(Q24646169)

English

Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

scientific article (published 2005-12-01)

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scholarly article

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Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder (English)

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obsessive-compulsive disorder

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J Melke

11

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Thomas Bourgeron

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T Bourgeron

24

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Catalina Betancur

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C Betancur

2

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Richard Delorme

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R Delorme

1

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Christopher Gillberg

22

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C Gillberg

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M Leboyer

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20

object named as

W Maier

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Henrik Anckarsäter

13

object named as

H Anckarsäter

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author name string

M O Krebs

4

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P Gorwood

5

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P Pearl

6

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G Nygren

7

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C M Durand

8

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F Buhtz

9

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P Pickering

10

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S Ruhrmann

12

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N Chabane

14

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A Kipman

15

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C Reck

16

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B Millet

17

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I Roy

18

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M C Mouren-Simeoni

19

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M Råstam

21

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M Wagner

3

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language of work or name

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publication date

December 2005

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Molecular Psychiatry

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10

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12

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1059-61

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2547479

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2547479

7 April 2017

Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2547479

27 September 2017

Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2547479

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2547479

27 September 2017

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2547479

27 September 2017

A human serotonin transporter mutation causes constitutive activation of transport activity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001728

21 January 2018

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001728

21 January 2018

Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons

1 reference

https://pubmed.ncbi.nlm.nih.gov/16088327

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retrospective assessment of prepubertal major depression with the Kiddie-SADS-e

1 reference

https://pubmed.ncbi.nlm.nih.gov/16088327

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/SJ.MP.4001728

1 reference

Consolidated OpenCitations Corpus – April 2017

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release_t74e2354pbgqdilcjqbf5hbpgq

1 reference

https://api.fatcat.wiki/v0/release/t74e2354pbgqdilcjqbf5hbpgq

24 November 2022

based on heuristic

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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