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Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhoodNeurexin 1 (NRXN1) deletions in schizophreniaSnoopCGH: software for visualizing comparative genomic hybridization dataIncreased de novo copy number variants in the offspring of older malesA genome-wide investigation of SNPs and CNVs in schizophrenia.Etiologies and molecular mechanisms of communication disorders.Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics?VCS: Tool for Visualizing Copy Number Variation and Single Nucleotide Polymorphism.Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants.Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia.Copy number variations of chromosome 16p13.1 region associated with schizophrenia.Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language ImpairmentAssociation of genetic variants on 15q12 with cortical thickness and cognition in schizophreniaA genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.Autism risk across generations: a population-based study of advancing grandpaternal and paternal age.Psychosis genetics: modeling the relationship between schizophrenia, bipolar disorder, and mixed (or "schizoaffective") psychosesPsychopathology and cognition in children with 22q11.2 deletion syndromeHigh rate of disease-related copy number variations in childhood onset schizophrenia.The clinical context of copy number variation in the human genome.Beyond the first episode: candidate factors for a risk prediction model of schizophrenia.Annual research review: impact of advances in genetics in understanding developmental psychopathology.Genes and Small RNA Transcripts Exhibit Dosage-Dependent Expression Pattern in Maize Copy-Number Alterations.Genetic insights into the neurodevelopmental origins of schizophrenia.Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders.Penetrance for copy number variants associated with schizophrenia.Reduced burden of very large and rare CNVs in bipolar affective disorder.Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.
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P2860
description
im Dezember 2008 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 2008
@uk
name
Phenotypic variations on the theme of CNVs
@en
Phenotypic variations on the theme of CNVs
@nl
type
label
Phenotypic variations on the theme of CNVs
@en
Phenotypic variations on the theme of CNVs
@nl
prefLabel
Phenotypic variations on the theme of CNVs
@en
Phenotypic variations on the theme of CNVs
@nl
P2860
P356
P1433
P1476
Phenotypic variations on the theme of CNVs
@en
P2093
Michael J Owen
P2860
P2888
P304
P356
10.1038/NG1208-1392
P407
P577
2008-12-01T00:00:00Z