Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Hearing Loss and TMPRSS3[original query] |
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| Genetic analysis of TMPRSS3 gene in the Korean population with autosomal recessive nonsyndromic hearing loss. Gene 2013 Dec 532 (2): 276-80. Lee Jinwook, Baek Jeong-In, Choi Jae Young, Kim Un-Kyung, Lee Sang-Heun, Lee Kyu-Y |
| Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations. Clinical genetics 2015 Jun 87 (6): 588-93. Gu X, Guo L, Ji H, Sun S, Chai R, Wang L, Li |
| TMPRSS3 mutations in autosomal recessive nonsyndromic hearing loss. 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 Jun . Battelino Saba, Klancar Gasper, Kovac Jernej, Battelino Tadej, Trebusak Podkrajsek Katari |
| The patients associated with TMPRSS3 mutations are good candidates for electric acoustic stimulation. The Annals of otology, rhinology, and laryngology 2015 May 124 Suppl 1 193S-204S. Miyagawa Maiko, Nishio Shin-Ya, Sakurai Yuika, Hattori Mitsuru, Tsukada Keita, Moteki Hideaki, Kojima Hiromi, Usami Shin-Ic |
| 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 |
| The Analysis of A Frequent TMPRSS3 Allele Containing P.V116M and P.V291L in A Cis Configuration among Deaf Koreans. International journal of molecular sciences 2017 Oct 18 (11): . Kim Ah Reum, Chung Juyong, Kim Nayoung K D, Lee Chung, Park Woong-Yang, Oh Doo-Yi, Choi Byung Yo |
| Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation. Ear and hearing 2019 5 41 (1): 114-124. Song Mee Hyun, Jung Jinsei, Rim John Hoon, Choi Hye Ji, Lee Hack June, Noh Byunghwa, Lee Jun Suk, Gee Heon Yung, Choi Jae You |
| Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss. Molecular genetics & genomic medicine 2019 4 7 (6): e685. Li Xinlei, Tan Bo, Wang Xiaoqian, Xu Xiaofei, Wang Cuicui, Zhong Mingjun, Zhao Qiuling, Bao Zhongwei, Peng Weihua, Zhang Lei, Cheng Jing, Lu Yu, Wu Peina, Yuan Huij |
| Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria. European journal of human genetics : EJHG 2021 Nov . Adeyemo Adebolajo, Faridi Rabia, Chattaraj Parna, Yousaf Rizwan, Tona Risa, Okorie Samuel, Bharadwaj Thashi, Nouel-Saied Liz M, Acharya Anushree, Schrauwen Isabelle, Morell Robert J, Leal Suzanne M, Friedman Thomas B, Griffith Andrew J, Roux Isabel |
| Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss. Scientific reports 2021 11 11 (1): 22488. Pavlenkova Zuzana, Varga Lukas, Borecka Silvia, Karhanek Miloslav, Huckova Miloslava, Skopkova Martina, Profant Milan, Gasperikova Danie |
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults.
Communications biology 2022 06 5 (1): 540. Praveen Kavita, Dobbyn Lee, Gurski Lauren, Ayer Ariane H, Staples Jeffrey, Mishra Shawn, Bai Yu, Kaufman Alexandra, Moscati Arden, Benner Christian, Chen Esteban, Chen Siying, Popov Alexander, Smith Janell, , , , Melander Olle, Jones Marcus B, Marchini Jonathan, Balasubramanian Suganthi, Zambrowicz Brian, Drummond Meghan C, Baras Aris, Abecasis Goncalo R, Ferreira Manuel A, Stahl Eli A, Coppola Giovan |
| A frameshift mutation of TMPRSS3 in a Chinese family with non-syndromic hearing loss. Frontiers in pediatrics 2022 12 10 1032659. Liang Jingwen, Yu Zhuoheng, Wang Zhangxing, Chen Jianxia, Liu Yihuan, Yin Zhaoqing, Xu Ruihu |
| Cochlear Implants in Deaf Patients with Novel TMPRSS3 Gene Mutation. Alternative therapies in health and medicine 2023 4 . Yu Rong, Wang Kai, You Liujun, Kang Junxin, Ai Honghui, Jiang Hongq |
| Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes. JAMA otolaryngology-- head & neck surgery 2023 1 149 (3): 212-222. Carlson Ryan J, Walsh Tom, Mandell Jessica B, Aburayyan Amal, Lee Ming K, Gulsuner Suleyman, Horn David L, Ou Henry C, Sie Kathleen C Y, Mancl Lisa, Rubinstein Jay, King Mary-Clai |
| Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis. Clinical genetics 2024 8 . Masoome Alerasool, Atieh Eslahi, Barbara Vona, Mir Salar Kahaei, Nasrin Kaseb Mojaver, Mohsen Rajati, Alireza Pasdar, Mohammad Mehdi Ghasemi, Ehsan Saburi, Reza Mousavi Ardehaie, Majid Hadadi Aval, Mohammad Reza Tale, Navid Nourizadeh, Mohammad Reza Afzalzadeh, Hamid Tayarani Niknezhad, Majid Mojarr |
| Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia. Croatian medical journal 2024 6 65 (3): 198-208. Ivona Sansovi?, Ana-Maria Meaši?, Adriana Bobinec, Leona Morožin Pohovski, Ljubica Odak, Katarina Vulin, Bernarda Lozi?, Mijana Kero, Sanda Huljev Frkovi?, Silvija Pušelj |
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