Min‐Xin Guan - Concepedia

Author

Min‐Xin Guan

Cincinnati Children's Hospital Medical Center ORCID

Also Known As

Freedman, B.I., G. Minxin, Guan Min-Xin, Guan Min-xin, Guan Minxin, Guan Min–Xin, Guan, Min-Xin, Jia Qu, Jianxin Lu, M X Guan

325

Publications

10.7K

Citations

H-Index

118

Concepts

All Affiliations

Cincinnati Children's Hospital Medical Center Zhejiang University Wenzhou Medical University University of Cincinnati Medical Center Children's Hospital of Zhejiang University

About

Min‐Xin Guan is an author at Cincinnati Children's Hospital Medical Center specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	43	100	5.5K
2	Natural Sciences	21	28	1.6K
3	Arts	14	14	891
4	Health Sciences	1	1	98
5	Public Health	1	1	37

Min‐Xin Guan

173

Publications

9.5K

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
Biochemical evidence for nuclear gene involvement in phenotype of non- syndromic deafness associated with mitochondrial 12S rRNA mutation Min‐Xin Guan Human Molecular Genetics	1996	234
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
A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity Min‐Xin Guan Human Molecular Genetics	2000	197
Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation Min‐Xin Guan Human Molecular Genetics	2001	193
Mitochondrial Stress Engages E2F1 Apoptotic Signaling to Cause Deafness Nuno Raimundo, Lei Song, Timothy E. Shutt, Cell Cause DeafnessSignal TransductionMitochondrial FunctionPhysiologyAutophagy	2012	187
The Deafness-Associated Mitochondrial DNA Mutation at Position 7445, Which Affects tRNA<sup>Ser(UCN)</sup> Precursor Processing, Has Long-Range Effects on NADH Dehydrogenase Subunit ND6 Gene Expression Min‐Xin Guan, José Antonio Enrı́quez, Nathan Fischel‐Ghodsian, Molecular and Cellular Biology	1998	185
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

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