Wan-Jin Chen (Wanjin Chen, W Chen)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 20

Top Venues

Annals of neurology

Movement disorders : official journal of the Movement Disorder Society

Annals of clinical and translational neurology

Human mutation

This page only lists publications with an associated author ORCID identifier.

Publications

Aowei Lv, Yaofeng Fang, Xiaohong Lin, Jiaying Chen, Huanhuan Song, Ning Wang, Wan-Jin Chen, Ying Fu, Rui Li, Yi Lin
B-cell depletion limits HTLV-1-infected T-cell expansion and ameliorate HTLV-1-associated myelopathy. Annals of clinical and translational neurology (2024)
Zhi-Xian Ye, Hao-Ling Xu, Na-Ping Chen, Xin-Yuan Chen, Meng-Cheng Li, Ru-Ying Yuan, Wei Lin, Liangliang Qiu, Minting Lin, Wan-Jin Chen, Ning Wang, Jian-Ping Hu, Ying Fu, Shi-Rui Gan, null null
Disease Progression and Multiparametric Imaging Characteristics of Spinocerebellar Ataxia Type 3 With Spastic Paraplegia. Neurology. Genetics 10 (3) (2024)
Zhi-Xian Ye, Hao-Ling Xu, Na-Ping Chen, Xin-Yuan Chen, Meng-Cheng Li, Ru-Ying Yuan, Wei Lin, Liangliang Qiu, Minting Lin, Wan-Jin Chen, Ning Wang, Jian-Ping Hu, Ying Fu, Shi-Rui Gan, null null
Disease Progression and Multiparametric Imaging Characteristics of Spinocerebellar Ataxia Type 3 With Spastic Paraplegia. Neurology. Genetics 10 (3) (2024)
Yun-Lu Li, Jingjing Lin, Xuejing Huang, Rui-Huang Zeng, Guangyu Zhang, Jie-Ni Xu, Kai-Jun Lin, Xin-Shuo Chen, Ming-Feng He, Jing-Da Qiao, Xuewen Cheng, Dengna Zhu, Zhi-Qi Xiong, Wan-Jin Chen
Heterozygous Variants in KCNJ10 Cause Paroxysmal Kinesigenic Dyskinesia Via Haploinsufficiency. Annals of neurology (2024)
Jin He, Xiao-Xuan Liu, Dong-Sheng Fan, Wan-Jin Chen
Reply to SARS1 (SerRS) causing de novo dominant Charcot-Marie-Tooth disease with slow conduction. Annals of neurology (2023)
Xiang Lin, Jun-Yi Jiang, Dao-Jun Hong, Kai-Jun Lin, Jin-Jing Li, Yi-Jun Chen, Yu-Sen Qiu, Zishuai Wang, Yi-Chu Liao, Kang Yang, Yan Shi, Meng-Wen Wang, Shao-Lun Hsu, Shunyan Hong, Yi-Heng Zeng, Xiao-Chun Chen, Ning Wang, Yi-Chung Lee, Wan-Jin Chen
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization. Movement disorders : official journal of the Movement Disorder Society (2023)
Yi-Jun Chen, Meng-Wen Wang, Yu-Sen Qiu, Ru-Ying Yuan, Ning Wang, Xiang Lin, Wan-Jin Chen
Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia. Movement disorders : official journal of the Movement Disorder Society (2023)
Jin He, Xiao-Xuan Liu, Ming-Ming Ma, Jing-Jing Lin, Jun Fu, Yi-Kun Chen, Guo-Rong Xu, Liu-Qing Xu, Zhi-Fei Fu, Dan Xu, Wen-Feng Chen, Chun-Yan Cao, Yan Shi, Yi-Heng Zeng, Jing Zhang, Xiao-Chun Chen, Ru-Xu Zhang, Ning Wang, Marina Kennerson, Dong-Sheng Fan, Wan-Jin Chen
Heterozygous Seryl-tRNA Synthetase 1 Variants Cause Charcot-Marie-Tooth Disease. Annals of neurology (2022)
Miao Zhao, Xiao-Hong Lin, Yi-Heng Zeng, Hui-Zhen Su, Chong Wang, Kang Yang, Yi-Kun Chen, Bi-Wei Lin, Xiang-Ping Yao, Wan-Jin Chen
Knockdown of myorg leads to brain calcification in zebrafish. Molecular brain 15 (1) (2022)
Yu-Sen Qiu, Yi-Heng Zeng, Ru-Ying Yuan, Zhi-Xian Ye, Jin Bi, Xiao-Hong Lin, Yi-Jun Chen, Meng-Wen Wang, Ying Liu, Shao-Bo Yao, Yi-Kun Chen, Jun-Yi Jiang, Yi Lin, Xiang Lin, Ning Wang, Ying Fu, Wan-Jin Chen
Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort study. BMJ open 12 (1) (2022)
