catechol-O-methyltransferase COMT gene
Catechol-O-Methyltransferase (COMT) Gene (Val158Met) and Brain-Derived Neurotropic Factor (BDNF) (Val66Met) Genes Polymorphism in Schizophrenia: A Case-Control Study
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Original Article Association of catechol-O-methyltransferase val158Met polymorphism with postoperative analgesic opioid use
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Depression and anxiety in relation to catechol O methyltransferase Val158Met genotype in the general population: The Nord Trøndelag Health Study (HUNT)
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<em>COMT </em>Val158Met, but not <em>BDNF </em>Val66Met, is associated with white matter abnormalities of the temporal lobe in patients with first-episode, treatment-naïve major depressive disorder: a diffusion tensor imaging study
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The influence of dopamine-beta-hydroxylase and catechol O-methyltransferase gene polymorphism on the efficacy of insulin detemir therapy in patients with type 2 diabetes mellitus
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Original Article Meta-analysis reveals a lack of association between a common catechol-O-methyltransferase (COMT) polymorphism val 158 met and fibromyalgia
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No association between chronic musculoskeletal complaints and Val158Met polymorphism in the Catechol O methyltransferase gene The HUNT study
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Genetic Analysis of Mu and Kappa Opioid Receptor and COMT Enzyme in Cancer Pain Tunisian Patients Under Opioid Treatment
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Identifying molecular mechanisms of catechol o-methyltransferase activity and regulation
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The association between headache and Val158Met polymorphism in the catechol–O–methyltransferase gene: the HUNT Study
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Identification of candidate genes associated with fibromyalgia susceptibility in southern Spanish women: the al Ándalus project
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Effect of minor SNPs on enzymatic activity regulated by common human haplotypes of the catechol-O-methyltransferase gene
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Association between Catechol-O-methyltransferase rs4680 (G > A) polymorphism and lung cancer risk
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Stress, COMT polymorphisms, and depressive symptoms in older Australian women: an exploratory study
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Roles of functional catechol O methyltransferase genotypes in Chinese patients with Parkinson’s disease
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Catechol-<em>O</em>-methyltransferase Val158Met genotype and the clinical responses to duloxetine treatment or plasma levels of 3-methoxy-4-hydroxyphenylglycol and homovanillic acid in Japanese patients with major depressive disorder
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Look beyond Catechol-O-Methyltransferase genotype for cathecolamines derangement in migraine: the BioBIM rs4818 and rs4680 polymorphisms study
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Genetic contribution of catechol O methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study
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Catechol O methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia
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Linkage studies of catechol O methyltransferase (COMT) and dopamine beta hydroxylase (DBH) cDNA expression levels
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