Jing Zhang

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 6

Top Topics

Hypertrophic Cardiomyopathy

Hepatitis C Virus

Top Venues

Molecular genetics & genomic medicine

Disease markers

Experimental biology and medicine (Maywood, N.J.)

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

Publications

Qing-Bing He, Cai-Hong Wu, Dong-Lan Sun, Jia-Yu Yuan, Hua-Ying Hu, Kai Yang, Wen-Qi Chen, You-Sheng Yan, Guang-Yue Yin, Jing Zhang, Ya-Zhou Li
Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B). Molecular genetics & genomic medicine 12 (3) (2024)
Qing-Bing He, Cai-Hong Wu, Dong-Lan Sun, Jia-Yu Yuan, Hua-Ying Hu, Kai Yang, Wen-Qi Chen, You-Sheng Yan, Guang-Yue Yin, Jing Zhang, Ya-Zhou Li
Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B). Molecular genetics & genomic medicine 12 (3) (2024)
Jing Zhang, Wen-Qi Chen, Kai Yang, Zhao-Xi Wang, Dong-Lan Sun, Yuan-Yuan Peng, Mei Yu, Shao-Xiong Wang, Qing Guo
RBM25 induces trophoblast epithelial-mesenchymal transition and preeclampsia disorder by enhancing the positive feedback loop between Grhl2 and RBM25. Experimental biology and medicine (Maywood, N.J.) (2023)
Kai Yang, Li-Man Fu, Xiao-Yang Chu, Jing Zhang, Wen-Qi Chen, You-Sheng Yan, Yi-Peng Wang, Dong-Liang Zhang, Cheng-Hong Yin, Qing Guo
Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population. Molecular genetics & genomic medicine (2023)
Xiaohui Wen, Huan-Xia Xing, Keyan Qi, Hao Wang, Xiaojun Li, Jianjiang Zhu, Wenqi Chen, Limin Cui, Jing Zhang, Hong Qi
Analysis of 17 Prenatal Cases with the Chromosomal 1q21.1 Copy Number Variation. Disease markers 2022 (2022)
Jing Zhang, Wen-Qi Chen, Si-Wen Wang, Shao-Xiong Wang, Mei Yu, Qing Guo, Ya-Dong Yu
Identification of a novel pathogenic variant in the MYH3 gene in a five-generation family with CPSFS1A (Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1A). Molecular genetics & genomic medicine 8 (10) (2020)