Zhidong Cen - Concepedia

Author

Zhidong Cen

Second Affiliated Hospital of Zhejiang University ORCID

Also Known As

Bo Wang, Z Cen, Zhaowei Cen, Zhi-Dong Cen, Zhi-dong Cen, Zhidong Cen, Zhi‐dong Cen, Zhuo Cen, Zongxiao Cen, Zuxi Cen

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Second Affiliated Hospital of Zhejiang University Zhejiang University Sir Run Run Shaw Hospital Zhejiang Hospital Lishui City People's Hospital

About

Zhidong Cen is an author at Second Affiliated Hospital of Zhejiang University specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	14	374
2	Public Health	3	3	143
3	Health Sciences	2	2	36
4	Social Sciences	2	2	43
5	Natural Sciences	1	1	25

Zhidong Cen

Publications

889

Citations

H-Index

Page 1

	Year	Citations
Altered brain network centrality in depressed Parkinson's disease patients Yuting Lou, Peiyu Huang, Dan Li, Movement Disorders	2015	97
Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1 Zhidong Cen, Zhengwen Jiang, You Chen, Brain	2018	97
Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcification Zhidong Cen, You Chen, Si Chen, Brain Developmental BiologyMendelian DisorderJam2 GeneMedicineGenetics	2019	91
Loss of function of CMPK2 causes mitochondria deficiency and brain calcification Miao Zhao, Hui‐Zhen Su, Yi‐Heng Zeng, Cell Discovery	2022	51
Abnormal baseline brain activity in Parkinson's disease with and without REM sleep behavior disorder: A resting‐state functional MRI study Dan Li, Peiyu Huang, Yu‐Feng Zang, Journal of Magnetic Resonance Imaging	2016	50
Prevalence and clinical correlation of dysphagia in Parkinson disease: a study on Chinese patients Xin-Yuan Ding, Jixiang Gao, Chengrong Xie, European Journal of Clinical Nutrition Clinical CorrelationMotor DysfunctionCorticobasal DegenerationNeurological DisorderParkinson Disease	2017	37
Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from China Si Chen, Zhidong Cen, Feng Fu, Parkinsonism & Related Disorders Biallelic VariantsGenetic DisorderDisease PrevalenceGenetic EpidemiologySevere Phenotypes	2019	36
Evaluation of <i>MYORG</i> mutations as a novel cause of primary familial brain calcification You Chen, Feng Fu, Si Chen, Movement Disorders	2018	31
SLC7A11 is an unconventional H+ transporter in lysosomes Nan Zhou, Jingzhi Chen, Meiqin Hu, Cell	2025	27
Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy Zhidong Cen, Chunping Huang, Houmin Yin, Movement Disorders	2016	26

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