Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders

Cited by (1,001)

Items 501–600 of 1,001

1. COMT polymorphisms as predictors of cognitive dysfunction during manic and mixed episodes in bipolar I disorder
   Márcio Gerhardt Soeiro‐de‐Souza, Rodrigo Machado‐Vieira, Danielle Soares Bio, Carolina Martins do Prado, Ricardo Alberto Moreno · 2012 · Bipolar Disorders
2. Inhibition of catechol-O-methyltransferase increases estrogen–DNA adduct formation
   Muhammad Zahid, MUHAMMAD KHALID SAEED, Fang Lu · 2007 · Free Radical Biology and Medicine
3. A Transposon in Comt Generates mRNA Variants and Causes Widespread Expression and Behavioral Differences among Mice
   Zhengsheng Li, Megan K. Mulligan, Xusheng Wang, Michael F. Miles, Lu Lu, Robert W. Williams · 2010 · PLoS ONE
4. The activity of catechol-O-methyltransferase (COMT) is not impaired by high doses of epigallocatechin-3-gallate (EGCG) in vivo
   Mario Lorenz, Friedemann Paul, Minoo Moobed, Gert Baumann, Benno F. Zimmermann, Karl Stangl, Verena Stangl · 2014 · European Journal of Pharmacology
5. Association of functional catechol O-methyl transferase (COMT) Val108Met polymorphism with smoking severity and age of smoking initiation in Chinese male smokers
   Song Guo, Da Fang Chen, Dong Feng Zhou, Hong Qiang Sun, Gui Ying Wu, Colin N. Haile, Therese A. Kosten, Thomas R. Kosten, Xiangyang Zhang · 2007 · Psychopharmacology
6. Catechol-O-methyltransferase and Monoamine Oxidase A Genotypes and Drug Response to Conventional Neuroleptics in Schizophrenia
   Ari Illi, Kari M. Mattila, Olli Kampman, Sami A. K. Anttila, Markus Roivas, Terho J. Lehtimäki, Esa V. J. Leinonen · 2003 · Journal of Clinical Psychopharmacology
7. No association between functional catechol O-methyl transferase 1947A>G polymorphism and smoking initiation, persistent smoking or smoking cessation
   Sean P. David, Elaine C Johnstone, Siân-Elin Griffiths, Michael F. Murphy, Patricia L Yudkin, David Mant, Robert T. Walton · 2002 · Pharmacogenetics
8. Genetics of affective disorders
   Carolina Hertzman Johansson, Mårten Jansson, Love Linnér, Qiuping Yuan, Nancy L. Pedersen, Douglas Blackwood, Nicholas Barden, John R. Kelsoe, Martin Schalling · 2001 · European Neuropsychopharmacology
9. Limited association between a catechol-O-methyltransferase (COMT) polymorphism and breast cancer risk in Japan
   Nobuyuki Hamajima, Keitaro Matsuo, Kazuo Tajima, M. Mizutani, Hiroji Iwata, Takuji Iwase, Shigeto Miura, H. Oya, Yuuki Obata · 2001 · International Journal of Clinical Oncology
10. Altered inhibition-related frontolimbic connectivity in obsessive–compulsive disorder
    van Velzen, Laura S., de Wit, Stella J., Ćurĉić‐Blake, Branislava, Cath, Daniëlle C., de Vries, Froukje E., Veltman, Dick J., van der Werf, Ysbrand D., van den Heuvel, Odile A. · 2015 · Human Brain Mapping
11. Imaging genetics of cognitive functions: Focus on episodic memory
    Björn Rasch, Andreas Papassotiropoulos, Dominique J.‐F. de Quervain · 2010 · NeuroImage
12. An association study of catechol-O-methyltransferase and monoamine oxidase A polymorphisms and personality traits in Koreans
    Se Joo Kim, Young Shin Kim, Shin Young Kim, Hong Shick Lee, Chan‐Hyung Kim · 2006 · Neuroscience Letters
13. Decreased Catecholamine Degradation Associates with Shock and Kidney Injury after Cardiac Surgery
    Anja Haase‐Fielitz, Michael Haase, Rinaldo Bellomo, Gavin William Lambert, George S. Matalanis, David Story, Laurie Doolan, Brian Buxton, Geoff A. Gutteridge, Friedrich Cameron Luft et al. · 2009 · Journal of the American Society of Nephrology
14. Catechol‐O‐methyltransferase val158met and cognitive function in Parkinson's disease
    Jeroen Hoogland, Rob M. A. de Bie, Caroline H. Williams‐Gray, D. Muslimović, Ben A. Schmand, Bart Post · 2010 · Movement Disorders
15. Monoamine Oxidase A (MAOA) and Catechol-O-Methyltransferase (COMT) Gene Polymorphisms Interact with Maternal Parenting in Association with Adolescent Reactive Aggression but not Proactive Aggression: Evidence of Differential Susceptibility
    Zhang, Wenxin, Cao, Cong, Wang, Meiping, Ji, Linqin, Cao, Yanmiao · 2016 · Journal of Youth and Adolescence
16. Depressive symptoms in schizophrenia and dopamine and serotonin gene polymorphisms
    Peitl, Vjekoslav, Štefanović, Mario, Karlović, Dalibor · 2017 · Progress in Neuro-Psychopharmacology and Biological Psychiatry
17. Genetic Association Between the COMT Genotype and Urinary Levels of Tea Polyphenols and Their Metabolites among Daily Green Tea Drinkers.
