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

No abstract is available for this paper.

• Publication year

  2000

• Venue

  American journal of medical genetics

• Publication date

  2000-06-12

• Fields of study

  Medicine, Psychology

• Identifiers
  DOI 10.1002/1096-8628(20000612)96:3<285::AID-AJMG10>3.0.CO;2-DPMID 10898901
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• 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.

  1999cited by this paper
• Genetic basis of attention deficit and hyperactivity

  1999cited by this paper
• A logistic regression extension of the transmission disequilibrium test for continuous traits: Application to linkage disequilibrium between alcoholism and the candidate genes DRD2 and ADH3

  1999cited by this paper
• Mapping susceptibility loci in attention deficit hyperactivity disorder: preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children

  1999cited by this paper
• Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity.

  1999cited by this paper
• Dopamine D4 gene 7-repeat allele and attention deficit hyperactivity disorder.

  1999cited by this paper
• Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severity.

  1998cited by this paper
• Charting some challenges in the art and science of nursing.

  1998cited by this paper
• Attention-deficit hyperactivity disorder and hyperkinetic disorder

  1998cited by this paper
• Dopamine DRD4 receptor polymorphism and attention deficit hyperactivity disorder

  1998cited by this paper
• Association of the dopamine receptor D4 (DRD4) gene with a refined phenotype of attention deficit hyperactivity disorder (ADHD): a family-based approach

  1998cited by this paper
• Evidence that the dopamine D4 receptor is a susceptibility gene in attention deficit hyperactivity disorder

  1998cited by this paper
• Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data.

  1997cited by this paper
• Confirmation of association between attention deficit hyperactivity disorder and a dopamine transporter polymorphism

  1997cited by this paper
• National Institute of Mental Health Collaborative Multimodal Treatment Study of Children with ADHD (the MTA). Design challenges and choices.

  1997cited by this paper
• The TDT and other family-based tests for linkage disequilibrium and association.

  1996cited by this paper
• Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

  1996cited by this paper
• Dopamine D4 receptor gene polymorphism is associated with attention deficit hyperactivity disorder.

  1996cited by this paper
• Hyperactivity and conduct problems as risk factors for adolescent development.

  1996cited by this paper
• The transmission/disequilibrium test: history, subdivision, and admixture.

  1995cited by this paper
• Association of attention-deficit disorder and the dopamine transporter gene.

  1995cited by this paper
• Modulation of Intracellular Cyclic AMP Levels by Different Human Dopamine D4 Receptor Variants

  1995cited by this paper
• Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme.

  1995cited by this paper
• Dominant inheritance in two families with familial Mediterranean fever (FMF).

  1995cited by this paper
• Dopamine D4 receptor repeat: analysis of different native and mutant forms of the human and rat genes.

  1994cited by this paper
• Comparison of statistics for candidate-gene association studies using cases and parents.

  1994cited by this paper
• Genotype relative risks: methods for design and analysis of candidate-gene association studies.

  1993cited by this paper
• Further evidence for family-genetic risk factors in attention deficit hyperactivity disorder. Patterns of comorbidity in probands and relatives psychiatrically and pediatrically referred samples.

  1992cited by this paper
• Manual for the child behavior checklist/4-18 and 1991 profile

  1991cited by this paper
• Family-genetic and psychosocial risk factors in DSM-III attention deficit disorder.

  1990cited by this paper
• Topography of cognition: parallel distributed networks in primate association cortex.

  1988cited by this paper
• Urinary 3-methoxy-4-hydroxyphenylglycol sulfate excretion in seventy-three schoolchildren with minimal brain dysfunction syndrome.

  1984cited by this paper
• Urinary 3-methoxy-4-hydroxyphenylglycol sulfate excretion in seventy-three schoolchildren with minimal brain dysfunction syndrome.

  1984cited by this paper
• Phenylethylamine excretion in attention deficit disorder.

  1984cited by this paper
• CSF monoamine metabolites in children with minimal brain dysfunction: evidence for alteration of brain dopamine. A preliminary report.

  1977cited by this paper
• Psychiatric illness in the families of hyperactive children.

  1972cited by this paper

• 2 Scanning the Genome for Attention Deficit Hyperactivity Disorder

  2019cites this paper
• Attention Deficit Hyperactivity Disorder and Genetics

  2018cites this paper
• Genetic Variations in Attention Deficit Hyperactivity Disorder Subtypes and Treatment Resistant Cases

  2016cites this paper
• The Effect of Single Dose Methylphenidate on Neurometabolites according to COMT Gene Val158Met Polymorphism in the Patient with Attention Deficit Hyperactivity Disorder: A Study Using Magnetic Resonance Spectroscopy

  2016cites this paper
• of attention-deficit / hyperactivity disorder : the search for endophenotypes . Nat Rev Neurosci

  2015cites this paper
• Working Memory Deficits and Emotion Dysregulation in Youth with Attention-Deficit/Hyperactivity Disorder: Understanding Relationships and Treatment Implications

  2015cites this paper
• No association between catechol-O-methyltransferase (COMT) genotype and attention deficit hyperactivity disorder (ADHD) in Japanese children.

