Rare copy number variations are associated with poorer cognition in schizophrenia

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SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse

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Examining cognition across the bipolar/schizophrenia diagnostic spectrum

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

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Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples

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Analysis of protein-coding genetic variation in 60,706 humans

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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

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Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

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CNVs in neuropsychiatric disorders

(2015) George Kirov   HUMAN MOLECULAR GENETICS

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(2015) Wolfgang Viechtbauer   Journal of Statistical Software

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

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The phenotypic manifestations of rare CNVs in schizophrenia

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Analysis of copy number variations at 15 schizophrenia-associated loci

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Cognitive remediation in schizophrenia: efficacy and effectiveness in patients with early versus long-term course of illness

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CNVs conferring risk of autism or schizophrenia affect cognition in controls

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The Impact of Copy Number Deletions on General Cognitive Ability and Ventricle Size in Patients with Schizophrenia and Healthy Control Subjects

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Static and Dynamic Cognitive Deficits in Childhood Preceding Adult Schizophrenia: A 30-Year Study

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The MATRICS Consensus Cognitive Battery, Part 1: Test Selection, Reliability, and Validity

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General and Specific Cognitive Deficits in Schizophrenia: Goliath Defeats David?

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Phenotypic variations on the theme of CNVs

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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

(2008) Joshua M Korn et al.   NATURE GENETICS