Associated Papers
Genetic complexity underlies clinical heterogeneity: YWTD β-propeller mutations and second-hit modifier mutations in LRP6-related tooth agenesis and ectodermal dysplasia in human.
Dong X et al.
Genes & Diseases, 2025
Genetic-environmental Risk Factors for Tooth Agenesis: A Familial Case-control Study in China.
Guo X et al.
International Dental Journal, 2025
Exonic and Intronic WNT10A Variants Isolated from Korean Children with Non-Syndromic Tooth Agenesis.
Ju Y et al.
Diagnostics (basel, Switzerland), 2025
Critical Considerations in Calling Disease-Causing EDAR Mutations in Nonsyndromic Oligodontia.
Kim YJ et al.
Journal of Clinical Medicine, 2024
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
Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia.
Liu Y et al.
Bmc Oral Health, 2024
The oligodontia phenotype in a X-linked hypohidrotic ectodermal dysplasia patient with a novel EVC2 variant.
Wu Y et al.
Heliyon, 2024
Whole exome sequencing identifies genetic markers of enterovirus susceptibility in East Asians.
Sung CC et al.
Frontiers in Microbiology, 2024
PAX9 mutations and genetic synergism in familial tooth agenesis.
Chu KY et al.
Annals of the New York Academy of Sciences, 2023
A Genome-wide association study of premolar agenesis in a chinese population.
Fan L et al.
Oral Diseases, 2023
Network expansion of genetic associations defines a pleiotropy map of human cell biology.
Barrio-Hernandez I et al.
Nature Genetics, 2023
Novel Dental Anomaly-associated Mutations in WNT10A Protein Binding Sites.
Kantaputra P et al.
International Dental Journal, 2023
Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification.
Bloch-Zupan A et al.
Frontiers in Physiology, 2023
Dose Dependence Effect in Biallelic WNT10A Variant-Associated Tooth Agenesis Phenotype.
Liu H et al.
Diagnostics (basel, Switzerland), 2022
A case of hidrotic ectodermal dysplasia with developing eccrine syringofibroadenoma with heterozygous mutation of GJB6 gene.
Nishibu A et al.
The Journal of Dermatology, 2022
Novel LRP6 Mutations Causing Non-Syndromic Oligodontia.
Lee Y et al.
Journal of Personalized Medicine, 2022
Two Novel Mutations in Ectodysplasin-A Identified in Syndromic Tooth Agenesis.
Xie W et al.
Journal of the College of Physicians and Surgeons--pakistan : Jcpsp, 2022
WNT10A, dermatology and dentistry.
Doolan BJ et al.
The British Journal of Dermatology, 2021
Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis.
Chu KY et al.
Journal of Personalized Medicine, 2021
Costello syndrome with special cutaneous manifestations and HRAS G12D mutation: A case report and literature review.
Qian W et al.
Molecular Genetics & Genomic Medicine, 2021
Functional Effects of WNT10A Rare Variants Associated with Tooth Agenesis.
Zeng Y et al.
Journal of Dental Research, 2021
Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family.
Li Y et al.
Molecular Medicine Reports, 2020
Phenotypic and Genotypic Features of Thai Patients With Nonsyndromic Tooth Agenesis and WNT10A Variants.
Kanchanasevee C et al.
Frontiers in Physiology, 2020
The GenomeAsia 100K Project enables genetic discoveries across Asia.
Unknown Author
Nature, 2019
Predicting disease-causing variant combinations.
Papadimitriou S et al.
Proceedings of the National Academy of Sciences of the United States of America, 2019
Novel mutations identified in patients with tooth agenesis by whole-exome sequencing.
Zhao K et al.
Oral Diseases, 2019
Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia.
Yu M et al.
American Journal of Medical Genetics. Part A, 2019
WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population.
Grejtakova D et al.
Journal of Genetics, 2018
Patterns of Dental Agenesis Highlight the Nature of the Causative Mutated Genes.
Fournier BP et al.
Journal of Dental Research, 2018
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
The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.
Williams MA et al.
Genes, 2018
Gene screening facilitates diagnosis of complicated symptoms: A case report.
Duan H et al.
Molecular Medicine Reports, 2017
Role of WNT10A in failure of tooth development in humans and zebrafish.
Yuan Q et al.
Molecular Genetics & Genomic Medicine, 2017
Comprehensive genetic exploration of selective tooth agenesis of mandibular incisors by exome sequencing.
Yamaguchi T et al.
Human Genome Variation, 2017
WNT10A variants isolated from Japanese patients with congenital tooth agenesis.
Machida J et al.
Human Genome Variation, 2017
Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients.
Zeng B et al.
Genes, 2016
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.
Prasad MK et al.
Journal of Medical Genetics, 2016
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.
Yang J et al.
Molecular Genetics & Genomic Medicine, 2015
The WNT10A gene in ectodermal dysplasias and selective tooth agenesis.
Mues G et al.
American Journal of Medical Genetics. Part A, 2014