Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Hearing and OTOG[original query] |
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| 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 |
| Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease. Ear and hearing 2020 11 41 (6): 1598-1605. Roman-Naranjo Pablo, Gallego-Martinez Alvaro, Soto-Varela Andrés, Aran Ismael, Moleon Maria Del Carmen, Espinosa-Sanchez Juan Manuel, Amor-Dorado Juan Carlos, Batuecas-Caletrio Angel, Perez-Vazquez Paz, Lopez-Escamez Jose Anton |
| 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 |
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.
Communications biology 2021 Oct 4 (1): 1148. Skuladottir Astros Th, Bjornsdottir Gyda, Nawaz Muhammad Sulaman, Petersen Hannes, Rognvaldsson Solvi, Moore Kristjan Helgi Swerford, Olafsson Pall I, Magnusson Sigurður H, Bjornsdottir Anna, Sveinsson Olafur A, Sigurdardottir Gudrun R, Saevarsdottir Saedis, Ivarsdottir Erna V, Stefansdottir Lilja, Gunnarsson Bjarni, Muhlestein Joseph B, Knowlton Kirk U, Jones David A, Nadauld Lincoln D, Hartmann Annette M, Rujescu Dan, Strupp Michael, Walters G Bragi, Thorgeirsson Thorgeir E, Jonsdottir Ingileif, Holm Hilma, Thorleifsson Gudmar, Gudbjartsson Daniel F, Sulem Patrick, Stefansson Hreinn, Stefansson Ka |
| 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 |
| Whole Exome Sequencing of Non-Syndromic Hearing Loss Patients. Iranian journal of public health 2024 6 53 (2): 453-461. Hossein Naddafnia, Zahra Noormohammadi, Shiva Irani, Iman Salahshoorif |
| MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population. BMC medical genomics 2024 1 17 (1): 32. Lang Zhang, Jin-Yuan Yang, Qiu-Quan Wang, Xue Gao, Guo-Jian Wang, Ming-Yu Han, Dong-Yang Kang, Dong-Yi Han, Sha-Sha Huang, Yong-Yi Yu |
- Page last reviewed:Feb 1, 2024
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