Wanjin Chen

Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China

Yan Hu, Xiong Zhang, Zhi-ying Wu, 2012, Neuroscience Letters.

ATP1A1 mutations cause intermediate Charcot‐Marie‐Tooth disease

Ning Wang, Jin He, Wenfeng Chen, 2019, Human mutation.

Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson’s disease in a Han-Chinese population in south-eastern China

Ning Wang, Yi Lin, Wei-hong Zheng, 2013, Neurological Sciences.

miR-29c Suppresses the Malignant Phenotype of Hepatocellular Carcinoma Cells In Vitro by Mediating TPX2 Associated with Immune Infiltration

Haibo Wang, Wenyong Wu, Wanjin Chen, 2022, Digestive Diseases and Sciences.

Let-7c-5p down-regulates immune-related CDCA8 to inhibit hepatocellular carcinoma

Shouwen Wang, Haibo Wang, X. Geng, 2023, Functional & Integrative Genomics.

Mini-dCas13X–mediated RNA editing restores dystrophin expression in a humanized mouse model of Duchenne muscular dystrophy

Erwei Zuo, Wenqin Ying, Hui Yang, 2022, The Journal of clinical investigation.