Ronghua Li - Concepedia

Author

Ronghua Li

Ningbo University ORCID

Also Known As

Li Ronghua, Li, Ronghua, Rong-Hua LI, Rong-Hua Li, Rong-hua LI, Rong-hua Li, Ronghua Li, Ronghua, Li, Xinjian Wang

223

Publications

4.8K

Citations

H-Index

148

Concepts

All Affiliations

Ningbo University Cincinnati Children's Hospital Medical Center University of Cincinnati Medical Center Wenzhou Medical University Guangzhou University

About

Ronghua Li is an author at Ningbo University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	55	2.9K
2	Engineering	8	8	142
3	Arts	6	6	495
4	Health Sciences	4	4	142
5	Management	1	1	11

Ronghua Li

Publications

4.4K

Citations

H-Index

Page 1

	Year	Citations
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, The American Journal of Human Genetics Mendelian DisorderMitochondrial FunctionGenetic DisorderGeneticsInherited Metabolic Disease	2004	422
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, The American Journal of Human Genetics Rna ModificationMitochondrial BiogenesisMitochondrial FunctionNatural SciencesGenetics	2006	222
Species identification through mitochondrial rRNA genetic analysis Li Yang, Zongqing Tan, Daren Wang, Scientific Reports Animal TaxonomyRibosomal RnaComparative GenomicsGeneticsTaxonomy	2014	220
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, Human Genetics Mitochondrial BiogenesisMitochondrial FunctionMitochondrial 12SPediatric OtolaryngologyGenetics	2005	172
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, American Journal of Medical Genetics Part A	2003	138
Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss Jianxin Lü, Zhiyuan Li, Yi Zhu, Mitochondrion Mitochondrial BiogenesisMitochondrial FunctionRrna VariantsGeneticsPhysiology	2010	138
Isolation and Characterization of the Putative Nuclear Modifier Gene MTO1 Involved in the Pathogenesis of Deafness-associated Mitochondrial 12 S rRNA A1555G Mutation Xiaoming Li, Ronghua Li, Xinhua Lin, Journal of Biological Chemistry	2002	133
Human Mitochondrial Leucyl-tRNA Synthetase Corrects Mitochondrial Dysfunctions Due to the tRNA<sup>Leu(UUR)</sup> A3243G Mutation, Associated with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Symptoms and Diabetes Ronghua Li, Min‐Xin Guan Molecular and Cellular Biology Mitochondrial DysfunctionGeneticsMolecular BiologyMolecular GeneticsMitochondrial Biology	2010	132
Maternally Inherited Essential Hypertension Is Associated With the Novel 4263A>G Mutation in the Mitochondrial tRNA <sup>Ile</sup> Gene in a Large Han Chinese Family Shiwen Wang, Ronghua Li, Andrea Fettermann, Circulation Research	2011	125
The Novel A4435G Mutation in the Mitochondrial tRNA<sup>Met</sup>May Modulate the Phenotypic Expression of the LHON-Associated ND4 G11778A Mutation Jia Qu, Ronghua Li, Xiangtian Zhou, Investigative Ophthalmology & Visual Science	2006	121

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