A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss

由 Huang, Bang-qing, Zeng, Jia-ling, Yuan, Yong-yi, Dai, Pu
發表在 J Otol (2015)

Granulation Tissue-type Hemangioma in the Internal Jugular Vein

由 Li, Jian-Hui, Yuan, Yong-Yi, Yuan, Jing, Huang, De-Liang, Liu, Ming-Bo
發表在 Chin Med J (Engl) (2018)

Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment

由 Gao, Xue, Yuan, Yong-Yi, Wang, Guo-Jian, Xu, Jin-Cao, Su, Yu, Lin, Xi, Dai, Pu
發表在 Biomed Res Int (2017)

Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling

由 Li Qi, Zhu Qing-wen, Yuan Yong-yi, Huang Sha-sha, Han Dong-yi, Huang De-liang, Dai Pu
出版 2012-11-01

Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling

由 Li, Qi, Zhu, Qing-wen, Yuan, Yong-yi, Huang, Sha-sha, Han, Dong-yi, Huang, De-liang, Dai, Pu
出版 2012

Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation

由 Guo, Chang, Huang, Sha-Sha, Yuan, Yong-Yi, Zhou, Ying, Wang, Ning, Kang, Dong-Yang, Yang, Su-Yan, Zhang, Xin, Gao, Xue, Dai, Pu
發表在 Neural Plast (2020)

Targeted Gene Capture and Massively Parallel Sequencing Identify TMC1 as the Causative Gene in a Six-generation Chinese Family with Autosomal Dominant Hearing Loss

由 Gao, Xue, Huang, Sha-Sha, Yuan, Yong-Yi, Wang, Guo-Jian, Xu, Jin-Cao, Ji, Yu-Bin, Han, Ming-Yu, Yu, Fei, Kang, Dong-Yang, Lin, Xi, Dai, Pu
發表在 Am J Med Genet A (2015)

Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss

由 Cui, Tian-Yi, Gao, Xue, Huang, Sha-Sha, Sun, Yan-Yan, Zhang, Si-Qi, Jiang, Xin-Xia, Yang, Yan-Zhong, Kang, Dong-Yang, Zhu, Qing-Wen, Yuan, Yong-Yi
發表在 Neural Plast (2020)

Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

由 Gao, Xue, Huang, Sha-Sha, Yuan, Yong-Yi, Xu, Jin-Cao, Gu, Ping, Bai, Dan, Kang, Dong-Yang, Han, Ming-Yu, Wang, Guo-Jian, Zhang, Mei-Guang, Li, Jia, Dai, Pu
發表在 Neural Plast (2017)

Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

由 Gao, Xue, Wang, Guo-Jian, Yuan, Yong-Yi, Xin, Feng, Han, Ming-Yu, Lu, Jing-Qiao, Zhao, Hui, Yu, Fei, Xu, Jin-Cao, Zhang, Mei-Guang, Dong, Jiang, Lin, Xi, Dai, Pu
出版 2014

Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

由 Gao, Xue, Wang, Guo-Jian, Yuan, Yong-Yi, Xin, Feng, Han, Ming-Yu, Lu, Jing-Qiao, Zhao, Hui, Yu, Fei, Xu, Jin-Cao, Zhang, Mei-Guang, Dong, Jiang, Lin, Xi, Dai, Pu
發表在 PLoS One (2015)

Novel Compound Heterozygous TMC1 Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family

由 Gao, Xue, Su, Yu, Guan, Li-Ping, Yuan, Yong-Yi, Huang, Sha-Sha, Lu, Yu, Wang, Guo-Jian, Han, Ming-Yu, Yu, Fei, Song, Yue-Shuai, Zhu, Qing-Yan, Wu, Jing, Dai, Pu
出版 2013

Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing

由 Gao, Xue, Zhu, Qing-yan, Song, Yue-Shuai, Wang, Guo-Jian, Yuan, Yong-Yi, Xin, Feng, Huang, Sha-Sha, Kang, Dong-Yang, Han, Ming-Yu, Guan, Li-ping, Zhang, Jian-guo, Dai, Pu
出版 2013

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

由 Gao, Xue, Xu, Jin-Cao, Wang, Wei-Qian, Yuan, Yong-Yi, Bai, Dan, Huang, Sha-Sha, Wang, Guo-Jian, Su, Yu, Li, Jia, Kang, Dong-Yang, Zhang, Mei-Guang, Lin, Xi, Dai, Pu
發表在 Biomed Res Int (2018)

Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family

由 Gao, Xue, Su, Yu, Chen, Yu-Lan, Han, Ming-Yu, Yuan, Yong-Yi, Xu, Jin-Cao, Xin, Feng, Zhang, Mei-Guang, Huang, Sha-Sha, Wang, Guo-Jian, Kang, Dong-Yang, Guan, Li-Ping, Zhang, Jian-Guo, Dai, Pu
發表在 PLoS One (2015)

A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss

由 Su, Yu, Tang, Wen-Xue, Gao, Xue, Yu, Fei, Dai, Zhi-Yao, Zhao, Jian-Dong, Lu, Yu, Ji, Fei, Huang, Sha-Sha, Yuan, Yong-Yi, Han, Ming-Yu, Song, Yue-Shuai, Zhu, Yu-Hua, Kang, Dong-Yang, HAN, Dong-Yi, Dai, Pu
出版 2014

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

由 Gao, Xue, Yuan, Yong-Yi, Lin, Qiong-Fen, Xu, Jin-Cao, Wang, Wei-Qian, Qiao, Yue-Hua, Kang, Dong-Yang, Bai, Dan, Xin, Feng, Huang, Sha-Sha, Qiu, Shi-Wei, Guan, Li-Ping, Su, Yu, Wang, Guo-Jian, Han, Ming-Yu, Jiang, Yi, Liu, Han-Kui, Dai, Pu
發表在 J Med Genet (2018)

Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China

由 Dai, Pu, Huang, Li-Hui, Wang, Guo-Jian, Gao, Xue, Qu, Chun-Yan, Chen, Xiao-Wei, Ma, Fu-Rong, Zhang, Jie, Xing, Wan-Li, Xi, Shu-Yan, Ma, Bin-Rong, Pan, Ying, Cheng, Xiao-Hua, Duan, Hong, Yuan, Yong-Yi, Zhao, Li-Ping, Chang, Liang, Gao, Ru-Zhen, Liu, Hai-Hong, Zhang, Wei, Huang, Sha-Sha, Kang, Dong-Yang, Liang, Wei, Zhang, Ke, Jiang, Hong, Guo, Yong-Li, Zhou, Yi, Zhang, Wan-Xia, Lyu, Fan, Jin, Ying-Nan, Zhou, Zhen, Lu, Hong-Li, Zhang, Xin, Liu, Ping, Ke, Jia, Hao, Jin-Sheng, Huang, Hai-Meng, Jiang, Di, Ni, Xin, Long, Mo, Zhang, Luo, Qiao, Jie, Morton, Cynthia Casson, Liu, Xue-Zhong, Cheng, Jing, Han, De-Min
發表在 Am J Hum Genet (2019)