Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: KCNQ4[original query] |
---|
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 |
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment. Journal of medical genetics 2007 Sep 44 (9): 570-8. Van Eyken E, Van Camp G, Fransen E, Topsakal V, Hendrickx J J, Demeester K, Van de Heyning P, Mäki-Torkko E, Hannula S, Sorri M, Jensen M, Parving A, Bille M, Baur M, Pfister M, Bonaconsa A, Mazzoli M, Orzan E, Espeso A, Stephens D, Verbruggen K, Huyghe J, Dhooge I, Huygen P, Kremer H, Cremers C W R J, Kunst S, Manninen M, Pyykkö I, Lacava A, Steffens M, Wienker T F, Van Laer |
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 |
A genome-wide association study of aging.
Neurobiology of aging 2011 Nov 32 (11): 2109.e15-28. Walter Stefan, Atzmon Gil, Demerath Ellen W, Garcia Melissa E, Kaplan Robert C, Kumari Meena, Lunetta Kathryn L, Milaneschi Yuri, Tanaka Toshiko, Tranah Gregory J, Völker Uwe, Yu Lei, Arnold Alice, Benjamin Emelia J, Biffar Reiner, Buchman Aron S, Boerwinkle Eric, Couper David, De Jager Philip L, Evans Denis A, Harris Tamara B, Hoffmann Wolfgang, Hofman Albert, Karasik David, Kiel Douglas P, Kocher Thomas, Kuningas Maris, Launer Lenore J, Lohman Kurt K, Lutsey Pamela L, Mackenbach Johan, Marciante Kristin, Psaty Bruce M, Reiman Eric M, Rotter Jerome I, Seshadri Sudha, Shardell Michelle D, Smith Albert V, van Duijn Cornelia, Walston Jeremy, Zillikens M Carola, Bandinelli Stefania, Baumeister Sebastian E, Bennett David A, Ferrucci Luigi, Gudnason Vilmundur, Kivimaki Mika, Liu Yongmei, Murabito Joanne M, Newman Anne B, Tiemeier Henning, Franceschini No |
Application of a combination of a knowledge-based algorithm and 2-stage screening to hypothesis-free genomic data on irinotecan-treated patients for identification of a candidate single nucleotide polymorphism related to an adverse effect. PloS one 2014 9 (8): e105160. Takahashi Hiro, Sai Kimie, Saito Yoshiro, Kaniwa Nahoko, Matsumura Yasuhiro, Hamaguchi Tetsuya, Shimada Yasuhiro, Ohtsu Atsushi, Yoshino Takayuki, Doi Toshihiko, Okuda Haruhiro, Ichinohe Risa, Takahashi Anna, Doi Ayano, Odaka Yoko, Okuyama Misuzu, Saijo Nagahiro, Sawada Jun-ichi, Sakamoto Hiromi, Yoshida Teruhi |
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 mutation of familial dilated cardiomyopathy based on next?generation semiconductor sequencing. Molecular medicine reports 2018 9 18 (5): 4271-4280. Lin Xin-Fu, Luo Jie-Wei, Liu Gui, Zhu Yao-Bin, Jin Zhao, Lin Xi |
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 |
Genetic Basis and Prognostic Value of Exercise QT Dynamics.
Circulation. Genomic and precision medicine 2020 Aug 13 (4): e002774. van Duijvenboden Stefan, Ramírez Julia, Young William J, Mifsud Borbala, Orini Michele, Tinker Andrew, Munroe Patricia B, Lambiase Pier |
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 |
Cholinergic Synapse Pathway Gene Polymorphisms Associated With Late-Phase Responses in Allergic Rhinitis. Frontiers in allergy 2022 4 2 724328. Samra Simranjit K, Rajasekaran Ashwini, Sandford Andrew J, Ellis Anne K, Tebbutt Scott |
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 |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: