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The World Journal of Biological Psychiatry Volume 16, 2015 - Issue 3
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ORIGINAL INVESTIGATION

Structural correlates of COMT Val158Met polymorphism in childhood ADHD: a voxel-based morphometry study

Thomas VillemonteixINSERM, U894, Team 1, Centre Psychiatrie et Neurosciences, Paris, FranceCorrespondence[email protected]
,
Stéphane A. De BritoSchool of Psychology, University of Birmingham, Edgbaston, Birmingham, UK
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Hichem SlamaUR2NF - Neuropsychology and Functional Neuroimaging Research Unit, Centre de Recherche Cognition et Neurosciences, Université Libre de Bruxelles (ULB), Belgium;UNESCOG – Research Unit in Cognitive Neurosciences, ULB, Belgium;Department of Clinical and Cognitive Neuropsychology, Erasme Hospital, Belgium
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Martin KavecDepartment of Radiology, Clinics of Magnetic Resonance, Erasme Hospital, Brussels, Belgium
,
Danielle BalériauxDepartment of Radiology, Clinics of Magnetic Resonance, Erasme Hospital, Brussels, Belgium
,
Thierry MetensDepartment of Radiology, Clinics of Magnetic Resonance, Erasme Hospital, Brussels, Belgium
,
Simon BaijotUR2NF - Neuropsychology and Functional Neuroimaging Research Unit, Centre de Recherche Cognition et Neurosciences, Université Libre de Bruxelles (ULB), Belgium;UNESCOG – Research Unit in Cognitive Neurosciences, ULB, Belgium
,
Alison MaryUR2NF - Neuropsychology and Functional Neuroimaging Research Unit, Centre de Recherche Cognition et Neurosciences, Université Libre de Bruxelles (ULB), Belgium
,
Nicolas RamozINSERM, U894, Team 1, Centre Psychiatrie et Neurosciences, Paris, France
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Mathilde SeptierAssistance Publique-Hôpitaux de Paris, Department of Child and Adolescent Psychiatry, Robert Debre Hospital, Paris Diderot, Université Paris, France
,
Philip GorwoodINSERM, U894, Team 1, Centre Psychiatrie et Neurosciences, Paris, France
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Philippe PeigneuxUR2NF - Neuropsychology and Functional Neuroimaging Research Unit, Centre de Recherche Cognition et Neurosciences, Université Libre de Bruxelles (ULB), Belgium;UNI – ULB Neurosciences Institute, ULB, Belgium
&
Isabelle MassatUR2NF - Neuropsychology and Functional Neuroimaging Research Unit, Centre de Recherche Cognition et Neurosciences, Université Libre de Bruxelles (ULB), Belgium;UNI – ULB Neurosciences Institute, ULB, Belgium;Laboratory of Experimental Neurology, ULB, Belgium
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Pages 190-199 | Received 08 Apr 2014, Accepted 03 Nov 2014, Published online: 15 Dec 2014

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Koji Shimada, Takashi X. Fujisawa, Shinichiro Takiguchi, Hiroaki Naruse, Hirotaka Kosaka, Hidehiko Okazawa & Akemi Tomoda. (2017) Ethnic differences in COMT genetic effects on striatal grey matter alterations associated with childhood ADHD: A voxel-based morphometry study in a Japanese sample. The World Journal of Biological Psychiatry 18:4, pages 322-328.
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Burge Kabukcu Basay, Ahmet Buber, Omer Basay, Huseyin Alacam, Onder Ozturk, Serkan Suren, Ozlem Izci Ay, Cengizhan Acikel, Kadir Agladıoglu, Mehmet Emin Erdal, Eyup Sabri Ercan & Hasan Herken. (2016) White matter alterations related to attention-deficit hyperactivity disorder and COMT val158met polymorphism: children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (cingulate gyrus). Neuropsychiatric Disease and Treatment 12, pages 969-981.
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Articles from other publishers (11)

