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dc.contributor.author Forde NJ
dc.contributor.author Kanaan AS
dc.contributor.author Widomska J
dc.contributor.author Padmanabhuni SS
dc.contributor.author Nespoli E
dc.contributor.author Alexander J
dc.contributor.author Rodriguez Arranz JI
dc.contributor.author Fan S
dc.contributor.author Houssari R
dc.contributor.author Nawaz MS
dc.contributor.author Rizzo F
dc.contributor.author Pagliaroli, Luca
dc.contributor.author Zilhäo NR
dc.contributor.author Arányi, Tamás
dc.contributor.author Barta, Csaba
dc.contributor.author Boeckers TM
dc.contributor.author Boomsma DI
dc.contributor.author Buisman WR
dc.contributor.author Buitelaar JK
dc.contributor.author Cath D
dc.contributor.author Dietrich A
dc.contributor.author Driessen N
dc.contributor.author Drineas P
dc.contributor.author Dunlap M
dc.contributor.author Gerasch S
dc.contributor.author Glennon J
dc.contributor.author Hengerer B
dc.contributor.author Van den Heuvel OA
dc.contributor.author Jespersgaard C
dc.contributor.author Möller HE
dc.contributor.author Müller-Vahl KR
dc.contributor.author Openneer TJC
dc.contributor.author Poelmans G
dc.contributor.author Pouwels PJW
dc.contributor.author Scharf JM
dc.contributor.author Stefansson H
dc.contributor.author Tümer Z
dc.contributor.author Veltman DJ
dc.contributor.author Van der Werf YD
dc.contributor.author Hoekstra PJ
dc.contributor.author Ludolph A
dc.contributor.author Paschou P
dc.date.accessioned 2018-06-27T11:35:00Z
dc.date.available 2018-06-27T11:35:00Z
dc.date.issued 2016
dc.identifier 84988350326
dc.identifier.citation pagination=384, pages: 9; journalVolume=10; journalTitle=FRONTIERS IN NEUROSCIENCE;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4849
dc.identifier.uri doi:10.3389/fnins.2016.00384
dc.description.abstract Gilles de la Tourette Syndrome (GTS) is characterized by the presence of multiple motor and phonic tics with a fluctuating course of intensity, frequency, and severity. Up to 90% of patients with GTS present with comorbid conditions, most commonly attention-deficit/hyperactivity disorder (ADHD), and obsessive-compulsive disorder (OCD), thus providing an excellent model for the exploration of shared etiology across disorders. TS-EUROTRAIN (FP7-PEOPLE-2012-ITN, Grant Agr. No. 316978) is a Marie Curie Initial Training Network (http://ts-eurotrain.eu) that aims to elucidate the complex etiology of the onset and clinical course of GTS, investigate the neurobiological underpinnings of GTS and related disorders, translate research findings into clinical applications, and establish a pan-European infrastructure for the study of GTS. This includes the challenges of (i) assembling a large genetic database for the evaluation of the genetic architecture with high statistical power; (ii) exploring the role of gene-environment interactions including the effects of epigenetic phenomena; (iii) employing endophenotype-based approaches to understand the shared etiology between GTS, OCD, and ADHD; (iv) establishing a developmental animal model for GTS; (v) gaining new insights into the neurobiological mechanisms of GTS via cross-sectional and longitudinal neuroimaging studies; and (vi) partaking in outreach activities including the dissemination of scientific knowledge about GTS to the public. Fifteen partners from academia and industry and 12 PhD candidates pursue the project. Here, we aim to share the design of an interdisciplinary project, showcasing the potential of large-scale collaborative efforts in the field of GTS. Our ultimate aims are to elucidate the complex etiology and neurobiological underpinnings of GTS, translate research findings into clinical applications, and establish Pan-European infrastructure for the study of GTS and associated disorders. © 2016 Forde, et al.
dc.relation.ispartof urn:issn:1662-4548
dc.title TS-EUROTRAIN: A European-wide investigation and training network on the etiology and pathophysiology of Gilles de la Tourette Syndrome
dc.type Journal Article
dc.date.updated 2018-02-19T13:07:09Z
dc.language.rfc3066 en
dc.identifier.mtmt 3126680
dc.identifier.wos WOS:000381802600001
dc.identifier.pubmed 27601976
dc.contributor.department SE/AOK/I/Orvosi Vegytani, Molekuláris Biológiai és Patobiokémiai Intézet
dc.contributor.institution Semmelweis Egyetem


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