[HTML][HTML] European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part I: assessment

N Szejko, S Robinson, A Hartmann, C Ganos… - European child & …, 2022 - Springer
In 2011 a working group of the European Society for the Study of Tourette Syndrome
(ESSTS) has developed the first European assessment guidelines for Tourette syndrome …

Gilles de la Tourette syndrome

MM Robertson, V Eapen, HS Singer… - Nature reviews Disease …, 2017 - nature.com
Gilles de la Tourette syndrome (GTS) is a childhood-onset neurodevelopmental disorder
that is characterized by several motor and phonic tics. Tics usually develop before 10 years …

Association between telomere length and risk of cancer and non-neoplastic diseases: a Mendelian randomization study

PC Haycock, S Burgess, A Nounu, J Zheng… - JAMA …, 2017 - jamanetwork.com
Importance The causal direction and magnitude of the association between telomere length
and incidence of cancer and non-neoplastic diseases is uncertain owing to the susceptibility …

Interrogating the genetic determinants of Tourette's syndrome and other tic disorders through genome-wide association studies

D Yu, JH Sul, F Tsetsos, MS Nawaz… - American Journal of …, 2019 - Am Psychiatric Assoc
Objective: Tourette's syndrome is polygenic and highly heritable. Genome-wide association
study (GWAS) approaches are useful for interrogating the genetic architecture and …

[HTML][HTML] Admixture in Latin America: geographic structure, phenotypic diversity and self-perception of ancestry based on 7,342 individuals

A Ruiz-Linares, K Adhikari, V Acuña-Alonzo… - PLoS …, 2014 - journals.plos.org
The current genetic makeup of Latin America has been shaped by a history of extensive
admixture between Africans, Europeans and Native Americans, a process taking place …

Genome-wide association study of obsessive-compulsive disorder

SE Stewart, D Yu, JM Scharf, BM Neale… - Molecular …, 2013 - nature.com
Obsessive-compulsive disorder (OCD) is a common, debilitating neuropsychiatric illness
with complex genetic etiology. The International OCD Foundation Genetics Collaborative …

[HTML][HTML] Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

LK Davis, D Yu, CL Keenan, ER Gamazon… - PLoS …, 2013 - journals.plos.org
The direct estimation of heritability from genome-wide common variant data as implemented
in the program Genome-wide Complex Trait Analysis (GCTA) has provided a means to …

[PDF][PDF] De novo coding variants are strongly associated with Tourette disorder

AJ Willsey, TV Fernandez, D Yu, RA King, A Dietrich… - Neuron, 2017 - cell.com
Whole-exome sequencing (WES) and de novo variant detection have proven a powerful
approach to gene discovery in complex neurodevelopmental disorders. We have completed …

[PDF][PDF] Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and mice

LC Baldan, KA Williams, JD Gallezot, V Pogorelov… - Neuron, 2014 - cell.com
Tourette syndrome (TS) is characterized by tics, sensorimotor gating deficiencies, and
abnormalities of cortico-basal ganglia circuits. A mutation in histidine decarboxylase (Hdc) …

Tourette's syndrome

J Jankovic - New England Journal of Medicine, 2001 - Mass Medical Soc
The French neurologist Georges Gilles de la Tourette first described this syndrome, which
consists of motor tics sometimes accompanied by uncontrollable noises or utterances …