Associated Papers
Familial Oculoauriculovertebral Spectrum: A Genomic Investigation of Autosomal Dominant Inheritance.
Petrin AL et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2025
Genotypic and phenotypic correlations in tooth agenesis: insights from WNT10A and EDA mutations in syndromic and non-syndromic forms.
Wu Y et al.
Human Genetics, 2024
Whole genome sequencing of a family with autosomal dominant features within the oculoauriculovertebral spectrum.
Petrin AL et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Omenn syndrome in a 10-month-old male with athymia and VACTERL association.
Pangli BK et al.
The Journal of Allergy and Clinical Immunology. Global, 2023
Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia family.
Zhao Y et al.
Archives of Oral Biology, 2023
WNT10A variants: following the pattern of inheritance in tooth agenesis and self-reported family history of cancer.
Bielik P et al.
Clinical Oral Investigations, 2022
WNT10A and RUNX2 mutations associated with non-syndromic tooth agenesis.
Živković M et al.
European Journal of Oral Sciences, 2022
Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting.
Wright CF et al.
American Journal of Human Genetics, 2019
Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis.
Du R et al.
Human Genetics, 2018
Genetic Basis of Nonsyndromic and Syndromic Tooth Agenesis.
Ye X et al.
Journal of Pediatric Genetics, 2016
GESPA: classifying nsSNPs to predict disease association.
Khurana JK et al.
Bmc Bioinformatics, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.
Yang J et al.
Molecular Genetics & Genomic Medicine, 2015
Variability in dentofacial phenotypes in four families with WNT10A mutations.
Vink CP et al.
European Journal of Human Genetics : Ejhg, 2014
A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice.
Maupin KA et al.
Bone Research, 2013
WNT10A and isolated hypodontia.
Kantaputra P et al.
American Journal of Medical Genetics. Part A, 2011