Evaluation of the Genetics of Bipolar Disorder

Status Recruiting

Clinical Trial Summary

This study looks to identify genes that may affect a person's chances of developing bipolar disorder (BP) and related conditions.

Clinical Trial Description

Bipolar affective disorder is a severe, heritable condition affecting about one percent of the population. The mode of inheritance is poorly understood and probably involves multiple loci of small to moderate effect. In this project, we use genetic mapping and sequencing methods to identify genetic markers and variations that contribute to the risk of bipolar disorder. Individuals diagnosed with bipolar disorder are studied, along with their relatives. Phenotypic information obtained from clinical interviews and family history is correlated with genotypic information obtained from genetic marker and sequencing methods. The goal is to identify genes involved in bipolar disorder and related conditions so that better methods of diagnosis, treatment, and prevention can be developed. ;

Study Design

Related Conditions & MeSH terms

Bipolar Disorder

Clinical Trial Details

NCT number	NCT00001174
Study type	Observational
Source	National Institutes of Health Clinical Center (CC)
Contact	Emily Besancon
Phone	(866) 644-4363
Email	emily.besancon@nih.gov
Status	Recruiting
Phase
Start date	August 11, 1994

View Details

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