(Q35851031)

10 August 2017

Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder (English)

1 reference

10 August 2017

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1

1 reference

10 August 2017

7

C Gillberg

1 reference

10 August 2017

12

M Leboyer

1 reference

10 August 2017

M Corbex

2

1 reference

10 August 2017

C Spielewoy

3

1 reference

10 August 2017

A Philippe

4

1 reference

10 August 2017

J L Laplanche

5

1 reference

10 August 2017

J M Launay

6

1 reference

10 August 2017

M C Mouren-Siméoni

8

1 reference

10 August 2017

M Hamon

9

1 reference

10 August 2017

B Giros

10

1 reference

10 August 2017

M Nosten-Bertrand

11

1 reference

10 August 2017

language of work or name

English

0 references

publication date

1 January 2002

1 reference

10 August 2017

1 reference

10 August 2017

7

1 reference

10 August 2017

1

1 reference

10 August 2017

67-71

1 reference

A serotonin transporter gene intron 2 polymorphic region, correlated with affective disorders, has allele-dependent differential enhancer-like properties in the mouse embryo

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Transmission/disequilibrium tests for extended marker haplotypes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Evidence of linkage between the serotonin transporter and autistic disorder.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Effects of tryptophan depletion in drug-free adults with autistic disorder.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Parametric and nonparametric linkage analysis: a unified multipoint approach

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Allelic variation of human serotonin transporter gene expression

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

A modified enzymatic-isotopic microassay for serotonin (5HT) using 5HT-N-acetyltransferase partially purified from Drosophila.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Kinetics of 3H-serotonin uptake by platelets in infantile autism and developmental language disorder (including five pairs of twins).

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Whole blood serotonin in autistic and normal subjects.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Relationships of whole blood serotonin and plasma norepinephrine within families.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

5-HTTLPR variants not associated with autistic spectrum disorders.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Genetic variation in the serotonin transporter promoter region affects serotonin uptake in human blood platelets

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

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

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Autism: the phenotype in relatives.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

A double-blind comparison of clomipramine, desipramine, and placebo in the treatment of autistic disorder.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1896269

Tetrahydropterin-dependent amino acid hydroxylases

24 September 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

The spectrum of behaviors influenced by serotonin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Synthesis of serotonin by a second tryptophan hydroxylase isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Analysis of tryptophan hydroxylase I and II mRNA expression in the human brain: a post-mortem study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Neuronal tryptophan hydroxylase mRNA expression in the human dorsal and median raphe nuclei: major depression and suicide

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Identification of genetic variants in the neuronal form of tryptophan hydroxylase (TPH2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Functional polymorphisms of the brain serotonin synthesizing enzyme tryptophan hydroxylase-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Allelic Variation in Human Gene Expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Genetic variants of the human H+/dipeptide transporter PEPT2: analysis of haplotype functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Allelic expression imbalance of human mu opioid receptor (OPRM1) caused by variant A118G.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Allelic expression of serotonin transporter (SERT) mRNA in human pons: lack of correlation with the polymorphism SERTLPR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Haplotype-based linkage of tryptophan hydroxylase 2 to suicide attempt, major depression, and cerebrospinal fluid 5-hydroxyindoleacetic acid in 4 populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Control elements of muscarinic receptor gene expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Mfold web server for nucleic acid folding and hybridization prediction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

PupaSNP Finder: a web tool for finding SNPs with putative effect at transcriptional level.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Listening to silence and understanding nonsense: exonic mutations that affect splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Global landscape of recent inferred Darwinian selection for Homo sapiens

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Recent developments and current controversies in depression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

SNP and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene provide evidence for association with major depression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Support for the involvement of TPH2 gene in affective disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

The novel brain-specific tryptophan hydroxylase-2 gene in panic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Possible association between autism and variants in the brain-expressed tryptophan hydroxylase gene (TPH2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Single nucleotide polymorphism and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene in suicide victims

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Analysis of the novel TPH2 gene in bipolar disorder and suicidality

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Promoter polymorphism of second tryptophan hydroxylase isoform (TPH2) in schizophrenia and suicidality

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

The interaction between TPH2 promoter haplotypes and clinical-demographic risk factors in suicide victims with major psychoses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Lack of association between the serotonin transporter and tryptophan hydroxylase gene polymorphisms and completed suicide

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Lack of association of TPH2 exon XI polymorphisms with major depression and treatment resistance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

A regulatory variant of the human tryptophan hydroxylase-2 gene biases amygdala reactivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Amygdala responsiveness is modulated by tryptophan hydroxylase-2 gene variation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Additive effects of serotonin transporter and tryptophan hydroxylase-2 gene variation on emotional processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Functional promoter and polyadenylation site mapping of the human serotonin (5-HT) transporter gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Serotonin and brain development: role in human developmental diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

The developmental role of serotonin: news from mouse molecular genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Neuroticism mediates the association of the serotonin transporter gene with lifetime major depression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: dissection of epigenetic and genetic factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001923

Genetic control of serotonin uptake in blood platelets: a twin study

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11803447

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Organization of the human serotonin transporter gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11803447

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/SJ.MP.4001923

1 reference

Dimensions Publication ID

10 August 2017

0 references

1 reference

10 August 2017

PubMed publication ID

11803447

1 reference