Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder. - Wikidata - wikimedia - TriplyDB

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.

http://www.wikidata.org/entity/Q37216372

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Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis Analysis of four DLX homeobox genes in autistic probands The genetics of autistic disorders and its clinical relevance: a review of the literature Genetics of autism spectrum disorder Advances in autism genetics: on the threshold of a new neurobiology Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27 Developmental cognitive genetics: how psychology can inform genetics and vice versa Current developments in the genetics of autism: from phenome to genome Genome-wide linkage analyses of quantitative and categorical autism subphenotypes Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates Sodium channels SCN1A, SCN2A and SCN3A in familial autism Autism: the quest for the genes Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample Family-based association study of DYX1C1 variants in autism Epac2-mediated dendritic spine remodeling: implications for disease.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.Telescoping of caregiver report on the Autism Diagnostic Interview--Revised Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.Dissecting trait heterogeneity: a comparison of three clustering methods applied to genotypic data Genetic and neurodevelopmental influences in autistic disorder.Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.Genetic investigation of quantitative traits related to autism: use of multivariate polygenic models with ascertainment adjustment.Developmental trajectories of restricted and repetitive behaviors and interests in children with autism spectrum disorders.The use of genetic epidemiology to guide classification in child and adult psychopathology.A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene.Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment Narrowing the broader autism phenotype: a study using the Communication Checklist-Adult Version (CC-A).The genetic relationship between individual differences in social and nonsocial behaviours characteristic of autism.New complexities in the genetics of stuttering: significant sex-specific linkage signals.A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16 Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.Autism risk assessment in siblings of affected children using sex-specific genetic scores.A genome scan for loci shared by autism spectrum disorder and language impairment.

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Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.

http://www.wikidata.org/entity/Q37216372

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bilimsel makale

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scientific article published on March 2002

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vetenskaplig artikel

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Phenotypic homogeneity provide ...... mosome 2 in autistic disorder.

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Phenotypic homogeneity provide ...... mosome 2 in autistic disorder.

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Phenotypic homogeneity provide ...... mosome 2 in autistic disorder.

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American Journal of Human Genetics

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Phenotypic homogeneity provide ...... mosome 2 in autistic disorder.

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Chantelle M Wolpert

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Harry H Wright

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Heidi A Cope

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John R Gilbert

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Kimberly L Raiford

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Michael L Cuccaro

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Robert G DeLong

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Ruth K Abramson

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Sarah A Ravan

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Yujun Shao

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P2860

Chromosome 7q: where autism meets language disorder?

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

Genetic studies of autistic disorder and chromosome 7

Effects of stratification in the analysis of affected-sib-pair data: benefits and costs.

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.

Allele-sharing models: LOD scores and accurate linkage tests.

Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives.

Genomic screen and follow-up analysis for autistic disorder.

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

Two-year outcome of preschool children with autism or Asperger's syndrome.

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1058-1061

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10.1086/339765

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Margaret A. Pericak-Vance

Allison Ashley-Koch

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2002-03-01T00:00:00Z

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11486454

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