(Q35170630)

6 August 2017

1 reference

title

Disease susceptibility genes for autism (English)

1 reference

6 August 2017

0 references

2

1 reference

6 August 2017

Irina N Bespalova

1

1 reference

6 August 2017

language of work or name

English

0 references

publication date

1 January 2003

1 reference

6 August 2017

1 reference

6 August 2017

volume

35

1 reference

6 August 2017

issue

4

1 reference

6 August 2017

page(s)

274-281

1 reference

The epidemiology of autism: a review.

6 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

The neuropsychology of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Familial autism and the fragile-X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Autism: the point of view from fragile X studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Angelman syndrome: mimicking conditions and phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Routes from research to clinical practice in child psychiatry: retrospect and prospect

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Are rare variants responsible for susceptibility to complex diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Genetics of autism: overview and new directions

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Infantile autism: a genetic study of 21 twin pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Autism: the phenotype in relatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Genetic studies of autistic disorder and chromosome 7

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

A genomewide screen for autism susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Presence of large deletions in kindreds with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Chromosome 7q: where autism meets language disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

FOXP2 is not a major susceptibility gene for autism or specific language impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Evidence supporting WNT2 as an autism susceptibility gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Auditory Brainstem Evoked Responses in Autistic Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Hypoplasia of Cerebellar Vermal Lobules VI and VII in Autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Dysregulation of Reelin and Bcl-2 proteins in autistic cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

A clinicopathological study of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Isolation and chromosomal localization of the human En-2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Neurotrophic activity of the Antennapedia homeodomain depends on its specific DNA-binding properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Subtle Cerebellar Phenotype in Mice Homozygous for a Targeted Deletion of the En-2 Homeobox

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Association study with two markers of a human homeogene in infantile autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Incorporating language phenotypes strengthens evidence of linkage to autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Genetic studies in autistic disorder and chromosome 15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype Correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Structure and organization of GABRB3 and GABRA5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Association between a GABRB3 polymorphism and autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Angelman syndrome: a review of clinical and genetic aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Mutation screening of the UBE3A/E6-AP gene in autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Serotonin and amino acid content in platelets of autistic children

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Linkage and association of the glutamate receptor 6 gene with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

The hyperserotonemia of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Psychiatric Disorders in the Parents of Autistic Individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Evidence of linkage between the serotonin transporter and autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Evidence for an association with the serotonin transporter promoter region polymorphism and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Role of the serotonin transporter gene in the behavioral expression of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Adenosine deaminase activity decreased in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Autism: evidence of association with adenosine deaminase genetic polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Two-loci ADA haplotypes in autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

A radio pulsar with an 8.5-second period that challenges emission models

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Transmission disequilibrium testing of arginine vasopressin receptor 1A (AVPR1A) polymorphisms in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Autism and genetics: clinical approach and association study with two markers of HRAS gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Studies of the c-Harvey-Ras gene in psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

GABA-transaminase, the liver and infantile autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Genetic dissection of complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Disease-causing mutations in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

The homeo box: A key to the understanding of development?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

The serotonin system in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Autism and tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Twin and adoption studies in child and adolescent psychiatric disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Autism in thalidomide embryopathy: a population study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Discovery of allelic variants ofHOXA1 andHOXB1: Genetic susceptibility to autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Adenosine deaminase alleles and autistic disorder: Case-control and family-based association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Population genetics--making sense out of sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

Association of the interleukin-1 gene cluster on chromosome 2q13 with knee osteoarthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310005966

10.1080/07853890310005966

21 January 2018

Identifiers

DOI

1 reference

6 August 2017

1 reference