Accès ouvert
2025
article
OpenAlex
Marisela Dy-Hollins, Lori B. Chibnik, Natasha Tracy, Lisa Osiecki et autres
OBJECTIVES: To analyze sex differences in outcomes in Tourette syndrome (TS) and Persistent Motor or Vocal tic disorders (PMVT) in the Tourette Association of America International Consortium for Genetics (TAAICG) dataset. METHODS: The relationship between sex and clinical measures was explored in …
us, nl, ca
(code pays fourni par la source)
Accès ouvert
2022
preprint
OpenAlex
Irene A. C. Malaty, Seonaid Anderson, Shannon M. Bennett, Cathy L. Budman et autres
Over the past 3 years, a global phenomenon has emerged characterized by the sudden onset and frequently rapid escalation of tics and tic-like movements and phonations. These symptoms have occurred not only in youth known to have tics or Tourette syndrome (TS), …
us
(code pays fourni par la source)
Accès ouvert
2020
preprint
OpenAlex
Fotis Tsetsos, Dongmei Yu, Jae Hoon Sul, Alden Y. Huang et autres
Abstract Tourette Syndrome (TS) is a neuropsychiatric disorder of complex genetic architecture involving multiple interacting genes. Here, we sought to elucidate the pathways that underlie the neurobiology of the disorder through genome-wide analysis. We analyzed genome-wide genotypic data of 3581 individuals with …
gr, us, de, ca, gb, at, hu, fr, pl, it, nl, ru
(code pays fourni par la source)
Accès ouvert
2019
article
OpenAlex
Phil H. Lee, Verneri Anttila, Hyejung Won, Yen‐Chen Anne Feng et autres
us, gb, cn, se, de, br, fi
(code pays fourni par la source)
Accès ouvert
2019
article
OpenAlex
Dongmei Yu, Jae Hoon Sul, Fotis Tsetsos, Muhammad Sulaman Nawaz et autres
OBJECTIVE: Tourette's syndrome is polygenic and highly heritable. Genome-wide association study (GWAS) approaches are useful for interrogating the genetic architecture and determinants of Tourette's syndrome and other tic disorders. The authors conducted a GWAS meta-analysis and probed aggregated Tourette's syndrome polygenic risk …
us
(code pays fourni par la source)
Accès ouvert
2017
article
OpenAlex
Erica Greenberg, Esther S. Tung, Caitlin Gauvin, Lisa Osiecki et autres
us, ca
(code pays fourni par la source)
Accès ouvert
2017
article
OpenAlex
Matthew E. Hirschtritt, Sabrina M. Darrow, Cornelia Illmann, Lisa Osiecki et autres
BACKGROUND: The unique phenotypic and genetic aspects of obsessive-compulsive (OCD) and attention-deficit/hyperactivity disorder (ADHD) among individuals with Tourette syndrome (TS) are not well characterized. Here, we examine symptom patterns and heritability of OCD and ADHD in TS families. METHOD: OCD and ADHD …
us, ca, nl
(code pays fourni par la source)
Accès ouvert
2017
article
OpenAlex
Sabrina M. Darrow, Marco A. Grados, Paul Sandor, Matthew E. Hirschtritt et autres
us, ca, nl
(code pays fourni par la source)
2017
article
OpenAlex
Matthew E. Hirschtritt, Sabrina M. Darrow, Cornelia Illmann, Lisa Osiecki et autres
us, ca, nl
(code pays fourni par la source)
Accès ouvert
2016
article
OpenAlex
Sabrina M. Darrow, Matthew E. Hirschtritt, Lea K. Davis, Cornelia Illmann et autres
OBJECTIVE: Phenotypic heterogeneity in Tourette syndrome is partly due to complex genetic relationships among Tourette syndrome, obsessive-compulsive disorder (OCD), and attention deficit hyperactivity disorder (ADHD). Identifying symptom-based endophenotypes across diagnoses may aid gene-finding efforts. METHOD: Assessments for Tourette syndrome, OCD, and ADHD …
ca, us
(code pays fourni par la source)
Accès ouvert
2016
article
OpenAlex
Matthew E. Hirschtritt, Sabrina M. Darrow, Cornelia Illmann, Lisa Osiecki et autres
OBJECTIVE: To identify heritable symptom-based subtypes of Tourette syndrome (TS). METHODS: Forty-nine motor and phonic tics were examined in 3,494 individuals (1,191 TS probands and 2,303 first-degree relatives). Item-level exploratory factor and latent class analyses (LCA) were used to identify tic-based subtypes. …
us
(code pays fourni par la source)
Accès ouvert
2014
article
OpenAlex
Peristera Paschou, Dongmei Yu, Gloria F. Gerber, Patrick Evans et autres
Tourette syndrome (TS) is a neurodevelopmental disorder with a complex genetic etiology. Through an international collaboration, we genotyped 42 single nucleotide polymorphisms (p < 10(-3) ) from the recent TS genomewide association study (GWAS) in 609 independent cases and 610 ancestry-matched controls. …
gr, us, de, at, hu, it, fr, nl, ca, pl, tw
(code pays fourni par la source)