AAV-ie enables safe and efficient gene transfer to inner ear cellsFangzhi Tan, Guisheng Zhong, Cenfeng Chu et al.|Nature Communications|2019Cited by 228
Hearing of Otof-deficient mice restored by trans-splicing of N- and C-terminal otoferlinHonghai Tang, Hui Wang, Shengyi Wang et al.|Human Genetics|2022Cited by 82
Prevention of acquired sensorineural hearing loss in mice by in vivo Htra2 gene editingXi Gu, Huawei Li|Genome biology|2021Cited by 52
Precise detection of CRISPR-Cas9 editing in hair cells in the treatment of autosomal dominant hearing lossChong Cui, Yilai Shu, Bowei Huang et al.|Molecular Therapy — Nucleic Acids|2022Cited by 51
The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in miceQing Li, Yilai Shu, Chong Cui et al.|Cellular and Molecular Life Sciences|2023Cited by 27