    Maki Inoue‐Choi, Jian‐Min Yuan, Chung Shu Yang · 2010 · PubMed
18. Performance on the Wisconsin Card Sorting Test in schizophrenia and genes of dopaminergic inactivation (COMT, DAT, NET).
    J. Rybakowski, A. Borkowska, P. Czerski, M. Dmitrzak-Węglarz, M. Skibińska, P. Kapelski, J. Hauser · 2006 · Psychiatry Research
19. Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome
    Thérèse van Amelsvoort, Janneke Zinkstok, Martijn Figee, Eileen Daly, Robin G. Morris, Michael John Owen, Kieran C. Murphy, Lieuwe de Haan, D.H. Linszen, Bronwyn Glaser et al. · 2007 · Psychological Medicine
20. Family-based association studies of monoaminergic gene polymorphisms among North Indians with schizophrenia
    Prachi Semwal, S Prasad, Triptish Bhatia · 2001 · Molecular Psychiatry
21. Ultradian rapid cycling in prepubertal and early adolescent bipolarity is not in transmission disequilibrium with val/met COMT alleles
    Barbara Geller, Edwin H. Cook · 2000 · Biological Psychiatry
22. Gene-sex interactions in schizophrenia: focus on dopamine neurotransmission
    Sean C. Godar, Marco Bortolato · 2014 · Frontiers in Behavioral Neuroscience
23. The Val/Met functional polymorphism in COMT confers susceptibility to bipolar disorder: evidence from an association study and a meta-analysis
    Zhao Zhang, Klaus Lindpaintner, Ronglin Che, Zangdong He, Peng Wang, Ping Yang, Guoyin Feng, Lin He, Yongyong Shi · 2009 · Journal of Neural Transmission
24. Dopamine receptor D4 gene variation predicts preschoolers’ developing theory of mind
    Christine L. Lackner, Mark A. Sabbagh, Elizabeth V. Hallinan, Xudong Liu, Jeanette J. A. Holden · 2011 · Developmental Science
25. Effects of Modafinil on the Sleep EEG Depend on Val158Met Genotype of COMT
    Sereina Bodenmann, Hans‐Peter Landolt · 2010 · SLEEP
26. Polymorphisms in the catechol‐ O ‐methyltransferase (COMT) gene influence plasma total homocysteine levels
    Elizabeth M. Tunbridge, Paul J. Harrison, Donald R. Warden, Carole Johnston, Helga Refsum, A. David Smith · 2008 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
27. Inhibition of catechol-Ο-methyltransferase activity in human breast cancer cells enhances the biological effect of the green tea polyphenol (-)-EGCG
    Dou · 2010 · Oncology Reports
28. Neurocognitive Profiles of Older Adults with Working-Memory Dysfunction
    Alireza Salami, Anna Rieckmann, Nina Karalija, Bárbara Avelar‐Pereira, Micael Andersson, Anders Wåhlin, Goran Papenberg, Douglas D. Garrett, Katrine Riklund, Martin Lövdén et al. · 2018 · Cerebral Cortex
29. Combined family trio and case‐control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa
    Mojca Gabrovsek, Marija Brecelj Anderluh, Laura Bellodi, Elena Cellini, Daniela Di Bella, Xavier Estivill, Fernando Fernández‐Aranda, Bernard Freeman, Frank Geller, Mónica Gratacòs et al. · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
30. Effects of several dioxin-like compounds on estrogen metabolism in the malignant MCF-7 and nontumorigenic MCF-10A human mammary epithelial cell lines
    Majorie B.M. van Duursen, J. Thomas Sanderson, Marieke van der Bruggen, Jeroen van der Linden, Martin van den Berg · 2003 · Toxicology and Applied Pharmacology
