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International Journal of Audiology Volume 51, 2012 - Issue 11
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Research Article

A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies

Elina Hietikko *Oulu Center for Cell-Matrix Research, Biocenter and Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Oulu, Finland;Department of Otorhinolaryngology, Institute of Clinical Medicine, University of Oulu, FinlandCorrespondence[email protected] [email protected]
,
Jouko KotimäkiDepartment of Otorhinolaryngology, Central Hospital of Kainuu, Finland;Department of Otorhinolaryngology, Institute of Clinical Medicine, University of Oulu, Finland
,
Annaleena Okuloff *Oulu Center for Cell-Matrix Research, Biocenter and Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Oulu, Finland;Department of Otorhinolaryngology, Institute of Clinical Medicine, University of Oulu, Finland
,
Martti Sorri *Oulu Center for Cell-Matrix Research, Biocenter and Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Oulu, Finland;Department of Otorhinolaryngology, Institute of Clinical Medicine, University of Oulu, Finland
&
Minna Männikkö *Oulu Center for Cell-Matrix Research, Biocenter and Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Oulu, Finland;Department of Otorhinolaryngology, Institute of Clinical Medicine, University of Oulu, Finland
Pages 841-845 | Received 16 Jun 2012, Accepted 20 Jul 2012, Published online: 30 Aug 2012

