Author: Carlos Pato

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Preprints

Characterization of Age and Polarity at Onset in Bipolar Disorder

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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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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses

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Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome

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Gene expression in patient-derived neural progenitors implicates WNT5A signaling in the etiology of schizophrenia

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Evolutionary and functional data power search for obsessive-compulsive disorder genes

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Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

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Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

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Investigation of convergent and divergent genetic influences underlying schizophrenia and alcohol use disorder

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Polygenic risk scores lack prognostic value for adults with severe mental illness

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