31. Manipulation of catechol-O-methyl-transferase (COMT) activity to influence the attenuation of substance seeking behavior, a subtype of Reward Deficiency Syndrome (RDS), is dependent upon gene polymorphisms: A hypothesis
    Kenneth Blum, Thomas J.H. Chen, Brian Meshkin, Roger L. Waite, Bernard William Downs, Seth H. Blum, Julie F. Mengucci, Vanessa Arcuri, Eric R. Braverman, Tomás Palomo · 2007 · Medical Hypotheses
32. Oligogenic combinations associated with breast cancer risk in women under 53�years of age
    Christopher E. Aston, David A. Ralph, Dominique Lalo, Sharmila Manjeshwar, Bobby A. Gramling, Daniele C. DeFreese, Amy D. West, Dannielle E. Branam, Linda F. Thompson, Melissa Craft et al. · 2004 · Human Genetics
33. Val158Met Polymorphism in catechol-O-methyltransferase gene associated with risk factors for breast cancer.
    Chi Chen Hong, Henry J. Thompson, Cheng Jiang, Geoffrey L. Hammond, David Tritchler, Martin J. Yaffe, Norman F. Boyd · 2003 · PubMed
34. Family‐based and case–control study of catechol‐O‐methyltransferase in schizophrenia among Palestinian Arabs
    Ilana Kremer, M. Pinto, Ibrahim Murad, M. Muhaheed, Issam Bannoura, D Müller, Thomas G. Schulze, Alon Reshef, Monica Blanaru, S. Gathas et al. · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
35. Relationship between the catechol-O-methyl transferase Val108/158Met genotype and brain volume in treatment-naive major depressive disorder: Voxel-based morphometry analysis
    Keita Watanabe, Shingo Kakeda, Reiji Yoshimura, Osamu Abe, Satoru Ide, Kenji Hayashi, Asuka Katsuki, Wakako Umene‐Nakano, Rieko Watanabe, Jun Nakamura et al. · 2015 · Psychiatry Research Neuroimaging
36. Estrogen pathway polymorphisms and mammographic density.
    Isabelle Dumas, Caroline Diorio · 2011 · PubMed
37. Unique features of breast cancer in Asian women—Breast cancer in Taiwan as an example
    Chiun‐Sheng Huang, Ching‐Hung Lin, Yen‐Shen Lu · 2010 · The Journal of Steroid Biochemistry and Molecular Biology
38. Gender‐specificCOMTVal158Met polymorphism association in Spanish schizophrenic patients
    Janet Hoenicka, Elena Garrido, Isabel Martínez, Guillermo Ponce, María Aragüés, Roberto Rodríguez–Jiménez, Laura España‐Serrano, Ximena Alvira, José Luis Santos, Gabriel Rubio et al. · 2009 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
39. Lack of Association of Alcohol Dependence and Habitual Smoking With Catechol‐O‐methyltransferase
    Tatiana Foroud, Leah Flury Wetherill, Danielle M. Dick, VICTOR M. HESSELBROCK, John I. Nürnberger, John Kramer, Jay A. Tischfield, Marc Alan Schuckit, Laura Jean Bierut, Xiaoling Xuei et al. · 2007 · Alcoholism Clinical and Experimental Research
40. Age‐specific association of steroid hormone pathway gene polymorphisms with breast cancer risk
    David A. Ralph, Lue Ping Zhao, Christopher E. Aston · 2007 · Cancer
41. Variation in the catechol-O-methyltransferase Val158Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents
    Colin G. DeYoung, Marya Getchell, Roman A. Koposov, Carolyn M. Yrigollen, Gerald J. Haeffel, Britt af Klinteberg, Lars Oreland, Vladislav V. Ruchkin, ANDREW J. PAKSTIS, Elena L. Grigorenko · 2009 · Psychiatric Genetics
