[HTML][HTML] Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis

L Slavec, N Karas Kuželički, I Locatelli, K Geršak - Scientific Reports, 2022 - nature.com
To date, the involvement of various genetic markers in the aetiopathogenesis of non-
syndromic orofacial cleft (nsOFC) has been extensively studied. In the present study, we …

The genetic factors contributing to the risk of cleft lip-cleft palate and their clinical utility

S Askarian, M Gholami, G Khalili-Tanha… - Oral and Maxillofacial …, 2023 - Springer
Cleft lip and cleft palate (CL/P) are among the most common congenital malformations in
neonates and have syndromic or nonsyndromic forms. Nonsyndromic forms of malformation …

Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non‐syndromic tooth agenesis

A Mostowska, B Biedziak, M Zadurska… - Clinical …, 2013 - Wiley Online Library
Tooth agenesis is one of the most common dental anomalies, with a complex and not yet
fully elucidated aetiology. Given the crucial role of the Wnt signalling pathway during tooth …

Association studies and direct DNA sequencing implicate genetic susceptibility loci in the etiology of nonsyndromic orofacial clefts in sub-Saharan African populations

LJJ Gowans, WL Adeyemo, M Eshete… - Journal of dental …, 2016 - journals.sagepub.com
Orofacial clefts (OFCs) are congenital dysmorphologies of the human face and oral cavity,
with a global incidence of 1 per 700 live births. These anomalies exhibit a multifactorial …

A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population

TK de Araujo, R Secolin, TM Félix, LT De Souza… - Journal of Cranio …, 2016 - Elsevier
Purpose The aim of this study was to use the TaqMan OpenArray system to evaluate
associations between 39 genes and the etiology of nonsyndromic cleft lip and palate …

Analysis of PRICKLE 1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations

T Yang, Z Jia, W Bryant‐Pike… - Molecular genetics & …, 2014 - Wiley Online Library
Palate development is shaped by multiple molecular signaling pathways, including the Wnt
pathway. In mice and humans, mutations in both the canonical and noncanonical arms of …

Association of WNT pathway genes with nonsyndromic cleft lip with or without cleft palate

V Vijayan, R Ummer, R Weber… - The Cleft Palate …, 2018 - journals.sagepub.com
Objective: Nonsyndromic cleft lip with or without cleft palate (NSCL±P) is a common
craniofacial anomaly with multifactorial etiology. Evidence suggests that variations in WNT …

[HTML][HTML] Clinical relevance of breast and gastric cancer-associated polymorphisms as potential susceptibility markers for oral clefts in the Brazilian population

RA Machado, EM de Freitas, SN de Aquino… - BMC Medical …, 2017 - Springer
Background Epidemiological studies have indicated a higher incidence of breast and gastric
cancer in patients with nonsyndromic cleft lip with or without cleft palate (NSCL±P) and their …

[HTML][HTML] Association of single nucleotide polymorphisms in AXIN2, BMP4, and IRF6 with Non-Syndromic Cleft Lip with or without Cleft Palate in a sample of the …

H Rafighdoost, M Hashemi, H Danesh… - Journal of Applied Oral …, 2017 - SciELO Brasil
Non-syndromic cleft lip with or without palate (NSCL/P) is a common congenital
malformation worldwide, with complex etiology. It has been proposed that interaction of …

Genetic polymorphisms in APC, DVL2, and AXIN1 are associated with susceptibility, advanced TNM stage or tumor location in colorectal cancer

MA Rosales-Reynoso… - The Tohoku journal of …, 2019 - jstage.jst.go.jp
Colorectal cancer (CRC) is the third most common cancer and the second leading cause of
death worldwide. The named “destruction complex” has a critical function in the Wnt/β …