H
Hong Jiang
Researcher at Central South University
Publications - 393
Citations - 23057
Hong Jiang is an academic researcher from Central South University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 51, co-authored 280 publications receiving 18722 citations. Previous affiliations of Hong Jiang include University of Texas at Austin & City University of New York.
Papers
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Journal ArticleDOI
Blood Neurofilament Light Chain in Genetic Ataxia: A Meta-Analysis.
Linliu Peng,Shang Wang,Zhao Chen,Yun Peng,Chunrong Wang,Zhe Long,Huirong Peng,Yuting Shi,Xuan Hou,Lijing Lei,Linlin Wan,Mingjie Liu,Guangdong Zou,Lu Shen,Kun Xia,Rong Qiu,Beisha Tang,Tetsuo Ashizawa,Thomas Klockgether,Thomas Klockgether,Hong Jiang +20 more
TL;DR: In this paper, the authors conducted a meta-analysis to assess the value of neurofilament light chain (NfL) as a biomarker in genetic ataxia and found that NfL levels correlated with disease severity in SCA3.
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C9orf72 hexanucleotide expansion analysis in Chinese patients with multiple system atrophy.
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Mutation Detection in Candidate Genes for Benign Familial Infantile Seizures on a Novel Locus
Nan Li,Haiyan Li,Hong Jiang,Lu Shen,Xinxiang Yan,Jifeng Guo,Yanmin Song,Qian Yang,Ya-qin Wang,Xiaobo Li,Ruping Xiang,Xiaohong Zi,Xiaoyan Long,Zhengmao Hu,Qian Pan,Kun Xia,Beisha Tang +16 more
TL;DR: Mutation analysis of candidate genes for the mapped chromosome region suggest those candidate genes that were detected might not be involved in the epileptogenesis of pure BFIS, at least in the Chinese family studied.
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Clinical findings of autosomal-dominant striatal degeneration and PDE8B mutation screening in parkinsonism and related disorders.
Jie Ni,Xiaoping Yi,Zhen Liu,Weining Sun,Yanchun Yuan,Jie Yang,Hong Jiang,Lu Shen,Beisha Tang,Yunhai Liu,Junling Wang +10 more
TL;DR: The typical ataxia phenotype in ADSD is described for the first time, and three PDE8B missense variants were identified that were unlikely to be the cause of the parkinsonism phenotype according to the functional prediction and mutation types reported in ADSS.
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Mutation analysis of CAPN1 in Chinese populations with spastic paraplegia and related neurodegenerative diseases.
Zheng-cai Xia,Zhenhua Liu,Xiaoxia Zhou,Zhen Liu,Junling Wang,Zhengmao Hu,Jieqiong Tan,Lu Shen,Hong Jiang,Beisha Tang,Lifang Lei +10 more
TL;DR: The data reveal a novel CAPN1 mutation found in patients with SPG/SCA and emphasize the spastic and ataxic phenotypes of SPG76, butCAPN1 may not play a major role in EOPD and ALS.