Hong-Fu Li

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 11

Top Topics

Mild Cognitive Impairment

Top Venues

CNS neuroscience & therapeutics

Clinical genetics

Molecular genetics & genomic medicine

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

Publications

Qiao Wei, Hao Yu, Pei-Shan Wang, Juan-Juan Xie, Hai-Lin Dong, Zhi-Ying Wu, Hong-Fu Li
Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype. CNS neuroscience & therapeutics (2023)
Hao-Ling Cheng, Yi-Jun Chen, Yan-Yan Xue, Zhi-Ying Wu, Hong-Fu Li, Ning Wang
Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration. Brain sciences 12 (5) (2022)
Qiao Wei, Pei-Shan Wang, Hai-Lin Dong, Wen-Jiao Luo, Zhi-Ying Wu, Hong-Fu Li
A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia. Molecular genetics & genomic medicine 10 (5) (2022)
Jing-Xin Fu, Qiao Wei, Yu-Lan Chen, Hong-Fu Li
Novel stop-gain RNF170 variation detected in a Chinese family with adolescent-onset hereditary spastic paraplegia. Clinical genetics (2022)
Lu-Xi Chen, Gong-Lu Liu, Hao Yu, Zhi-Ying Wu, Hong-Fu Li
Taste loss as the sole presenting symptom in Chinese patient with facial onset sensory and motor neuronopathy. CNS neuroscience & therapeutics 27 (12) (2021)
Yan-Yan Xue, Zhi-Ying Wu, Hong-Fu Li
Identification of pathogenic C9orf72 hexanucleotide repeat expansion in a Chinese patient with frontotemporal dementia: A case report. CNS neuroscience & therapeutics 27 (6) (2021)
Yan-Yan Xue, Xue-Rong Huang, Hai-Lin Dong, Zhi-Ying Wu, Hong-Fu Li
Identification of a large homozygous SPG21 deletion in a Chinese patient with Mast syndrome. CNS neuroscience & therapeutics 27 (10) (2021)
Yang-Tian Yan, Qiao Wei, Yicen Zheng, Wen-Jiao Luo, Hai-Lin Dong, Cong Lu, Juan Zhang, Mei-Jiao Chen, Ying-Xiao Bao, Hong-Fu Li
Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegia. Clinical genetics 95 (5) (2019)
Wen-Jiao Luo, Qiao Wei, Hai-Lin Dong, Yang-Tian Yan, Mei-Jiao Chen, Hong-Fu Li
Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy. Molecular genetics & genomic medicine 8 (1) (2019)
Mei-Jiao Chen, Hong-Fu Li, Shanying Mao
Trigeminal Autonomic Cephalalgias Manifested As The Only Initial Symptom Of Ehlers-Danlos Syndrome Type IV. Journal of pain research 12 (2019)
Cong-Xin Chen, Hai-Lin Dong, Qiao Wei, Li-Xi Li, Hao Yu, Jia-Qi Li, Gong-Lu Liu, Hong-Fu Li, Ge Bai, Huan Ma, Zhi-Ying Wu
Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth disease. Clinical genetics 96 (5) (2019)