Hong Zhang

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 16

Top Topics

Embryonic Stem Cells

Intellectual Disability

Tyrosine Kinase

Artificial Intelligence

Top Venues

Journal of personalized medicine

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Shih-Kai Wang, Hong Zhang, Hua-Chieh Lin, Yin-Lin Wang, Shu-Chun Lin, Figen Seymen, Mine Koruyucu, James P Simmer, Jan C-C Hu
AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta. International journal of molecular sciences 25 (11) (2024)
Shih-Kai Wang, Hong Zhang, Hua-Chieh Lin, Yin-Lin Wang, Shu-Chun Lin, Figen Seymen, Mine Koruyucu, James P Simmer, Jan C-C Hu
AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta. International journal of molecular sciences 25 (11) (2024)
Shih-Kai Wang, Hong Zhang, Hua-Chieh Lin, Yin-Lin Wang, Shu-Chun Lin, Figen Seymen, Mine Koruyucu, James P Simmer, Jan C-C Hu
AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta. International journal of molecular sciences 25 (11) (2024)
Shih-Kai Wang, Hong Zhang, Hua-Chieh Lin, Yin-Lin Wang, Shu-Chun Lin, Figen Seymen, Mine Koruyucu, James P Simmer, Jan C-C Hu
AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta. International journal of molecular sciences 25 (11) (2024)
Youn Jung Kim, Hong Zhang, Yejin Lee, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, James P Simmer, Jan C-C Hu, Jung-Wook Kim
Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta. Journal of personalized medicine 13 (2) (2023)
Youn Jung Kim, Hong Zhang, Yejin Lee, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, James P Simmer, Jan C-C Hu, Jung-Wook Kim
Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta. Journal of personalized medicine 13 (2) (2023)
Youn Jung Kim, Hong Zhang, Yejin Lee, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, James P Simmer, Jan C-C Hu, Jung-Wook Kim
Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta. Journal of personalized medicine 13 (2) (2023)
Youn Jung Kim, Hong Zhang, Yejin Lee, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, James P Simmer, Jan C-C Hu, Jung-Wook Kim
Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta. Journal of personalized medicine 13 (2) (2023)
Youn Jung Kim, Hong Zhang, Yejin Lee, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, James P Simmer, Jan C-C Hu, Jung-Wook Kim
Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta. Journal of personalized medicine 13 (2) (2023)
Youn Jung Kim, Yejin Lee, Hong Zhang, Figen Seymen, Mine Koruyucu, Sule Bayrak, Nuray Tuloglu, James P Simmer, Jan C-C Hu, Jung-Wook Kim
Translated Mutant DSPP mRNA Expression Level Impacts the Severity of Dentin Defects. Journal of personalized medicine 12 (6) (2022)
James P Simmer, Hong Zhang, Sophie J H Moon, Lori A-J Donnelly, Yuan-Ling Lee, Figen Seymen, Mine Koruyucu, Hui-Chen Chan, Kevin Y Lee, Suwei Wu, Chia-Lan Hsiang, Anthony T P Tsai, Rebecca L Slayton, Melissa Morrow, Shih-Kai Wang, Edward D Shields, Jan C-C Hu
The Modified Shields Classification and 12 Families with Defined DSPP Mutations. Genes 13 (5) (2022)
Yejin Lee, Hong Zhang, Figen Seymen, Youn Jung Kim, Yelda Kasimoglu, Mine Koruyucu, James P Simmer, Jan C-C Hu, Jung-Wook Kim
Novel KLK4 Mutations Cause Hypomaturation Amelogenesis Imperfecta. Journal of personalized medicine 12 (2) (2022)
Figen Seymen, Hong Zhang, Yelda Kasimoglu, Mine Koruyucu, James P Simmer, Jan C-C Hu, Jung-Wook Kim
Novel Mutations in GPR68 and SLC24A4 Cause Hypomaturation Amelogenesis Imperfecta. Journal of personalized medicine 12 (1) (2021)
Youn Jung Kim, Yejin Lee, Hong Zhang, John Timothy Wright, James P Simmer, Jan C-C Hu, Jung-Wook Kim
Translational Attenuation by an Intron Retention in the 5' UTR of ENAM Causes Amelogenesis Imperfecta. Biomedicines 9 (5) (2021)
Youn Jung Kim, Yejin Lee, Hong Zhang, Ji-Soo Song, Jan C-C Hu, James P Simmer, Jung-Wook Kim
A Novel De Novo SP6 Mutation Causes Severe Hypoplastic Amelogenesis Imperfecta Genes 12 (3) (2021)
Xiang Zhang, Misaki Mizukoshi, Hong Zhang, Engkong Tan, Yoji Igarashi, Yutaka Suzuki, Susumu Mitsuyama, Shigeharu Kinoshita, Kazuyoshi Saito, Shugo Watabe, Shuichi Asakawa
Ultrahigh-Density Linkage Map Construction Using Low-Coverage Whole-Genome Sequencing of a Doubled Haploid Population: Case Study of Torafugu (Takifugu rubripes). Genes 9 (3) (2018)