Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.
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The effect of DSM-5 criteria on externalizing, internalizing, behavioral and adaptive symptoms in children diagnosed with autismThe 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 neurobiologyAllelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviorsCurrent developments in the genetics of autism: from phenome to genomeGenome-wide linkage analyses of quantitative and categorical autism subphenotypesA 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 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 DisorderEssential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Autism: the quest for the genesPassive transfer of streptococcus-induced antibodies reproduces behavioral disturbances in a mouse model of pediatric autoimmune neuropsychiatric disorders associated with streptococcal infectionHaplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autismA heterogeneity-based genome search meta-analysis for autism-spectrum disordersA genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe IslandsIdentification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control populationVariants in several genomic regions associated with asperger disorderCombined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci.Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex.Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.Gene-network analysis identifies susceptibility genes related to glycobiology in autismA genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples.Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.Bio-collections in autism research.Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.Systematic genotype-phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autismIdentification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.Genome-wide association scan of korean autism spectrum disorders with language delay: a preliminary study.Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16Analysis 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.Convergent functional genomics of anxiety disorders: translational identification of genes, biomarkers, pathways and mechanisms.Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder.Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.Stratification based on language-related endophenotypes in autism: attempt to replicate reported linkage.Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder.Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder
P2860
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P2860
Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
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name
Linkage analysis for autism in ...... genes on chromosome 6 and 19.
@en
Linkage analysis for autism in ...... genes on chromosome 6 and 19.
@nl
type
label
Linkage analysis for autism in ...... genes on chromosome 6 and 19.
@en
Linkage analysis for autism in ...... genes on chromosome 6 and 19.
@nl
prefLabel
Linkage analysis for autism in ...... genes on chromosome 6 and 19.
@en
Linkage analysis for autism in ...... genes on chromosome 6 and 19.
@nl
P2093
P2860
P356
P1433
P1476
Linkage analysis for autism in ...... y genes on chromosome 6 and 19
@en
P2093
Hollander E
Keddache M
Reichert JG
Silverman J
P2860
P2888
P304
P356
10.1038/SJ.MP.4001465
P407
P577
2004-02-01T00:00:00Z