The role of COMT gene variants in depression: Bridging neuropsychological, behavioral and clinical phenotypes-Reference-Cited by-同舟云学术

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The role of COMT gene variants in depression: Bridging neuropsychological, behavioral and clinical phenotypes

Published:2013-09 Issue:8 Volume:37 Page:1597-1610
ISSN:0149-7634
Container-title:Neuroscience & Biobehavioral Reviews
language:en
Short-container-title:Neuroscience & Biobehavioral Reviews

Author:

Antypa Niki,Drago Antonio,Serretti Alessandro

Funder

Netherlands Organization for Scientific Research and the Marie Curie Cofund Action

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Cognitive Neuroscience,Neuropsychology and Physiological Psychology

Reference137 articles.

1. Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder;Abdolmaleky;Hum. Mol. Genet.,2006

2. The functional Val158Met polymorphism in catechol-O-methyltransferase (COMT) is associated with depression and motivation in men from a Swedish population-based study;Aberg;J. Affect. Disord.,2011

3. Analysis of COMT gene (Val 158 Met polymorphism) in the clinical response to SSRIs in depressive patients of European origin;Arias;J. Affect. Disord.,2006

4. A neuropsychological theory of positive affect and its influence on cognition;Ashby;Psychol. Rev.,1999

5. Enzymatic O-methylation of epinephrine and other catechols;Axelrod;J. Biol. Chem.,1958

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