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Single-Cell mRNA Profiling Reveals Cell-Type-Specific Expression of Neurexin IsoformsConverging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndromeHidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping MicroarraysDe novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.New copy number variations in schizophrenia.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.SVM²: an improved paired-end-based tool for the detection of small genomic structural variations using high-throughput single-genome resequencing dataDe novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining.A comprehensive survey of copy number variation in 18 diverse pig populations and identification of candidate copy number variable genes associated with complex traits.RNA-Seq analysis implicates dysregulation of the immune system in schizophreniaA pilot study on collective effects of 22q13.31 deletions on gray matter concentration in schizophreniaSNPranker 2.0: a gene-centric data mining tool for diseases associated SNP prioritization in GWAS.Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.Comparison of constitutional and replication stress-induced genome structural variation by SNP array and mate-pair sequencingPsychiatrists' views of the genetic bases of mental disorders and behavioral traits and their use of genetic testsGenome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.Hydroxyurea induces de novo copy number variants in human cells.A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.Family-based association study of early growth response gene 3 with child bipolar I disorderEthics and neuropsychiatric genetics: a review of major issues.Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia Risk.Implications of genetic findings for understanding schizophrenia.The dynamics of DNA methylation in schizophrenia and related psychiatric disorders.Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese populationThe genomically mosaic brain: aneuploidy and more in neural diversity and disease.Genome-wide association studies of schizophrenia: does bigger lead to better results?A stochastic inference of de novo CNV detection and association test in multiplex schizophrenia families.Identifying Potential Regions of Copy Number Variation for Bipolar Disorder.Copy number variants: a new molecular frontier in clinical psychiatry.Proteomic investigations of the synaptic vesicle interactome.Progress in defining the biological causes of schizophrenia.Recent genomic advances in schizophrenia.A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease.Pathogenic or not? Assessing the clinical relevance of copy number variants.Next-generation sequencing in schizophrenia and other neuropsychiatric disorders.Whole genome/exome sequencing in mood and psychotic disorders.Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity.Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies.Glutathione S-Transferase Deletion Polymorphisms in Early-Onset Psychotic and Bipolar Disorders: A Case-Control Study.Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 12 September 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The role of DNA copy number variation in schizophrenia.
@en
The role of DNA copy number variation in schizophrenia.
@nl
type
label
The role of DNA copy number variation in schizophrenia.
@en
The role of DNA copy number variation in schizophrenia.
@nl
prefLabel
The role of DNA copy number variation in schizophrenia.
@en
The role of DNA copy number variation in schizophrenia.
@nl
P1476
The role of DNA copy number variation in schizophrenia
@en
P2093
Gloria W C Tam
Nigel P Carter
P304
P356
10.1016/J.BIOPSYCH.2009.07.027
P407
P577
2009-09-12T00:00:00Z