The past two decades of research have demonstrated that Tourette's syndrome
(TS) is likely to be more genetically heterogeneous than initially appreci
ated. Nonetheless, important progress toward the understanding of genetic i
nfluences in TS has been made by the combination of family and twin studies
, segregation analyses, parametric and nonparametric linkage analyses, and
association studies. The identification of genetic factors involved in TS w
ill have important implications for clinical research. Once it is possible
to stratify patients meaningfully with respect to known genetic markers, a
reassessment of diagnostic nosology, neuroimaging findings, psychopharmacol
ogy, and disease course will be possible. Another result of gene identifica
tion will be the rapid clarification of additional environmental factors in
fluencing the development of the disorder. Because it may be easier to infl
uence the environment and behavior rather than to change genes, exploration
of such gene-environment interactions may lead to the most significant cli
nical contributions in the near term.