Records 1 - 26
| Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo.
Current medical science 2021 Aug 41 (4): 673-679.
Gao Yun, Wang Hong-Yang, Guan Jing, Lan Lan, Zhao Cui, Xie Lin-Yi, Wang Da-Yong, Wang Qiu-
| PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India.
Annals of human genetics 2021 Aug .
Vanniya S Paridhy, Chandru Jayasankaran, Jeffrey Justin Margret, Rabinowitz Tom, Brownstein Zippora, Krishnamoorthy Mathuravalli, Avraham Karen B, Cheng Le, Shomron Noam, Srisailapathy C R Srikuma
| Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Jul .
Bhatt Ishan Sunilkumar, Dias Raquel, Torkamani A
| Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.
Molecular genetics & genomic medicine 2020 Oct e1539.
Xiang Yan-Bao, Xu Chen-Yang, Xu Yun-Zhi, Li Huan-Zheng, Zhou Li-Li, Xu Xue-Qin, Chen Zi-Hui, Tang Shao-H
| The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China.
International journal of pediatric otorhinolaryngology 2020 May 136 110143.
Liu Xiao-Wen, Wang Jian-Chao, Wang Su-Yang, Li Shu-Juan, Zhu Yi-Ming, Ding Wen-Juan, Xu Chen-Yang, Duan Lei, Xu Bai-Cheng, Guo Yu-F
| Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
Orphanet journal of rare diseases 2020 Jan 15 (1): 29.
Yu Xiaoyu, Lin Yun, Xu Jun, Che Tuanjie, Li Lin, Yang Tao, Wu H
| Identification of a novel CDH23 gene variant associated with non-syndromic progressive hearing loss in a Chinese family: Individualized hearing rehabilitation guided by genetic diagnosis.
International journal of pediatric otorhinolaryngology 2019 Aug 127 109649.
Chen Ying, Li Yun, Ren Yan, Li Haifeng, Huang Meiping, Jia Huan, Yang Tao, Wang Zhaoyan, Huang Zhiwu, Wu H
| Screening of noise-induced hearing loss (NIHL)-associated SNPs and the assessment of its genetic susceptibility.
Environmental health : a global access science source 2019 Apr 18 (1): 30.
Zhang Xuhui, Ni Yaqin, Liu Yi, Zhang Lei, Zhang Meibian, Fang Xinyan, Yang Zhangping, Wang Qiang, Li Hao, Xia Yuyong, Zhu Yim
| Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss.
Fetal and pediatric pathology 2019 Apr 38 (2): 93-102.
Alimardani Maliheh, Hosseini Seyed Mojtaba, Khaniani Mahmoud Shekari, Haghi Mohsen Rajati, Eslahi Atieh, Farjami Mashsa, Chezgi Javad, Derakhshan Sima Mansoori, Mojarrad Maj
| The p.P240L variant of CDH23 and the risk of nonsyndromic hearing loss: a meta-analysis.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2019 Jan 276 (1): 11-16.
Xu Tianni, Zhu Wei, Wang Pi
| Comprehensive Molecular Screening in Chinese Usher Syndrome Patients.
Investigative ophthalmology & visual science 2018 Mar 59 (3): 1229-1237.
Sun Tengyang, Xu Ke, Ren Yanfan, Xie Yue, Zhang Xiaohui, Tian Lu, Li Ya
| Recurrence of reported CDH23 mutations causing DFNB12 in a special cohort of South Indian hearing impaired assortative mating families - an evaluation.
Annals of human genetics 2017 Nov .
Vanniya S Paridhy, Chandru Jayasankaran, Pavithra Amritkumar, Jeffrey Justin Margret, Kalaimathi Murugesan, Ramakrishnan Rajagopalan, Karthikeyen Natarajan P, C R Srikumari Srisailapat
| [Association between CDH23 gene polymorphisms and susceptibility to noise-induced hearing loss in the Chinese population: a meta-analysis].
Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases 2016 Dec 34 (12): 920-923.
Yu J N, Wu S S, He C H, Zhang C Y, Mu H X, Ma W S, Liu B, Zhang Y, Yu S
| Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family.
Iranian journal of basic medical sciences 2016 Jul 19 (7): 772-8.
Reiisi Somayeh, Tabatabaiefar Mohammad Amin, Sanati Mohammad Hosein, Chaleshtori Morteza Hashemzad
| Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans.
PloS one 2016 11 (10): e0165680.
Kim Bong Jik, Kim Ah Reum, Lee Chung, Kim So Young, Kim Nayoung K D, Chang Mun Young, Rhee Jihye, Park Mi-Hyun, Koo Soo Kyung, Kim Min Young, Han Jin Hee, Oh Seung-Ha, Park Woong-Yang, Choi Byung Yo
| Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss population.
Clinical genetics 2015 Sep .
Moteki Hideaki, Azaiez Hela, Booth Kevin T, Shearer A Eliot, Sloan Christina M, Kolbe Diana L, Nishio Shin-Ya, Hattori Mitsuru, Usami Shin-Ichi, Smith Richard J
| Deafness gene variations in a 1120 nonsyndromic hearing loss cohort: molecular epidemiology and deafness mutation spectrum of patients in Japan.
The Annals of otology, rhinology, and laryngology 2015 May 124 Suppl 1 49S-60S.
Nishio Shin-Ya, Usami Shin-Ic
| Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss.
PloS one 2015 10 (11): e0142154.
Atik Tahir, Onay Huseyin, Aykut Ayca, Bademci Guney, Kirazli Tayfun, Tekin Mustafa, Ozkinay Fer
| High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss.
Orphanet journal of rare diseases 2015 10 (1): 60.
Mizutari Kunio, Mutai Hideki, Namba Kazunori, Miyanaga Yuko, Nakano Atsuko, Arimoto Yukiko, Masuda Sawako, Morimoto Noriko, Sakamoto Hirokazu, Kaga Kimitaka, Matsunaga Tats
| Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology.
BMC medical genetics 2015 16 (1): 85.
Svidnicki Maria Carolina Costa Melo, Silva-Costa Sueli Matilde, Ramos Priscila Zonzini, Dos Santos Nathalia Zocal Pereira, Martins Fábio Tadeu Arrojo, Castilho Arthur Menino, Sartorato Edi Lúc
| Strong founder effect of p.P240L in CDH23 in Koreans and its significant contribution to severe-to-profound nonsyndromic hearing loss in a Korean pediatric population.
Journal of translational medicine 2015 13 263.
Kim So Young, Kim Ah Reum, Kim Nayoung K D, Kim Min Young, Jeon Eun-Hee, Kim Bong Jik, Han Young Eun, Chang Mun Young, Park Woong-Yang, Choi Byung Yo
| Gene-gene interaction of GJB2, SOD2, and CAT on occupational noise-induced hearing loss in Chinese Han population.
Biomedical and environmental sciences : BES 2014 Dec 27 (12): 965-8.
Wang Sheng Li, Yu Lu Gang, Liu Ren Ping, Zhu Wan Zhan, Gao Wei Min, Xue Li Ping, Jiang Xu, Zhang Ya Han, Yi Ding, Chen Dong, Zhang Yong Ho
| Genetic variants of CDH23 associated with noise-induced hearing loss.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2014 Feb 35 (2): 358-65.
Kowalski Tomasz Jarema, Pawelczyk Malgorzata, Rajkowska Elzbieta, Dudarewicz Adam, Sliwinska-Kowalska Mario
| Targeted next generation sequencing for molecular diagnosis of Usher syndrome.
Orphanet journal of rare diseases 2014 9 168.
Aparisi María J, Aller Elena, Fuster-García Carla, García-García Gema, Rodrigo Regina, Vázquez-Manrique Rafael P, Blanco-Kelly Fiona, Ayuso Carmen, Roux Anne-Françoise, Jaijo Teresa, Millán José
| Novel mutations in the USH1C gene in Usher syndrome patients.
Molecular vision 2010 16 2948-54.
Aparisi María José, García-García Gema, Jaijo Teresa, Rodrigo Regina, Graziano Claudio, Seri Marco, Simsek Tulay, Simsek Enver, Bernal Sara, Baiget Montserrat, Pérez-Garrigues Herminio, Aller Elena, Millán José Mar
| [Association of cadherin CDH23 gene polymorphisms with noise induced hearing loss in Chinese workers].
Wei sheng yan jiu = Journal of hygiene research 2006 Jan 35 (1): 19-22.
Yang Miao, Tan Hao, Zheng Jian-Ru, Wang Feng, Jiang Changzheng, He Mei'an, Chen Yongwen, Wu Tangch