A genomewide screen of 345 families for autism-susceptibility loci.
about
The genetics of autistic disorders and its clinical relevance: a review of the literatureGenetics of autism spectrum disorderAdvances in autism genetics: on the threshold of a new neurobiologyEpigenetic 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 geneReplication of autism linkage: fine-mapping peak at 17q21.Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviorsIdentification of significant association and gene-gene interaction of GABA receptor subunit genes in autismSupport for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locusShared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorderHigh-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate geneCurrent developments in the genetics of autism: from phenome to genomeGenes controlling affiliative behavior as candidate genes for autismGenome-wide linkage analyses of quantitative and categorical autism subphenotypesA genetic variant that disrupts MET transcription is associated with autismA unified genetic theory for sporadic and inherited autismGenome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlatesA case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5RCytogenetic abnormalities and fragile-X syndrome in Autism Spectrum DisorderMolecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disordersThe role of glutamate and its receptors in autism and the use of glutamate receptor antagonists in treatment.Potential for treatment of severe autism in tuberous sclerosis complexThe Use of Induced Pluripotent Stem Cell Technology to Advance Autism Research and TreatmentAutism: the quest for the genesAssociation of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorderHaplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autismAutism and the serotonin transporter: the long and short of itDecreased Serum Hepatocyte Growth Factor (HGF) in Autistic Children with Severe Gastrointestinal DiseaseA heterogeneity-based genome search meta-analysis for autism-spectrum disordersThe serotonin system in autism spectrum disorder: From biomarker to animal modelsLoss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathologyHow the serotonin story is being rewritten by new gene-based discoveries principally related to SLC6A4, the serotonin transporter gene, which functions to influence all cellular serotonin systems.The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci.Genetic background modulates phenotypes of serotonin transporter Ala56 knock-in miceEffects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale.Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs.Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines.
P2860
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P2860
A genomewide screen of 345 families for autism-susceptibility loci.
description
2003 nî lūn-bûn
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2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年學術文章
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name
A genomewide screen of 345 families for autism-susceptibility loci
@nl
A genomewide screen of 345 families for autism-susceptibility loci.
@ast
A genomewide screen of 345 families for autism-susceptibility loci.
@en
A genomewide screen of 345 families for autism-susceptibility loci.
@en-gb
type
label
A genomewide screen of 345 families for autism-susceptibility loci
@nl
A genomewide screen of 345 families for autism-susceptibility loci.
@ast
A genomewide screen of 345 families for autism-susceptibility loci.
@en
A genomewide screen of 345 families for autism-susceptibility loci.
@en-gb
prefLabel
A genomewide screen of 345 families for autism-susceptibility loci
@nl
A genomewide screen of 345 families for autism-susceptibility loci.
@ast
A genomewide screen of 345 families for autism-susceptibility loci.
@en
A genomewide screen of 345 families for autism-susceptibility loci.
@en-gb
P2093
P2860
P50
P356
P1476
A genomewide screen of 345 families for autism-susceptibility loci.
@en
P2093
Abraham A Palmer
Adina Grunn
Joseph D Terwilliger
Maricela Alarcón
Rita M Cantor
Rong Cheng
Sarah J Spence
Suh-Hang Hank Juo
T Conrad Gilliam
P2860
P304
P356
10.1086/378778
P407
P577
2003-09-17T00:00:00Z