Records 1 - 30 (of 46 Records)
|Query Trace: Hearing Loss and CDH23[original query]|
| Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss.
Neural plasticity 2018 8 2018 4920980.
Hu Songqun, Sun Feifei, Zhang Jie, Tang Yan, Qiu Jinhong, Wang Zhixia, Zhang Lupi
| 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
| 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
| Whole-exome sequencing identifies rare pathogenic and candidate variants in sporadic Chinese Han deaf patients.
Clinical genetics 2019 9 97 (2): 352-356.
Zou Songfeng, Mei Xueshuang, Yang Weiqiang, Zhu Rvfei, Yang Tao, Hu Hong
| 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
| Genetic Screening of the Usher Syndrome in Cuba.
Frontiers in genetics 2019 6 10 501.
Santana Elayne E, Fuster-García Carla, Aller Elena, Jaijo Teresa, García-Bohórquez Belén, García-García Gema, Millán José M, Lantigua Arace
| 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
| 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
| [Relationship research among CDH23 gene and the risk of noise-induced hearing loss].
Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases 2020 4 38 (2): 84-90.
Jiao J, Gu G Z, Chen G S, Zhang H L, Wu H, Li Y H, Zhou W H, Yu S
| Genetic testing has the potential to impact hearing preservation following cochlear implantation.
Acta oto-laryngologica 2020 3 140 (6): 438-444.
Yoshimura Hidekane, Moteki Hideaki, Nishio Shin-Ya, Miyajima Hiroki, Miyagawa Maiko, Usami Shin-Ic
| Association Analysis of Candidate Gene Polymorphisms and Audiometric Measures of Noise-Induced Hearing Loss in Young Musicians.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2020 3 41 (5): e538-e547.
Bhatt Ishan Sunilkumar, Dias Raquel, Washnik Nilesh, Wang Jin, Guthrie O'neil, Skelton Michael, Lane Jeffery, Wilder Jas
| 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
| 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
| 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-
| 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
| Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss.
International journal of pediatric otorhinolaryngology 2021 7 148 110817.
Liang Pengfei, Chen Fengping, Wang Shujuan, Li Qiong, Li Wei, Wang Jian, Chen Jun, Zha Dingj
| Identifying genetic risk variants associated with noise-induced hearing loss based on a novel strategy for evaluating individual susceptibility.
Hearing research 2021 6 407 108281.
Jiang Zhuang, Fa Botao, Zhang Xunmiao, Wang Jiping, Feng Yanmei, Shi Haibo, Zhang Yue, Sun Daoyuan, Wang Hui, Yin Shank
| Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.
Frontiers in genetics 2021 6 12 641925.
Fareed Mohd, Sharma Varun, Singh Inderpal, Rehman Sayeed Ur, Singh Gurdarshan, Afzal Mohamm
| Mitochondrial calcium uniporter is essential for hearing and hair cell preservation in congenic FVB/NJ mice.
Scientific reports 2021 5 11 (1): 9660.
Manikandan Mayakannan, Walker Steven, Deshmukh Aditi R, Perea Elizabeth, Wang Danqi, Alagramam Kumar N, Stepanyan Rub
| Cochlear Implantation Outcomes in Children With CDH23 Mutations-Associated Hearing Loss.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2021 11 167 (3): 560-565.
Chen Kaitian, Huang Bixue, Sun Jincangjian, Liang Yue, Xiong Guanx
| [Analysis of result of gene screening of neonatal deafness in Huizhou and surrounding urban areas].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 11 38 (12): 1176-1179.
Zeng Yun, Lu Xuanting, Wu Lifang, Zheng Y
| Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria.
European journal of human genetics : EJHG 2021 Nov .
Adeyemo Adebolajo, Faridi Rabia, Chattaraj Parna, Yousaf Rizwan, Tona Risa, Okorie Samuel, Bharadwaj Thashi, Nouel-Saied Liz M, Acharya Anushree, Schrauwen Isabelle, Morell Robert J, Leal Suzanne M, Friedman Thomas B, Griffith Andrew J, Roux Isabel
| 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
| Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher Genes.
Genes 2022 8 13 (8): .
Feenstra Helena M, Al-Khuzaei Saoud, Shah Mital, Broadgate Suzanne, Shanks Morag, Kamath Archith, Yu Jing, Jolly Jasleen K, MacLaren Robert E, Clouston Penny, Halford Stephanie, Downes Susan
| Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study.
Cytogenetic and genome research 2022 5 162 (1-2): 1-9.
Reis Cláudia Sousa, Quental Sofia, Fernandes Susana, Castedo Sérgio, Moura Carla Pin
| Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes.
Orphanet journal of rare diseases 2022 3 17 (1): 114.
Mutai Hideki, Momozawa Yukihide, Kamatani Yoichiro, Nakano Atsuko, Sakamoto Hirokazu, Takiguchi Tetsuya, Nara Kiyomitsu, Kubo Michiaki, Matsunaga Tats
| Molecular etiology study of hearing loss in 13 Chinese Han families.
Frontiers in neurology 2022 12 13 1048218.
Sun Lianhua, Lin Zhengyu, Wang Xiaowen, Shen Jiali, Li Yue, Huang Yuyu, Yang J
| Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss.
Human genetics 2022 1 141 (3-4): 903-914.
Usami Shin-Ichi, Isaka Yuichi, Miyagawa Maiko, Nishio Shin-
| Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel.
Human genomics 2023 1 17 (1): 1.
Ma Jing, Ma Xiuli, Lin Ken, Huang Rui, Bi Xianyun, Ming Cheng, Li Li, Li Xia, Li Guo, Zhao Liping, Yang Tao, Gao Yingqin, Zhang Tieso