Hongfu Li

14PUBLICATIONS
5CO-AUTHORS
Neurology and neuromuscular diseasesSouth-East Asian languages (excl. Indonesian)Infant and child healthCancer geneticsCondensed matter imaging
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Publications (14)

|Jul 27, 2026
Pathogenicity Classification of TARDBP Variants of Uncertain Significance: An Integrative Clinical Characterization and Functional Validation.

|Oct 01, 2024
Clinical characterization and founder effect analysis in Chinese amyotrophic lateral sclerosis patients with SOD1 common variants.

Pei-Shan Wang, Xin-Xia Yang, Qiao Wei

|Sep 24, 2024
Blood diagnostic and prognostic biomarkers in amyotrophic lateral sclerosis.

Yongting Lv, Hongfu Li

|Nov 28, 2023
Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype.

Qiao Wei, Hao Yu, Pei-Shan Wang

|Sep 01, 2022
Novel stop-gain RNF170 variation detected in a Chinese family with adolescent-onset hereditary spastic paraplegia.

Jing-Xin Fu, Qiao Wei, Yu-Lan Chen

|May 28, 2022
Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration.

Hao-Ling Cheng, Yi-Jun Chen, Yan-Yan Xue

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Frequent Collaborators

6 joint publications

Zhi-Ying Wu

1 joint publications

Hai-Lin Dong

1 joint publications

Ning Wang

1 joint publications

Jia-Li Xie