The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD
- 15 January 2005
- journal article
- research article
- Published by Springer Nature in Experimental Brain Research
- Vol. 163 (3) , 352-360
- https://doi.org/10.1007/s00221-004-2180-y
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Genetic and Neurochemical Modulation of Prefrontal Cognitive Functions in ChildrenAmerican Journal of Psychiatry, 2004
- Enhancing the Sensitivity of a Sustained Attention Task to Frontal Damage: Convergent Clinical and Functional Imaging EvidenceNeurocase, 2003
- Dopaminergic System Genes in ADHD Toward a Biological HypothesisNeuropsychopharmacology, 2002
- Prefrontal blood flow dysregulation in drug naive ADHD children without structural abnormalitiesJournal Of Neural Transmission-Parkinsons Disease and Dementia Section, 2001
- Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity val allele with adhd impulsive-hyperactive phenotypeAmerican Journal of Medical Genetics, 1999
- Pharmacokinetics and Clinical Effectiveness of MethylphenidateClinical Pharmacokinetics, 1999
- Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in womenInternational Journal of Neuropsychopharmacology, 1999
- Sustained attention deficits in pat ients with right frontal lesionsNeuropsychologia, 1996
- Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disordersPharmacogenetics, 1996
- Frontal lesions and sustained attentionNeuropsychologia, 1987