Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Hearing Loss and meta-analysis and GJB2[original query] |
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| Is hearing loss due to mutations in the Connexin 26 gene progressive? International journal of audiology 2008 Jan 47 (1): 11-20. Gopalarao Deepika, Kimberling William J, Jesteadt Walt, Kelley Philip M, Beauchaine Kathryn L, Cohn Edward |
| Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequency. International journal of audiology 2009 48 (6): 363-70. Mahdieh Nejat, Rabbani Bahar |
| A systematic review and meta-analysis of 235delC mutation of GJB2 gene. Journal of translational medicine 2012 10 (1): 136. Yao Jun, Lu Yajie, Wei Qinjun, Cao Xin, Xing Guangqi |
| GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype. The Laryngoscope 2014 Feb 124 (2): E34-53. Chan Dylan K, Chang Kay |
| Systematic Review of Hearing Loss Genes in the African American Population. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2019 5 40 (5): e488-e496. Worden Cameron P, Jeyakumar Ani |
| The worldwide frequency of MYO15A gene mutations in patients with non-syndromic hearing loss: A meta-analysis. Iranian journal of basic medical sciences 2020 8 23 (7): 841-848. Farjami Mahsa, Assadi Reza, Afzal Javan Fahimeh, Alimardani Malihe, Eslami Saeid, Mansoori Derakhshan Sima, Eslahi Atieh, Mojarrad Maj |
| Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis. Frontiers in genetics 2021 10 12 707845. Han Shuang, Zhang Dejun, Guo Yingyuan, Fu Zeming, Guan Guofa |
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 |
| 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 |
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