High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
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Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryLinkage and candidate gene studies of autism spectrum disorders in European populationsMitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysisMutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathologyDemographically-Based Evaluation of Genomic Regions under Selection in Domestic DogsGenomic analysis of wig-1 pathwaysThe atypical guanine nucleotide exchange factor Dock4 regulates neurite differentiation through modulation of Rac1 GTPase and actin dynamicsA novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian familyGenome-wide association analysis of ischemic stroke in young adults.Disease gene characterization through large-scale co-expression analysisPopulation-based study of genetic variation in individuals with autism spectrum disorders from CroatiaUse of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approachRelative burden of large CNVs on a range of neurodevelopmental phenotypes.Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairmentIntragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.The genetics of Tourette disorderSocial Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autismIdentification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibilityA Pooled Genome-Wide Association Study of Asperger Syndrome.Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia.NCLscan: accurate identification of non-co-linear transcripts (fusion, trans-splicing and circular RNA) with a good balance between sensitivity and precisionPathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism.Triggers for autism: genetic and environmental factors.Rac GEF Dock4 interacts with cortactin to regulate dendritic spine formation.An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk.The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders.Penelope's web: using alpha-latrotoxin to untangle the mysteries of exocytosis.Dock protein family in brain development and neurological disease.Balance within the Neurexin Trans-Synaptic Connexus Stabilizes Behavioral Control.Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han populationMetabolic Dysfunction Underlying Autism Spectrum Disorder and Potential Treatment Approaches.Predicting the diagnosis of autism spectrum disorder using gene pathway analysis.A review of the evidence for the canonical Wnt pathway in autism spectrum disorders.Diagnostic yield of array comparative genomic hybridization in adults with autism spectrum disorders.-7/7q- syndrome in myeloid-lineage hematopoietic malignancies: attempts to understand this complex disease entity.Unifying Views of Autism Spectrum Disorders: A Consideration of Autoregulatory Feedback Loops.
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P2860
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
description
2009 nî lūn-bûn
@nan
2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին 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
High-density SNP association s ...... gion in autism susceptibility.
@ast
High-density SNP association s ...... gion in autism susceptibility.
@en
type
label
High-density SNP association s ...... gion in autism susceptibility.
@ast
High-density SNP association s ...... gion in autism susceptibility.
@en
prefLabel
High-density SNP association s ...... gion in autism susceptibility.
@ast
High-density SNP association s ...... gion in autism susceptibility.
@en
P2093
P2860
P356
P1433
P1476
High-density SNP association s ...... gion in autism susceptibility.
@en
P2093
A J Bailey
A P Morris
A T Pagnamenta
A de Bildt
E Bacchelli
E J Mulder
E Maestrini
F Minopoli
P2860
P2888
P304
P356
10.1038/MP.2009.34
P407
P577
2009-04-28T00:00:00Z
P5875
P6179
1028933507