(Q34126958)

31 July 2017

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

1 reference

31 July 2017

0 references

3

1 reference

Marlene Briciet Lauritsen

31 July 2017

Anne Philippe

4

0 references

object named as

Marlene B Lauritsen

1

0 references

Marion Leboyer

object named as

Marion Leboyer

6

0 references

author name string

Anders D Børglum

2

1 reference

PubMed ID

11992572

31 July 2017

Torben A Kruse

5

1 reference

PubMed ID

11992572

31 July 2017

Henrik Ewald

7

1 reference

31 July 2017

1 May 2002

1 reference

American Journal of Medical Genetics Part A

31 July 2017

1 reference

31 July 2017

114

1 reference

31 July 2017

466-470

1 reference

31 July 2017

4

1 reference

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

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

5 July 2018

The genetics of autism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

An autosomal genomic screen for autism. Collaborative linkage study of autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

Genetic studies of autistic disorder and chromosome 7

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

The epidemiology of autism: a review.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

A genomic screen of autism: evidence for a multilocus etiology

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

Autism: not an extremely rare disorder

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

Serotonin transporter (5-HTT) gene variants associated with autism?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

Evidence of linkage between the serotonin transporter and autistic disorder.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

A double-blind, placebo-controlled study of fluvoxamine in adults with autistic disorder.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

The future of genetic studies of complex human diseases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

A case-control family history study of autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

A note on the application of the transmission disequilibrium test when a parent is missing.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

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

5 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

5 July 2018

https://api.crossref.org/works/10.1002%2FAJMG.10379

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

An extended transmission/disequilibrium test (TDT) for multi-allele marker loci.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

On the identity of DOPA decarboxylase and 5-hydroxytryptophan decarboxylase (immunological titration-aromatic L-amino acid decarboxylase-serotonin-dopamine-norepinephrine).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

Whole blood serotonin in autistic and normal subjects.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

Elevated blood serotonin in autistic probands and their first-degree relatives

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

Self-injurious behavior: a review of the behavior and biology of self- mutilation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

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

5 July 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10379

Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10379

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/10.1002%2FAJMG.10379

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/10.1002%2FAJMG.10379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10379

Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4826443

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

28 October 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10379

21 January 2018

Identifiers

DOI

10.1002/AJMG.10379

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

PubMed ID

11992572