(Q22250993)

Dimensions Publication ID

Dimensions

1020755353

European Journal of Human Genetics

7 February 2023

language of work or name

English

0 references

publication date

June 2006

0 references

published in

0 references

volume

14

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issue

6

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page(s)

714-720

0 references

cites work

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Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

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Analysis of the RELN gene as a genetic risk factor for autism

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Association of Reelin gene polymorphisms with autism

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Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

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Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus

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Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

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Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene

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Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

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Large-scale copy number polymorphism in the human genome

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Detection of large-scale variation in the human genome

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Autism and the serotonin transporter: the long and short of it

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Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

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Disorder-associated mutations lead to functional inactivation of neuroligins

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X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

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Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

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Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

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NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

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Epidemiological surveys of autism and other pervasive developmental disorders: an update

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Autism as a strongly genetic disorder: evidence from a British twin study

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Genetic influences in childhood-onset psychiatric disorders: autism and attention-deficit/hyperactivity disorder

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The future of genetic studies of complex human diseases

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

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A genomewide screen for autism susceptibility loci

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Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.

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Incorporating language phenotypes strengthens evidence of linkage to autism.

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

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Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays

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SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample

21 January 2018

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Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

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Reelin gene alleles and susceptibility to autism spectrum disorders

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Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism

21 January 2018

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Analysis of reelin as a candidate gene for autism

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Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network

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Reelin signaling is impaired in autism

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Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

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Evidence for sex-specific risk alleles in autism spectrum disorder

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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.

21 January 2018

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21 January 2018

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Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes

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Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

21 January 2018

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21 January 2018

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Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

21 January 2018

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Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

21 January 2018

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Association between a GABRB3 polymorphism and autism.

21 January 2018

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A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism.

21 January 2018

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An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder.

21 January 2018

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Deletion of chromosome 2q37 and autism: a distinct subtype?

21 January 2018

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Pilot assessment of the subtelomeric regions of children with autism: detection of a 2q deletion.

21 January 2018

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Simultaneous genotyping of four functional loci of human SLC6A4, with a reappraisal of 5-HTTLPR and rs25531.

21 January 2018

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Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder

21 January 2018

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Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype

21 January 2018

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Xp deletions associated with autism in three females.

21 January 2018

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Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?

21 January 2018

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Analysis of four neuroligin genes as candidates for autism.

21 January 2018

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Mapping complex disease loci in whole-genome association studies

21 January 2018

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The Autism Genome Project: goals and strategies

21 January 2018

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2-year-old boy who has been diagnosed with autism

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201610

inferred from DOI database lookup

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201610