Copy-number variations associated with neuropsychiatric conditions
about
Genome-wide association studies: a primerDisruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityRare deletions at the neurexin 3 locus in autism spectrum disorderAnalysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individualsMutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardationSHANK1 Deletions in Males with Autism Spectrum DisorderFunctional impact of global rare copy number variation in autism spectrum disordersMedicine. The future of psychiatric research: genomes and neural circuitsAbnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autismUsing ERDS to infer copy-number variants in high-coverage genomesAutismMultiple rare variants in the etiology of autism spectrum disordersCommon variants on chromosome 6p22.1 are associated with schizophreniaThe genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disordersGenetic Syndromes, Maternal Diseases and Antenatal Factors Associated with Autism Spectrum Disorders (ASD)Drug Repurposing Is a New Opportunity for Developing Drugs against Neuropsychiatric DisordersBehavioral phenotypes of genetic mouse models of autism.Toward developmental models of psychiatric disorders in zebrafishClinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concernsHuman genetics of diabetic vascular complicationsInsights on the functional interactions between miRNAs and copy number variations in the aging brainMutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathologyCopy number variations and strokeDiscovery of Rare Mutations in Autism: Elucidating Neurodevelopmental MechanismsCrh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndromeInfant siblings and the investigation of autism risk factorsUsing mouse models of autism spectrum disorders to study the neurotoxicology of gene-environment interactionsFast Bayesian Inference of Copy Number Variants using Hidden Markov Models with Wavelet CompressionRecurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.Rapid birth-and-death evolution of imprinted snoRNAs in the Prader-Willi syndrome locus: implications for neural development in EuarchontogliresSex bias in copy number variation of olfactory receptor gene family depends on ethnicityConfluence of genes, environment, development, and behavior in a post Genome-Wide Association Study worldGenome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanicsA family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3Individual common variants exert weak effects on the risk for autism spectrum disordersA genome-wide scan for common alleles affecting risk for autismA genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.Behavioural phenotyping assays for mouse models of autismGenome-wide association study of copy number variations (CNVs) with opioid dependence.The Neurobiological Basis for Social Affiliation in Autism Spectrum Disorder and Schizophrenia.
P2860
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P2860
Copy-number variations associated with neuropsychiatric conditions
description
2008 nî lūn-bûn
@nan
2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Copy-number variations associated with neuropsychiatric conditions
@ast
Copy-number variations associated with neuropsychiatric conditions
@en
Copy-number variations associated with neuropsychiatric conditions
@en-gb
Copy-number variations associated with neuropsychiatric conditions
@nl
type
label
Copy-number variations associated with neuropsychiatric conditions
@ast
Copy-number variations associated with neuropsychiatric conditions
@en
Copy-number variations associated with neuropsychiatric conditions
@en-gb
Copy-number variations associated with neuropsychiatric conditions
@nl
prefLabel
Copy-number variations associated with neuropsychiatric conditions
@ast
Copy-number variations associated with neuropsychiatric conditions
@en
Copy-number variations associated with neuropsychiatric conditions
@en-gb
Copy-number variations associated with neuropsychiatric conditions
@nl
P3181
P356
P1433
P1476
Copy-number variations associated with neuropsychiatric conditions
@en
P2093
Edwin H. Cook Jr
P2888
P304
P3181
P356
10.1038/NATURE07458
P407
P577
2008-10-01T00:00:00Z
P5875
P6179
1002940116