O. Xiao

Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.

X. Liu, K. Johnson, D. Yan, 2005, Human molecular genetics.

Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.

K. Arnos, A. Pandya, D. Corey, 2003, Human molecular genetics.

A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12

A. Pandya, S. Blanton, D. Yan, 2005, Journal of Medical Genetics.

Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians

A. Pandya, X. Liu, N. Matsushiro, 2003, Human Genetics.

The prevalence of connexin 26 (GJB2) mutations in the Chinese population

F. Telischi, X. Liu, T. Balkany, 2002, Human Genetics.

Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

X. Liu, Shoeb Ahmad, D. Yan, 2008, Human Genetics.

Refinement of the DFNA41 locus and candidate genes analysis

Xiaofeng Zhu, X. Liu, D. Yan, 2005, Journal of Human Genetics.