Hong‐Fu Li - Concepedia

Author

Hong‐Fu Li

Second Affiliated Hospital of Zhejiang University ORCID

Also Known As

Hong-Fu Li, Hong-fu Li, Hongfu Li, Hong‐Fu Li, Huiwen Wu, Li Hong-Fu, Li, Hong-Fu

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Second Affiliated Hospital of Zhejiang University Fudan University Huashan Hospital Fujian Medical University First Affiliated Hospital of Fujian Medical University

About

Hong‐Fu Li is an author at Second Affiliated Hospital of Zhejiang University specializing in medicine, neuropathology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	19	1K
2	Health Sciences	3	3	88
3	Engineering	2	2	47
4	Natural Sciences	1	1	12
5	Public Health	1	1	12

Hong‐Fu Li

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia Wan‐Jin Chen, Yu Lin, Zhi‐Qi Xiong, Nature Genetics Transcriptional RegulationMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	2011	477
Lithium reduced neural progenitor apoptosis in the hippocampus and ameliorated functional deficits after irradiation to the immature mouse brain Kaiming Huo, Yanyan Sun, Hong‐Fu Li, Molecular and Cellular Neuroscience NeurophysiologyCell DeathNeuropharmacologyNeural Progenitor ApoptosisNeurogenesis	2012	99
PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellum Guohe Tan, Yuan-Yuan Liu, Lu Wang, Cell Research Specific Prrt2 DeletionNeurological DisorderSynaptic TransmissionNeurotransmitterNeurotransmission	2017	97
Clinical features and mutation spectrum in Chinese patients with <scp>CADASIL</scp>: A multicenter retrospective study Sheng Chen, Ni Wang, Xinzhen Yin, CNS Neuroscience & Therapeutics	2017	60
<i>PRRT2</i> mutation correlated with phenotype of paroxysmal kinesigenic dyskinesia and drug response Hong‐Fu Li, Wan‐Jin Chen, Ni Wang, Neurology Neurological DisorderGeneticsDiagnosisDisease Gene IdentificationMedical Diagnosis	2013	57
Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system Zhijun Liu, Hong‐Fu Li, Guohe Tan, Neurobiology of Aging Neurodegenerative DiseasesIdentify MutationAmyotrophic Lateral SclerosisNeurological DisorderGenetics	2014	54
Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia Qiao Wei, Hai‐Lin Dong, Li-Ying Pan, Translational Neurodegeneration	2019	43
Bi-allelic loss of function variants in <i>COX20</i> gene cause autosomal recessive sensory neuronopathy Hai‐Lin Dong, Yin Ma, Hao Yu, Brain GeneticsPathologyDisease Gene IdentificationComplex IvDegenerative Pathology	2021	33
SOD1 Mutation Spectrum and Natural History of ALS Patients in a 15-Year Cohort in Southeastern China Luxi Chen, Haifeng Xu, Pei‐Shan Wang, Frontiers in Genetics	2021	32
Typing and evaluating heat resistance of Bacillus cereus sensu stricto isolated from the processing environment of powdered infant formula Kejin Zhuang, Hong‐Fu Li, Ziwei Zhang, Journal of Dairy Science	2019	31

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