Support for the association between the rare functional variant 1425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder
(2005) In Molecular Psychiatry 10(12). p.61-1059
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1454332
- author
- Delorme, Richard
; Betancur, Catalina
; Wagner, Michael
; Krebs, Marie-Odile
; Gorwood, Philip
; Pearl, Philip
; Nygren, Gudrun
; Durand, Christelle M
; Buhtz, Friederike
; Pickering, P
; Melke, Jonas
; Ruhrmann, Stephan
; Anckarsäter, Henrik
LU
; Chabane, Nadia
; Kipman, Amélie
; Reck, Claudia
; Millet, Bruno
; Roy, Isabelle
; Mouren-Simeoni, Marie-Christine
; Maier, Wolfgang
; Råstam, Maria
LU
; Gillberg, Christopher
; Leboyer, Marion
and Bourgeron, Thomas
(Less) - publishing date
- 2005
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Adolescent Adult Alcoholism/genetics Anorexia Nervosa/genetics Child Child Development Disorders, Genetic/genetics Reference Values Serotonin Plasma Membrane Transport Proteins/genetics* Serotonin Uptake Inhibitors/therapeutic use, Pervasive/genetics Drug Resistance/genetics Family Female Genetic Predisposition to Disease/genetics* Humans Male Middle Aged Obsessive-Compulsive Disorder/drug therapy Obsessive-Compulsive Disorder/genetics* Pedigree Polymorphism
- in
- Molecular Psychiatry
- volume
- 10
- issue
- 12
- pages
- 61 - 1059
- publisher
- Nature Publishing Group
- external identifiers
-
- pmid:16088327
- scopus:32844455970
- pmid:16088327
- ISSN
- 1359-4184
- DOI
- 10.1038/sj.mp.4001728
- language
- English
- LU publication?
- no
- id
- e1ea654f-4057-4afd-b51c-7aa3614b0d66 (old id 1454332)
- alternative location
- http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2547479/?tool=pubmed
- date added to LUP
- 2016-04-04 08:25:45
- date last changed
- 2022-04-23 17:27:08
@article{e1ea654f-4057-4afd-b51c-7aa3614b0d66,
author = {{Delorme, Richard and Betancur, Catalina and Wagner, Michael and Krebs, Marie-Odile and Gorwood, Philip and Pearl, Philip and Nygren, Gudrun and Durand, Christelle M and Buhtz, Friederike and Pickering, P and Melke, Jonas and Ruhrmann, Stephan and Anckarsäter, Henrik and Chabane, Nadia and Kipman, Amélie and Reck, Claudia and Millet, Bruno and Roy, Isabelle and Mouren-Simeoni, Marie-Christine and Maier, Wolfgang and Råstam, Maria and Gillberg, Christopher and Leboyer, Marion and Bourgeron, Thomas}},
issn = {{1359-4184}},
keywords = {{Adolescent Adult Alcoholism/genetics Anorexia Nervosa/genetics Child Child Development Disorders; Genetic/genetics Reference Values Serotonin Plasma Membrane Transport Proteins/genetics* Serotonin Uptake Inhibitors/therapeutic use; Pervasive/genetics Drug Resistance/genetics Family Female Genetic Predisposition to Disease/genetics* Humans Male Middle Aged Obsessive-Compulsive Disorder/drug therapy Obsessive-Compulsive Disorder/genetics* Pedigree Polymorphism}},
language = {{eng}},
number = {{12}},
pages = {{61--1059}},
publisher = {{Nature Publishing Group}},
series = {{Molecular Psychiatry}},
title = {{Support for the association between the rare functional variant 1425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder}},
url = {{http://dx.doi.org/10.1038/sj.mp.4001728}},
doi = {{10.1038/sj.mp.4001728}},
volume = {{10}},
year = {{2005}},
}