Hearing Loss ► Public Health Genomics Knowledge Base (v1.0)

Public Health Genomics Knowledge Base (v1.0)

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Last Updated: Feb 18, 2016

• Cytomegalovirus Infection in Ireland: Seroprevalence, HLA Class I Alleles, and Implications.
  Hassan Jaythoon, et al. Medicine 2016 2 (6) e2735 (From HuGE Literature Finder)
• GRHL2 genetic polymorphisms may confer a protective effect against sudden sensorineural hearing loss.
  Lin Xiaojiang, et al. Molecular medicine reports 2016 2 (From HuGE Literature Finder)
• Studies underlying pharmacogenomics-based safety labeling can have inconsistent results.
  Thompson Cheryl A et al. American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists 2015 May 72(10) 768-9, 771 (From Genomics & Health Impact Scan Database)
• [Children's hearing behavior observations and high risk individual genetic screening for late-onset hearing loss early detection and intervention exploring a basic-level hospitals model].
  Guo Yilian et al. Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2015 Sep 29(18) 1618-21 (From Genomics & Health Impact Scan Database)
• [Clinical and genetic features of X-linked Alport syndrome in men positive for the collagen ? ?5 chain in epidermal basement membrane].
  Zhang Y Q, et al. Zhonghua er ke za zhi. Chinese journal of pediatrics 2016 1 (1) 61-4 (From HuGE Literature Finder)
• Auditory phenotype in Stickler syndrome: results of audiometric analysis in 20 patients.
  Acke Frederic R, et al. 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 1 (From HuGE Literature Finder)
• Prevalence and audiological profiles of GJB2 mutations in a large collective of hearing impaired patients.
  Burke W F, et al. Hearing research 2016 1 (From HuGE Literature Finder)
• An effective screening strategy for deafness in combination with a next-generation sequencing platform: a consecutive analysis.
  Sakuma Naoko et al. Journal of human genetics 2016 Jan (From Genomics & Health Impact Scan Database)
• Deafness gene mutations in newborns in Beijing.
  Han Shujing, et al. Acta oto-laryngologica 2016 1 1-5 (From HuGE Literature Finder)
• Distinct vestibular phenotypes in DFNA9 families with COCH variants.
  Kim Bong Jik, et al. 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 1 (From HuGE Literature Finder)
• Advances in the Understanding of the Genetic Causes of Hearing Loss in Children Inform a Rational Approach to Evaluation.
  Carey John C et al. Indian journal of pediatrics 2016 Jan (From Genomics & Health Impact Scan Database)
• Targeted Next-Generation Sequencing Analysis of a Pendred Syndrome-Associated Thyroid Carcinoma.
  Tong Guo-Xia, et al. Endocrine pathology 2016 1 (From HuGE Literature Finder)
• Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis.
  Lu Ya-Jie, et al. Medicine 2015 12 (50) e2248 (From HuGE Literature Finder)
• Newborn Screening Program (Minnesota)
  Disease: NA; Type: Program; State: Minnesota (From Implementation Database)
• State of Kansas Genetics Plan 2010[PDF 6.71 MB]
  Disease: Multiple Diseases; Type: Data|Policy|Program; State: Kansas (From Implementation Database)
• Center for Congenital and Inherited Disorders (CCID) 
  Disease: Birth defects; Type: General Information; State: Iowa (From Implementation Database)
• Newborn Screening Home
  Disease: NA; Type: Program; State: Indiana (From Implementation Database)
• Newborn Screening Program (New Mexico)
  Disease: NA; Type: Program; State: New Mexico (From Implementation Database)