Miaomiao Yu, Xinyu Gao, Xiaoyu Niu, Mengzhe Zhang, Zhengui Yang, Shaoqiang Han, Jingliang Cheng & Yong Zhang. (2023) Meta-analysis of structural and functional alterations of brain in patients with attention-deficit/hyperactivity disorder. Frontiers in Psychiatry 13.
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Salma N. Younes, Rana Al-Jurf, Sara Hammuda, Gheyath K. Nasrallah, Amal Al-Jurf, Ayah Ziyada, Palli Valapila Abdulrouf, M. Walid Qoronfleh, Muthanna Samara & Nader Al-Dewik. 2022. Proteins Associated with Neurodevelopmental Disorders. Proteins Associated with Neurodevelopmental Disorders 135 189 .
Xinyu Gao, Mengzhe Zhang, Zhengui Yang, Mengmeng Wen, Huiyu Huang, Ruiping Zheng, Weijian Wang, Yarui Wei, Jingliang Cheng, Shaoqiang Han & Yong Zhang. (2021) Structural and Functional Brain Abnormalities in Internet Gaming Disorder and Attention-Deficit/Hyperactivity Disorder: A Comparative Meta-Analysis. Frontiers in Psychiatry 12.
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Santosh K. Yadav, Ajaz A. Bhat, Sheema Hashem, Sabah Nisar, Madeeha Kamal, Najeeb Syed, Mohamed-Ramzi Temanni, Rakesh K. Gupta, Saddat Kamran, Muhammad Waqar Azeem, Amit K. Srivastava, Puneet Bagga, Sanjeev Chawla, Ravinder Reddy, Michael P. Frenneaux, Khalid Fakhro & Mohammad Haris. (2021) Genetic variations influence brain changes in patients with attention-deficit hyperactivity disorder. Translational Psychiatry 11:1.
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Carles Soriano-Mas & Ben J. Harrison. 2018. A Transdiagnostic Approach to Obsessions, Compulsions and Related Phenomena. A Transdiagnostic Approach to Obsessions, Compulsions and Related Phenomena 74 84 .
Bernis Sutcubasi Kaya, Baris Metin, Zeynep Cubukcuoglu Tas, Ayse Buyukaslan, Aysegul Soysal, Deniz Hatiloglu & Nevzat Tarhan. (2016) Gray Matter Increase in Motor Cortex in Pediatric ADHD: A Voxel-Based Morphometry Study. Journal of Attention Disorders 22:7, pages 611-618.
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Ping-yuan Yang, Ya-jing Menga, Tao Li & Yi Huang. (2017) Associations of endocrine stress-related gene polymorphisms with risk of autism spectrum disorders: Evidence from an integrated meta-analysis. Autism Research 10:11, pages 1722-1736.
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Marieke Klein, Marten Onnink, Marjolein van Donkelaar, Thomas Wolfers, Benjamin Harich, Yan Shi, Janneke Dammers, Alejandro Arias-Vásquez, Martine Hoogman & Barbara Franke. (2017) Brain imaging genetics in ADHD and beyond – Mapping pathways from gene to disorder at different levels of complexity. Neuroscience & Biobehavioral Reviews 80, pages 115-155.
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Yoshifumi Mizuno, Minyoung Jung, Takashi X. Fujisawa, Shinichiro Takiguchi, Koji Shimada, Daisuke N. Saito, Hirotaka Kosaka & Akemi Tomoda. (2017) Catechol-O-methyltransferase polymorphism is associated with the cortico-cerebellar functional connectivity of executive function in children with attention-deficit/hyperactivity disorder. Scientific Reports 7:1.
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Anirban Ray, Subhamita Maitra, Mahasweta Chatterjee, Paramita Ghosh, Arijit Karmakar, Swagata Sinha & Kanchan Mukhopadhyay. (2017) Dimorphic association of dopaminergic transporter gene variants with treatment outcome: Pilot study in Indian ADHD probands. Meta Gene 11, pages 64-69.
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Hang Su, Zhibin Li, Jiang Du, Haifeng Jiang, Zhikang Chen, Haiming Sun & Min Zhao. (2015) Predictors of heroin relapse: Personality traits, impulsivity, COMT gene Val158met polymorphism in a 5-year prospective study in Shanghai, China. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168:8, pages 712-719.
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