High rate of disease-related copy number variations in childhood onset schizophrenia. - Wikidata - wikimedia - TriplyDB

High rate of disease-related copy number variations in childhood onset schizophrenia.

High rate of disease-related copy number variations in childhood onset schizophrenia.

http://www.wikidata.org/entity/Q37505079

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The dysconnection hypothesis (2016)N100 Repetition Suppression Indexes Neuroplastic Defects in Clinical High Risk and Psychotic Youth.Collection of developmental history in the evaluation of schizophrenia spectrum disorders Neurogenetic analysis of childhood disintegrative disorder.Neuroimaging findings from childhood onset schizophrenia patients and their non-psychotic siblings.Functional and clinical insights from neuroimaging studies in childhood-onset schizophrenia.Inhibition of STEP61 ameliorates deficits in mouse and hiPSC-based schizophrenia models.Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders.Potential Value of Genomic Copy Number Variations in Schizophrenia.An inherited small microdeletion at 15q13.3 in a patient with early-onset obsessive-compulsive disorder Genetic epidemiology and insights into interactive genetic and environmental effects in autism spectrum disorders Gene dosage in the dysbindin schizophrenia susceptibility network differentially affect synaptic function and plasticity Heat shock alters the expression of schizophrenia and autism candidate genes in an induced pluripotent stem cell model of the human telencephalon Childhood-onset schizophrenia case with 2.2 Mb deletion at chromosome 3p12.2-p12.1 and two large chromosomal abnormalities at 16q22.3-q24.3 and Xq23-q28 MicroRNA Profiling of Neurons Generated Using Induced Pluripotent Stem Cells Derived from Patients with Schizophrenia and Schizoaffective Disorder, and 22q11.2 Del.Disrupted sensorimotor and social-cognitive networks underlie symptoms in childhood-onset schizophrenia.Severity of Cortical Thinning Correlates With Schizophrenia Spectrum Symptoms.Enhanced conversion of induced neuronal cells (iN cells) from human fibroblasts: Utility in uncovering cellular deficits in mental illness-associated chromosomal abnormalities De novo variants in sporadic cases of childhood onset schizophrenia.Strong Treatment Response and High Maintenance Rates of Clozapine in Childhood-Onset Schizophrenia.15q13.3 duplication in two patients with childhood-onset schizophrenia.Serotonin-related pathways and developmental plasticity: relevance for psychiatric disorders.Development of novel therapy of schizophrenia in children and adolescents.Genetics in child and adolescent psychiatry: methodological advances and conceptual issues.Using hiPSCs to model neuropsychiatric copy number variations (CNVs) has potential to reveal underlying disease mechanisms.Trans-acting epigenetic effects of chromosomal aneuploidies: lessons from Down syndrome and mouse models.Application of induced pluripotent stem cells to understand neurobiological basis of bipolar disorder and schizophrenia.Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder.Lack of Gender-Related Differences in Childhood-Onset Schizophrenia.Common polygenic variation and risk for childhood-onset schizophrenia.The 3q29 deletion confers >40-fold increase in risk for schizophrenia Neurodevelopmental disease mechanisms, primary cilia, and endosomes converge on the BLOC-1 and BORC complexes.Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with post-mortem adult brains.Attenuated resting-state functional connectivity in patients with childhood- and adult-onset schizophrenia.Symptom dimensions and subgroups in childhood-onset schizophrenia.Genomic trade-offs: are autism and schizophrenia the steep price of the human brain?Gene-environment interplay in the etiology of psychosis.Altered intra- and inter-network dynamics reflect symptom dimensions in childhood-onset schizophrenia.Reduced Functional Brain Activation and Connectivity During a Working Memory Task in Childhood-Onset Schizophrenia.Genome-wide Purification of Extrachromosomal Circular DNA from Eukaryotic Cells.

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High rate of disease-related copy number variations in childhood onset schizophrenia.

http://www.wikidata.org/entity/Q37505079

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 21 May 2013

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

@cs

name

High rate of disease-related copy number variations in childhood onset schizophrenia.

@en

High rate of disease-related copy number variations in childhood onset schizophrenia.

@nl

type

label

High rate of disease-related copy number variations in childhood onset schizophrenia.

@en

High rate of disease-related copy number variations in childhood onset schizophrenia.

@nl

prefLabel

High rate of disease-related copy number variations in childhood onset schizophrenia.

@en

High rate of disease-related copy number variations in childhood onset schizophrenia.

@nl

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Molecular Psychiatry

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High rate of disease-related copy number variations in childhood onset schizophrenia

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A A Anvari

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A Darvasi

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H Hakonarson

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J L Rapoport

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K Ahn

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M W State

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N Gotay

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P Gochman

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T M Andersen

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Y Lee

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P2860

Rare chromosomal deletions and duplications increase risk of schizophrenia

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

Common variants conferring risk of schizophrenia

Strong synaptic transmission impact by copy number variations in schizophrenia.

Microduplications of 16p11.2 are associated with schizophrenia

Disruption of the neurexin 1 gene is associated with schizophrenia

Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited

Large recurrent microdeletions associated with schizophrenia

PLINK: a tool set for whole-genome association and population-based linkage analyses

Association between microdeletion and microduplication at 16p11.2 and autism

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568-572

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scholarly article

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10.1038/MP.2013.59

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5

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19

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Stephan J. Sanders

Joseph Glessner

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2013-05-21T00:00:00Z

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23689535

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