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Fanxi Xu
Observed name:
Xu, Fanxi
Institutions:
Capital Medical University,
Xuan Wu Hospital of the Capital Medical University
Observed institutions:
Central South University,
Capital Medical University,
Xuan Wu Hospital of the Capital Medical University,
Second Xiangya Hospital of Central South University,
Xiangya Hospital Central South University
ORCID:
0000-0003-1915-1530
Observed ORCID:
0000-0003-1915-1530
OpenAlex ID:
A5010752142
ACO2 deficiency increases vulnerability to Parkinson’s disease via dysregulating mitochondrial function and histone acetylation-mediated transcription of autophagy genes
2023
·
Junge Zhu
, Fanxi Xu
, et al.
·
Communications Biology
·
33
PDF
Efficacy and Tolerability of Intravenous Immunoglobulin and Subcutaneous Immunoglobulin in Neurologic Diseases
2019
·
Yun Chen
, Chunyu Wang
, et al.
·
Clinical Therapeutics
·
18
Applications of Machine Learning to Diagnosis of Parkinson’s Disease
2023
·
Hong Lai
, Xu-Ying Li
, et al.
·
Brain Sciences
·
15
PDF
Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China
2022
·
Fanxi Xu
, Sen Huang
, et al.
·
BMC Medical Genomics
·
11
PDF
Genetic, clinical and neuroimaging profiles of sporadic and autosomal recessive hereditary spastic paraplegia cases in Chinese
2021
·
Yue Dong
, Xu-Ying Li
, et al.
·
Neuroscience Letters
·
10
A novel FBXO7-R345P mutation in a Chinese family with autosomal recessive parkinsonian-pyramidal syndrome
2021
·
Zhanjun Wang
, Yang Song
, et al.
·
Parkinsonism & Related Disorders
·
7
Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families
2021
·
Zhanjun Wang
, Yang Song
, et al.
·
Neuroscience Letters
·
5
PDF
Genetic profiles of multiple system atrophy revealed by exome sequencing, long‐read sequencing and spinocerebellar ataxia repeat expansion analysis
2024
·
Xu‐Ying Li
, Hong Lai
, et al.
·
European Journal of Neurology
·
4
PDF
Multidisciplinary molecular consultation increases the diagnosis of pediatric epileptic encephalopathy and neurodevelopmental disorders
2023
·
Liping Zhang
, Xu‐Ying Li
, et al.
·
Molecular Genetics & Genomic Medicine
·
4
PDF
Clinical and Preclinical Neuroimaging Changes in Spinocerebellar Ataxia Type 12: A Study of Three Chinese Pedigrees
2022
·
Tingyan Yao
, Hongwen Qiao
, et al.
·
European Neurology
·
4
Pyruvate is modified by tea/coffee metabolites and reversely correlated with multiple system atrophy and Parkinson's disease
2024
·
Xu-Ying Li
, Teng Xue
, et al.
·
Heliyon
·
2
Development and Validation of a Predictive Nomogram for Possible REM Sleep Behavior Disorders
2022
·
Hong Lai
, Xu-Ying Li
, et al.
·
Frontiers in Neurology
·
2
PDF
A novel loss-of-function compound heterozygous mutation of MYORG causes idiopathic basal ganglia calcification 7
2022
·
Junge Zhu
, Fanxi Xu
, et al.
·
Parkinsonism & Related Disorders
Identification of TARDBP Gly298Ser as a Founder Mutation for Amyotrophic Lateral Sclerosis in Southern China
2022
·
Fanxi Xu
, Sen Huang
, et al.
·
Research Square
PDF
Relationship between blood lipid level and Parkinson′s Disease: A Meta-analysis
2019
·
Fanxi Xu
, Hainan Zhang
, et al.
·
中国医师杂志
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Works count:
17
Citation count:
115
H-index:
6
I10-index:
5
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