Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Hearing Loss and EYA4[original query] |
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| Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study. Environmental health : a global access science source 2015 14 (1): 77. Zhang Xuhui, Liu Yi, Zhang Lei, Yang Zhangping, Yang Luoxian, Wang Xuchu, Jiang CaiXia, Wang Qiang, Xia Yuyong, Chen Yanjuan, Wu Ou, Zhu Yim |
| Identification of a novel truncation mutation of EYA4 in moderate degree hearing loss by targeted exome sequencing. 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 2015 May . Choi Hyun Seok, Kim Ah Reum, Kim Shin Hye, Choi Byung Yo |
| Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss. PloS one 2015 10 (3): e0119443. Kim Ye-Ri, Kim Min-A, Sagong Borum, Bae Seung-Hyun, Lee Hyo-Jeong, Kim Hyung-Jong, Choi Jae Young, Lee Kyu-Yup, Kim Un-Kyu |
| Genetic variation in EYA4 on the risk of noise-induced hearing loss in Chinese steelworks firm sample. Occupational and environmental medicine 2016 Dec 73 (12): 823-828. Yang Qiuyue, Xu Xiangrong, Jiao Jie, Zheng Yuxin, He Lihua, Yu Shanfa, Gu Guizhen, Chen Guoshun, Zhou Wenhui, Wu Hui, Li Yanhong, Zhang Huanling, Zhang Zengr |
A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records.
PLoS genetics 2016 Oct 12 (10): e1006371. Hoffmann Thomas J, Keats Bronya J, Yoshikawa Noriko, Schaefer Catherine, Risch Neil, Lustig Lawrence |
| [Association between eye absent homolog 4 gene polymorphisms and occupational noise-induced hearing loss]. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] 2017 Jan 51 (1): 27-33. Yang Q Y, Xu X R, Jiao J, Zheng Y X, He L H, Yu S F, Gu G Z, Chen G S, Zhou W H, Wu H, Li Y H, Zhang H L, Zhang Z |
| 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 |
| 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 |
| Prevalence and clinical features of hearing loss caused by EYA4 variants. Scientific reports 2020 Feb 10 (1): 3662. Shinagawa Jun, Moteki Hideaki, Nishio Shin-Ya, Ohyama Kenji, Otsuki Koshi, Iwasaki Satoshi, Masuda Shin, Oshikawa Chie, Ohta Yumi, Arai Yasuhiro, Takahashi Masahiro, Sakuma Naoko, Abe Satoko, Sakurai Yuika, Sakaguchi Hirofumi, Ishino Takashi, Uehara Natsumi, Usami Shin-Ic |
| Single gene variants causing deafness in Asian Indians. Journal of genetics 2021 7 100 . Panigrahi Inusha, Kumari Divya, Anil Kumar B |
| Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults. Human genetics 2021 Mar . Ahmadmehrabi Shadi, Li Binglan, Park Joseph, Devkota Batsal, Vujkovic Marijana, Ko Yi-An, Van Wagoner David, Tang W H Wilson, Krantz Ian, Ritchie Marylyn, , Brant Jason, Ruckenstein Michael J, Epstein Douglas J, Rader Daniel |
| Polymorphisms and NIHL: a systematic review and meta-analyses. Frontiers in cellular neuroscience 2023 7 17 1175427. Lu Wang, HanYu Wang, Feng Xiang, YuLu Xiang, Feng Xiong, QinXiu Zha |
| Identification of mutations on the EMD and EYA4 genes associated with Emery-Dreifuss muscular dystrophy and deafness: a case report. Frontiers in neurology 2023 5 14 1183147. Ana Karina Zambrano, Elius Paz-Cruz, Santiago Cadena-Ullauri, Patricia Guevara-Ramírez, Viviana A Ruiz-Pozo, Rafael Tamayo-Trujillo, Rita Ibarra-Castillo, José Luis Laso-Bayas, Nieves Doménech, Adriana Alexandra Ibarra-Rodríguez, Ricardo Hidal |
| Rare-variant association analysis reveals known and new age-related hearing loss genes. European journal of human genetics : EJHG 2023 2 . Cornejo-Sanchez Diana M, Li Guangyou, Fabiha Tabassum, Wang Ran, Acharya Anushree, Everard Jenna L, Kadlubowska Magda K, Huang Yin, Schrauwen Isabelle, Wang Gao T, DeWan Andrew T, Leal Suzanne |
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