Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant. (Q43233918)

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13 February 2020

title

Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant (English)

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13 February 2020

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attention deficit hyperactivity disorder

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4

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13 February 2020

author name string

Haukur Pálmason

1

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13 February 2020

Dirk Moser

2

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13 February 2020

Jessica Sigmund

3

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13 February 2020

Susann Hänig

5

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13 February 2020

Anna Schneider

6

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13 February 2020

Christiane Seitz

7

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13 February 2020

Alexander Marcus

8

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13 February 2020

Jobst Meyer

9

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13 February 2020

Christine M Freitag

10

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13 February 2020

publication date

28 November 2009

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Journal of Neural Transmission

13 February 2020

published in

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13 February 2020

volume

117

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issue

2

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13 February 2020

page(s)

259-267

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On the distinction between attentional deficits/hyperactivity and conduct problems/aggression in child psychopathology

13 February 2020

cites work

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12 December 2020

Neurobiology of executive functions: catecholamine influences on prefrontal cortical functions

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Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study

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Maternal smoking and hyperactivity in 8-year-old children

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No association between low- and high-activity catecholamine-methyl-transferase (COMT) and attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children

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Catecholamines and aggression: the role of COMT and MAO polymorphisms.

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Determinants of low birth weight: methodological assessment and meta-analysis

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COMT Val108/158Met gene variant, birth weight, and conduct disorder in children with ADHD.

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Gene-environment interplay in relation to emotional and behavioral disturbance

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Further evidence of an association between maternal smoking during pregnancy and attention deficit hyperactivity disorder: findings from a high-risk sample of siblings

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[Reliability and validity of the Wender-Utah-Rating-Scale short form. Retrospective assessment of symptoms for attention deficit/hyperactivity disorder]

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Bizarre social behaviour in rats induced by a combination of a peripheral decarboxylase inhibitor and DOPA

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Dopamine Axon Varicosities in the Prelimbic Division of the Rat Prefrontal Cortex Exhibit Sparse Immunoreactivity for the Dopamine Transporter

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The role of lifestyle in preventing low birth weight.

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Cognitive and behavioral outcomes of school-aged children who were born preterm: a meta-analysis.

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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 phenotype

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Behavioral and neural consequences of prenatal exposure to nicotine

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Molecular genetics of attention-deficit/hyperactivity disorder

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The timing of child physical maltreatment: a cross-domain growth analysis of impact on adolescent externalizing and internalizing problems.

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Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior

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Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data

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Impact of executive function deficits and attention-deficit/hyperactivity disorder (ADHD) on academic outcomes in children

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No association between catechol-O-methyltransferase (COMT) gene polymorphism and attention deficit hyperactivity disorder (ADHD) in an Irish sample

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Hyperactivity and conduct problems as risk factors for adolescent development

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A functional single nucleotide polymorphism (V158M) in the COMT gene is associated with aggressive personality traits

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12 December 2020

Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

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12 December 2020

A simple salting out procedure for extracting DNA from human nucleated cells

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12 December 2020

Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder.

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12 December 2020

Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2

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12 December 2020

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome

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Executive functions in attention-deficit/hyperactivity disorder

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Psychiatric comorbidity associated with DSM-IV ADHD in a nonreferred sample of twins

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12 December 2020

Meta-analysis of association between a catechol-O-methyltransferase gene polymorphism and attention deficit hyperactivity disorder

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12 December 2020

Development of the alpha7 nicotinic cholinergic receptor in rat hippocampal formation

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12 December 2020

Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder

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12 December 2020

Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism

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12 December 2020

Failure to replicate an association between the catechol-O-methyltransferase polymorphism and attention deficit hyperactivity disorder in a second, independently recruited Israeli cohort

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Predictors of antisocial behaviour in children with attention deficit hyperactivity disorder.

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Impact of comorbid oppositional or conduct problems on attention-deficit hyperactivity disorder

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Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome

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[Tools for the diagnosis of attention-deficit/hyperactivity disorder in adults. Self-rating behaviour questionnaire and diagnostic checklist]

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

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The reliability of axis V of the multiaxial classification scheme.

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Early experience and serotonin transporter gene variation interact to influence primate CNS function

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[3H](-)nicotine binding sites in fetal human brain

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Inferring candidate genes for attention deficit hyperactivity disorder (ADHD) assessed by the World Health Organization Adult ADHD Self-Report Scale (ASRS).

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The Worldwide Prevalence of ADHD: A Systematic Review and Metaregression Analysis

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Schizotypy, attention deficit hyperactivity disorder, and dopamine genes

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Is fetal brain monoamine oxidase inhibition the missing link between maternal smoking and conduct disorders?

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Fetal growth and childhood behavioral problems: results from the ALSPAC cohort

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12 December 2020

Annotation: the role of prefrontal deficits, low autonomic arousal, and early health factors in the development of antisocial and aggressive behavior in children

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12 December 2020

Prenatal Smoking Exposure and Dopaminergic Genotypes Interact to Cause a Severe ADHD Subtype

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12 December 2020

Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.

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12 December 2020

Nicotinic acetylcholine receptors and nicotinic cholinergic mechanisms of the central nervous system

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12 December 2020

10.1007/S00702-009-0338-2

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19946713%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

13 February 2020

1050150548

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