paperKB
coga / coga-kb
Help
Sign in

Chunk #5 — METHODS AND MATERIALS — Study Subjects

Source
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.
Embedded
yes

Text

Patients who met Diagnostic and Statistical Manual of Mental Disorders, fourth edition, text revision (DSM-IV-TR) criteria for Tourette’s Disorder (50) and their parents, if available, were included. Two cohorts of Caucasian TS patients (n=645, including 248 trios) from independent studies in the United States and Netherlands were ascertained (see Methods in Supplement 1). Control subjects were comprised of unrelated children (n=546) and parents (n=1098) of European ancestry from the Simons Simplex Collection (SSC) who were extensively phenotyped (https://sfari.org/ssc-instruments) and showed no evidence of ASD (51), as well as a group of unrelated healthy subjects collected as part of a separate genetic study of intracranial aneurysms (YNIA, n=786) (Figure 1, Table S1 in Supplement 1).