funded by the Tourette Syndrome Association, Inc.
Project Aims
The
following specific aims are going to be pursued:
»
Creation of a network of geneticists and psychiatrists in seven
different countries in Eastern and Southern Europe with a goal to
promote the study of TS genomics and educate both the public and
professionals about the disorder. Countries that will initially
participate will include Greece, Albania, Hungary, Italy, Poland,
Ukraine and Russia. An open call for additional collaborators will be
announced.
» Establishment of biobank of
samples from individuals with TS and their parents.
» Standardization of diagnostic
criteria used for characterization of patients according to the standards
set forth by the TSAICG.
» Creation of database
containing detailed phenotypic information about participating
individuals.
» Collection of blood and
plasma samples from approximately 350 families with one affected child
with TS from all six countries. Blood samples are going to be used for
DNA extraction. These samples are going to be added to the DNA samples
from 100 families with one child affected with TS, already collected in Hungary (total of 450 families).
» Genotyping of collected
samples for variants reported to be associated/linked to TS by the recent
TSAICG genome screen and recent studies of genes in the dopaminergic and
serotonergic pathways (monoamine oxidase-A, dopamine transporter and
tryptophan hydroxylase-2).
» Analysis of results using
existing and novel statistical techniques.
» Creation of project website
that will serve as a forum for researchers interested in TS genetics in
Eastern and Southern Europe as well as
individuals with TS and educators in this region.
» Description of the project
aims and invitation for new collaborations.
» Posting of TS related
articles addressing both scientists and the general public.
» Dissemination of study results.