Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients. - Wikidata - awgldk - TriplyDB

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.

http://www.wikidata.org/entity/Q35109411

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CNVs: harbingers of a rare variant revolution in psychiatric genetics Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci Animal models of gene-environment interaction in schizophrenia: A dimensional perspective.Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.Genomic structural variation in psychiatric disorders.Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders.Copy number variation in schizophrenia in Sweden Exposure to prenatal infection and risk of schizophrenia A New Method for Detecting Associations with Rare Copy-Number Variants.Genome-wide burden of deleterious coding variants increased in schizophrenia.Quantitative proteomic and genetic analyses of the schizophrenia susceptibility factor dysbindin identify novel roles of the biogenesis of lysosome-related organelles complex 1.Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia.Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes Cheek swabs, SNP chips, and CNVs: assessing the quality of copy number variant calls generated with subject-collected mail-in buccal brush DNA samples on a high-density genotyping microarray.Schizophrenia genetic variants are not associated with intelligence.Molecular characteristics of Human Endogenous Retrovirus type-W in schizophrenia and bipolar disorder.Genetic schizophrenia risk variants jointly modulate total brain and white matter volume.DISC1 genetics, biology and psychiatric illness Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness.Common alleles contribute to schizophrenia in CNV carriers.Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets.Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndrome.Recent genomic advances in schizophrenia.Novel treatment strategies for schizophrenia from improved understanding of genetic risk.Increased rare duplication burden genomewide in patients with treatment-resistant schizophrenia.Associations of common copy number variants in glutathione S-transferase mu 1 and D-dopachrome tautomerase-like protein genes with risk of schizophrenia in a Japanese population.The 3q29 deletion confers >40-fold increase in risk for schizophrenia Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia.Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?Behavior genetics and postgenomics.Increased paternal age and the influence on burden of genomic copy number variation in the general population.No evidence that common genetic risk variation is shared between schizophrenia and autism.Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families.Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia.Replication analyses of four chromosomal deletions with schizophrenia via independent large-scale meta-analyses.Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart Syndrome

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Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.

http://www.wikidata.org/entity/Q35109411

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2011 թվականի ապրիլին հրատարակված գիտական հոդված

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2011年の論文

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Genome-wide analysis shows inc ...... Dutch schizophrenia patients.

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Genome-wide analysis shows inc ...... Dutch schizophrenia patients.

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Genome-wide analysis shows inc ...... Dutch schizophrenia patients.

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Genome-wide analysis shows inc ...... Dutch schizophrenia patients.

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Genome-wide analysis shows inc ...... Dutch schizophrenia patients.

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J.BIOPSYCH.2011.02.015

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Biological Psychiatry

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Genome-wide analysis shows inc ...... Dutch schizophrenia patients.

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Chiara Sabatti

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Eric Strengman

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Genetic Risk and Outcome in Psychosis (GROUP) Consortium Members

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Jacob A S Vorstman

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Jacobine E Buizer-Voskamp

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Jan-Willem Muntjewerff

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Roel A Ophoff

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P2860

Finding the missing heritability of complex diseases

Rare chromosomal deletions and duplications increase risk of schizophrenia

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

Common variants conferring risk of schizophrenia

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

Large recurrent microdeletions associated with schizophrenia

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

The genetics of schizophrenia

Detection of large-scale variation in the human genome

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10.1016/J.BIOPSYCH.2011.02.015

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Hreinn Stefansson

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