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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disordersNovel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in SchizophreniaDe novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.The penetrance of copy number variations for schizophrenia and developmental delay.De novo mutations in schizophrenia implicate synaptic networksDe novo CNVs in bipolar affective disorder and schizophrenia.Copy number variation in schizophrenia in SwedenNo Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci.Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsyParental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.Exome arrays capture polygenic rare variant contributions to schizophrenia.Gender differences in CNV burden do not confound schizophrenia CNV associations.Implication of a rare deletion at distal 16p11.2 in schizophrenia.Common alleles contribute to schizophrenia in CNV carriers.Copy number variation in bipolar disorder.Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.Evidence that duplications of 22q11.2 protect against schizophreniaAnalysis of copy number variations at 15 schizophrenia-associated loci.De novo rates and selection of schizophrenia-associated copy number variants.Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.De novo mutation in schizophrenia.Schizophrenia copy number variants and associative learningGenome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.Erratum: Common alleles contribute to schizophrenia in CNV carriers
P50
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P50
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Elliott Rees
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P106
P21
P31
P496
0000-0002-6168-9222