AMELX Mutations and Genotype–Phenotype Correlation in X-Linked Amelogenesis Imperfecta SK Wang, H Zhang, HC Lin, YL Wang, SC Lin, F Seymen, M Koruyucu, ... International Journal of Molecular Sciences 25 (11), 6132, 2024 | | 2024 |
ENAM Mutations Can Cause Hypomaturation Amelogenesis Imperfecta YL Wang, HC Lin, T Liang, JCY Lin, JP Simmer, JCC Hu, SK Wang Journal of Dental Research 103 (6), 662-671, 2024 | 1 | 2024 |
Phenotypic variability in LAMA3‐associated amelogenesis imperfecta SK Wang, H Zhang, YL Wang, F Seymen, M Koruyucu, JP Simmer, ... Oral diseases 29 (8), 3514-3524, 2023 | 7 | 2023 |
The Characterization of Hydroxyapatite and Octa-calcium Phosphate with Electron Energy Loss Spectroscopy YH Hsu, A Hassan, A Trout, JD Bartlett, CE Smith, JP Simmer, ... Microscopy and Microanalysis 29 (Supplement_1), 1223-1225, 2023 | | 2023 |
FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome SK Wang, H Zhang, YL Wang, HY Lin, F Seymen, M Koruyucu, JT Wright, ... International Endodontic Journal 56 (8), 943-954, 2023 | 6 | 2023 |
PAX9 mutations and genetic synergism in familial tooth agenesis KY Chu, YL Wang, JT Chen, CH Lin, CCJ Yao, YJ Chen, HW Chen, ... Annals of the New York Academy of Sciences 1524 (1), 87-96, 2023 | 7 | 2023 |
Dentin defects caused by a Dspp−1 frameshift mutation are associated with the activation of autophagy T Liang, CE Smith, Y Hu, H Zhang, C Zhang, Q Xu, Y Lu, L Qi, JCC Hu, ... Scientific Reports 13 (1), 6393, 2023 | 4 | 2023 |
Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta YJ Kim, H Zhang, Y Lee, F Seymen, M Koruyucu, Y Kasimoglu, ... Journal of Personalized Medicine 13 (2), 326, 2023 | 2 | 2023 |
Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations T Liang, SK Wang, C Smith, H Zhang, Y Hu, F Seymen, M Koruyucu, ... Scientific Reports 12 (1), 16477, 2022 | 6 | 2022 |
Translated Mutant DSPP mRNA Expression Level Impacts the Severity of Dentin Defects YJ Kim, Y Lee, H Zhang, F Seymen, M Koruyucu, S Bayrak, N Tuloglu, ... Journal of Personalized Medicine 12 (6), 1002, 2022 | 8 | 2022 |
The Modified Shields Classification and 12 Families with Defined DSPP Mutations JP Simmer, H Zhang, SJH Moon, LAJ Donnelly, YL Lee, F Seymen, ... Genes 13 (5), 858, 2022 | 10 | 2022 |
Novel homozygous KREMEN1 mutation causes ectodermal dysplasia Y Lee, H Zhang, F Seymen, M Koruyucu, Y Kasimoglu, ZH Lee, JCC Hu, ... Oral diseases 28 (3), 843, 2022 | | 2022 |
Novel KLK4 Mutations Cause Hypomaturation Amelogenesis Imperfecta Y Lee, H Zhang, F Seymen, YJ Kim, Y Kasimoglu, M Koruyucu, ... Journal of Personalized Medicine 12 (2), 150, 2022 | 2 | 2022 |
Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta YJ Kim, Y Lee, Y Kasimoglu, F Seymen, JP Simmer, JCC Hu, ES Cho, ... Journal of Dental Research 101 (1), 37-45, 2022 | 12 | 2022 |
Novel Mutations in GPR68 and SLC24A4 Cause Hypomaturation Amelogenesis Imperfecta F Seymen, H Zhang, Y Kasimoglu, M Koruyucu, JP Simmer, JCC Hu, ... Journal of Personalized Medicine 12 (1), 13, 2021 | 12 | 2021 |
A genetic model for the secretory stage of dental enamel formation JP Simmer, JCC Hu, Y Hu, S Zhang, T Liang, SK Wang, JW Kim, ... Journal of structural biology 213 (4), 107805, 2021 | 27 | 2021 |
Analyses of oligodontia phenotypes and genetic etiologies M Zhou, H Zhang, H Camhi, F Seymen, M Koruyucu, Y Kasimoglu, ... International journal of oral science 13 (1), 32, 2021 | 47 | 2021 |
Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis KY Chu, YL Wang, YR Chou, JT Chen, YP Wang, JP Simmer, JCC Hu, ... Journal of Personalized Medicine 11 (11), 1217, 2021 | 22 | 2021 |
Mouse Dspp frameshift model of human dentinogenesis imperfecta T Liang, Y Hu, H Zhang, Q Xu, CE Smith, C Zhang, JW Kim, SK Wang, ... Scientific Reports 11 (1), 20653, 2021 | 16 | 2021 |
MMP20-generated amelogenin cleavage products prevent formation of fan-shaped enamel malformations JD Bartlett, CE Smith, Y Hu, A Ikeda, M Strauss, T Liang, YH Hsu, ... Scientific Reports 11 (1), 10570, 2021 | 14 | 2021 |