James Simmer
University of Michigan
H-index: 78
North America-United States
Top articles of James Simmer
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta | Journal of Personalized Medicine | Youn Jung Kim Hong Zhang Yejin Lee Figen Seymen Mine Koruyucu | 2023/2/14 |
Phenotypic variability in LAMA3‐associated amelogenesis imperfecta | Oral Diseases | Shih‐Kai Wang Hong Zhang Yin‐Lin Wang Figen Seymen Mine Koruyucu | 2023/11 |
The Characterization of Hydroxyapatite and Octa-calcium Phosphate with Electron Energy Loss Spectroscopy | Ya-Hsiang Hsu Asra Hassan Amanda Trout John D Bartlett Charles E Smith | 2023/8/1 | |
FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome | International Endodontic Journal | Shih‐Kai Wang Hong Zhang Yin‐Lin Wang Hung‐Ying Lin Figen Seymen | 2023/8 |
PAX9 mutations and genetic synergism in familial tooth agenesis | Annals of the New York Academy of Sciences | Kuan‐Yu Chu Yin‐Lin Wang Jung‐Tsu Chen Chia‐Hui Lin Chung‐Chen Jane Yao | 2023/6 |
Dentin defects caused by a Dspp−1 frameshift mutation are associated with the activation of autophagy | Scientific Reports | Tian Liang Charles E Smith Yuanyuan Hu Hong Zhang Chuhua Zhang | 2023/4/19 |
Novel KLK4 Mutations Cause Hypomaturation Amelogenesis Imperfecta | Journal of Personalized Medicine | Yejin Lee Hong Zhang Figen Seymen Youn Jung Kim Yelda Kasimoglu | 2022/1/24 |
Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta | Journal of Dental Research | Youn Jung Kim Yejin Lee Yelda Kasimoglu Figen Seymen James P Simmer | 2022/1 |
Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations | Scientific Reports | Tian Liang Shih-Kai Wang Charles Smith Hong Zhang Yuanyuan Hu | 2022/10/1 |
Translated Mutant DSPP mRNA Expression Level Impacts the Severity of Dentin Defects | Journal of Personalized Medicine | Youn Jung Kim Yejin Lee Hong Zhang Figen Seymen Mine Koruyucu | 2022/6/19 |
The Modified Shields Classification and 12 Families with Defined DSPP Mutations | Genes | James P Simmer Hong Zhang Sophie JH Moon Lori AJ Donnelly Yuan-Ling Lee | 2022/5/12 |
Novel homozygous KREMEN1 mutation causes ectodermal dysplasia | Oral diseases | Yejin Lee Hong Zhang Figen Seymen Mine Koruyucu Yelda Kasimoglu | 2022/4 |
FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta | Journal of Dental Research | Shih-Kai Wang Hong Zhang Chia-Yuan Hu Jeng-Fen Liu Sagar Chadha | 2021/3 |
Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis | Journal of Personalized Medicine | Kuan-Yu Chu Yin-Lin Wang Yu-Ren Chou Jung-Tsu Chen Yi-Ping Wang | 2021/11/17 |
A Novel De Novo SP6 Mutation Causes Severe Hypoplastic Amelogenesis Imperfecta | Genes | Youn Jung Kim Yejin Lee Hong Zhang Ji-Soo Song Jan C-C Hu | 2021/2/26 |
Mouse Dspp frameshift model of human dentinogenesis imperfecta | Scientific Reports | Tian Liang Yuanyuan Hu Hong Zhang Qian Xu Charles E Smith | 2021/10/19 |
Odontogenesis-associated phosphoprotein truncation blocks ameloblast transition into maturation in OdaphC41*/C41* mice | Scientific reports | Tian Liang Yuanyuan Hu Kazuhiko Kawasaki Hong Zhang Chuhua Zhang | 2021/1/13 |
MMP20-generated amelogenin cleavage products prevent formation of fan-shaped enamel malformations | Scientific Reports | John D Bartlett Charles E Smith Yuanyuan Hu Atsushi Ikeda Mike Strauss | 2021/5/19 |
Novel Mutations in GPR68 and SLC24A4 Cause Hypomaturation Amelogenesis Imperfecta | Journal of Personalized Medicine | Figen Seymen Hong Zhang Yelda Kasimoglu Mine Koruyucu James P Simmer | 2021/12/28 |
Correction: Analyses of oligodontia phenotypes and genetic etiologies | International journal of oral science | Mengqi Zhou Hong Zhang Heather Camhi Figen Seymen Mine Koruyucu | 2021 |
