Orthodontic treatment, genetic factors, and risk of temporomandibular disorder

GD Slade, L Diatchenko, R Ohrbach, W Maixner - Seminars in orthodontics, 2008 - Elsevier
Traditionally, four groups of factors have been identified in the etiology of
temporomandibular disorder (TMD): anatomical variation in the masticatory system; …

Shared genetics of temporomandibular disorder pain and neck pain: results of a twin study

CM Visscher, MJ Schouten, L Ligthart… - Journal of oral & facial …, 2018 - research.vu.nl
AIMS:(1) To examine the heritability of TMD pain and of neck pain; and (2) to estimate the
potential overlap in genetic and environmental factors influencing TMD pain and neck pain …

[HTML][HTML] Genetic variation in genes involved in folate and drug metabolism in a south Indian population

PS Rai, TS Murali, TG Vasudevan… - Indian Journal of …, 2011 - ncbi.nlm.nih.gov
BACKGROUND: Genetic variations represented as single nucleotide polymorphisms (SNPs)
vary across the world population. This genetic polymorphism (such as SNPs) plays an …

Analysis of the MTHFD1 promoter and risk of neural tube defects

N Carroll, F Pangilinan, AM Molloy, J Troendle, JL Mills… - Human genetics, 2009 - Springer
Abstract Genetic variants in MTHFD1 (5, 10-methylenetetrahydrofolate dehydrogenase/5, 10-
methenyltetrahydrofolate cyclohydrolase/10-formyltetrahydrofolate synthetase), an important …

[HTML][HTML] Significant association of MTHFD1 1958G> A single nucleotide polymorphism with nonsyndromic cleft lip and palate in Indian population

J Murthy, VB Gurramkonda… - Medicina oral, patologia …, 2014 - ncbi.nlm.nih.gov
Objectives: Nonsyndromic cleft lip and palate (NSCLP) is genetically distinct from those with
syndromic clefts, and accounts for~ 70% of cases with Oral clefts. Folate, or vitamin B9, is an …

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

N Mutlu, ME Erdal, H Herken, G Oz, YA Bayazıt - Oral diseases, 2004 - Wiley Online Library
Objective: To assess whether a relationship existed between the T102C polymorphism of 5‐
HT2A receptor gene and temporomandibular dysfunction. Methods: Sixty‐three patients with …

Genetic Polymorphisms of Catechol-O-Methyltransferase: Association with Temporomandibular Disorders and Postoperative Pain.

I Mladenovic, G Supic, R Kozomara… - Journal of Oral & …, 2016 - search.ebscohost.com
Aims: To evaluate the association between catechol-O-methyltransferase (COMT) gene
polymorphisms and temporomandibular disorders (TMD), TMD pain, psychosocial …

[HTML][HTML] Gene polymorphisms involved in folate metabolism and DNA methylation with the risk of head and neck cancer

TB De Castro, GH Rodrigues-Fleming… - Asian Pacific Journal …, 2020 - ncbi.nlm.nih.gov
Background: Folate is essential for DNA synthesis, repair, and methylation. Polymorphisms
in genes associated with folate metabolism may alter these processes and, consequently …

[HTML][HTML] Summary of findings from the OPPERA prospective cohort study of incidence of first-onset temporomandibular disorder: implications and future directions

GD Slade, RB Fillingim, AE Sanders, E Bair… - The Journal of …, 2013 - Elsevier
Papers in this issue investigate when and how putative risk factors influence development of
first-onset, painful temporomandibular disorder (TMD). The results represent first findings …

Role of inflammatory and pain genes polymorphisms in temporomandibular disorder and pressure pain sensitivity

LMSP Fiamengui, BDA Furquim… - Archives of Oral …, 2020 - Elsevier
Objective The aim of this study was to assess the correlation of inflammatory and pain genes
polymorphisms with the presence of temporomandibular disorder (TMD) patients and with …