Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications - Wikidata - wikimedia - TriplyDB

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

http://www.wikidata.org/entity/Q28304430

about

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 Evolutionary history and genome organization of DUF1220 protein domains Neuromodulation of thought: flexibilities and vulnerabilities in prefrontal cortical network synapses Rate of de novo mutations and the importance of father's age to disease risk Genetics and genomics of psychiatric disease Neuronal migration abnormalities and its possible implications for schizophrenia Following the genes: a framework for animal modeling of psychiatric disorders A genetic model for neurodevelopmental disease RNA Sequencing in Schizophrenia Two patients walk into a clinic...a genomics perspective on the future of schizophrenia The impact of NMDA receptor hypofunction on GABAergic neurons in the pathophysiology of schizophrenia Evaluating historical candidate genes for schizophrenia CNVs in neuropsychiatric disorders Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia CNVs leading to fusion transcripts in individuals with autism spectrum disorder Confluence of genes, environment, development, and behavior in a post Genome-Wide Association Study world Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Targeting of vasoactive intestinal peptide receptor 2, VPAC2, a secretin family G-protein coupled receptor, to primary cilia.Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.Animal models of gene-environment interaction in schizophrenia: A dimensional perspective.Reductions in synaptic proteins and selective alteration of prepulse inhibition in male C57BL/6 mice after postnatal administration of a VIP receptor (VIPR2) agonist.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.Mice with reduced NMDA receptor expression: more consistent with autism than schizophrenia?Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa.Integrating Diverse Types of Genomic Data to Identify Genes that Underlie Adverse Pregnancy Phenotypes Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics.Genomic structural variation in psychiatric disorders.De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes The translationally relevant mouse model of the 15q13.3 microdeletion syndrome reveals deficits in neuronal spike firing matching clinical neurophysiological biomarkers seen in schizophrenia.An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders.Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome.De novo non-synonymous TBL1XR1 mutation alters Wnt signaling activity.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Potential Value of Genomic Copy Number Variations in Schizophrenia.

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Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

http://www.wikidata.org/entity/Q28304430

description

2011 nî lūn-bûn

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2011 թուականի Մարտին հրատարակուած գիտական յօդուած

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2011 թվականի մարտին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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Copy number variants in schizo ...... letions and VIPR2 duplications

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Copy number variants in schizo ...... letions and VIPR2 duplications

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Copy number variants in schizo ...... letions and VIPR2 duplications

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Copy number variants in schizo ...... letions and VIPR2 duplications

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Copy number variants in schizo ...... letions and VIPR2 duplications

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Copy number variants in schizo ...... letions and VIPR2 duplications

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Copy number variants in schizo ...... letions and VIPR2 duplications

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Copy number variants in schizo ...... letions and VIPR2 duplications

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APPI.AJP.2010.10060876

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American Journal of Psychiatry

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Copy number variants in schizo ...... letions and VIPR2 duplications

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Alan R Sanders

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Ayman H Fanous

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Bryan J Mowry

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Douglas F Levinson

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Farooq Amin

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Jeremy M Silverman

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Jianxin Shi

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Jubao Duan

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Kai Wang

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Nancy Zhang

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P2860

Rare chromosomal deletions and duplications increase risk of schizophrenia

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila

Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.

3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome.

Common variants conferring risk of schizophrenia

Microduplications of 16p11.2 are associated with schizophrenia

Common variants on chromosome 6p22.1 are associated with schizophrenia

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

Disruption of the neurexin 1 gene is associated with schizophrenia

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

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C. Robert Cloninger

Hakon Hakonarson

Nancy G. Buccola

Donald W. Black

Frank Dudbridge

Kenneth S. Kendler

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2011-03-01T00:00:00Z

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