Complex multilocus effects of catechol-O-methyltransferase haplotypes predict pain and pain interference 6 weeks after motor vehicle collision (Q37624141)

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scientific article published on 21 August 2013

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English	Complex multilocus effects of catechol-O-methyltransferase haplotypes predict pain and pain interference 6 weeks after motor vehicle collision	scientific article published on 21 August 2013

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scholarly article

1 reference

Europe PubMed Central

21 August 2017

Complex multilocus effects of catechol-O-methyltransferase haplotypes predict pain and pain interference 6 weeks after motor vehicle collision (English)

1 reference

Europe PubMed Central

21 August 2017

Samuel A McLean

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Samuel A McLean

3

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Andrey V Bortsov

1

1 reference

Europe PubMed Central

21 August 2017

Luda Diatchenko

2

1 reference

Europe PubMed Central

21 August 2017

publication date

21 August 2013

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Europe PubMed Central

21 August 2017

NeuroMolecular Medicine

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Europe PubMed Central

21 August 2017

16

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Europe PubMed Central

21 August 2017

1

1 reference

Europe PubMed Central

21 August 2017

83-93

1 reference

Europe PubMed Central

21 August 2017

https://scigraph.springernature.com/pub.10.1007/s12017-013-8255-9

0 references

The catechol-O-methyltransferase gene (COMT) and cognitive function from childhood through adolescence

1 reference

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23 August 2017

Potential genetic risk factors for chronic TMD: genetic associations from the OPPERA case control study

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23 August 2017

Using emergency department-based inception cohorts to determine genetic characteristics associated with long term patient outcomes after motor vehicle collision: methodology of the CRASH study

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23 August 2017

Effects of catechol-O-methyltransferase on normal variation in the cognitive function of children

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23 August 2017

Biopsychosocial influence on exercise-induced delayed onset muscle soreness at the shoulder: pain catastrophizing and catechol-o-methyltransferase (COMT) diplotype predict pain ratings.

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23 August 2017

Haplotype associations with quantitative traits in the presence of complex multilocus and heterogeneous effects

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23 August 2017

Polymorphisms of the serotonin-2A receptor and catechol-O-methyltransferase genes: a study on fibromyalgia susceptibility

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A network of dopaminergic gene variations implicated as risk factors for schizophrenia

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Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia

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23 August 2017

Responses to Drs. Kim and Dionne regarding comments on Diatchenko, et al. Catechol-O-methyltransferase gene polymorphisms are associated with multiple pain-evoking stimuli. Pain 2006; 125: 216-24.

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23 August 2017

Evidence for a biopsychosocial influence on shoulder pain: pain catastrophizing and catechol-O-methyltransferase (COMT) diplotype predict clinical pain ratings.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3946256

23 August 2017

Catechol-O-methyltransferase inhibition increases pain sensitivity through activation of both beta2- and beta3-adrenergic receptors

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23 August 2017

Association of the functional catechol-O-methyltransferase VAL158MET polymorphism with the personality trait of extraversion

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23 August 2017

Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies

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23 August 2017

Core outcome measures for chronic pain clinical trials: IMMPACT recommendations

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23 August 2017

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain

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23 August 2017

Haploview: analysis and visualization of LD and haplotype maps

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23 August 2017

COMT val158met genotype affects mu-opioid neurotransmitter responses to a pain stressor

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23 August 2017

A highly significant association between a COMT haplotype and schizophrenia.

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23 August 2017

Haplotype inference in random population samples.

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23 August 2017

The structure of haplotype blocks in the human genome

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23 August 2017

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

1 reference

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23 August 2017

Pain assessment: global use of the Brief Pain Inventory

1 reference

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23 August 2017

Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme

1 reference

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23 August 2017

The American College of Rheumatology 1990 Criteria for the Classification of Fibromyalgia. Report of the Multicenter Criteria Committee

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23 August 2017

Membrane-bound catechol-O-methyltransferase: a reevaluation of its role in the O-methylation of the catecholamine neurotransmitters

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23 August 2017

Importance of the COMT gene for sex differences in brain function and predisposition to psychiatric disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3946256

6 September 2017

Validation of a verbally administered numerical rating scale of acute pain for use in the emergency department

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3946256

14 September 2017

COMT haplotypes suggest P2 promoter region relevance for schizophrenia.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3946256

14 September 2017

Human catechol-O-methyltransferase down-regulation by estradiol

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14 September 2017

The COMT rs4680 Met allele contributes to long-lasting low back pain, sciatica and disability after lumbar disc herniation.

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The relationship between a common catechol-O-methyltransferase (COMT) polymorphism val(158) met and fibromyalgia.

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1 September 2018

The role of the COMT Val(158)Met polymorphism in the phenotypic expression of obsessive-compulsive disorder.

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1 September 2018

Re: the use of inferred haplotypes in downstream analysis

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3946256

1 September 2018

The met(158) allele of catechol-O-methyltransferase (COMT) is associated with obsessive-compulsive disorder in men: case-control study and meta-analysis.

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1 September 2018

Gene-gene effects on central processing of aversive stimuli.

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1 September 2018

Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3946256

1 September 2018

Impact of complex genetic variation in COMT on human brain function.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3946256

1 September 2018

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3946256

1 September 2018

Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3946256

1 September 2018

No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain

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https://api.crossref.org/works/10.1007%2FS12017-013-8255-9

21 January 2018

Genetic variation in the beta2-adrenergic receptor but not catecholamine-O-methyltransferase predisposes to chronic pain: Results from the 1958 British Birth Cohort Study

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https://api.crossref.org/works/10.1007%2FS12017-013-8255-9

21 January 2018

Validity of the brief pain inventory for use in documenting the outcomes of patients with noncancer pain

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12 December 2020

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A functional polymorphism in the catechol-O-methyltransferase gene is associated with osteoarthritis-related pain

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Identifiers

10.1007/S12017-013-8255-9

1 reference

Europe PubMed Central

21 August 2017

1 reference

Europe PubMed Central

21 August 2017

1 reference

Europe PubMed Central

21 August 2017

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