  2014cites this paper
• Attention-deficit/hyperactivity disorder.

  2012cites this paper
• Dikkat Eksikliği Hiperaktivite Bozukluğunun Genetik Boyutu

  2011cites this paper
• Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant

  2010cites this paper
• CAPÍTULO 2 – GENÉTICA DEL TDAH

  2010cites this paper
• Association Between Catechol-O-Methyltransferase Gene Polymorphism and Attention-Deficit Hyperactivity Disorder in Korean Population

  2009cites this paper
• Candidate gene studies of ADHD: a meta-analytic review

  2009cites this paper
• Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A

  2009cites this paper
• COMT Val108/158Met Polymorphism and the Modulation of Task-Oriented Behavior in Children with ADHD

  2008cites this paper
• Catechol‐O‐methyltransferase Val158Met polymorphism is associated with methylphenidate response in ADHD children

  2008cites this paper
• Association of the catechol-O-methyltransferase polymorphism with methylphenidate response in a classroom setting in children with attention-deficit hyperactivity disorder

  2008cites this paper
• Endophenotypes and genetic risk factors for psychosis

  2007cites this paper
• Evaluation of potential gene–gene interactions for attention deficit hyperactivity disorder in the Han Chinese population

  2007cites this paper
• Pharmacogenomics versus Aetiology in ADHD

  2007cites this paper
• Neurobiologie hyperkinetické poruchy

  2007cites this paper
• What do Dopamine Transporter and Catechol-O-Methyltransferase Tell us About Attention Deficit–Hyperactivity Disorder? Pharmacogenomic Implications

  2007cites this paper
• Functional polymorphisms in dopamine and serotonin pathway genes

  2006cites this paper
• Molecular genetic studies of ADHD: 1991 to 2004

  2006cites this paper
• Two candidate gene polymorphisms in ADHD children: a case-control study of catechol-O-methyltransferase (COMT) and monoamine oxidase B (MAOB) genes

  2006cites this paper
• Candidate gene studies of attention-deficit/hyperactivity disorder.

  2006cites this paper
• The genetics of attention deficit hyperactivity disorder.

  2006cites this paper
• Meta-analysis of Association Between a Catechol-O-Methyltransferase Gene Polymorphism and Attention Deficit Hyperactivity Disorder

  2006cites this paper
• Association of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sample

  2005cites this paper
• Molecular genetics of attention-deficit/hyperactivity disorder.

  2005cites this paper
• The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD

  2005cites this paper
• [Meta-analysis of candidate genes in attention-deficit hyperactivity disorder].

  2005cites this paper
• A family based study of catechol‐O‐methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD)

  2005cites this paper
• Scanning the Genome for Attention Deficit Hyperactivity Disorder

  2005cites this paper
• Méta-analyse des gènes candidats dans le trouble déficit attentionnel avec hyperactivité (TDAH)

  2005cites this paper
• The Catechol-O-Methyltransferase Polymorphism: Relations to the Tonic–Phasic Dopamine Hypothesis and Neuropsychiatric Phenotypes

  2004cites this paper
• Attention-Deficit Hyperactivity Disorder (ADHD)

  2004cites this paper
• Molecular genetics of attention-deficit hyperactivity disorder (ADHD): an update.

  2004cites this paper
• The Etiology of ADHD: Behavioral and Molecular Genetic Approaches

  2004cites this paper
• Genetics of adult attention-deficit/hyperactivity disorder.

  2004cites this paper
• Attention deficit/hyperactivity disorder (ADHD): Complex phenotype, simple genotype?

  2004cites this paper
• No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: A case-control study

  2004cites this paper
• Family‐based and case‐control association studies of catechol‐O‐methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism

  2003cites this paper
• Attention deficit and hyperactivity disorder: review of genetic association studies.

  2003cites this paper
• Attention deficit hyperactivity disorder: new genetic findings, new directions

  2003cites this paper
• Dopamine genes and attention-deficit hyperactivity disorder: a review.

  2003cites this paper
• Recent genetic advances in ADHD and diagnostic and therapeutic prospects

  2003cites this paper
• Genes de suscetibilidade no transtorno de déficit de atenção e hiperatividade

  2002cites this paper
• Significance of Serotonin Transporter Gene 5-HTTLPR and Variable Number of Tandem Repeat Polymorphism in Attention Deficit Hyperactivity Disorder

  2002cites this paper
• Dopaminergic System Genes in ADHD: Toward a Biological Hypothesis

  2002cites this paper
• PATHOPHYSIOLOGY OF ATTENTION-DEFICIT / HYPERACTIVITY DISORDER

  2002cites this paper
• Neuroscience of attention-deficit/hyperactivity disorder: the search for endophenotypes

  2002cites this paper
• Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study.

  2001cites this paper
• The nature and heritability of attention-deficit/hyperactivity disorder.

  2001cites this paper
• Nature, Nurture, and Attention Deficit Hyperactivity Disorder

  2000cites this paper