42. Child exposure to serious life events, COMT, and aggression: Testing differential susceptibility theory.
    Hygen, Beate Wold, Belsky, Jay, Stenseng, Frode, Lydersen, Stian, Guzey, Ismail Cuneyt, Wichstrøm, Lars · 2015 · Developmental Psychology
43. Latent-Profile Analysis Reveals Behavioral and Brain Correlates of Dopamine-Cognition Associations
    Martin Lövdén, Nina Karalija, Micael Andersson, Anders Wåhlin, Jan Axelsson, Ylva Köhncke, Lars Stiernman Jonasson, Anna Rieckmann, Goran Papenberg, Douglas D. Garrett et al. · 2017 · Cerebral Cortex
44. Polymorphism in SNAP29 gene promoter region associated with schizophrenia
    Takuya Saito, F Guan, Demitri F. Papolos, N Rajouria, Cathy S.J. Fann, Herbert M. Lachman · 2001 · Molecular Psychiatry
45. Gene–gene interaction between MAOA and COMT in suicidal behavior: Analysis in schizophrenia
    Vincenzo De Luca, Subi Tharmalingam, Daniel J. Müller, Greg Wong, Andrea de Bartolomeis, James L. Kennedy · 2006 · Brain Research
46. COMT Val158Met and BDNF C270T polymorphisms in schizophrenia: a case-control study
    Silvana Galderisi, Mario Maj, Brian W Kirkpatrick et al. · 2004 · Schizophrenia Research
47. Association of the Catechol-O-Methyl Transferase Gene Val158Met Polymorphism With Blood Pressure and Prevalence of Hypertension: Interaction With Dietary Energy Intake
    Nay Chi Htun, Koichi Miyaki, Yaling Song · 2011 · American Journal of Hypertension
48. Cannabis controversies: how genetics can inform the study of comorbidity
    Arpana Agrawal A, Michael T. Lynskey · 2014 · Addiction
49. Association analysis of the COMT/MTHFR genes and geriatric depression: An MRI study of the putamen
    Chih‐Chuan Pan, Douglas R. McQuoid, Warren D. Taylor, Martha E. Payne, Allison E. Ashley‐Koch, David C. Steffens · 2009 · International Journal of Geriatric Psychiatry
50. Lack of Association of catechol-O-Methyltransferase Gene Polymorphism in Obsessive-Compulsive Disorder
    Mehmet Emin Erdal, Şenel Tot, Kemal Utku Yazıcı, Aylin Yazıcı, Hasan Herken, Pervin Erdem, Ebru Derici, Handan Çamdeviren Ankaralı · 2003 · Depression and Anxiety
51. Catechol-O-methyltransferase Val158Met polymorphism is associated with somatosensory amplification and nocebo responses
    Wendt, Laura, Albring, Antje, Benson, Sven, Engler, Harald, Engler, Andrea, Hinney, Anke, Rief, Winfried, Witzke, Oliver, Schedlowski, Manfred · 2014 · PLoS ONE
52. Association of COMT and COMT-DRD2 interaction with creative potential
    Shun Zhang, Muzi Zhang, Jinghuan Zhang · 2014 · Frontiers in Human Neuroscience
53. The effect of COMT Val158 Met genotype on decision-making and preliminary findings on its interaction with the 5-HTTLPR in healthy females
    Ruud van den Bos, Judith Regina Homberg, Ellen Gijsbers, Esther den Heijer, Edwin P. J. G. Cuppen · 2008 · Neuropharmacology
54. Design of Electrochemical Biosensor Systems for the Detection of Specific DNA Sequences in PCR-Amplified Nucleic Acids Related to the Catechol-O-methyltransferase Val108/158Met Polymorphism Based on Intrinsic Guanine Signal
    Dilsat Ozkan‐Ariksoysal, Burçin Tezcanlı Kaymaz, Buket Kosova, Mehmet Özsöz · 2008 · Analytical Chemistry
55. Interaction between gene variants of the serotonin transporter promoter region (5‐HTTLPR) and catechol O‐methyltransferase (COMT) in borderline personality disorder
    André Tadić, Anja Victor, Ömür Başkaya, Robert von Cube, Julia Höch, Ioanna Kouti, Nina J. Anicker, Wolfgang Höppner, Klaus Lieb, Norbert Dahmen · 2008 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
56. Aversive stimuli lead to differential amygdala activation and connectivity patterns depending on catechol-O-methyltransferase Val158Met genotype
    Björn Rasch, Klara Spalek, S. Buholzer, Roger Luechinger, Peter Boesiger, Dominique J.‐F. de Quervain, Andreas Papassotiropoulos · 2010 · NeuroImage
57. Effects of two dopamine-modulating genes (DAT1 9/10 and COMT Val/Met) on n-back working memory performance in healthy volunteers
    Mathieu M. Blanchard, Samuel R. Chamberlain, J. Roiser, Trevor W. Robbins, Ulrich Müller · 2010 · Psychological Medicine
58. Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands.
