Genetics of Disorders Affecting Tooth Structure, Number, Morphology and Eruption

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds

Jie Yang, Jie Yang, Shih-Kai Wang, et al.. (2014). Molecular Genetics & Genomic Medicine. Cited 103 times. https://doi.org/10.1002/mgg3.111

STIM1 and SLC24A4 Are Critical for Enamel Maturation

Shih-Kai Wang, Murim Choi, Murim Choi, et al.. (2014). Journal of Dental Research. Cited 98 times. https://doi.org/10.1177/0022034514527971

FAM20A Mutations Can Cause Enamel-Renal Syndrome (ERS)

Shih-Kai Wang, P. Aref, Yuanyuan Hu, et al.. (2013). PLoS Genetics. Cited 95 times. https://doi.org/10.1371/journal.pgen.1003302

FAM20A Mutations Associated with Enamel Renal Syndrome

Shih-Kai Wang, B. M. Reid, S. Dugan, et al.. (2014). Journal of Dental Research. Cited 72 times. https://doi.org/10.1177/0022034513512653

ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta.

Shih-Kai Wang, Murim Choi, A. S. Richardson, et al.. (2014). Human molecular genetics. Cited 69 times. https://doi.org/10.1093/hmg/ddt611

LAMB3 Mutations Causing Autosomal-dominant Amelogenesis Imperfecta

Jung-Wook Kim, F. Seymen, Kyu Eun Lee, et al.. (2013). Journal of Dental Research. Cited 67 times. https://doi.org/10.1177/0022034513502054

Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta

David A. Parry, Claire E L Smith, W. El-Sayed, et al.. (2016). American Journal of Human Genetics. Cited 63 times. https://doi.org/10.1016/j.ajhg.2016.08.020

Mutations in RELT cause autosomal recessive amelogenesis imperfecta

Jung‐Wook Kim, Hong Zhang, F. Seymen, et al.. (2018). Clinical Genetics. Cited 50 times. https://doi.org/10.1111/cge.13487

Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta.

F. Seymen, Y. J. Kim, Yejin Lee, et al.. (2016). American journal of human genetics. Cited 43 times. https://doi.org/10.1016/j.ajhg.2016.09.018

WDR72 Mutations Associated with Amelogenesis Imperfecta and Acidosis

Hong Zhang, M. Koruyucu, F. Seymen, et al.. (2019). Journal of Dental Research. Cited 42 times. https://doi.org/10.1177/0022034518824571

Amelogenesis Imperfecta in Two Families with Defined AMELX Deletions in ARHGAP6

J. Hu, Hui-chen Chan, S. Simmer, et al.. (2012). PLoS ONE. Cited 41 times. https://doi.org/10.1371/journal.pone.0052052

Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation.

Curtis R Herzog, B. M. Reid, F. Seymen, et al.. (2015). Oral surgery, oral medicine, oral pathology and oral radiology. Cited 32 times. https://doi.org/10.1016/j.oooo.2014.09.003

Novel PAX9 and COL1A2 Missense Mutations Causing Tooth Agenesis and OI/DGI without Skeletal Abnormalities

Shih-Kai Wang, Hui-chen Chan, I. Makovey, et al.. (2012). PLoS ONE. Cited 28 times. https://doi.org/10.1371/journal.pone.0051533

FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta

S.K. Wang, H. Zhang, C. Hu, et al.. (2020). Journal of Dental Research. Cited 23 times. https://doi.org/10.1177/0022034520962731

Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta

Y. J. Kim, Jenny Kang, F. Seymen, et al.. (2017). Frontiers in Physiology. Cited 23 times. https://doi.org/10.3389/fphys.2017.00229

Alteration of Exon Definition Causes Amelogenesis Imperfecta

Yong-Ik Kim, Jenny Kang, F. Seymen, et al.. (2020). Journal of Dental Research. Cited 22 times. https://doi.org/10.1177/0022034520901708

Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis

Kuan‐Yu Chu, Yin-Lin Wang, Yu-Ren Chou, et al.. (2021). Journal of Personalized Medicine. Cited 21 times. https://doi.org/10.3390/jpm11111217

FAM20C Functions Intracellularly Within Both Ameloblasts and Odontoblasts In Vivo

Shih-Kai Wang, Andrew C Samann, J. Hu, et al.. (2013). Journal of Bone and Mineral Research. Cited 19 times. https://doi.org/10.1002/jbmr.1990

The Modified Shields Classification and 12 Families with Defined DSPP Mutations

J. Simmer, Hong Zhang, Sophie J. H. Moon, et al.. (2022). Genes. Cited 16 times. https://doi.org/10.3390/genes13050858

Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta

Y. Kim, Y. Lee, Y. Kasımoğlu, et al.. (2021). Journal of Dental Research. Cited 12 times. https://doi.org/10.1177/00220345211015119

Novel Mutations in GPR68 and SLC24A4 Cause Hypomaturation Amelogenesis Imperfecta

F. Seymen, Hong Zhang, Y. Kasımoğlu, et al.. (2021). Journal of Personalized Medicine. Cited 9 times. https://doi.org/10.3390/jpm12010013

Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta

Y. J. Kim, Hong Zhang, Yejin Lee, et al.. (2023). Journal of Personalized Medicine. Cited 4 times. https://doi.org/10.3390/jpm13020326