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Giuseppe Chiarella, C Petrolo & E Cassandro. (2015) The genetics of Ménière’s disease. The Application of Clinical Genetics 8, pages 9-17.
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Qingqing Dai, Lili Long, Hui Zhao, Ruikai Wang, Hong Zheng & Maoli Duan. (2022) Genetic advances in Meniere Disease. Molecular Biology Reports 50:3, pages 2901-2908.
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Hitomi Sakano & Benjamin T. Crane. 2023. Disorders of the Vestibular System. Disorders of the Vestibular System 63 90 .
Habib G. Rizk, Neil K. Mehta, Uneeb Qureshi, Erick Yuen, Kathy Zhang, Yaw Nkrumah, Paul R. Lambert, Yuan F. Liu, Theodore R. McRackan, Shaun A. Nguyen & Ted A. Meyer. (2022) Pathogenesis and Etiology of Ménière Disease. JAMA Otolaryngology–Head & Neck Surgery 148:4, pages 360.
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Shoujun Gu, Rafal Olszewski, Lacey Nelson, Alvaro Gallego-Martinez, Jose Antonio Lopez-Escamez & Michael Hoa. (2021) Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis. Frontiers in Neurology 12.
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Alvaro Gallego-Martinez & Jose A. Lopez-Escamez. (2020) Genetic architecture of Meniere’s disease. Hearing Research 397, pages 107872.
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Estrella Martinez-Gomez, Alvaro Gallego-Martinez, Pablo Roman-Naranjo & Jose A. Lopez-Escamez. (2020) Clinical and molecular genetics of Meniere disease. Medizinische Genetik 32:2, pages 141-148.
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Eun Hye Oh, Jin-Hong Shin, Hyang-Sook Kim, Jae Wook Cho, Seo Young Choi, Kwang-Dong Choi, Je-Keun Rhee, Seowhang Lee, Changwook Lee & Jae-Hwan Choi. (2020) Rare Variants of Putative Candidate Genes Associated With Sporadic Meniere's Disease in East Asian Population. Frontiers in Neurology 10.
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Alexander L. Luryi, Elliot Morse & Elias Michaelides. 2019. Diagnosis and Treatment of Vestibular Disorders. Diagnosis and Treatment of Vestibular Disorders 165 188 .
Rabia Faridi, Risa Tona, Alessandra Brofferio, Michael Hoa, Rafal Olszewski, Isabelle Schrauwen, Muhammad Z.K. Assir, Akhtar A. Bandesha, Asma A. Khan, Atteeq U. Rehman, Carmen Brewer, Wasim Ahmed, Suzanne M. Leal, Sheikh Riazuddin, Steven E. Boyden & Thomas B. Friedman. (2018) Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome . Human Mutation.
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Marc‐Henri Asmar, Louis Gaboury & Issam Saliba. (2018) Ménière's Disease Pathophysiology: Endolymphatic Sac Immunohistochemical Study of Aquaporin‐2, V2R Vasopressin Receptor, NKCC2, and TRPV4. Otolaryngology–Head and Neck Surgery 158:4, pages 721-728.
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Marisa Flook & Jose A. Lopez Escamez. (2018) Meniere’s Disease: Genetics and the Immune System. Current Otorhinolaryngology Reports 6:1, pages 24-31.
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Jose Antonio Lopez-Escamez, Angel Batuecas-Caletrio & Alexandre Bisdorff. (2018) Towards personalized medicine in Ménière’s disease. F1000Research 7, pages 1295.
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Lidia Frejo, Teresa Requena, Satoshi Okawa, Alvaro Gallego-Martinez, Manuel Martinez-Bueno, Ismael Aran, Angel Batuecas-Caletrio, Jesus Benitez-Rosario, Juan M. Espinosa-Sanchez, Jesus José Fraile-Rodrigo, Ana María García-Arumi, Rocío González-Aguado, Pedro Marques, Eduardo Martin-Sanz, Nicolas Perez-Fernandez, Paz Pérez-Vázquez, Herminio Perez-Garrigues, Sofía Santos-Perez, Andres Soto-Varela, Maria C. Tapia, Gabriel Trinidad-Ruiz, Antonio del Sol, Marta E. Alarcon Riquelme & Jose A. Lopez-Escamez. (2017) Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere’s Disease. Frontiers in Immunology 8.
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Sung-Il Nam. (2017) Recent Research Trend for Ménièreʼs Disease. Research in Vestibular Science 16:2, pages 39-46.
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Rahul Mittal, Mayank Aranke, Luca H. Debs, Desiree Nguyen, Amit P. Patel, M'hamed Grati, Jeenu Mittal, Denise Yan, Prem Chapagain, Adrien A. Eshraghi & Xue Zhong Liu. (2017) Indispensable Role of Ion Channels and Transporters in the Auditory System. Journal of Cellular Physiology 232:4, pages 743-758.
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Roberto Teggi, Laura Zagato, Simona Delli Carpini, Lorena Citterio, Claudia Cassandro, Roberto Albera, Wen-Yi Yang, Jan A. Staessen, Mario Bussi, Paolo Manunta & Chiara Lanzani. (2016) Genetics of ion homeostasis in Ménière’s Disease. European Archives of Oto-Rhino-Laryngology 274:2, pages 757-763.
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Michael D. Puricelli, Henrique Furlan Pauna & Michael M. Paparella. (2016) Endolymphatic sac surgery for Meniere’s Disease. Operative Techniques in Otolaryngology-Head and Neck Surgery 27:4, pages 235-239.
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Karen de Carvalho Lopes, Edi Lúcia Sartorato, Sueli M. da Silva-Costa, Nadya Soares de Macedo Adamov & Fernando Freitas Ganança. (2016) Ménière's Disease. Otology & Neurotology 37:8, pages 1117-1121.
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Tsutomu Nakashima, Ilmari Pyykkö, Megan A. Arroll, Margaretha L. Casselbrant, Carol A. Foster, Nauman F. Manzoor, Cliff A. Megerian, Shinji Naganawa & Yi-Ho Young. (2016) Meniere's disease. Nature Reviews Disease Primers 2:1.
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Lidia Frejo, Ina Giegling, Roberto Teggi, Jose A. Lopez-Escamez & Dan Rujescu. (2016) Genetics of vestibular disorders: pathophysiological insights. Journal of Neurology 263:S1, pages 45-53.
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Yuan-Jun Li, Zhan-Guo Jin & Xian-Rong Xu. (2016) Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis. Journal of Vestibular Research 25:5-6, pages 211-218.
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N. V. Boiko & N. L. Kunel’skaya. (2016) The current problems related to Meniere’s disease. Vestnik otorinolaringologii 81:5, pages 89.
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J.M. Espinosa-Sanchez & J.A. Lopez-Escamez. 2016. Neuro-Otology. Neuro-Otology 257 277 .
Katsumi Doi. (2015) Meniere's disease. Equilibrium Research 74:2, pages 51-57.
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Sonia Cabrera, Elena Sanchez, Teresa Requena, Manuel Martinez-Bueno, Jesus Benitez, Nicolas Perez, Gabriel Trinidad, Andrés Soto-Varela, Sofía Santos-Perez, Eduardo Martin-Sanz, Jesus Fraile, Paz Perez, Marta E. Alarcon-Riquelme, Angel Batuecas, Juan M. Espinosa-Sanchez, Ismael Aran & Jose A. Lopez-Escamez. (2014) Intronic Variants in the NFKB1 Gene May Influence Hearing Forecast in Patients with Unilateral Sensorineural Hearing Loss in Meniere's Disease. PLoS ONE 9:11, pages e112171.
Crossref
Elina Hietikko, Jouko Kotimäki & Minna Männikkö. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences.
Elina Hietikko, Jouko Kotimäki, Martti Sorri & Minna Männikkö. (2013) High incidence of Meniere-like symptoms in relatives of Meniere patients in the areas of Oulu University Hospital and Kainuu Central Hospital in Finland. European Journal of Medical Genetics 56:6, pages 279-285.
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