    M. Das, A. Das Bhowmik, N. Bhaduri, Kanyakumarika Sarkar, Paramita Ghosh, S. Sinha, Anirban Ray, A. Chatterjee, Kanchan Mukhopadhyay · 2011 · Progress in Neuro-psychopharmacology and Biological Psychiatry
59. COMT Val158Met and 5HTTLPR functional loci interact to predict persistence of anxiety across adolescence: results from the Victorian Adolescent Health Cohort Study
    Craig A. Olsson, Graham B Byrnes, Richard Anney, V. Collins, S. A. Hemphill, R. Williamson, George C. Patton · 2007 · Genes Brain & Behavior
60. Genetic features of antidepressant induced mania and hypo-mania in bipolar disorder
    Alessandro Serretti, Paola Artioli, Raffaella Zanardi, Cristina Lorenzi, David Rossini, Cristina Cusin, Alessia Arnoldi, Marco Catalano · 2004 · Psychopharmacology
61. A functional variant of the tryptophan hydroxylase 2 gene impacts working memory: A genetic imaging study
    Martin Reuter, Christine Esslinger, Christian Montag, Stefanie Lis, B. Gallhofer, Peter Kirsch · 2007 · Biological Psychology
62. Pharmacogenetics of lithium prophylaxis in mood disorders: Analysis of COMT, MAO‐A, and Gβ3 variants
    Alessandro Serretti, Cristina Lorenzi, Roberta Lilli, Laura Mandelli, Adele Pirovano, Enrico Smeraldi · 2002 · American Journal of Medical Genetics
63. Genetic modelling of the estrogen metabolism as a risk factor of hormone-dependent disorders
    J. Huber, Christian Schneeberger, Clemens Tempfer · 2002 · Maturitas
64. Reviewing pharmacogenetics to advance precision medicine for opioids
    Leen Magarbeh, Ilona Gorbovskaya, Bernard Le Foll, Reuven Jhirad, Daniel J. Müller · 2021 · Biomedicine & Pharmacotherapy
65. Adverse childhood experiences influence white matter microstructure in patients with schizophrenia
    Sara Poletti, Elena Beatrice Mazza, Irene Bollettini, Clara Locatelli, Roberto Cavallaro, Enrico Smeraldi, Francesco Benedetti · 2015 · Psychiatry Research Neuroimaging
66. Dopamine 2 receptor C957T and catechol-o-methyltransferase Val158Met polymorphisms are associated with treatment response in electroconvulsive therapy
    Kaija Huuhka, Sami A. K. Anttila, Martti Huuhka, Jarmo A. Hietala, Heini Huhtala, Nina Mononen, Terho J. Lehtimäki, Esa V. J. Leinonen · 2008 · Neuroscience Letters
67. The impact of COMT gene polymorphisms on suicidality in treatment resistant major depressive disorder — A European Multicenter Study
    Alexandra Schosser, Raffaella Calati, Alessandro Serretti, Isabelle Massat, Neslihan Aygün Kocabaş, K. Papageorgiou, Sylvie Linotte, Julien Mendlewicz, Daniel Souery, Joseph Zohar et al. · 2011 · European Neuropsychopharmacology
68. An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD
    A. Boonstra, J. J. Sandra Kooij, J. Buitelaar, J. Oosterlaan, J. Sergeant, J. G. A. M. Angelien Heister, B. Franke · 2008 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
69. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism
    Stephan Klebe, Jean‐Louis Golmard, Mike A. Nalls, Mohamad Saad, Andrew Singleton, José Brás, John Hardy, Javier Simón‐Sánchez, Peter Heutink, Gregor Kuhlenbäumer et al. · 2013 · Journal of Neurology Neurosurgery & Psychiatry
70. Modulation of impulsivity and reward sensitivity in intertemporal choice by striatal and midbrain dopamine synthesis in healthy adults
    Christopher T. Smith, Deanna L. Wallace, Linh C. Dang, Esther Aarts, William J. Jagust, Mark D’Esposito, Charlotte A. Boettiger · 2015 · Journal of Neurophysiology
71. Clinical and genetic factors associated with suicide in mood disorder patients
    N. Antypa, D. Souery, Mario Tomasini, D. Albani, Federica Fusco, J. Mendlewicz, A. Serretti · 2016 · European Archives of Psychiatry and Clinical Neuroscience
