[HTML][HTML] European clinical guidelines for Tourette syndrome and other tic disorders—Version 2.0. Part II: Psychological interventions

…, E Jakubovski, TL Murphy, K Woitecki, Z Tarnok… - European child & …, 2022 - Springer
Part II of the European clinical guidelines for Tourette syndrome and other tic disorders (ECAP
journal, 2011) provides updated information and recommendations for psychological …

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

…, A Dietrich, TL Murphy, D Martino, Z Tarnok… - 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 (TS). Now…

Semantide-and chemotaxonomy-based analyses of some problematic phenotypic clusters of slowly growing mycobacteria, a cooperative study of the International …

…, E Stackebrandt, I Tarnok, Z Tarnok… - … of Systematic and …, 1996 - microbiologyresearch.org
During previous cooperative numerical taxonomic studies of slowly growing mycobacteria,
the International Working Group on Mycobacterial Taxonomy described a number of strains …

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

…, TV Fernandez, C Barta, Z Tarnok… - 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 …

[PDF][PDF] Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome

…, GJ Lyon, WM McMahon, C Barta, Z Tarnok… - Neuron, 2017 - cell.com
… First, we extracted the LRR intensity Z-scores for all probes in the region across all samples.
The Z-scores for all probes spanning the CNV locus were then subjected to second round of …

[PDF][PDF] De novo sequence and copy number variants are strongly associated with tourette disorder and implicate cell polarity in pathogenesis

…, J Puchala, R Rizzo, N Szejko, U Szymanska, Z Tarnok… - Cell reports, 2018 - cell.com
We previously established the contribution of de novo damaging sequence variants to
Tourette disorder (TD) through whole-exome sequencing of 511 trios. Here, we sequence an …

Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families

…, S Dehning, P Sandor, Z Tarnok… - Journal of medical …, 2013 - jmg.bmj.com
Background Gilles de la Tourette Syndrome is a neurodevelopmental disorder that is caused
by the interaction of environment with a complex genetic background. The genetic etiology …

Catechol‐O‐methyltransferase Val158Met polymorphism is associated with methylphenidate response in ADHD children

E Kereszturi, Z Tarnok, E Bognar… - American Journal of …, 2008 - Wiley Online Library
… Please cite this article as follows: Kereszturi E, Tarnok Z, Bognar E, Lakatos K, Farkas L,
Gadoros J, Sasvari-Szekely M, Nemoda Z. 2008. Catechol-O-Methyltransferase Val158Met …

[PDF][PDF] Geographically separate increases in the frequency of the derived ADH1B* 47His allele in eastern and western Asia

H Li, N Mukherjee, U Soundararajan, Z Tárnok… - The American Journal of …, 2007 - cell.com
The ADH1B Arg47His polymorphism has been convincingly associated with alcoholism in
numerous studies of several populations in Asia and Europe. In a review of literature from the …

Carboxylesterase 1 gene polymorphism and methylphenidate response in ADHD

Z Nemoda, N Angyal, Z Tarnok, J Gadoros… - …, 2009 - Elsevier
Methylphenidate (MPH) is the most frequently prescribed drug in the treatment of attention
deficit hyperactivity disorder (ADHD). Several pharmacogenetic studies suggested that …