Objective: Tourette’s syndrome is polygenic and highly heritable. Genome-wide association
study (GWAS) approaches are useful for interrogating the genetic architecture and …

Tourette syndrome (TS) is a model neuropsychiatric disorder thought to arise from abnormal
development and/or maintenance of cortico-striato-thalamo-cortical circuits. TS is highly …

The Neolithic populations, which colonized Europe approximately 9,000 y ago, presumably
migrated from Near East to Anatolia and from there to Central Europe through Thrace and …

Background Tourette syndrome (TS) is often found comorbid with other
neurodevelopmental disorders across the impulsivity-compulsivity spectrum, with attention-deficit/hyperactivity …

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 …

Tourette syndrome (TS) is a neurodevelopmental disorder with a complex genetic etiology.
Through an international collaboration, we genotyped 42 single nucleotide polymorphisms (p …

Diabetic type 2 patients compared to nondiabetic patients exhibit an increased risk of
developing diabetic kidney disease (DKD), the leading cause of end-stage renal disease. …

Gilles de la Tourette Sydrome (TS) is a childhood onset neurodevelopmental disorder,
characterized phenotypically by the presence of multiple motor and vocal tics. It is often …

Soluble epoxide hydrolase 2 (EPHX2) is an enzyme promoting increased cellular apoptosis
through induction of oxidative stress (OS) and inflammation. The EPHX2 gene which …

Peloponnese has been one of the cradles of the Classical European civilization and an
important contributor to the ancient European history. It has also been the subject of a …