Yuhua Zhu - Concepedia

Author

Yuhua Zhu

Chinese PLA General Hospital

Also Known As

Y H Zhu, Yu-Hua Zhu, Yu-Hua Zhu (525993), Yu-hua ZHU, Yu-hua Zhu, Yuhua Zhu, Zhu Yuhua, Zhu, Yuhua

Publications

277

Citations

H-Index

Concepts

All Affiliations

Chinese PLA General Hospital University of Miami Massachusetts Eye and Ear Infirmary Harvard University

About

Yuhua Zhu is an author at Chinese PLA General Hospital specializing in genetics, hearing loss, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	131
2	Arts	2	2	49
3	Public Health	1	1	26
4	Biostatistics	1	1	26
5	Molecular Biology	1	1	56

Yuhua Zhu

Publications

237

Citations

H-Index

Page 1

	Year	Citations
Functional Mutation of SMAC/DIABLO, Encoding a Mitochondrial Proapoptotic Protein, Causes Human Progressive Hearing Loss DFNA64 Jing Cheng, Yuhua Zhu, Sudan He, The American Journal of Human Genetics Mitochondrial FunctionFunctional MutationGeneticsMolecular BiologyDegenerative Disease	2011	56
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China Yi Sun, Jing Chen, Han-Jun Sun, Journal of Human Genetics Genetic DisorderGeneticsAudiologyHearing DisordersAuditory Research	2010	36
Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation Yuhua Zhu, Qi Li, Zheng‐Yi Chen, Mitochondrion Mitochondrial FunctionGenetic DisorderMedicineGeneticsEvolutionary Biology	2009	36
Machine learning-based dynamic prediction of lateral lymph node metastasis in patients with papillary thyroid cancer Sheng-wei Lai, Yunlong Fan, Yuhua Zhu, Frontiers in Endocrinology	2022	36
Correlation analysis of phenotype and genotype of GJB2 in patients with non-syndromic hearing loss in China Zhiyao Dai, Baochun Sun, Shasha Huang, Gene Non-syndromic Hearing LossGeneticsGenetic EpidemiologyAudiologyBiostatistics	2015	26
Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation Yuhua Zhu, Shasha Huang, Dongyang Kang, BMC Genetics	2014	22
Exome Sequencing Identifies a Novel Frameshift Mutation of<i>MYO6</i>as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family Jing Cheng, Xueya Zhou, Yu Lu, Annals of Human Genetics Family MembersExome SequencingGeneticsLarge Chinese FamilyMolecular Genetics	2014	13
Mutations in the mitochondrial 12S rRNA gene in elderly Chinese people Yuhua Zhu, Jiandong Zhao, Bo Feng, Acta Oto-Laryngologica	2014	12

Page 1