Yongyi Yuan
12PUBLICATIONS
10CO-AUTHORS
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Publications (12)
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|Mar 28, 2026
Therapeutic potential of cAMP-mediated lysosomal pH modulation in ATP6V1B2-related neuropathology.Lu Zheng, Weihao Zhao, Guang Yang
|Mar 16, 2026
Genotype-phenotype correlation-driven precision management in hereditary conductive and mixed hearing loss.Qin Wang, Xiedong Wu, Guojie Dong
|Dec 06, 2025
A Novel Frameshift Variant c.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss.Li-Ting Peng, Wei-Qian Wang, Sha-Sha Huang
|Mar 11, 2025
Single Administration of AAV-mAtp6v1b2 Gene Therapy Rescues Hearing and Vestibular Disorders Caused by Atp6v1b2-Induced Lysosomal Dysfunction in Hair Cells.Gege Wei, Shiwei Qiu, Xue Gao
|Nov 14, 2022
A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3-4.Kun Yang, Xi Wang, Wei-Qian Wang
|Jul 07, 2021
Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.Xue Gao, Pu Dai, Yong-Yi Yuan
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