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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Xue Zhong Liu

Department of Otolaryngology (D-48)

University of Miami

1666 NW 12th Avenue




Name/email consistency: high



  • Department of Otolaryngology (D-48), University of Miami, 1666 NW 12th Avenue, Miami, USA. 2002 - 2009
  • Department of Human Genetics, Medical College of Virginia of Virginia Commonwealth University, Richmond, VA 23298-0033, USA. 2001


  1. Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31. Liu, X.Z., Yuan, Y., Yan, D., Ding, E.H., Ouyang, X.M., Fei, Y., Tang, W., Yuan, H., Chang, Q., Du, L.L., Zhang, X., Wang, G., Ahmad, S., Kang, D.Y., Lin, X., Dai, P. Hum. Genet. (2009) [Pubmed]
  2. Cochlear implantation in individuals with Usher type 1 syndrome. Liu, X.Z., Angeli, S.I., Rajput, K., Yan, D., Hodges, A.V., Eshraghi, A., Telischi, F.F., Balkany, T.J. Int. J. Pediatr. Otorhinolaryngol. (2008) [Pubmed]
  3. Audiological and genetic features of the mtDNA mutations. Liu, X.Z., Angeli, S., Ouyang, X.M., Liu, W., Ke, X.M., Liu, Y.H., Liu, S.X., Du, L.L., Deng, X.W., Yuan, H., Yan, D. Acta Otolaryngol. (2008) [Pubmed]
  4. Ageing and hearing loss. Liu, X.Z., Yan, D. J. Pathol. (2007) [Pubmed]
  5. Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss. Liu, X.Z., Ouyang, X.M., Xia, X.J., Zheng, J., Pandya, A., Li, F., Du, L.L., Welch, K.O., Petit, C., Smith, R.J., Webb, B.T., Yan, D., Arnos, K.S., Corey, D., Dallos, P., Nance, W.E., Chen, Z.Y. Hum. Mol. Genet. (2003) [Pubmed]
  6. The prevalence of connexin 26 ( GJB2) mutations in the Chinese population. Liu, X.Z., Xia, X.J., Ke, X.M., Ouyang, X.M., Du, L.L., Liu, Y.H., Angeli, S., Telischi, F.F., Nance, W.E., Balkany, T., Xu, L.R. Hum. Genet. (2002) [Pubmed]
  7. The clinical presentation of DFNB2. Liu, X.Z. Adv. Otorhinolaryngol. (2002) [Pubmed]
  8. Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness. Liu, X.Z., Xia, X.J., Adams, J., Chen, Z.Y., Welch, K.O., Tekin, M., Ouyang, X.M., Kristiansen, A., Pandya, A., Balkany, T., Arnos, K.S., Nance, W.E. Hum. Mol. Genet. (2001) [Pubmed]
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