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Molecular Medicine Reports|April 13, 2021
A novel KCNQ4 gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non‑syndromic deafness 2AQiong Li, Pengfei Liang, Shujuan Wang, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 4, 2014
Filtering of acoustic signals within the hearing organSripriya Ramamoorthy, Dingjun Zha, Fangyi Chen, et al.Ear, Nose, & Throat Journal|January 9, 2026
Investigation of Eustachian Tube Dysfunction by Different Methods in Children with Otitis Media with EffusionRui Li, Jiawei Chen, Runqin Yang, et al.Ear, Nose, & Throat Journal|October 31, 2024
Management of Acquired Aural Atresia and Stenosis: A Case SeriesRunqin Yang, Yu Zhao, Rui Li, et al.Frontiers in Neurology|September 12, 2022
Effects of aging on ocular vestibular-evoked myogenic potential using ER-3A insert earphone and B81 bone vibratorZhuo Xu, Zhilin Wang, Bo Zhong, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|October 11, 2021
[Clinical features and prognostic factors for early-stage external auditory canal carcinoma]Yu Han, Rui Li, Runqin Yang, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|April 2, 2021
[Comparative analysis of the hearing of three type reconstruction material in type Ⅱ tympanoplasty of 286 cases]Bo Yue, Xi Wang, Chanjuan Zhang, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|April 30, 2024
[Analysis of clinical manifestations and imaging features of facial nerve schwannomas]Yu Han, Hongsheng Liu, Runqin Yang, et al.Journal of Cancer Research and Clinical Oncology|August 28, 2023
Cuproptosis-related LINC02454 as a biomarker for laryngeal squamous cell carcinoma based on a novel risk model and in vitro and in vivo analysesQingwen Zhu, Ruyue Zhang, Fei Lu, et al.ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|January 25, 2022
De novo Splice Site Mutation of the CHD7 Gene in a Chinese Patient with Typical CHARGE SyndromeShujuan Wang, Ying Lin, Pengfei Liang, et al.Pageof 10