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Journal of Translational Medicine|October 4, 2011
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueductShasha Huang, Dongyi Han, Yongyi Yuan, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype]Guojian Wang, Yongyi Yuan, Rong Li, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|September 30, 2009
Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueductSamuel Reyes, Guojian Wang, Xiaomei Ouyang, et al.
Plos One|March 6, 2012
Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairmentYongyi Yuan, Xun Zhang, Shasha Huang, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 10, 2024
Clinical Application of the 4K-3D Exoscope System in Cochlear ImplantationHonglei Zhang, Guojian Wang, Xin Zhang, et al.
Journal of Translational Medicine|December 18, 2013
Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, ChinaFeng Xin, Yongyi Yuan, Xiaoming Deng, et al.
Clinical Chemistry|November 14, 2023
Exploration of a Novel Noninvasive Prenatal Testing Approach for Monogenic Disorders Based on Fetal Nucleated Red Blood CellsXiaoge Li, Dejun Zhang, Xing Zhao, et al.
Orphanet Journal of Rare Diseases|September 13, 2024
Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese populationHaifeng Feng, Shasha Huang, Ying Ma, et al.
Scientific Reports|June 17, 2026
An in situ non-contact 3D microscopic measurement system for temporal bone anatomy based on stereo imagingHonglei Zhang, Wei Liu, Junhui Tang, et al.
Stem Cell Research|June 12, 2022
Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10Xiaohong Li, Xue Gao, Shasha Huang, et al.
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