,248 (rank: 236 out of 31,252)
    • genomics: 935 (rank: 15,505 (tie) out of 35,539)

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 8,078 times
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    • Site-wide: 154 out of 73,229
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Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation

genetics more details view paper
  • Downloaded 7,048 times
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    • In genetics: 26 out of 4,023
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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 1,674 times
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De novo Variants In Neurodevelopmental Disorders With Epilepsy

genetics more details view paper
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ASD and ADHD have a similar burden of rare protein-truncating variants

genetics more details view paper
  • Downloaded 1,409 times
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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
  • Downloaded 935 times
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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
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Schizophrenia risk conferred by protein-coding de novo mutations

genetics more details view paper
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Contribution of Retrotransposition to Developmental Disorders

genetics more details view paper
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Meta-analysis of Scandinavian Schizophrenia Exomes

genetics more details view paper
  • Downloaded 239 times
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