72. Pharmacogenetics-guided analgesics in major abdominal surgery: Further benefits within an enhanced recovery protocol
    Anthony J. Senagore, Bradley J. Champagne, Eslam Dosokey · 2016 · The American Journal of Surgery
73. Investigational and Experimental Drugs to Treat Obsessive-Compulsive Disorder
    Grassi, Giacomo, Cecchelli, Chiara, Vignozzi, Luisa, Pacini, Silvia · 2021 · Journal of Experimental Pharmacology
74. A Comprehensive Review of the Genetic and Epigenetic Contributions to the Development of Fibromyalgia
    Erik A. Ovrom, Karson Mostert, Shivani Khakhkhar, Daniel P. McKee, Padao Yang, Yeng F Her · 2023 · Biomedicines
75. Catechol-O-methyltransferase: characteristics, polymorphisms and role in breast cancer
    James D. Yager · 2012 · Drug Discovery Today Disease Mechanisms
76. Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes
    Patricia A. Brennan, Constance L. Hammen, Patrick D. Sylvers, William Bor, Jake Moses Najman, Penelope A. Lind, Grant W. Montgomery, Alicia K. Smith · 2011 · Biological Psychology
77. MAO-A and COMT genotypes as possible regulators of perinatal serotonergic symptoms after in utero exposure to SSRIs
    Johanna Hilli, Tuija Heikkinen, Riikka Rontu, Terho J. Lehtimäki, Ikuko Kishida, Eleni Aklillu, Leif Bertilsson, Tero J. Vahlberg, Kari Laine · 2009 · European Neuropsychopharmacology
78. Proteasome inhibition in human breast cancer cells with high catechol-O-methyltransferase activity by green tea polyphenol EGCG analogs
    Congde Huo, Huanjie Yang, Qiuzhi Cindy Cui · 2009 · Bioorganic & Medicinal Chemistry
79. Early Institutionalization: Neurobiological Consequences and Genetic Modifiers
    Margaret A. Sheridan, Stacy S. Drury, Katie A. McLaughlin, Alisa N. Almas · 2010 · Neuropsychology Review
80. Modeling neurodevelopmental cognitive deficits in tasks with cross‐species translational validity
    Zackary A. Cope, Susan B. Powell, Jared W. Young · 2015 · Genes Brain & Behavior
81. Expression of multiple catechol‐o‐methyltransferase (COMT) mRNA variants in human brain
    Elizabeth M. Tunbridge, Tracy A. Lane, Paul J. Harrison · 2007 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
82. Genetic polymorphisms in dopamine-related genes and smoking cessation in women: a prospective cohort study
    Thanh G.N. Ton, Mary Anne Rossing, Deborah J. Bowen, Sengkeo Srinouanprachan, Kristine G. Wicklund, Federico M. Farin · 2007 · Behavioral and Brain Functions
83. Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario
    Laurent Briollais, Yuanyuan Wang, Isaac Rajendram, Venus Onay, Ellen Shi, Julia A. Knight, Hilmi Özçelik · 2007 · BMC Medicine
84. No evidence of association between Catechol-O-Methyltransferase (COMT) Val 158 Met genotype and performance on neuropsychological tasks in children with ADHD: A case-control study
    Sophie Mills, K. Langley, Marianne B. M. van den Bree, Eddy Street, Darko Turic, Michael John Owen, Michael C. O’Donovan, Anita Thapar · 2004 · BMC Psychiatry
85. Pharmacogenetics: inherited variation in amino acid sequence and altered protein quantity*1
    Richard M. Weinshilboum · 2004 · Clinical Pharmacology & Therapeutics
86. Association between the low activity genotype of catechol-O-methyltransferase and myocardial infarction in a hypertensive population
    Anna‐Lena Eriksson · 2004 · European Heart Journal
87. Generation and Characterization of Humanized Mice Carrying COMT158 Met/Val Alleles
    Victoria B. Risbrough, Baohu Ji, Richard Hauger, Xianjin Zhou · 2014 · Neuropsychopharmacology
