Ronghua Li

Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family

Hui Zhao, Ronghua Li, Qiuju Wang et al. · The American Journal of Human Genetics · 2004 · 422 citations · Full text

Mendelian Disorder, Mitochondrial Function, Genetic Disorder +10

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

Min‐Xin Guan, Qingfeng Yan, Xiaoming Li et al. · The American Journal of Human Genetics · 2006 · 222 citations · Full text

Rna Modification, Mitochondrial Biogenesis, Mitochondrial Function +10

Species identification through mitochondrial rRNA genetic analysis

Li Yang, Zongqing Tan, Daren Wang et al. · Scientific Reports · 2014 · 220 citations · Full text

Animal Taxonomy, Ribosomal Rna, Comparative Genomics +17

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss

Zhiyuan Li, Ronghua Li, Jian‐Fu Chen et al. · Human Genetics · 2005 · 172 citations · Full text

Mitochondrial Biogenesis, Mitochondrial Function, Mitochondrial 12S +11

Cosegregation of C‐insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss

Ronghua Li, Guangqian Xing, Ming Yan et al. · American Journal of Medical Genetics Part A · 2003 · 138 citations