(Q50303536)

English

[Autism: genetics].

scientific article published in May 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

1 reference

Europe PubMed Central

[Autism: genetics]. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

0 references

author name string

Abha R Gupta

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

Matthew W State

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

language of work or name

0 references

publication date

1 May 2006

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

Brazilian Journal of Psychiatry

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

28 Suppl 1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

S29-38

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Genetics of autism: overview and new directions

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

A genomic screen of autism: evidence for a multilocus etiology

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

The search for autism disease genes

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

A genomewide screen of 345 families for autism-susceptibility loci

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

A forkhead-domain gene is mutated in a severe speech and language disorder

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Evidence for sex-specific risk alleles in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Replication of autism linkage: fine-mapping peak at 17q21.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Relationships of whole blood serotonin and plasma norepinephrine within families.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Autism as a paradigmatic complex genetic disorder

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Advances in molecular cytogenetics for the evaluation of mental retardation

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disorders.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Xp deletions associated with autism in three females.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Neuropsychiatric disorders in the 22q11 deletion syndrome

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

A comprehensive review of genetic association studies

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Autism spectrum disorders: molecular genetic advances

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

The genetics of autism

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Linkage and association of the glutamate receptor 6 gene with autism

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Three autism candidate genes: a synthesis of human genetic analysis with other disciplines

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Complement factor H polymorphism in age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Genome-wide scan for loci of Asperger syndrome

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

A genomewide screen for autism susceptibility loci

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Incorporating language phenotypes strengthens evidence of linkage to autism.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Genetic studies of autistic disorder and chromosome 7

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Genomic screen and follow-up analysis for autistic disorder.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Genetic linkage analysis of the X chromosome in autism, with emphasis on the fragile X region.

1 reference

https://api.crossref.org/works/10.1590%2FS1516-44462006000500005

21 January 2018

Identifiers

10.1590/S1516-44462006000500005

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16791389

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