Author: Wei J. Chen

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Preprints

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

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Comparative genetic architectures of schizophrenia in East Asian and European populations

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Schizophrenia risk conferred by protein-coding de novo mutations

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Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations

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Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

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