Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
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Why are autism spectrum conditions more prevalent in males?Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryGenomic and epigenetic evidence for oxytocin receptor deficiency in autismAssociation of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysisExamination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genesAnalysis of four DLX homeobox genes in autistic probandsThe genetics of autistic disorders and its clinical relevance: a review of the literatureGenetics of autism spectrum disorderGenetics of austim: complex aetiology for a heterogeneous disorderEpigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.Genomewide scans of complex human diseases: true linkage is hard to findDisorder-associated mutations lead to functional inactivation of neuroliginsLinkage, 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 behaviorsA genomewide screen of 345 families for autism-susceptibility loci.Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autismX-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin familyThe autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditionsExcess of twins among affected sibling pairs with autism: implications for the etiology of autism.Chromosome 7q: where autism meets language disorder?Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorderFOXP2 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 3q25-27Identification and characterization of a second melanin-concentrating hormone receptor, MCH-2RConstitutional downregulation of SEMA5A expression in autismExamination of association of genes in the serotonin system to autismThe genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disordersGenes controlling affiliative behavior as candidate genes for autismGenome-wide linkage analyses of quantitative and categorical autism subphenotypesGenome-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 DisorderBehavioral phenotypes of genetic mouse models of autism.Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.Common Genetic Variants Found in HLA and KIR Immune Genes in Autism Spectrum DisorderMicroRNA-183 Family in Inner Ear: Hair Cell Development and Deafness.Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families
P2860
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P2860
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
description
1999 nî lūn-bûn
@nan
1999 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Genome-wide scan for autism su ...... ch International Sibpair Study
@ast
Genome-wide scan for autism su ...... ch International Sibpair Study
@en
Genome-wide scan for autism su ...... ch International Sibpair Study
@nl
type
label
Genome-wide scan for autism su ...... ch International Sibpair Study
@ast
Genome-wide scan for autism su ...... ch International Sibpair Study
@en
Genome-wide scan for autism su ...... ch International Sibpair Study
@nl
altLabel
Genome-Wide Scan for Autism Susceptibility Genes
@ast
Genome-Wide Scan for Autism Susceptibility Genes
@en
prefLabel
Genome-wide scan for autism su ...... ch International Sibpair Study
@ast
Genome-wide scan for autism su ...... ch International Sibpair Study
@en
Genome-wide scan for autism su ...... ch International Sibpair Study
@nl
P2093
P2860
P50
P3181
P356
P1476
Genome-wide scan for autism su ...... ch International Sibpair Study
@en
P2093
C Gillberg
E Sponheim
J Feingold
L Van Maldergem
M Guilloud-Bataille
M Zappella
P2860
P304
P3181
P356
10.1093/HMG/8.5.805
P407
P577
1999-05-01T00:00:00Z