Professor | Hongfu Li | Asia Growth Partners

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Name	Hongfu Li
Contact Information	hongfuli@zju.edu.cn
Language ability	Chinese, English
Province	Zhejiang

Upload Avatar (500 x 500)

Name

Hongfu Li

Contact Information

hongfuli@zju.edu.cn

Language ability

Chinese, English

Province

Zhejiang

University/Lab Affiliation and Title	Zhejiang University
Faculty	Medical
Academic Background & Achievements	2014 - PhD: Fudan University Deputy Director of the Department of Medical Genetics Deputy Director of the Key Laboratory of Medical Neurobiology of Zhejiang Province

University/Lab Affiliation and Title

Zhejiang University

Faculty

Medical

Academic Background & Achievements

2014 - PhD: Fudan University
Deputy Director of the Department of Medical Genetics
Deputy Director of the Key Laboratory of Medical Neurobiology of Zhejiang Province

Areas of Focus	Precision diagnosis and pathogenesis of neurogenetic diseases Clinical and basic research of motor neuron diseases
Publications	Features Differ Between Paroxysmal Kinesigenic Dyskinesia Patients with PRRT2 and TMEM151A Variants, Chen YL, Chen DF, Li HF, Wu ZY, 2022 Paroxysmal Kinesigenic Dyskinesia Caused by 16p11.2 Microdeletion and Related Clinical Features, Chen YL, Chen DF, Ke HZ, Zhao SY, Li HF, Wu ZY, 2022 TMEM151A variants cause paroxysmal kinesigenic dyskinesia, Li HF, Chen YL, Zhuang L, Chen DF, Ke HZ, Luo WJ, Liu GL, Wu SN, Zhou WH, Xiong ZQ, Wu ZY, 2021 SOD1 Mutation Spectrum and Natural History of ALS Patients in a 15-Year Cohort in Southeastern China, Chen LX, Xu HF, Wang PS, Yang XX, Wu ZY, Li HF, 2021 Identification of a large homozygous SPG21 deletion in a Chinese patient with Mast syndrome, Xue YY, Huang XR, Dong HL, Wu ZY, Li HF, 2021 Taste loss as the sole presenting symptom in Chinese patient with facial onset sensory and motor neuronopathy, Chen LX, Liu GL, Yu H, Wu ZY, Li HF, 2021 Penetrance estimation of PRRT2 variants in paroxysmal kinesigenic dyskinesia and infantile convulsions, Chen Y, Chen D, Zhao S, Liu G, Li HF, Wu ZY, 2021 Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy, Luo WJ, Wei Q, Dong HL, Yan YT, Chen MJ, Li HF, 2020 Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2-related disorders, Zhao SY, Li LX, Chen YL, Chen YJ, Liu GL, Dong HL, Chen DF, Li HF, Wu ZY, 2020 Associations between neuroanatomical abnormality and motor symptoms in paroxysmal kinesigenic dyskinesia, Li HF, Yang L, Yin D, Chen WJ, Liu GL, Ni W, Wang N, Yu W, Wu ZY, Wang Z, 2019 Genetic spectrum and variability in Chinese patients with amyotrophic lateral sclerosis, Liu ZJ, Lin HX, Wei Q, Zhang QJ, Chen CX, Tao QQ, Liu GL, Ni W, Aaron D. Gitler, Li HF, Wu ZY, 2019 Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegia, Yan YT, Wei Q, Zheng Y, Luo WJ, Dong HL, Lu C, Zhang J, Chen MJ, Bao YX, Li HF, 2019 Novel PLA2G6 mutations and clinical heterogeneity in Chinese cases with phospholipase A2-associated neurodegeneration, Chen YJ, Chen YC, Dong HL, Li LX, Ni W, Li HF, Wu ZY, 2018 Clinical features of Chinese patients with Gerstmann-Sträussler-Scheinker identified by targeted next-generation sequencing, Li HF, Liu ZJ, Dong HL, Xie JJ, Zhao SY, Ni W, Dong Y, Wu ZY, 2017 Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective study, Chen S, Ni W, Yin XZ, Liu HQ, Lu C, Zheng QJ, Zhao GX, Xu YF, Wu L, Zhang L, Wang N, Li HF, Wu ZY, 2017

