Strong association of de novo copy number mutations with autism
about
Novel association strategy with copy number variation for identifying new risk Loci of human diseasesA common and unstable copy number variant is associated with differences in Glo1 expression and anxiety-like behaviorAdvanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhoodA novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogsWhy are autism spectrum conditions more prevalent in males?Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryMutation screening of melatonin-related genes in patients with autism spectrum disordersGenomic and epigenetic evidence for oxytocin receptor deficiency in autismArray-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberrationMutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephalyRecent advances in the pathogenesis of syndromic autismsChronic cocaine-regulated epigenomic changes in mouse nucleus accumbens.Finding the missing heritability of complex diseasesMapping and sequencing of structural variation from eight human genomesAdvances in autismAutistic phenotypes and genetic testing: state-of-the-art for the clinical geneticistWhat causes attention deficit hyperactivity disorder?Genetics evaluation for the etiologic diagnosis of autism spectrum disordersEvolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophreniaAdvances in autism genetics: on the threshold of a new neurobiologyMinor physical anomalies in autism: a meta-analysisThe genetics of bipolar disorderAutism: many genes, common pathways?Autism and brain developmentRare chromosomal deletions and duplications increase risk of schizophreniaAutism, fever, epigenetics and the locus coeruleusMeta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsDisruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityRare deletions at the neurexin 3 locus in autism spectrum disorderLinkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneMolecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersReduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.SHANK1 Deletions in Males with Autism Spectrum DisorderMouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Functional impact of global rare copy number variation in autism spectrum disordersAbnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autismCommon genetic variants on 5p14.1 associate with autism spectrum disordersAutism risk factors: genes, environment, and gene-environment interactionsChildhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
P2860
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P2860
Strong association of de novo copy number mutations with autism
description
2007 nî lūn-bûn
@nan
2007 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Strong association of de novo copy number mutations with autism
@ast
Strong association of de novo copy number mutations with autism
@en
Strong association of de novo copy number mutations with autism
@nl
type
label
Strong association of de novo copy number mutations with autism
@ast
Strong association of de novo copy number mutations with autism
@en
Strong association of de novo copy number mutations with autism
@nl
prefLabel
Strong association of de novo copy number mutations with autism
@ast
Strong association of de novo copy number mutations with autism
@en
Strong association of de novo copy number mutations with autism
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
Strong association of de novo copy number mutations with autism
@en
P2093
Alex Krasnitz
Annette T Lee
Anthony Leotta
Boris Yamrom
Christa Lese-Martin
David Ledbetter
David Skuse
Dheeraj Malhotra
P2860
P3181
P356
10.1126/SCIENCE.1138659
P407
P50
P5008
P577
2007-04-20T00:00:00Z