Genomic screen and follow-up analysis for autistic disorder. - Wikidata - awgldk - TriplyDB

Genomic screen and follow-up analysis for autistic disorder.

Genomic screen and follow-up analysis for autistic disorder.

http://www.wikidata.org/entity/Q50310138

about

Why are autism spectrum conditions more prevalent in males?The genetics of autistic disorders and its clinical relevance: a review of the literature Genetics of autism spectrum disorder Disorder-associated mutations lead to functional inactivation of neuroligins Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism Replication of autism linkage: fine-mapping peak at 17q21.Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors A genomewide screen of 345 families for autism-susceptibility loci.Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism On the twin risk in autism A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27 A genome-wide association study of autism reveals a common novel risk locus at 5p14.1 Examination of association of genes in the serotonin system to autism Current developments in the genetics of autism: from phenome to genome Genes controlling affiliative behavior as candidate genes for autism Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates Is Oxytocin Application for Autism Spectrum Disorder Evidence-Based?A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?MicroRNA-183 Family in Inner Ear: Hair Cell Development and Deafness.Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network Autism: the quest for the genes Genome-wide scan for loci of Asperger syndrome Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism A heterogeneity-based genome search meta-analysis for autism-spectrum disorders A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands Analysis of the RELN gene as a genetic risk factor for autism Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT Neuroligin1 drives synaptic and behavioral maturation through intracellular interactions.Multiple autism-like behaviors in a novel transgenic mouse model.Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.Genetic and neurodevelopmental influences in autistic disorder.GABAA receptor subunit gene polymorphisms predict symptom-based and developmental deficits in Chinese Han children and adolescents with autistic spectrum disorders Communication, interventions, and scientific advances in autism: a commentary.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.Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.Plasma oxytocin concentrations and OXTR polymorphisms predict social impairments in children with and without autism spectrum disorder.Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.

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Genomic screen and follow-up analysis for autistic disorder.

http://www.wikidata.org/entity/Q50310138

description

2002 nî lūn-bûn

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2002年の論文

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年學術文章

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2002年學術文章

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name

Genomic screen and follow-up analysis for autistic disorder.

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Genomic screen and follow-up analysis for autistic disorder.

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type

label

Genomic screen and follow-up analysis for autistic disorder.

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Genomic screen and follow-up analysis for autistic disorder.

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prefLabel

Genomic screen and follow-up analysis for autistic disorder.

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Genomic screen and follow-up analysis for autistic disorder.

@nl

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P1433

American Journal of Medical Genetics Part A

P1476

Genomic screen and follow-up analysis for autistic disorder.

@en

P2093

Cate McClain

http://www.w3.org/2001/XMLSchema#string

Chantelle M Wolpert

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Harry H Wright

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John R Gilbert

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Kimberly L Raiford

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Lennart von Wendt

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Margaret A Pericak-Vance

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Marisa M Menold

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Meredyth P Bass

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Michael L Cuccaro

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P2860

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder

A genomic screen of autism: evidence for a multilocus etiology.

Strategies for multilocus linkage analysis in humans

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

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

The human secretin receptor gene: genomic organization and promoter characterization

Genetic studies of autistic disorder and chromosome 7

A case-control family history study of autism

Localisation of a gene implicated in a severe speech and language disorder

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

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99-105

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10.1002/AJMG.10153

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1

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114

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Jeffery M. Vance

Allison Ashley-Koch

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2002-01-01T00:00:00Z

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11840513

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