Areas of Focus

Precision diagnosis and pathogenesis of neurogenetic diseases
Clinical and basic research of motor neuron diseases

Publications

Features Differ Between Paroxysmal Kinesigenic Dyskinesia Patients with PRRT2 and TMEM151A Variants, Chen YL, Chen DF, Li HF*, Wu ZY*, 2022
Paroxysmal Kinesigenic Dyskinesia Caused by 16p11.2 Microdeletion and Related Clinical Features, Chen YL, Chen DF, Ke HZ, Zhao SY, Li HF*, Wu ZY*, 2022
TMEM151A variants cause paroxysmal kinesigenic dyskinesia, Li HF, Chen YL, Zhuang L, Chen DF, Ke HZ, Luo WJ, Liu GL, Wu SN, Zhou WH, Xiong ZQ*, Wu ZY*, 2021
SOD1 Mutation Spectrum and Natural History of ALS Patients in a 15-Year Cohort in Southeastern China, Chen LX, Xu HF, Wang PS, Yang XX, Wu ZY*, Li HF*, 2021
Identification of a large homozygous SPG21 deletion in a Chinese patient with Mast syndrome, Xue YY, Huang XR, Dong HL, Wu ZY, Li HF*, 2021
Taste loss as the sole presenting symptom in Chinese patient with facial onset sensory and motor neuronopathy, Chen LX, Liu GL, Yu H, Wu ZY, Li HF, 2021
Penetrance estimation of PRRT2 variants in paroxysmal kinesigenic dyskinesia and infantile convulsions, Chen Y, Chen D, Zhao S, Liu G, Li HF*, Wu ZY*, 2021
Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy, Luo WJ, Wei Q, Dong HL, Yan YT, Chen MJ, Li HF*, 2020
Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2-related disorders, Zhao SY, Li LX, Chen YL, Chen YJ, Liu GL, Dong HL, Chen DF, Li HF*, Wu ZY*, 2020
Associations between neuroanatomical abnormality and motor symptoms in paroxysmal kinesigenic dyskinesia, Li HF, Yang L, Yin D, Chen WJ, Liu GL, Ni W, Wang N, Yu W, Wu ZY*, Wang Z*, 2019
Genetic spectrum and variability in Chinese patients with amyotrophic lateral sclerosis, Liu ZJ, Lin HX, Wei Q, Zhang QJ, Chen CX, Tao QQ, Liu GL, Ni W, Aaron D. Gitler, Li HF*, Wu ZY*, 2019
Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegia, Yan YT, Wei Q, Zheng Y, Luo WJ, Dong HL, Lu C, Zhang J, Chen MJ, Bao YX, Li HF*, 2019
Novel PLA2G6 mutations and clinical heterogeneity in Chinese cases with phospholipase A2-associated neurodegeneration, Chen YJ, Chen YC, Dong HL, Li LX, Ni W, Li HF*, Wu ZY*, 2018
Clinical features of Chinese patients with Gerstmann-Sträussler-Scheinker identified by targeted next-generation sequencing, Li HF, Liu ZJ, Dong HL, Xie JJ, Zhao SY, Ni W, Dong Y, Wu ZY*, 2017
Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective study, Chen S, Ni W, Yin XZ, Liu HQ, Lu C, Zheng QJ, Zhao GX, Xu YF, Wu L, Zhang L, Wang N, Li HF*, Wu ZY*, 2017

Neurogenetic Diseases Precision Diagnosis Pathogenesis Motor Neuron Diseases Clinical Research Basic Research Genetics Neurology Neurobiology Disease Mechanisms

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