Xiaomei Ouyang

Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

Xue Zhong Liu, Dongyi Han, Jianzhong Li et al. · The American Journal of Human Genetics · 2009 · 123 citations · Full text

Developmental Biology, Genetic Disorder, Prps1 Gene Cause +5

Antioxidant enzymes, presbycusis, and ethnic variability

Anthony Bared, Xiaomei Ouyang, Simón I. Angeli et al. · Otolaryngology · 2010 · 70 citations · Full text

Proxy activation of protein ErbB2 by heterologous ligands implies a heterotetrameric mode of receptor tyrosine kinase interaction

Guo Huang, Xiaomei Ouyang, Richard J. Epstein · Biochemical Journal · 1998 · 58 citations · Full text

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene

Nele Hilgert, Matthew J. Huentelman, Ashley Q. Thorburn et al. · European Journal of Human Genetics · 2008 · 53 citations · Full text

Genetic Analysis, Allelic Variant, Phenotypic Variation +8

Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population

Rosemary I. Kabahuma, Xiaomei Ouyang, Li Du et al. · International Journal of Pediatric Otorhinolaryngology · 2011 · 48 citations · Full text

Gjb6 Deletion, Genetic Disorder, Genetics +11