Quick Search:

uzh logo
Browse by:

Zurich Open Repository and Archive

Walitza, S; Renner, T J; Wewetzer, C; Warnke, A (2008). Genetische Befunde bei Zwangsstörungen im Kindes- und Jugendalter und bei Erwachsenen. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie, 36(1):45-52.

Full text not available from this repository.

View at publisher


Obsessive-compulsive disorders (OCD) are on the rise, and affected children, 1-2% of the general population, often are seriously impaired in their development. OCD is characterized by recurrent, intrusive and disturbing thoughts as well as by repetitive stereotypic behaviours. Depending on their age and developmental status, patients usually try unsuccessfully to suppress the obsessive thoughts and compulsive behaviours. The current state of genetic research on OCD and early-onset OCD is presented and discussed. OCD, especially early-onset OCD, has been shown to be familial. Convincing evidence indicates that both environmental and genetic factors substantially influence OCD. Various approaches, including linkage and association studies, yielded conflicting results as well as the notion that multiple genes of modest effect sizes, in interaction with environmental factors, cause vulnerability to the disorder. The phenotypic and genetic heterogeneity of OCD complicate the identification of specific genetic factors. Further studies have to be designed in consideration of subtypes, e.g. age at onset, symptom dimensions, or comorbid disorders.


7 citations in Web of Science®
6 citations in Scopus®
Google Scholar™


Additional indexing

Other titles:Genetic findings in obsessive-compulsive disorder in childhood and adolescence and in adulthood
Item Type:Journal Article, refereed, further contribution
Communities & Collections:04 Faculty of Medicine > Center for Child and Adolescent Psychiatry
Dewey Decimal Classification:610 Medicine & health
Date:January 2008
Deposited On:26 Jan 2009 19:46
Last Modified:05 Apr 2016 12:54
Publisher:Hans Huber
Publisher DOI:10.1024/1422-4917.36.1.45
PubMed ID:18476602

Users (please log in): suggest update or correction for this item

Repository Staff Only: item control page