Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
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HERVs expression in Autism Spectrum DisordersWhy are autism spectrum conditions more prevalent in males?Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigreesGenomic and epigenetic evidence for oxytocin receptor deficiency in autismMutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephalyExpanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1Alterations of GABAergic signaling in autism spectrum disordersRecent advances in the pathogenesis of syndromic autismsAdvances in autismAutistic phenotypes and genetic testing: state-of-the-art for the clinical geneticistGenetics 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 neurobiologyNeuroligins and neurexins link synaptic function to cognitive diseaseMinor physical anomalies in autism: a meta-analysisAutism: many genes, common pathways?DUF1220 domains, cognitive disease, and human brain evolutionMeta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsTruncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophreniaDisruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityPhenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controlsRare 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 individualsLinkage, 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.A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum exportMutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardationSHANK1 Deletions in Males with Autism Spectrum DisorderStructural insights into the exquisite selectivity of neurexin/neuroligin synaptic interactions.CASK Functions as a Mg2+-independent neurexin kinaseMouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.The human language-associated gene SRPX2 regulates synapse formation and vocalization in miceThe comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Functional impact of global rare copy number variation in autism spectrum disordersLinkage and candidate gene studies of autism spectrum disorders in European populationsCommon genetic variants on 5p14.1 associate with autism spectrum disordersAutism risk factors: genes, environment, and gene-environment interactionsRare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
P2860
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P2860
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
description
2007 nî lūn-bûn
@nan
2007 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի փետրվարին 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
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
@nl
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
@ast
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
@en
type
label
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
@nl
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
@ast
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
@en
prefLabel
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
@nl
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
@ast
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
@en
P2093
P2860
P50
P3181
P356
P1433
P1476
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
@en
P2093
Aislinn Hutchinson
Alberto Segre
Ann Le Couteur
Ann P Thompson
Anthony J Bailey
Autism Genome Project Consortium
Bernadette Rogé
Bernie Devlin
Bärbel Felder
P2507
P2860
P2888
P304
P3181
P356
10.1038/NG1985
P407
P50
P577
2007-02-18T00:00:00Z
P5875
P6179
1036967594