Areas of Focus
- Pathogenic mechanisms of rare diseases
- Genetic and epigenetic regulation of reproductive disorders
Publications
- Research progress of in vitro activation of follicles in patients with premature ovarian insufficiency in assisted reproduction, Liu Zhan'ao, Chen Chen, 2023
- Research progress of CRISPR-Cas9 gene editing technology in tumor treatment, Ding Yidan, Chen Chen, 2022
- Recurrent Stroke-Like Symptoms After Cesarean Section Deliveries in a Female Patient With X-Linked Charcot-Marie-Tooth Type 1, Qu Li, Chen Chen, Yan Ren, Xu Liu, 2020
- Novel homozygous nonsense mutations in LHCGR lead to empty follicle syndrome and 46, XY disorder of sex development, Chen C, Xu X, Kong L, Li P, Zhou F, Zhao S, Xin X, Tan J, Zhang X, 2018
- A Novel Splicing Mutation Identified in a Chinese Family with X-linked Alport Syndrome Using Targeted Next-Generation Sequencing, Chen C, Lu CX, Wang Q, Cao LH, Luo Y, Zhang X, 2016
- Screening of Duchenne Muscular Dystrophy (DMD) Mutations and Investigating Its Mutational Mechanism in Chinese Patients, Chen C, Ma H, Zhang F, Chen L, Xing X, Wang S, Zhang X, Luo Y, 2014
- TERT Promoter Mutations Lead to High Transcriptional Activity under Hypoxia and Temozolomide Treatment and Predict Poor Prognosis in Gliomas, Chen C, Han S, Meng L, Li Z, Zhang X, Wu A, 2014