Hearing Loss, Genomics and Public Health [NEW TOPIC PAGE]

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From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• Absence of KCNQ4 mutation in Bengali families with ADNSHL originated from West Bengal, India.  
  International journal of pediatric otorhinolaryngology 2017 Sep 100 35-38.
  Adhikary Bidisha, Bankura Biswabandhu, Biswas Subhradev, Paul Silpita, Das Madhusud
• A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct.  
  Journal of medical genetics 2017 Aug .
  Chattaraj Parna, Munjal Tina, Honda Keiji, Rendtorff Nanna D, Ratay Jessica S, Muskett Julie A, Risso Davide S, Roux Isabelle, Gertz E Michael, Schäffer Alejandro A, Friedman Thomas B, Morell Robert J, Tranebjærg Lisbeth, Griffith Andrew
• A mutation in Nischarin causes otitis media via LIMK1 and NF-?B pathways.  
  PLoS genetics 2017 Aug 13 (8): e1006969.
  Crompton Michael, Purnell Tom, Tyrer Hayley E, Parker Andrew, Ball Greg, Hardisty-Hughes Rachel E, Gale Richard, Williams Debbie, Dean Charlotte H, Simon Michelle M, Mallon Ann-Marie, Wells Sara, Bhutta Mahmood F, Burton Martin J, Tateossian Hilda, Brown Steve D
• Glutathione peroxidase 3 gene polymorphisms and the risk of sudden sensorineural hearing loss.  
  The Kaohsiung journal of medical sciences 2017 Jul 33 (7): 359-364.
  Chien Chen-Yu, Huang Tzu-Yen, Tai Shu-Yu, Chang Ning-Chia, Wang Hsun-Mo, Wang Ling-Feng, Ho Kuen-Y
• Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China.  
  International journal of pediatric otorhinolaryngology 2017 Jul 98 39-42.
  Pan Jing, Xu Ping, Tang Weibo, Cui Zhongtao, Feng Miao, Wang Chunyi

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