Author: Ming T Tsuang

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Preprints

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

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  • Site-wide: 3,493
  • In genetic and genomic medicine: 11
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  • Site-wide: 846

Comparative genetic architectures of schizophrenia in East Asian and European populations

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  • In genetics: 287
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Schizophrenia risk conferred by protein-coding de novo mutations

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  • In genetics: 1,307
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  • Site-wide: 90,588
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Identification of de novo mutations in prenatal neurodevelopment-associated genes in schizophrenia in two Han Chinese patient-sibling family-based cohorts

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  • In psychiatry and clinical psychology: 118
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Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations

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  • Site-wide: 48,724
  • In genetics: 2,288
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Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

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  • In genetic and genomic medicine: 166
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Reliability of Mismatch Negativity Event-Related Potentials in a Multisite, Traveling Subjects Study

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  • Site-wide: 91,579
  • In neuroscience: 14,161
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BrainGENIE: The Brain Gene Expression and Network Imputation Engine

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  • Site-wide: 117,993
  • In bioinformatics: 9,617
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