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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 12, 2018
[Analysis of DSPP gene mutation in a Chinese pedigree affected with hereditary dentinogenesis imperfecta]Aiqin Hu, Xiaocong Li, Danna Chen, et al.
BMC Ophthalmology|December 12, 2025
Iron-associated central macular ganglion cell complex thinning and choroidal vascularity index elevation in transfusion-dependent β-thalassemia: potential OCT/OCTA biomarkersNingfeng Li, Liang Liang, Wenzhi Huang, et al.
Cancer Medicine|March 30, 2026
A Disproportionality Analysis of Immune Checkpoint Inhibitors in Combination With Platinum-Based Agents Using the FDA Adverse Event Reporting System DatabaseBoyi Liu, Wenchao Zhang, Ruizhe Huang, et al.
Genesis (New York, N.Y. : 2000)|March 8, 2021
VPS4B deficiency causes early embryonic lethality and induces signal transduction disorders of cell endocytosisDanna Chen, Fei He, Ting Lu, et al.
European Journal of Medicinal Chemistry|August 28, 2024
Discovery of AMPs from random peptides via deep learning-based model and biological activity validationJun Du, Changyan Yang, Yabo Deng, et al.
Experimental Eye Research|November 3, 2024
Integrative multiomic analysis unveils the molecular nexus of mitochondrial dysfunction in the pathogenesis of age-related macular degenerationJianqi Chen, Zhe Liu, Yingting Zhu, et al.
Bioinformatics (Oxford, England)|July 27, 2024
MuCoCP: a priori chemical knowledge-based multimodal contrastive learning pre-trained neural network for the prediction of cyclic peptide membrane penetration abilityYunxiang Yu, Mengyun Gu, Hai Guo, et al.
BMC Genetics|January 13, 2019
Vps4b heterozygous mice do not develop tooth defects that replicate human dentin dysplasia IAiqin Hu, Ting Lu, Danna Chen, et al.
Clinical Genetics|November 21, 2025
Functional Validation and Phenotypic Spectrum of Splice-Site Variants in CHD7, FGFR1, and ANOS1 in Congenital Hypogonadotropic HypogonadismYuting Li, Pingchuan Zhang, Jun Guan, et al.
Human Molecular Genetics|January 25, 2023
A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadismXinying Wang, Danna Chen, Yaguang Zhao, et al.
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