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

Richard Delorme; Catalina Betancur; Michael Wagner; Marie-Odile Krebs; Philip Gorwood; Phillip Pearl; Gudrun Nygren; Christelle M. Durand; Friederike Buhtz; P. Pickering; Jonas Melke; Stephan Ruhrmann; Henrik Anckarsäter; Nadia Chabane; Amélie Kipman; Claudia Reck; Bruno Millet; Isabelle Roy; Marie-Christine Mouren-Simeoni; Wolfgang Maier; Maria Råstam; Christopher Gillberg; Marion Leboyer; Thomas Bourgeron

doi:10.1038/sj.mp.4001728

Journal Articles Molecular Psychiatry Year : 2005

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

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Richard Delorme

Function : Correspondent author
PersonId : 837674

Connectez-vous pour contacter l'auteur

Génétique Humaine et Fonctions Cognitives

Neurobiologie et Psychiatrie

Service de psychopathologie de l'enfant et de l'adolescent

Catalina Betancur

Function : Author
PersonId : 13320
IdHAL : catalina-betancur
ORCID : 0000-0002-3327-4804
IdRef : 180835750

Neurobiologie et Psychiatrie

Michael Wagner

Function : Author

Department of Psychiatry

Marie-Odile Krebs

Function : Author
PersonId : 757581
ORCID : 0000-0002-4715-9890
IdRef : 069691010

Physiopathologie des Maladies Psychiatriques, Développement et Vulnérabilité

Philip Gorwood

Function : Author

Analyse Phenotypique, Developpementale et Genetique des Comportements Addictifs

Phillip Pearl

Function : Author

Children's National Medical Center

Gudrun Nygren

Function : Author

Department of Child and Adolescent Psychiatry

Christelle M. Durand

Function : Author

Génétique Humaine et Fonctions Cognitives

Friederike Buhtz

Function : Author

Department of Psychiatry

P. Pickering

Function : Author

Analyse Phenotypique, Developpementale et Genetique des Comportements Addictifs

Jonas Melke

Function : Author

Génétique Humaine et Fonctions Cognitives

Stephan Ruhrmann

Function : Author

Department of Psychiatry and Psychotherapy

Henrik Anckarsäter

Function : Author

Department of Child and Adolescent Psychiatry

Nadia Chabane

Function : Author

Neurobiologie et Psychiatrie

Service de psychopathologie de l'enfant et de l'adolescent

Amélie Kipman

Function : Author

Analyse Phenotypique, Developpementale et Genetique des Comportements Addictifs

Claudia Reck

Function : Author

Department of Psychiatry

Bruno Millet

Function : Author

Physiopathologie des Maladies Psychiatriques, Développement et Vulnérabilité

Isabelle Roy

Function : Author

Neurobiologie et Psychiatrie

Département de Psychiatrie

Marie-Christine Mouren-Simeoni

Function : Author

Service de psychopathologie de l'enfant et de l'adolescent

Wolfgang Maier

Function : Author

Department of Psychiatry

Maria Råstam

Function : Author

Department of Child and Adolescent Psychiatry

Christopher Gillberg

Function : Author

Department of Child and Adolescent Psychiatry

Saint George's Hospital Medical School

Marion Leboyer

Function : Author
PersonId : 756830
ORCID : 0000-0001-5473-3697
IdRef : 089352475

Neurobiologie et Psychiatrie

Département de Psychiatrie

Thomas Bourgeron

Function : Author
PersonId : 747963
IdHAL : thomas-bourgeron
ORCID : 0000-0001-8164-9220
IdRef : 119761955

Génétique Humaine et Fonctions Cognitives

Université Paris Diderot - Paris 7

Abstract

No abstract available.

Domains

Genetics

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Delorme_Mol_Psychiatry_2005.pdf (154.5 Ko)

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https://inserm.hal.science/inserm-00125111

Submitted on : Thursday, January 18, 2007-10:45:59 AM

Last modification on : Thursday, December 14, 2023-1:50:37 PM

Long-term archiving on: Tuesday, April 6, 2010-8:41:40 PM

Dates and versions

inserm-00125111 , version 1 (18-01-2007)

Identifiers

HAL Id : inserm-00125111 , version 1
DOI : 10.1038/sj.mp.4001728
PUBMED : 16088327

Cite

Richard Delorme, Catalina Betancur, Michael Wagner, Marie-Odile Krebs, Philip Gorwood, et al.. Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder.. Molecular Psychiatry, 2005, 10 (12), pp.1059-61. ⟨10.1038/sj.mp.4001728⟩. ⟨inserm-00125111⟩

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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.

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