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What have we learnt about the causes of ADHD?Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 MiceElusive copy number variation in the mouse genomeA pilot multivariate parallel ICA study to investigate differential linkage between neural networks and genetic profiles in schizophrenia.DUF1220 copy number is associated with schizophrenia risk and severity: implications for understanding autism and schizophrenia as related diseasesModeling read counts for CNV detection in exome sequencing data.DeAnnCNV: a tool for online detection and annotation of copy number variations from whole-exome sequencing dataPotential Value of Genomic Copy Number Variations in Schizophrenia.Detection of recurrent rearrangement breakpoints from copy number dataGenome-wide algorithm for detecting CNV associations with diseases.Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics?The hunt for gene effects pertinent to behavioral traits and psychiatric disorders: from mouse to human.Genetic associations of brain structural networks in schizophrenia: a preliminary studyCopy number variations of chromosome 16p13.1 region associated with schizophrenia.Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese populationTranscriptomics analysis of iPSC-derived neurons and modeling of neuropsychiatric disorders.Using latent class growth analysis to form trajectories of premorbid adjustment in schizophreniaProtein-protein interaction and pathway analyses of top schizophrenia genes reveal schizophrenia susceptibility genes converge on common molecular networks and enrichment of nucleosome (chromatin) assembly genes in schizophrenia susceptibility lociNeurobiology and phenotypic expression in early onset schizophrenia.Chromosomal microarray testing influences medical management.Toward understanding genetic risk for differential antipsychotic response in individuals with schizophrenia.Prevalence of Asperger syndrome among patients of an Early Intervention in Psychosis team.Global patterns of apparent copy number variation in birds revealed by cross-species comparative genomic hybridization.A copy number variation in PKD1L2 is associated with colorectal cancer predisposition in korean population.Absent smooth muscle actin immunoreactivity of the small bowel muscularis propria circular layer in association with chromosome 15q11 deletion in megacystis-microcolon-intestinal hypoperistalsis syndrome.Prospects for Modeling Abnormal Neuronal Function in Schizophrenia Using Human Induced Pluripotent Stem Cells.Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.Penetrance for copy number variants associated with schizophrenia.A remark on copy number variation detection methods.Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Copy number variation and schizophrenia
@ast
Copy number variation and schizophrenia
@en
Copy number variation and schizophrenia
@nl
type
label
Copy number variation and schizophrenia
@ast
Copy number variation and schizophrenia
@en
Copy number variation and schizophrenia
@nl
prefLabel
Copy number variation and schizophrenia
@ast
Copy number variation and schizophrenia
@en
Copy number variation and schizophrenia
@nl
P2860
P356
P1476
Copy number variation and schizophrenia
@en
P2093
David St Clair
P2860
P356
10.1093/SCHBUL/SBN147
P407
P577
2009-01-01T00:00:00Z