88. Catechol-O-methyl transferase and schizophrenia.
    Marina Šagud, Dorotea Mück‐Šeler, Alma Mihaljević-Peleš, Bjanka Vuksan‐Ćusa, Maja Živković, Miro Jakovljević, Nela Pivac · 2010 · PubMed
89. Catechol‐O‐methyltransferase Val 158 Met genotype, parenting practices and adolescent alcohol use: testing the differential susceptibility hypothesis
    Manfred Laucht, Dorothea Blomeyer, Arlette F. Buchmann, Jens Treutlein, Martin H. Schmidt, Günter Esser, Christine Jennen-Steinmetz, Marcella Rietschel, Ulrich S. Zimmermann, Tobias Banaschewski · 2011 · Journal of Child Psychology and Psychiatry
90. Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults
    Wolfgang Retz, Michael Rösler, Christian Kissling, Stefan Wiemann, Regina Hünnerkopf, Andrew N. Coogan, Johannes Thome, Christine Margarete Freitag · 2007 · Journal of Neural Transmission
91. The association of genetic polymorphisms in serotonin transporter and catechol‐O‐methyltransferase on temporomandibular disorders and anxiety in adolescents
    João Armando Brancher, Paula Porto Spada, Michelle Nascimento Meger, Aluhê Lopes Fatturi, Mariana Dalledone, Fernanda Mara de Paiva Bertoli, Kathleen B. Deeley, Rafaela Scariot, Alexandre Rezende Vieira, Érika Calvano Küchler et al. · 2019 · Journal of Oral Rehabilitation
92. The Role of Tryptophan and Tyrosine in Executive Function and Reward Processing
    Luca Aquili · 2020 · International Journal of Tryptophan Research
93. Adrenergic signalling in osteoarthritis
    Rebecca E. Sohn, Gundula Rösch, Marius Junker, Andrea Meurer, Frank Zaucke, Zsuzsa Jenei‐Lanzl · 2021 · Cellular Signalling
94. Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant
    Pálmason, Haukur, Moser, Dirk, Sigmund, Jessica, Vogler, Christian, Hänig, Susann, Schneider, Anna, Seitz, Christiane, Marcus, Alexander, Meyer, Jobst, Freitag, Christine M. · 2010 · Journal of Neural Transmission
95. Association study of a functional catechol- O-methyltransferase (COMT) Val108/158Met polymorphism and suicide attempts in patients with alcohol dependence
    Gordana Nedić Erjavec, Matea Nikolac Perković, Korona Nenadić Šviglin, Dorotea Mück‐Šeler, Fran Borovečki, Nela Pivac · 2010 · The International Journal of Neuropsychopharmacology
96. Interaction between COMT Val158Met polymorphism and childhood adversity affects reward processing in adulthood
    Boecker-Schlier, Regina, Holz, Nathalie E., Buchmann, Arlette F., Blomeyer, Dorothea, Plichta, Michael M., Jennen-Steinmetz, Christine, Wolf, Isabella, Baumeister, Sarah, Treutlein, Jens, Rietschel, Marcella et al. · 2016 · NeuroImage
97. Clinical and genetic characteristics of Korean male alcoholics with and without attention deficit hyperactivity disorder
    KIM, JAE-WON, PARK, CHURL-SOO, HWANG, JUN-WON, SHIN, MIN-SUP, HONG, KANG-E, CHO, SOO-CHURL, KIM, BOONG-NYUN · 2006 · Alcohol and Alcoholism
98. Task demands, tDCS intensity, and the COMT val158met polymorphism impact tDCS-linked working memory training gains
    Stephens, Jaclyn A., Jones, Kevin T., Berryhill, Marian E. · 2017 · Scientific Reports
99. The Minnesota Green Tea Trial (MGTT), a randomized controlled trial of the efficacy of green tea extract on biomarkers of breast cancer risk: study rationale, design, methods, and participant characteristics
    Hamed Samavat, Allison M. Dostal, Renwei Wang et al. · 2015 · Cancer Causes & Control
100. Sleep and COMT Polymorphism in ADHD Children: Preliminary Actigraphic Data
     Reut Gruber, Natalie Grizenko, George J. Schwartz, Leila Ben Amor, Julie Gauthier, Rosherrie de Guzman, Ridha Joober · 2006 · Journal of the American Academy of Child & Adolescent Psychiatry