A genomic screen of autism: evidence for a multilocus etiology.
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Confounding from cryptic relatedness in case-control association studies.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 ancestryAssociation of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysisThe Role of the Neurobiologist in Redefining the Diagnosis of AutismThe genetics of autistic disorders and its clinical relevance: a review of the literatureGenetics of autism spectrum disorderGenetics of austim: complex aetiology for a heterogeneous disorderAre rare variants responsible for susceptibility to complex diseases?Replication 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 conditionsSupport for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locusExcess of twins among affected sibling pairs with autism: implications for the etiology of autism.Investigation of autism and GABA receptor subunit genes in multiple ethnic groupsFOXP2 is not a major susceptibility gene for autism or specific language impairmentAutism risk factors: genes, environment, and gene-environment interactionsOn the twin risk in autismA genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysisHigh-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate geneOverlaps between autism and language impairment: phenomimicry or shared etiology?Constitutional downregulation of SEMA5A expression in autismExamination of association of genes in the serotonin system to autismCurrent developments in the genetics of autism: from phenome to genomemTOR signaling: at the crossroads of plasticity, memory and diseaseIdentifying autism loci and genes by tracing recent shared ancestryGenome-wide linkage analyses of quantitative and categorical autism subphenotypesWhole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back AgainA unified genetic theory for sporadic and inherited autismA 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 correlatesCytogenetic abnormalities and fragile-X syndrome in Autism Spectrum DisorderAlterations in sociability and functional brain connectivity caused by early-life seizures are prevented by bumetanide.Mapping autism risk loci using genetic linkage and chromosomal rearrangements.Function and regulation of AUTS2, a gene implicated in autism and human evolutionMicroRNA-183 Family in Inner Ear: Hair Cell Development and Deafness.
P2860
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P2860
A genomic screen of autism: evidence for a multilocus etiology.
description
1999 nî lūn-bûn
@nan
1999 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի օգոստոսին 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
A genomic screen of autism: evidence for a multilocus etiology
@nl
A genomic screen of autism: evidence for a multilocus etiology.
@ast
A genomic screen of autism: evidence for a multilocus etiology.
@en
type
label
A genomic screen of autism: evidence for a multilocus etiology
@nl
A genomic screen of autism: evidence for a multilocus etiology.
@ast
A genomic screen of autism: evidence for a multilocus etiology.
@en
prefLabel
A genomic screen of autism: evidence for a multilocus etiology
@nl
A genomic screen of autism: evidence for a multilocus etiology.
@ast
A genomic screen of autism: evidence for a multilocus etiology.
@en
P2093
P2860
P356
P1476
A genomic screen of autism: evidence for a multilocus etiology.
@en
P2093
H C Kraemer
P2860
P304
P356
10.1086/302497
P407
P577
1999-08-01T00:00:00Z