Objective This study aimed to evaluate the association of genetic variants inACTN3 and
MYO1H with craniofacial skeletal patterns in Brazilians. Design This cross-sectional study …

Introduction α-Actinins are myofibril anchor proteins that influence the contractile properties
of skeletal muscles. ACTN2 is expressed in slow type I and fast type II fibers, whereas …

Introduction Our goal was to verify the association between candidate polymorphisms and
skeletal Class III malocclusion in a well-characterized homogeneous sample set. Methods …

This study evaluated associations between craniofacial candidate genes and skeletal
variation in patients with malocclusion. Lateral cephalometric radiographs of 269 untreated …

Introduction We investigated whether ACTN3, ENPP1, ESR1, PITX1, and PITX2 genes
which contribute to sagittal and vertical malocclusions also contribute to facial asymmetries …

Objectives The present systematic review aims to report and critically assess the findings of
the available scientific evidence from genetic association studies examining the genetic …

Background The aim of the present study was to assess if genetic polymorphisms in tooth
agenesis (TA)-related genes are associated with craniofacial morphological patterns …

Aim: The aim of this study is to review studies evaluating the role of genetics in skeletal class
II malocclusion. Objective: To assess the scientific evidence associating the role of genes in …

Abstract Objective To investigate SNPs in bone‐and cartilage‐related genes and their
interaction in the aetiology of sagittal and vertical skeletal malocclusions. Settings and …

Craniofacial asymmetry, mandibular condylar modeling and temporomandibular joint
disorders are common comorbidities of skeletally disproportionate malocclusions, but …