(Q35785420)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

review article

1 reference

title

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

0 references

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

5

Jean-Pierre Fryns

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

author name string

Dries Castermans

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Valérie Wilquet

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Wim Van de Ven

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Koen Devriendt

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

publication date

1 June 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

page(s)

141-161

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

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

29 December 2019

cites work

1 reference

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

21 January 2018

1 reference

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Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland

21 January 2018

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

21 January 2018

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Autism: the phenotype in relatives.

21 January 2018

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Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

21 January 2018

1 reference

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A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

21 January 2018

1 reference

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How commonly are known medical conditions associated with autism?

21 January 2018

1 reference

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Genetic studies in autistic disorder and chromosome 15.

21 January 2018

1 reference

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A case-control family history study of autism

21 January 2018

1 reference

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The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders

21 January 2018

1 reference

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A family with a grand-maternally derived interstitial duplication of proximal 15q.

21 January 2018

1 reference

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Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

21 January 2018

1 reference

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The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings.

21 January 2018

1 reference

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

21 January 2018

1 reference

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Association between a GABRB3 polymorphism and autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism.

21 January 2018

1 reference

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Association of autism severity with a monoamine oxidase A functional polymorphism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Incorporating language phenotypes strengthens evidence of linkage to autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

The human genome project and its impact on psychiatry

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Mitochondrial dysfunction in autistic patients with 15q inverted duplication

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Genetics of austim: complex aetiology for a heterogeneous disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Infantile autism: a genetic study of 21 twin pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

The epidemiology of autism: a review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

The neurobiology of infantile autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Chromosomal disorders and autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Trinucleotide repeat expansions: do they contribute to bipolar disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Possible association of c-Harvey-Ras-1 (HRAS-1) marker with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

A case of autism associated with partial tetrasomy 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Defining the autism minimum candidate gene region on chromosome 7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Linkage and association of the glutamate receptor 6 gene with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

A risk-factor model of epistatic interaction, focusing on autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

21 January 2018

The genetics of autism.

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Investigation of two variants in the DOPA decarboxylase gene in patients with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

A genomewide screen for autism susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Identifying autism susceptibility genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Increased density of the platelet serotonin transporter in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Secretin for the treatment of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Platelet serotonin, a possible marker for familial autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Imprinting mechanisms in mammals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Genomic screen and follow-up analysis for autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Genetics of autism: overview and new directions

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Genetic and clinical characterization of patients with an interstitial duplication 15q11‐q13, emphasizing behavioral phenotype and response to treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Review article: the concept of entero-colonic encephalopathy, autism and opioid receptor ligands

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

Serotonin and brain development: role in human developmental diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

The autistic spectrum: subgroups, boundaries, and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

The epidemiology of autistic spectrum disorders: is the prevalence rising?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

A genomewide screen of 345 families for autism-susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1362361304042719

21 January 2018

Identifiers

DOI

10.1177/1362361304042719

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15165431%20AND%20SRC:MED&resulttype=core&format=json

release_zbb7qc2vrbhvpd63bbnypdb6ta

29 December 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/zbb7qc2vrbhvpd63bbnypdb6ta

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference