(Q37374588)

English

Genetic variants associated with development of TMD and its intermediate phenotypes: the genetic architecture of TMD in the OPPERA prospective cohort study.

scientific article published on December 2013

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1 March 2020

Genetic variants associated with development of TMD and its intermediate phenotypes: the genetic architecture of TMD in the OPPERA prospective cohort study (English)

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1 March 2020

The Journal of Pain

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1 March 2020

T91-101.e1-3

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1 March 2020

Psychological factors associated with development of TMD: the OPPERA prospective cohort study.

1 reference

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6 September 2017

Pain sensitivity and autonomic factors associated with development of TMD: the OPPERA prospective cohort study.

1 reference

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6 September 2017

General health status and incidence of first-onset temporomandibular disorder: the OPPERA prospective cohort study

1 reference

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6 September 2017

Clinical orofacial characteristics associated with risk of first-onset TMD: the OPPERA prospective cohort study

1 reference

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6 September 2017

Study protocol, sample characteristics, and loss to follow-up: the OPPERA prospective cohort study

1 reference

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6 September 2017

GCH1-polymorphism and pain sensitivity among women with provoked vestibulodynia

1 reference

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6 September 2017

Catechol-O-methyltransferase gene polymorphism and chronic human pain: a systematic review and meta-analysis

1 reference

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6 September 2017

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

1 reference

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6 September 2017

Pain sensitivity risk factors for chronic TMD: descriptive data and empirically identified domains from the OPPERA case control study.

1 reference

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6 September 2017

Potential psychosocial risk factors for chronic TMD: descriptive data and empirically identified domains from the OPPERA case-control study.

1 reference

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6 September 2017

Summary of findings from the OPPERA baseline case-control study: implications and future directions

1 reference

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6 September 2017

Genetics of migraine in the age of genome-wide association studies

1 reference

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6 September 2017

Large candidate gene association study reveals genetic risk factors and therapeutic targets for fibromyalgia.

1 reference

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6 September 2017

Genetic variability in the NMDA-dependent AMPA trafficking cascade is associated with alcohol dependence

1 reference

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6 September 2017

Candidate gene studies of fibromyalgia: a systematic review and meta-analysis

1 reference

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6 September 2017

A genome-wide Drosophila screen for heat nociception identifies α2δ3 as an evolutionarily conserved pain gene

1 reference

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6 September 2017

Gene expression profiling in the stress control brain region hypothalamic paraventricular nucleus reveals a novel gene network including amyloid beta precursor protein

1 reference

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6 September 2017

Association of catechol-O-methyltransferase genetic variants with outcome in patients undergoing surgical treatment for lumbar degenerative disc disease

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6 September 2017

Multiple chronic pain states are associated with a common amino acid-changing allele in KCNS1

1 reference

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6 September 2017

Pain perception is altered by a nucleotide polymorphism in SCN9A

1 reference

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6 September 2017

Estrogen receptor-alpha polymorphisms and predisposition to TMJ disorder

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6 September 2017

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6 September 2017

Current evidence for a modulation of low back pain by human genetic variants

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6 September 2017

The association between ACE inhibitors and the complex regional pain syndrome: Suggestions for a neuro-inflammatory pathogenesis of CRPS.

1 reference

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6 September 2017

Sequence variations of the human MPDZ gene and association with alcoholism in subjects with European ancestry

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6 September 2017

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6 September 2017

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

1 reference

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6 September 2017

PLINK: a tool set for whole-genome association and population-based linkage analyses

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6 September 2017

A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition

1 reference

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6 September 2017

GenABEL: an R library for genome-wide association analysis

1 reference

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6 September 2017

Temporomandibular disorder is associated with a serotonin transporter gene polymorphism in the Japanese population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855664

6 September 2017

Principal components analysis corrects for stratification in genome-wide association studies

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6 September 2017

Idiopathic pain disorders--pathways of vulnerability.

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6 September 2017

Three major haplotypes of the beta2 adrenergic receptor define psychological profile, blood pressure, and the risk for development of a common musculoskeletal pain disorder

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6 September 2017

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

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6 September 2017

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6 September 2017

The endophenotype concept in psychiatry: etymology and strategic intentions

1 reference

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6 September 2017

Genetic variation in cyclooxygenase 1: effects on response to aspirin

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6 September 2017

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6 September 2017

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.

1 reference

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6 September 2017

Interaction of serotonin 5-hydroxytryptamine type 2C receptors with PDZ10 of the multi-PDZ domain protein MUPP1

1 reference

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6 September 2017

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6 September 2017

Research diagnostic criteria for temporomandibular disorders: review, criteria, examinations and specifications, critique

1 reference

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6 September 2017

GABAB receptor association with the PDZ scaffold Mupp1 alters receptor stability and function

1 reference

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14 September 2017

Characterization of two APP gene promoter polymorphisms that appear to influence risk of late-onset Alzheimer's disease

1 reference

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14 September 2017

Association of 231G>A polymorphism of endothelin type A receptor gene with migraine: a meta-analysis

1 reference

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26 June 2018

Genetic polymorphisms of the beta2-adrenergic receptor relate to guanosine protein-coupled stimulator receptor dysfunction in fibromyalgia syndrome

1 reference

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26 June 2018

Epidemiology of signs and symptoms in temporomandibular disorders: clinical signs in cases and controls.

1 reference

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26 June 2018

Angiotensin-(1-7) induces peripheral antinociception through mas receptor activation in an opioid-independent pathway

1 reference

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2 September 2018

ACE2 gene polymorphism and essential hypertension: an updated meta-analysis involving 11,051 subjects

1 reference

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2 September 2018

Influence of the interaction between environmental quality and T102C SNP in the HTR2A gene on fibromyalgia susceptibility.

1 reference

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2 September 2018

Microinjection of angiotensin II in the caudal ventrolateral medulla induces hyperalgesia

1 reference

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2 September 2018

Association between tryptophan hydroxylase gene polymorphism and painful non-osseous temporomandibular disorders.

1 reference

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2 September 2018

Association between estrogen receptor polymorphism and pain susceptibility in female temporomandibular joint osteoarthritis patients.

1 reference

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2 September 2018

Variations in the APP gene promoter region and risk of Alzheimer disease.

1 reference

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2 September 2018

Estrogen receptor gene polymorphism and craniofacial morphology in female TMJ osteoarthritis patients.

1 reference

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2 September 2018

A new role for the renin-angiotensin system in the rat periaqueductal gray matter: angiotensin receptor-mediated modulation of nociception

1 reference

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2 September 2018

Restraint stress induces beta-amyloid precursor protein mRNA expression in the rat basolateral amygdala

1 reference

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2 September 2018

T102C polymorphism of the 5-HT2A receptor gene may be associated with temporomandibular dysfunction.

1 reference

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2 September 2018

Polymorphisms in the promoter of the human APP gene: functional evaluation and allele frequencies in Alzheimer disease

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2 September 2018

Congenic mapping of alcohol and pentobarbital withdrawal liability loci to a <1 centimorgan interval of murine chromosome 4: identification of Mpdz as a candidate gene.

1 reference

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2 September 2018

Confirmation of an association between fibromyalgia and serotonin transporter promoter region (5- HTTLPR) polymorphism, and relationship to anxiety-related personality traits

1 reference

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2 September 2018

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1 reference

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2 September 2018

Possible association of temporomandibular joint pain and dysfunction with a polymorphism in the serotonin transporter gene

1 reference

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2 September 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

1 reference

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3 December 2018

Genetic basis for individual variations in pain perception and the development of a chronic pain condition

1 reference

https://pubmed.ncbi.nlm.nih.gov/24275226

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible association of fibromyalgia with a polymorphism in the serotonin transporter gene regulatory region

1 reference

https://pubmed.ncbi.nlm.nih.gov/24275226

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effects of estrogen receptor α polymorphism on the prevalence of symptomatic temporomandibular disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/24275226

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between genetic polymorphisms in the cyclooxygenase-1 gene promoter and peptic ulcers in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/24275226

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pain sensitivity in fibromyalgia is associated with catechol-O-methyltransferase (COMT) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/24275226

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of catechol-O-methyltransferase (COMT) gene polymorphisms in pain sensibility of Brazilian fibromialgia patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/24275226

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the Vascular Endothelial Growth Factor Gene Polymorphisms (-460C/T, +405G/C and +936T/C) with Endometriosis: A Meta-Analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/24275226

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.JPAIN.2013.09.004

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24275226%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

release_5sahqemi5nbvtdjksgk4kqrlqq

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https://api.fatcat.wiki/v0/release/5sahqemi5nbvtdjksgk4kqrlqq

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24275226%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24275226%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

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