Yi-Heng Zeng, Kang Yang, Gan-Qin Du, Yi-Kun Chen, Chun-Yan Cao, Yu-Sen Qiu, Jin He, Hai-Dong Lv, Qian-Qian Qu, Jian-Nan Chen, Guo-Rong Xu, Long Chen, Fu-Ze Zheng, Miao Zhao, Min-Ting Lin, Wan-Jin Chen, Jing Hu, Zhi-Qiang Wang, Ning Wang
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy. Annals of neurology 92 (3) (2022)
Y Liu, Z Ye, Jianping Hu, Zebin Xiao, F Zhang, X Yang, Wan-Jin Chen, Ying Fu, Dairong Cao
White Matter Alterations in Spastic Paraplegia Type 5: A Multiparametric Structural MRI Study and Correlations with Biochemical Measurements. AJNR. American journal of neuroradiology (2021)
Ying-Xuan Xie, Wen-Qi Lv, Yi-Kun Chen, Shunyan Hong, Xiang-Ping Yao, Wan-Jin Chen, Miao Zhao
Advances in gene therapy for neurogenetic diseases: a brief review. Journal of molecular medicine (Berlin, Germany) (2021)
Yun-Lu Li, Wen-Qi Lv, Yi-Heng Zeng, Yi-Kun Chen, Xian-Long Wang, Kang Yang, Yuan-Liang Ding, Ru-Kai Chen, Ning Wang, Wan-Jin Chen
Exome-Wide Analyses in Paroxysmal Kinesigenic Dyskinesia Confirm TMEM151A as a Novel Causative Gene. Movement disorders : official journal of the Movement Disorder Society 37 (3) (2021)
Xia-Hua Liu, Ying Li, Hao-Ling Xu, Arif Sikandar, Wei-Hong Lin, Gui-He Li, Xiao-Fen Li, Alimire Alimu, Sheng-Bin Yu, Xiang-Hui Ye, Ning Wang, Jun Ni, Wan-Jin Chen, Shi-Rui Gan
Quantitative assessment of postural instability in spinocerebellar ataxia type 3 patients. Annals of clinical and translational neurology 7 (8) (2020)
Lu-Lu Lai, Yi-Jun Chen, Yun-Lu Li, Xiao-Hong Lin, Meng-Wen Wang, En-Lin Dong, Ning Wang, Wan-Jin Chen, Xiang Lin
Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia. Annals of clinical and translational neurology 7 (10) (2020)
Xin-Xin Guo, Hui-Zhen Su, Xiao-Huan Zou, Lu-Lu Lai, Ying-Qian Lu, Chong Wang, Yun-Lu Li, Jing-Mei Hong, Miao Zhao, Kun-Xin Lin, Jie Lin, Yi-Heng Zeng, Xiang-Ping Yao, Ning Wang, Wan-Jin Chen
Identification of SLC20A2 deletions in patients with primary familial brain calcification. Clinical genetics 96 (1) (2019)
Xin-Xin Guo, Xiao-Huan Zou, Chong Wang, Xiang-Ping Yao, Hui-Zhen Su, Lu-Lu Lai, Hai-Ting Chen, Jing-Hui Lai, Yao-Bin Liu, Dong-Ping Chen, Yu-Chun Deng, Pan Lin, Hua-Song Lin, Bing-Cong Hong, Qing-Yang Yao, Xue-Jiao Chen, Dan-Qin Huang, Hong-Xia Fu, Ji-Dong Peng, Yan-Fang Niu, Yu-Ying Zhao, Xiao-Qun Zhu, Xiao-Pei Lu, Hai-Liang Lin, Yong-Kun Li, Chang-Yun Liu, Gen-Bin Huang, Ning Wang, Wan-Jin Chen
Spectrum of SLC20A2, PDGFRB, PDGFB, and XPR1 mutations in a large cohort of patients with primary familial brain calcification. Human mutation 40 (4) (2019)
Jin He, Lingling Guo, Shan Lin, Wenfeng Chen, Guorong Xu, Bin Cai, Liuqing Xu, Jingmei Hong, Liangliang Qiu, Ning Wang, Wan-Jin Chen
ATP1A1 mutations cause intermediate Charcot-Marie-Tooth disease. Human mutation 40 (12) (2019)
Shuang Wu, Yun-Lu Li, Ning-Yi Cheng, Chong Wang, En-Lin Dong, Ying-Qian Lu, Jin-Jing Li, Xin-Xin Guo, Xiang Lin, Lu-Lu Lai, Zhi-Wei Liu, Ning Wang, Wan-Jin Chen
c.835-5T>G Variant in SMN1 Gene Causes Transcript Exclusion of Exon 7 and Spinal Muscular Atrophy. Journal of molecular neuroscience : MN 65 (2) (2018)

Wan-Jin Chen.css-eqlu8i{font-size:small;padding-left:4px;} (Wanjin Chen, W Chen)

Publication Activity (10 Years)

Top Topics

Top Venues

Wan-Jin Chen (Wanjin Chen, W Chen)