Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: EYA4[original query] |
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Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci. Arthritis and rheumatism 2011 Mar 63 (3): 645-53. Plant Darren, Bowes John, Potter Catherine, Hyrich Kimme L, Morgan Ann W, Wilson Anthony G, Isaacs John D, , , Barton An |
Audiometric Characteristics of a Dutch DFNA10 Family With Mid-Frequency Hearing Impairment. Ear and hearing 2015 Sep . van Beelen Eline, Oonk Anne M M, Leijendeckers Joop M, Hoefsloot Elisabeth H, Pennings Ronald J E, Feenstra Ilse, Dieker Hendrik-Jan, Huygen Patrick L M, Snik Ad F M, Kremer Hannie, Kunst Henricus P |
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 |
Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia. PloS one 2017 8 12 (8): e0181840. Fedida Joel, Fressart Veronique, Charron Philippe, Surget Elodie, Hery Tiphaine, Richard Pascale, Donal Erwan, Keren Boris, Duthoit Guillaume, Hidden-Lucet Françoise, Villard Eric, Gandjbakhch Estel |
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Scientific reports 2017 Apr 7 45040. Gorski Mathias, van der Most Peter J, Teumer Alexander, Chu Audrey Y, Li Man, Mijatovic Vladan, Nolte Ilja M, Cocca Massimiliano, Taliun Daniel, Gomez Felicia, Li Yong, Tayo Bamidele, Tin Adrienne, Feitosa Mary F, Aspelund Thor, Attia John, Biffar Reiner, Bochud Murielle, Boerwinkle Eric, Borecki Ingrid, Bottinger Erwin P, Chen Ming-Huei, Chouraki Vincent, Ciullo Marina, Coresh Josef, Cornelis Marilyn C, Curhan Gary C, d'Adamo Adamo Pio, Dehghan Abbas, Dengler Laura, Ding Jingzhong, Eiriksdottir Gudny, Endlich Karlhans, Enroth Stefan, Esko Tõnu, Franco Oscar H, Gasparini Paolo, Gieger Christian, Girotto Giorgia, Gottesman Omri, Gudnason Vilmundur, Gyllensten Ulf, Hancock Stephen J, Harris Tamara B, Helmer Catherine, Höllerer Simon, Hofer Edith, Hofman Albert, Holliday Elizabeth G, Homuth Georg, Hu Frank B, Huth Cornelia, Hutri-Kähönen Nina, Hwang Shih-Jen, Imboden Medea, Johansson Åsa, Kähönen Mika, König Wolfgang, Kramer Holly, Krämer Bernhard K, Kumar Ashish, Kutalik Zoltan, Lambert Jean-Charles, Launer Lenore J, Lehtimäki Terho, de Borst Martin, Navis Gerjan, Swertz Morris, Liu Yongmei, Lohman Kurt, Loos Ruth J F, Lu Yingchang, Lyytikäinen Leo-Pekka, McEvoy Mark A, Meisinger Christa, Meitinger Thomas, Metspalu Andres, Metzger Marie, Mihailov Evelin, Mitchell Paul, Nauck Matthias, Oldehinkel Albertine J, Olden Matthias, Wjh Penninx Brenda, Pistis Giorgio, Pramstaller Peter P, Probst-Hensch Nicole, Raitakari Olli T, Rettig Rainer, Ridker Paul M, Rivadeneira Fernando, Robino Antonietta, Rosas Sylvia E, Ruderfer Douglas, Ruggiero Daniela, Saba Yasaman, Sala Cinzia, Schmidt Helena, Schmidt Reinhold, Scott Rodney J, Sedaghat Sanaz, Smith Albert V, Sorice Rossella, Stengel Benedicte, Stracke Sylvia, Strauch Konstantin, Toniolo Daniela, Uitterlinden Andre G, Ulivi Sheila, Viikari Jorma S, Völker Uwe, Vollenweider Peter, Völzke Henry, Vuckovic Dragana, Waldenberger Melanie, Jin Wang Jie, Yang Qiong, Chasman Daniel I, Tromp Gerard, Snieder Harold, Heid Iris M, Fox Caroline S, Köttgen Anna, Pattaro Cristian, Böger Carsten A, Fuchsberger Christi |
[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 |
Targeted next generation sequencing reveals OTOF mutations in auditory neuropathy spectrum disorder. International journal of pediatric otorhinolaryngology 2018 10 115 19-23. Chen Kaitian, Liu Min, Wu Xuan, Zong Ling, Jiang Hongy |
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 |
Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2021 3 73 (10): 1860-1870. Jamieson Sarra E, Fakiola Michaela, Tang Dave, Scaman Elizabeth, Syn Genevieve, Francis Richard W, Coates Harvey L, Anderson Denise, Lassmann Timo, Cordell Heather J, Blackwell Jenefer |
Prognostic Role of EYA4 in Lower Grade Glioma with IDH1 Mutation and 1p19q Co-Deletion. World neurosurgery 2021 2 149 e1174-e1179. Zhu Jin, Hu Li-Bo, Zhao Ya-Peng, Zhang Yu- |
Genome-wide association study of brain tau deposition as measured by F-flortaucipir positron emission tomography imaging. Neurobiology of aging 2022 Sep 120 128-136. Guo Yu, Yang Yu-Xiang, Zhang Ya-Ru, Huang Yu-Yuan, Chen Ke-Liang, Chen Shi-Dong, Dong Prof Qiang, Yu Jin-Tai, |
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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- Page last updated:Apr 29, 2024
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