Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Hearing Loss and KCNQ4[original query] |
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KCNQ4: a gene for age-related hearing impairment? Human mutation 2006 Oct 27 (10): 1007-16. Van Eyken E, Van Laer L, Fransen E, Topsakal V, Lemkens N, Laureys W, Nelissen N, Vandevelde A, Wienker T, Van De Heyning P, Van Camp |
The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss. Human mutation 2006 Aug 27 (8): 786-95. Van Laer Lut, Carlsson Per-Inge, Ottschytsch Natacha, Bondeson Marie-Louise, Konings Annelies, Vandevelde Ann, Dieltjens Nele, Fransen Erik, Snyders Dirk, Borg Erik, Raes Adam, Van Camp G |
Identification of novel mutations in the KCNQ4 gene of patients with nonsyndromic deafness from Taiwan. Audiology & neuro-otology 2007 12 (1): 20-6. Su Ching-Chyuan, Yang Jiann-Jou, Shieh Jia-Ching, Su Mao-Chang, Li Shuan-Y |
Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss. Annals of human genetics 2009 Jul 73 (Pt 4): 411-21. Pawelczyk Malgorzata, Van Laer Lut, Fransen Erik, Rajkowska Elzbieta, Konings Annelies, Carlsson Per-Inge, Borg Erik, Van Camp Guy, Sliwinska-Kowalska Mario |
Absence of KCNQ4 mutation in Bengali families with ADNSHL originated from West Bengal, India. International journal of pediatric otorhinolaryngology 2017 Sep 100 35-38. Adhikary Bidisha, Bankura Biswabandhu, Biswas Subhradev, Paul Silpita, Das Madhusud |
STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2017 10 38 (10): e393-e400. Plevova Pavlina, Paprskarova Martina, Tvrda Petra, Turska Petra, Slavkovsky Rastislav, Mrazkova E |
Genetic variation in KCNQ4 gene is associated with susceptibility to noise-induced hearing loss in a Chinese population. Environmental toxicology and pharmacology 2018 Aug 63 55-59. Guo Haoran, Ding Enmin, Sheng Rongjian, Cheng Jian, Cai Wenyan, Guo Jiadi, Wang Ning, Zhang Hengdong, Zhu Bao |
Genetic Aetiology of Nonsyndromic Hearing Loss in Moravia-Silesia. Medicina (Kaunas, Lithuania) 2018 10 54 (2): . Plevova Pavlina, Tvrda Petra, Paprskarova Martina, Turska Petra, Kantorova Barbara, Mrazkova Eva, Zapletalova Ja |
Effect of GRM7 polymorphisms on the development of noise-induced hearing loss in Chinese Han workers: a nested case-control study. BMC medical genetics 2018 Jan 19 (1): 4. Yu Peipei, Jiao Jie, Chen Guoshun, Zhou Wenhui, Zhang Huanling, Wu Hui, Li Yanhong, Gu Guizhen, Zheng Yuxin, Yu Yue, Yu Shan |
A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. Human genetics 2020 5 139 (10): 1315-1323. Walls W Daniel, Moteki Hideaki, Thomas Taylor R, Nishio Shin-Ya, Yoshimura Hidekane, Iwasa Yoichiro, Frees Kathy L, Nishimura Carla J, Azaiez Hela, Booth Kevin T, Marini Robert J, Kolbe Diana L, Weaver A Monique, Schaefer Amanda M, Wang Kai, Braun Terry A, Usami Shin-Ichi, Barr-Gillespie Peter G, Richardson Guy P, Smith Richard J, Casavant Thomas |
[Prediction of KCNQ4gene polymorphism varies with CNE or noise exposure duration on the Risk of NIHL-Cox model analysis based on cohort study]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases 2020 Feb 38 (2): 111-116. Zhou W H, Gu G Z, Wu H, Li Y H, Chen G S, Zhang H L, Yu S F, Zheng Y |
A novel KCNQ4 gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non?syndromic deafness 2A. Molecular medicine reports 2021 4 23 (6): . Li Qiong, Liang Pengfei, Wang Shujuan, Li Wei, Wang Jian, Yang Yang, An Xiaogang, Chen Jun, Zha Dingj |
A KCNQ4 c.546C>G Genetic Variant Associated with Late Onset Non-Syndromic Hearing Loss in a Taiwanese Population. Genes 2021 11 12 (11): . Yen Ting-Ting, Chen I-Chieh, Hua Men-Wei, Wei Chia-Yi, Shih Kai-Hsiang, Li Jui-Lin, Lin Ching-Heng, Hsiao Tzu-Hung, Chen Yi-Ming, Jiang Rong-S |
Preimplantation genetic testing for hereditary hearing loss in Chinese population. Journal of assisted reproduction and genetics 2023 4 . Bi Qingling, Huang Shasha, Wang Hui, Gao Xue, Ma Minyue, Han Mingyu, Lu Sijia, Kang Dongyang, Nourbakhsh Aida, Yan Denise, Blanton Susan, Liu Xuezhong, Yuan Yongyi, Yao Yuanqing, Dai |
Overlooked KCNQ4 variants augment the risk of hearing loss. Experimental & molecular medicine 2023 4 . Oh Kyung Seok, Roh Jae Won, Joo Sun Young, Ryu Kunhi, Kim Jung Ah, Kim Se Jin, Jang Seung Hyun, Koh Young Ik, Kim Da Hye, Kim Hye-Youn, Choi Murim, Jung Jinsei, Namkung Wan, Nam Joo Hyun, Choi Jae Young, Gee Heon Yu |
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- Page last updated:May 06, 2024
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