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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: 25,529 (rank: 2,057 out of 404,161)
  • Categories:
    • genetics: 24,556 (rank: 227 out of 36,792)
    • genomics: 973 (rank: 18,581 (tie) out of 42,763)

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Preprints

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

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

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

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De novo Variants In Neurodevelopmental Disorders With Epilepsy

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

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

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

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Schizophrenia risk conferred by protein-coding de novo mutations

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Contribution of Retrotransposition to Developmental Disorders

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Meta-analysis of Scandinavian Schizophrenia Exomes

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