Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Hearing Loss and COCH[original query] |
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| Absence of COCH mutations in patients with Meniere disease. European journal of human genetics : EJHG 2004 1 12 (1): 75-8. Sanchez Elena, López-Escámez Jose A, López-Nevot Miguel A, López-Nevot Alicia, Cortes Rosario, Martin Javi |
| Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. Journal of translational medicine 2014 12 (1): 311. Wei Qinjun, Zhu Hongmei, Qian Xuli, Chen Zhibin, Yao Jun, Lu Yajie, Cao Xin, Xing Guangqi |
| Distinct vestibular phenotypes in DFNA9 families with COCH variants. 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 2016 Jan . Kim Bong Jik, Kim Ah Reum, Han Kyu-Hee, Rah Yoon Chan, Hyun Jaihwan, Ra Brandon S, Koo Ja-Won, Choi Byung Yo |
| 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 |
| Audiovestibular Phenotypes and Advanced Magnetic Resonance Imaging Features of Cochlin Gene Mutation Carriers. Audiology & neuro-otology 2019 8 24 (4): 166-173. Conte Giorgio, Lo Russo Francesco, Caschera Luca, Zanetti Diego, Castorina Pierangela, Sina Clara, Triulzi Fabio, Di Berardino Federi |
| COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype-genotype study. Human genetics 2021 9 141 (3-4): 889-901. Oh Kyung Seok, Walls Daniel, Joo Sun Young, Kim Jung Ah, Yoo Jee Eun, Koh Young Ik, Kim Da Hye, Rim John Hoon, Choi Hye Ji, Kim Hye-Youn, Yu Seyoung, Smith Richard J, Choi Jae Young, Gee Heon Yung, Jung Jins |
| Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo. Current medical science 2021 Aug 41 (4): 673-679. Gao Yun, Wang Hong-Yang, Guan Jing, Lan Lan, Zhao Cui, Xie Lin-Yi, Wang Da-Yong, Wang Qiu- |
| Predictive Sensitivity and Concordance of Machine-learning Tools for Diagnosing DFNA9 in a Large Series of p.Pro51Ser Variant Carriers in the COCH-gene. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 1 42 (5): 671-677. Salah Mahadi, de Varebeke Sebastien Janssens, Fransen Erik, Topsakal Vedat, Van Camp Guy, Van Rompaey Vince |
| Radiologic Features in Cochlear Implant Candidates: A Prospective Study Comparing Candidates Carrying the p.Pro51Ser Mutation in Coagulation Factor C Homology With Noncarriers. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2022 8 43 (9): e969-e975. Beerten Anneleen, Bosmans Helena, Lauwers Meindert, Vermeulen Helene, Janssens de Varebeke Sebastien Pier |
| Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis. Biomolecules 2022 2 12 (2): . Robijn Sybren M M, Smits Jeroen J, Sezer Kadriye, Huygen Patrick L M, Beynon Andy J, van Wijk Erwin, Kremer Hannie, de Vrieze Erik, Lanting Cornelis P, Pennings Ronald J |
| Accelerated Cognitive Decline Associated With Hearing Loss and Bilateral Vestibulopathy: Insights From a Prospective Cross-Sectional Study Using the Repeatable Battery for the Assessment of Neuropsychological Status Adjusted for the Hearing Impaired in the DFNA9 Population. Ear and hearing 2023 1 . Gommeren Hanne, Bosmans Joyce, Moyaert Julie, Mertens Griet, Cras Patrick, Engelborghs Sebastiaan, Van Ombergen Angelique, Gilles Annick, Fransen Erik, van de Berg Raymond, JanssensdeVarebeke Sebastien, Van Rompaey Vince |
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