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• Recent advances in genetic etiology of non-syndromic deafness in children.

  Feng Y, Hu S, Zhao S, Chen M. Feng Y, et al. Front Neurosci. 2023 Oct 19;17:1282663. doi: 10.3389/fnins.2023.1282663. eCollection 2023. Front Neurosci. 2023. PMID: 37928735 Free PMC article. Review.
• DTI study on rehabilitation of the congenital deafness auditory pathway and speech center by cochlear implantation.

  Wang H, Liang Y, Fan W, Zhou X, Huang M, Shi G, Yu H, Shen G. Wang H, et al. Eur Arch Otorhinolaryngol. 2019 Sep;276(9):2411-2417. doi: 10.1007/s00405-019-05477-7. Epub 2019 May 24. Eur Arch Otorhinolaryngol. 2019. PMID: 31127414 Free PMC article.
• Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling.

  Li Q, Zhu QW, Yuan YY, Huang SS, Han DY, Huang DL, Dai P. Li Q, et al. J Transl Med. 2012 Nov 14;10:225. doi: 10.1186/1479-5876-10-225. J Transl Med. 2012. PMID: 23151025 Free PMC article.
• Attitudes to genetic testing for deafness: the importance of informed choice.

  Guillemin M, Gillam L. Guillemin M, et al. J Genet Couns. 2006 Feb;15(1):51-9. doi: 10.1007/s10897-005-9003-6. J Genet Couns. 2006. PMID: 16525898
• Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.

  Riazuddin S, Khan SN, Ahmed ZM, Ghosh M, Caution K, Nazli S, Kabra M, Zafar AU, Chen K, Naz S, Antonellis A, Pavan WJ, Green ED, Wilcox ER, Friedman PL, Morell RJ, Riazuddin S, Friedman TB. Riazuddin S, et al. Am J Hum Genet. 2006 Jan;78(1):137-43. doi: 10.1086/499164. Epub 2005 Nov 21. Am J Hum Genet. 2006. PMID: 16385457 Free PMC article.