A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.
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Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigreesPolymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryAssociation of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysisAnalysis of four DLX homeobox genes in autistic probandsHow to diagnose autismThe genetics of autistic disorders and its clinical relevance: a review of the literatureAdvances in autism genetics: on the threshold of a new neurobiologyGenetics of austim: complex aetiology for a heterogeneous disorderEpigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneNYAP: a phosphoprotein family that links PI3K to WAVE1 signalling in neuronsReplication of autism linkage: fine-mapping peak at 17q21.Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviorsA genomewide screen of 345 families for autism-susceptibility loci.Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autismExcess of twins among affected sibling pairs with autism: implications for the etiology of autism.FOXP2 is not a major susceptibility gene for autism or specific language impairmentLinkage and candidate gene studies of autism spectrum disorders in European populationsOn the twin risk in autismA genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27A genome-wide association study of autism reveals a common novel risk locus at 5p14.1Constitutional downregulation of SEMA5A expression in autismExamination of association of genes in the serotonin system to autismCurrent developments in the genetics of autism: from phenome to genomeThe genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disordersIdentifying autism loci and genes by tracing recent shared ancestryGenome-wide linkage analyses of quantitative and categorical autism subphenotypesAbsence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaA unified genetic theory for sporadic and inherited autismA genetic study of autism in Costa Rica: multiple variables affecting IQ scores observed in a preliminary sample of autistic casesGenome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlatesCytogenetic abnormalities and fragile-X syndrome in Autism Spectrum DisorderRELN Mutations in Autism Spectrum DisorderUsing Sibling Designs to Understand Neurodevelopmental Disorders: From Genes and Environments to Prevention ProgrammingNetworking in autism: leveraging genetic, biomarker and model system findings in the search for new treatmentsThe role of glutamate and its receptors in autism and the use of glutamate receptor antagonists in treatment.Decreased left perisylvian GABA concentration in children with autism and unaffected siblingsEssential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 regionSodium channels SCN1A, SCN2A and SCN3A in familial autism
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P2860
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.
description
2001 nî lūn-bûn
@nan
2001 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հուլիսին հրատարակված գիտական հոդված
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2001年の論文
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2001年学术文章
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2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
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2001年学术文章
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2001年學術文章
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name
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@ast
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@en
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@nl
type
label
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@ast
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@en
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@nl
prefLabel
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@ast
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@en
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@nl
P2860
P356
P1476
A genomewide screen for autism ...... o chromosomes 2q, 7q, and 16p.
@en
P2093
International Molecular Genetic Study of Autism Consortium (IMGSAC)
P2860
P304
P356
10.1086/323264
P407
P577
2001-07-30T00:00:00Z