Author: Tarjinder Singh

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

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

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