Fanxi Xu

Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families

Yue Dong, Zhanjun Wang, Huapin Huang, 2021, Neuroscience Letters.

Efficacy and tolerability of intravenous immunoglobulin and subcutaneous immunoglobulin in neurologic diseases.

Chunyu Wang, Hai-nan Zhang, Fanxi Xu, 2019, Clinical therapeutics.

Development and Validation of a Predictive Nomogram for Possible REM Sleep Behavior Disorders

Lina Chen, Huidan Weng, Jiao Yu, 2022, Frontiers in Neurology.

Clinical and Preclinical Neuroimaging Changes in Spinocerebellar Ataxia Type 12: A Study of Three Chinese Pedigrees

Chenfei Ye, H. Lai, Tao Wu, 2022, European Neurology.

A novel FBXO7-R345P mutation in a Chinese family with autosomal recessive parkinsonian-pyramidal syndrome.

Wenjia Zhu, Zhanjun Wang, Junge Zhu, 2021, Parkinsonism & related disorders.

Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China

Xusheng Huang, Yan-ming Xu, Xiuli Feng, 2022, BMC Medical Genomics.

Multidisciplinary molecular consultation increases the diagnosis of pediatric epileptic encephalopathy and neurodevelopmental disorders

Guoguang Zhao, Jing Ye, Zhanjun Wang, 2023, Molecular genetics & genomic medicine.

Applications of Machine Learning to Diagnosis of Parkinson’s Disease

Zhanjun Wang, Xu-Ying Li, Yang Song, 2023, Brain sciences.