Linkage Studies
Table of Contents
Linkage is a genetic
mapping technique that identifies regions of chromosomes that are likely
to contain a risk gene. They also rule out chromosome areas where there
is a low chance of finding a risk gene. Linkage studies show
an association between two or more genes where the traits they control
tend to be inherited together. This type of study pinpoints the chromosomal
location of a gene that causes the manifested trait. As stated before,
researchers have not yet found a specific gene for the susceptibility of
bipolar disorder. Although, they have found some genes that have
potential for it.
"Linkage studies
have defined at least six potential BPD susceptibility loci which meet
suggested guidelines for initial identification and subsequent confirmation.
These loci, found on 18p11, 18q22, 21q21, 4p16, 12q24, and 22q11, are targets
for BPD candidate gene investigations." (Berrettini,
W. H., 2001) Literature shows there has been some research conducted
on many different chromosomes such as on chromosome 11, 15, and 22 but
the strongest evidence for genetic linkage in bipolar disorder is to chromosome
18, because there are several positive studies from independent research
groups (as cited by Millon, Blaney, & Davis, 1999)
**To see a presentation of a linkage study by Wade Berrettini go here-->Linkage Study by Berrettini **
**Some of the terms used in genetics are hard to understand so here is a helpful glossary that defines genetic terms Genetic Glossary **
Research Articles on Linkage Studies
Linkage Studies on Chromosome 22