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Enhancing neuroimaging genetics through meta-analysis for Tourette syndrome (ENIGMA-TS): A worldwide platform for collaboration

Authors :
National Institute of Mental Health (US)
National Science Foundation (US)
Innovative Medicines Initiative
National Institutes of Health (US)
Universidad de Sevilla
Lundbeck Foundation
Dagmar Marshall Foundation
Bohemia Fund
Jeff Hansen Memorial Foundation
Queen Louise's Children's Hospital Foundation
King Christian X’s Foundation
Paschou, Peristera
Jin, Yin
Müller-Vahl, Kirsten R.
Möller, Harald E.
Rizzo, Renata
Hoekstra, Pieter J.
Roessner, Veit
Mol Debes, Nanette
Worbe, Yulia
Hartmann, Andreas
Mir, Pablo
Cath, Danielle
Neuner, Irene
Eichele, Heike
Zhang, Chencheng
Lewandowska, Katarzyna
Münchau, Alexander
Verrel, Julius
Musil, Richard
Silk, Tim J.
Hanlon, Colleen A.
Bihun, Emily D.
Brandt, Valerie
Dietrich, Andrea
Forde, Natalie
Ganos, Christos
Greene, Deanna J.
Chu, Chunguang
Grothe, Michel J.
Hershey, Tamara
Janik, Piotr
Koller, Jonathan M.
Martín-Rodríguez, Juan Francisco
Müller, Karsten
Palmucci, Stefano
Prato, Adriana
Ramkiran, Shukti
Saia, Federica
Szejko, Natalia
Torrecuso, Renzo
Tumer, Zeynep
Uhlmann, Anne
Veselinovic, Tanja
Wolańczyk, Tomasz
Zouki, Jade Jocelyne
Jain, Pritesh
Topaloudi, Apostolia
Kaka, Mary
Yang, Zhiyu
Drineas, Petros
Thomopoulos, Sophia I.
White, Tonya
Veltman, Dick J.
Schmaal, Lianne
Stein, Dan J.
Buitelaar, Jan
Franke, Barbara
Heuvel, Odile van den
Jahanshad, Neda
Thompson, Paul M.
Black, Kevin J.
National Institute of Mental Health (US)
National Science Foundation (US)
Innovative Medicines Initiative
National Institutes of Health (US)
Universidad de Sevilla
Lundbeck Foundation
Dagmar Marshall Foundation
Bohemia Fund
Jeff Hansen Memorial Foundation
Queen Louise's Children's Hospital Foundation
King Christian X’s Foundation
Paschou, Peristera
Jin, Yin
Müller-Vahl, Kirsten R.
Möller, Harald E.
Rizzo, Renata
Hoekstra, Pieter J.
Roessner, Veit
Mol Debes, Nanette
Worbe, Yulia
Hartmann, Andreas
Mir, Pablo
Cath, Danielle
Neuner, Irene
Eichele, Heike
Zhang, Chencheng
Lewandowska, Katarzyna
Münchau, Alexander
Verrel, Julius
Musil, Richard
Silk, Tim J.
Hanlon, Colleen A.
Bihun, Emily D.
Brandt, Valerie
Dietrich, Andrea
Forde, Natalie
Ganos, Christos
Greene, Deanna J.
Chu, Chunguang
Grothe, Michel J.
Hershey, Tamara
Janik, Piotr
Koller, Jonathan M.
Martín-Rodríguez, Juan Francisco
Müller, Karsten
Palmucci, Stefano
Prato, Adriana
Ramkiran, Shukti
Saia, Federica
Szejko, Natalia
Torrecuso, Renzo
Tumer, Zeynep
Uhlmann, Anne
Veselinovic, Tanja
Wolańczyk, Tomasz
Zouki, Jade Jocelyne
Jain, Pritesh
Topaloudi, Apostolia
Kaka, Mary
Yang, Zhiyu
Drineas, Petros
Thomopoulos, Sophia I.
White, Tonya
Veltman, Dick J.
Schmaal, Lianne
Stein, Dan J.
Buitelaar, Jan
Franke, Barbara
Heuvel, Odile van den
Jahanshad, Neda
Thompson, Paul M.
Black, Kevin J.
Publication Year :
2022

Abstract

Tourette syndrome (TS) is characterized by multiple motor and vocal tics, and high-comorbidity rates with other neuropsychiatric disorders. Obsessive compulsive disorder (OCD), attention deficit hyperactivity disorder (ADHD), autism spectrum disorders (ASDs), major depressive disorder (MDD), and anxiety disorders (AXDs) are among the most prevalent TS comorbidities. To date, studies on TS brain structure and function have been limited in size with efforts mostly fragmented. This leads to low-statistical power, discordant results due to differences in approaches, and hinders the ability to stratify patients according to clinical parameters and investigate comorbidity patterns. Here, we present the scientific premise, perspectives, and key goals that have motivated the establishment of the Enhancing Neuroimaging Genetics through Meta-Analysis for TS (ENIGMA-TS) working group. The ENIGMA-TS working group is an international collaborative effort bringing together a large network of investigators who aim to understand brain structure and function in TS and dissect the underlying neurobiology that leads to observed comorbidity patterns and clinical heterogeneity. Previously collected TS neuroimaging data will be analyzed jointly and integrated with TS genomic data, as well as equivalently large and already existing studies of highly comorbid OCD, ADHD, ASD, MDD, and AXD. Our work highlights the power of collaborative efforts and transdiagnostic approaches, and points to the existence of different TS subtypes. ENIGMA-TS will offer large-scale, high-powered studies that will lead to important insights toward understanding brain structure and function and genetic effects in TS and related disorders, and the identification of biomarkers that could help inform improved clinical practice.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1380452337
Document Type :
Electronic Resource