Profiles of the auditory epithelia related microRNA expression in neonatal and adult rats

por Guo, Weiwei, Yuan, Yongyi, Hou, Zhaohui, Wang, Xiang, Yang, Shiming
Publicado 2014

A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafness

por Huang, Aiping, Yuan, Yongyi, Liu, Yanping, Zhu, Qingwen, Dai, Pu
Publicado 2015

The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals

por Huang, Shasha, Huang, Bangqing, Wang, Guojian, Yuan, Yongyi, Dai, Pu
Publicado 2015

Editorial: Hearing Loss: Mechanisms and Prevention

por Chai, Renjie, Li, Hongzhe, Yang, Tao, Sun, Shan, Yuan, Yongyi
Publicado 2022

Two SOX11 variants cause Coffin–Siris syndrome with a new feature of sensorineural hearing loss

por Wang, Qiuquan, Wu, Jie, Yang, Jinyuan, Huang, Shasha, Yuan, Yongyi, Dai, Pu
Publicado 2022

SLC26A4 gene copy number variations in Chinese patients with non-syndromic enlarged vestibular aqueduct

por Zhao, Jiandong, Yuan, Yongyi, Chen, Jing, Huang, Shasha, Wang, Guojian, Han, Dongyi, Dai, Pu
Publicado 2012

A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2

por Huang, Bangqing, Liu, Yanping, Gao, Xue, Xu, Jincao, Dai, Pu, Zhu, Qingwen, Yuan, Yongyi
Publicado 2017

Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation

por Yuan, Yongyi, Gao, Xue, Huang, Bangqing, Lu, Jingqiao, Wang, Guojian, Lin, Xi, Qu, Yan, Dai, Pu
Publicado 2016

Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients

por Fu, Ying, Huang, Shasha, Gao, Xue, Han, Mingyu, Wang, Guojian, Kang, Dongyang, Yuan, Yongyi, Dai, Pu
Publicado 2022

Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2

por Yuan, Yongyi, Yu, Fei, Wang, Guojian, Huang, Shasha, Yu, Ruili, Zhang, Xin, Huang, Deliang, Han, Dongyi, Dai, Pu
Publicado 2010

KCNJ10 May Not Be a Contributor to Nonsyndromic Enlargement of Vestibular Aqueduct (NSEVA) in Chinese Subjects

por Zhao, Jiandong, Yuan, Yongyi, Huang, Shasha, Huang, Bangqing, Cheng, Jing, Kang, Dongyang, Wang, Guojian, Han, Dongyi, Dai, Pu
Publicado 2014

A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss

por Zhang, Dejun, Wu, Jie, Yuan, Yongyi, Li, Xiaohong, Gao, Xue, Han, Mingyu, Gao, Song, Huang, Shasha, Dai, Pu
Publicado 2022

Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct

por Huang, Shasha, Han, Dongyi, Yuan, Yongyi, Wang, Guojian, Kang, Dongyang, Zhang, Xin, Yan, Xiaofei, Meng, Xiaoxiao, Dong, Min, Dai, Pu
Publicado 2011

Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation

por Zhu, Yuhua, Huang, Shasha, Kang, Dongyang, Han, Mingyu, Wang, Guojian, Yuan, Yongyi, Su, Yu, Yuan, Huijun, Zhai, Suoqiang, Dai, Pu
Publicado 2014

A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability

por Zhao, Weihao, Gao, Xue, Qiu, Shiwei, Gao, Bo, Gao, Song, Zhang, Xin, Kang, Dongyang, Han, Weiju, Dai, Pu, Yuan, Yongyi
Publicado 2019

Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

por Dai, Pu, Yuan, Yongyi, Huang, Deliang, Zhu, Xiuhui, Yu, Fei, Kang, Dongyang, Yuan, Huijun, Wu, Bailin, Han, Dongyi, Wong, Lee-Jun C
Publicado 2008

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

por Yuan, Yongyi, You, Yiwen, Huang, Deliang, Cui, Jinghong, Wang, Yong, Wang, Qiang, Yu, Fei, Kang, Dongyang, Yuan, Huijun, Han, Dongyi, Dai, Pu
Publicado 2009

Common Molecular Etiologies Are Rare in Nonsyndromic Tibetan Chinese Patients with Hearing Impairment

por Yuan, Yongyi, Zhang, Xun, Huang, Shasha, Zuo, Lujie, Zhang, Guozheng, Song, Yueshuai, Wang, Guojian, Wang, Hongtian, Huang, Deliang, Han, Dongyi, Dai, Pu
Publicado 2012

Molecular Epidemiology and Functional Assessment of Novel Allelic Variants of SLC26A4 in Non-Syndromic Hearing Loss Patients with Enlarged Vestibular Aqueduct in China

por Yuan, Yongyi, Guo, Weiwei, Tang, Jie, Zhang, Guozheng, Wang, Guojian, Han, Mingyu, Zhang, Xun, Yang, Shiming, He, David Z. Z., Dai, Pu
Publicado 2012

Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China

por Xin, Feng, Yuan, Yongyi, Deng, Xiaoming, Han, Mingyu, Wang, Guojian, Zhao, Jiandong, Gao, Xue, Liu, Jun, Yu, Fei, Han, Dongyi, Dai, Pu
Publicado 2013