Yongzhi Xie - Concepedia

Author

Yongzhi Xie

Also Known As

Ruxu Zhang, Shangwei Xie, Yi Zhan, Shushan Qiao, Xie Yongzhi, Xie, Yongzhi, Xie, Yumu, Y Xie, Y Z Xie, Y. Xie, Y. Z. Xie, Y.Z. Xie

Publications

642

Citations

H-Index

Concepts

All Affiliations

Central South University Third Xiangya Hospital Xiangya Hospital Central South University Second Xiangya Hospital of Central South University Nanjing Medical University

About

Yongzhi Xie is an author at Central South University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	219
2	Natural Sciences	2	2	170
3	Engineering	1	1	15
4	Public Health	1	1	20
5	Biochemistry	1	1	31

Yongzhi Xie

Publications

486

Citations

H-Index

Page 1

	Year	Citations
CRISPR-Cas9 Screens Identify the RNA Helicase DDX3X as a Repressor of C9ORF72 (GGGGCC)n Repeat-Associated Non-AUG Translation Weiwei Cheng, Shaopeng Wang, Zhe Zhang, Neuron Rna ProcessingNatural SciencesGeneticsRna Helicase Ddx3xMolecular Biology	2019	139
A <i>SIGMAR1</i> splice-site mutation causes distal hereditary motor neuropathy Xiaobo Li, Zhengmao Hu, Lei Liu, Neurology	2015	77
Genotype and phenotype distribution of 435 patients with Charcot–Marie–Tooth disease from central south China Yongzhi Xie, Zhiqiang Lin, Lei Liu, European Journal of Neurology	2021	35
Accelerated aging-related transcriptome alterations in neurovascular unit cells in the brain of Alzheimer’s disease Yan Zhao, Yongzhi Xie, You‐Shuo Liu Frontiers in Aging Neuroscience	2022	32
The importance of methionine residues for the catalysis of the biotin enzyme, transcarboxylase. Analysis by site-directed mutagenesis. Bhami C. Shenoy, Yongzhi Xie, V.L. Park, Journal of Biological Chemistry Methionine ResiduesBiosynthesisCellular EnzymologyBiochemistryNatural Sciences	1992	31
Autophagy induction regulates aquaporin 3‐mediated skin fibroblast ageing* Hongfu Xie, Liang Zhou, F. Liu, British Journal of Dermatology Cell AutophagySkin DevelopmentCell RegulationAutophagy InductionCell Signaling	2021	30
MFN2‐related genetic and clinical features in a cohort of Chinese CMT2 patients Yongzhi Xie, Xiaobo Li, Lei Liu, Journal of the Peripheral Nervous System	2016	23
Genotype–phenotype correlation and frequency of distribution in a cohort of Chinese Charcot–Marie–Tooth patients associated with GDAP1 mutations Pukar Singh Pakhrin, Yongzhi Xie, Zhengmao Hu, Journal of Neurology Genotype-phenotype AssociationGdap1 MutationsGeneticsGenetic EpidemiologyGenotype–phenotype Correlation	2018	20
A novel <i>WARS</i> mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family Binghao Wang, Xiaobo Li, Shunxiang Huang, Clinical Genetics	2019	20
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease Shun-Chang Sun, Di Ma, Meiyi Li, Brain	2019	20

Page 1