Xue Zhong Liu

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Julie M. Bork, Linda Peters, Saima Riazuddin et al. · The American Journal of Human Genetics · 2001 · 557 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Philomena Mburu, Mirna Mustapha, Anabel Varela et al. · Nature Genetics · 2003 · 342 citations

Life Sciences, Genetics, Neuroscience +11

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

Xue Zhong Liu · Human Molecular Genetics · 2003 · 205 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22

Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici et al. · Proceedings of the National Academy of Sciences · 2002 · 182 citations · Full text

Medicine, Molecular Biology, Molecular Genetics +12

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

Qing Yin Zheng, Denise Yan, Xiao Mei Ouyang et al. · Human Molecular Genetics · 2004 · 147 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17