(Q24794008)

English

No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study

scientific article

No evidence of association between Catechol-O-Methyltransferase (COMT) Val 158 Met genotype and performance on neuropsychological tasks in children with ADHD: A case-control study

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scholarly article

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No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study (English)

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neuropsychology

1 reference

based on heuristic

inferred from title

object named as

Kate Langley

2

0 references

Marianne Bernadette van den Bree

object named as

Marianne Van den Bree

3

0 references

object named as

Anita Thapar

8

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Michael C O'Donovan

object named as

Michael C O'Donovan

7

0 references

1

object named as

Sophie Mills

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5

object named as

Darko Turic

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author name string

Eddy Street

4

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Michael J Owen

6

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language of work or name

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publication date

2004

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4

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1

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15

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Assessing the molecular genetics of attention networks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

7 April 2017

Behavioral inhibition, sustained attention, and executive functions: constructing a unifying theory of ADHD

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

7 April 2017

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

7 April 2017

Neuropsychological analyses of impulsiveness in childhood hyperactivity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

28 September 2017

Hypofrontality in attention deficit hyperactivity disorder during higher-order motor control: a study with functional MRI.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

28 September 2017

Genetic basis of attention deficit and hyperactivity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

28 September 2017

Implication of right frontostriatal circuitry in response inhibition and attention-deficit/hyperactivity disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

28 September 2017

Is the Continuous Performance Task a valuable research tool for use with children with Attention-Deficit-Hyperactivity Disorder?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

28 September 2017

A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-4-15

21 January 2018

Neurocognitive correlates of the COMT Val(158)Met polymorphism in chronic schizophrenia.

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-4-15

21 January 2018

Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-4-15

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-4-15

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-4-15

21 January 2018

The Child Attention-Deficit Hyperactivity Disorder Teacher Telephone Interview (CHATTI): reliability and validity

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-4-15

21 January 2018

When is "impulsiveness" not impulsive? The case of hyperactive children's cognitive style.

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-4-15

21 January 2018

Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis.

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-4-15

21 January 2018

Cellular and subcellular localization of the dopamine transporter in rat cortex.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

28 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=425584

28 November 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15182372

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/15182372

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Universal SNP genotyping assay with fluorescence polarization detection

1 reference

https://pubmed.ncbi.nlm.nih.gov/15182372

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Child and Adolescent Psychiatric Assessment (CAPA)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15182372

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15182372

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-244X-4-15

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1186/1471-244X-4-15

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Dimensions Publication ID

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1471-244x-4-15

PMC publication ID

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PubMed publication ID

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