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Frontiers in Molecular Neuroscience|October 28, 2022
Kölliker's organ-supporting cells and cochlear auditory developmentJianyong Chen, Dekun Gao, Lianhua Sun, et al.
International Journal of Pediatric Otorhinolaryngology|December 1, 2019
Identification of MYO6 copy number variation associated with cochlear aplasia by targeted sequencingLianhua Sun, Xiaowen Wang, Shule Hou, et al.
Frontiers in Neurology|December 26, 2022
Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencingLianhua Sun, Zhengyu Lin, Jifang Zhang, et al.
Hearing Research|November 8, 2022
A liquid chromatography-mass spectroscopy-based untargeted metabolomic study of the rat cochlear nucleus at various stages of maturityJun Tan, Yue Li, Dekun Gao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 14, 2013
Mutation spectrum and differential gene expression in cystic and solid vestibular schwannomaZhihua Zhang, Zhaoyan Wang, Lianhua Sun, et al.
Frontiers in Neurology|December 12, 2022
Molecular etiology study of hearing loss in 13 Chinese Han familiesLianhua Sun, Zhengyu Lin, Xiaowen Wang, et al.
Scientific Reports|October 21, 2016
Molecular etiology and genotype-phenotype correlation of Chinese Han deaf patients with type I and type II Waardenburg SyndromeLianhua Sun, Xiaohua Li, Jun Shi, et al.
Plos One|June 20, 2014
Characterization of spectrum, de novo rate and genotype-phenotype correlation of dominant GJB2 mutations in Chinese hansXiuhong Pang, Yongchuan Chai, Lianhua Sun, et al.
Frontiers in Molecular Neuroscience|October 3, 2022
Pathological mechanisms of connexin26-related hearing loss: Potassium recycling, ATP-calcium signaling, or energy supply?Penghui Chen, Wenjin Wu, Jifang Zhang, et al.
International Journal of Pediatric Otorhinolaryngology|February 11, 2014
Identification of both MT-RNR1 m.1555A>G and bi-allelic GJB2 mutations in probands with non-syndromic hearing lossYongchuan Chai, Lianhua Sun, Xiuhong Pang, et al.
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