Lei Fu

1.1k total citations
46 papers, 808 citations indexed

About

Lei Fu is a scholar working on Molecular Biology, Immunology and Plant Science. According to data from OpenAlex, Lei Fu has authored 46 papers receiving a total of 808 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 10 papers in Immunology and 10 papers in Plant Science. Recurrent topics in Lei Fu's work include Streptococcal Infections and Treatments (8 papers), Antimicrobial Peptides and Activities (7 papers) and Neonatal and Maternal Infections (6 papers). Lei Fu is often cited by papers focused on Streptococcal Infections and Treatments (8 papers), Antimicrobial Peptides and Activities (7 papers) and Neonatal and Maternal Infections (6 papers). Lei Fu collaborates with scholars based in China, United States and United Kingdom. Lei Fu's co-authors include Anding Zhang, Meilin Jin, Lianghui Gao, Lan Lin, Li Han, Wei‐Hai Fang, Yaozu Xiang, Jianqing Zhao, Rui Zhou and Shan-Shan Pan and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and PLoS ONE.

In The Last Decade

Lei Fu

44 papers receiving 797 citations

Peers

Lei Fu

IMMUN

MICRO

PHEOH

Narumon Phaonakrop Thailand

Xifang Zhu China

Namarta Kalia India

Edgar Oliver López‐Villegas Mexico

Zhi-xue Cheng China

Corey P. Parlet United States

Giulio Petronio Petronio Italy

Shumin Yu China

Eric J. Haas-Stapleton United States

Xia Meng China

Narumon Phaonakrop Thailand

Lei Fu

361 ×1.1

68 ×0.3

IMMUN

119 ×0.7

MICRO

85 ×0.6

PHEOH

183 ×1.7

Citations per year, relative to Lei Fu Lei Fu (= 1×) peers Narumon Phaonakrop

Countries citing papers authored by Lei Fu

Since Specialization

Citations

This map shows the geographic impact of Lei Fu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Lei Fu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lei Fu more than expected).

Fields of papers citing papers by Lei Fu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lei Fu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Lei Fu. The network helps show where Lei Fu may publish in the future.

Co-authorship network of co-authors of Lei Fu

This figure shows the co-authorship network connecting the top 25 collaborators of Lei Fu. A scholar is included among the top collaborators of Lei Fu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lei Fu. Lei Fu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Fu, Lei, et al.. (2025). Research on the Design of a Short Video Recommendation System Based on Multimodal Information and Differential Privacy. 45–52. 8 indexed citations

Li, Qifa, Xiaoqin Luo, Jing Xu, et al.. (2025). Anticonvulsant effect of Stachydrine on pentylenetetrazole-induced kindling seizure mouse model via Notch and NMDAR signaling pathways. Journal of Ethnopharmacology. 349. 119975–119975.

Yuan, David Yu, et al.. (2024). A New Cloud-Native Tool for Pharmacogenetic Analysis. Genes. 15(3). 352–352. 2 indexed citations

Wang, Hui, Jing Dong, Yuanyuan Wu, et al.. (2023). Human umbilical cord mesenchymal stem cell‐derived exosomes attenuate neuroinflammation and oxidative stress through the NRF2/NF‐κB/NLRP3 pathway. CNS Neuroscience & Therapeutics. 30(3). e14454–e14454. 38 indexed citations

Fu, Lei, Mengqi Wu, Xinmeng Chen, et al.. (2023). Conformational cycle of human polyamine transporter ATP13A2. Nature Communications. 14(1). 1978–1978. 10 indexed citations

Li, Xiangyuan, et al.. (2023). How Alligator Immune Peptides Kill Gram-Negative Bacteria: A Lipid-Scrambling, Squeezing, and Extracting Mechanism Revealed by Theoretical Simulations. International Journal of Molecular Sciences. 24(13). 10962–10962. 1 indexed citations

Fu, Lei, Junjie Song, Shan Zhang, et al.. (2022). Thermodynamic Driving Forces for Divalent Cations Binding to Zwitterionic Phospholipid Membranes. The Journal of Physical Chemistry Letters. 13(48). 11237–11244. 5 indexed citations

Fu, Lei, et al.. (2022). Polymyxins induce lipid scrambling and disrupt the homeostasis of Gram-negative bacteria membrane. Biophysical Journal. 121(18). 3486–3498. 21 indexed citations

Zhang, Shan, et al.. (2019). Peripheral Antimicrobial Peptide Gomesin Induces Membrane Protrusion, Folding, and Laceration. Langmuir. 35(40). 13233–13242. 7 indexed citations

10.

Fu, Lei, et al.. (2019). Polymyxin B Loosens Lipopolysaccharide Bilayer but Stiffens Phospholipid Bilayer. Biophysical Journal. 118(1). 138–150. 45 indexed citations

11.

Fu, Lei, et al.. (2018). Peptide-Lipid Interaction Sites Affect Vesicles’ Responses to Antimicrobial Peptides. Biophysical Journal. 115(8). 1518–1529. 18 indexed citations

12.

Wang, Xiaoping, Jianqing Zhao, Cong Cai, et al.. (2018). A Label-Free Quantitative Proteomic Analysis of Mouse Neutrophil Extracellular Trap Formation Induced by Streptococcus suis or Phorbol Myristate Acetate (PMA). Frontiers in Immunology. 9. 2615–2615. 9 indexed citations

13.

Hou, Yiling, Xiang Ding, Hongqing Zhu, et al.. (2017). Comparative analysis of transcriptomes of macrophage revealing the mechanism of the immunoregulatory activities of a novel polysaccharide isolated from Boletus speciosus frost. Pharmacognosy Magazine. 13(51). 463–463. 3 indexed citations

14.

Fu, Lei, Jianqing Zhao, Lan Lin, et al.. (2016). Characterization of IgA1 protease as a surface protective antigen of Streptococcus suis serotype 2. Microbes and Infection. 18(4). 285–289. 14 indexed citations

15.

Yu, Chengjie, Sizhu Suolang, Qingping Luo, et al.. (2016). Genome sequencing of a virulent avian Pasteurella multocida strain GX-Pm reveals the candidate genes involved in the pathogenesis. Research in Veterinary Science. 105. 23–27. 14 indexed citations

16.

Wang, Zhihua, Juan Wang, Zeyuan Zhou, et al.. (2015). Extracellular Signal-regulated Kinase Mitogen-activated Protein Kinase and Phosphatidylinositol 3-Kinase/Akt Signaling Are Required for Lipopolysaccharide-mediated Mineralization in Murine Odontoblast-like Cells. Journal of Endodontics. 41(6). 871–876. 9 indexed citations

17.

Zhao, Jianqing, Shan-Shan Pan, Lan Lin, et al.. (2015). Streptococcus suis serotype 2 strains can induce the formation of neutrophil extracellular traps and evade trapping. FEMS Microbiology Letters. 362(6). 24 indexed citations

18.

Ding, Xiang, Yiling Hou, Panpan Wang, et al.. (2015). Structure elucidation, anticancer and antioxidant activities of a novel polysaccharide from Gomphus clavatus Gray. Oncology Reports. 33(6). 3162–3170. 14 indexed citations

19.

Hou, Yiling, et al.. (2015). Structure elucidation and anti-tumor activities of water-soluble oligosaccharides from Lactarius deliciosus (L. ex Fr.) Gray. Pharmacognosy Magazine. 11(44). 716–716. 13 indexed citations

20.

Yang, Chao, Jianqing Zhao, Lan Lin, et al.. (2015). Targeting TREM-1 Signaling in the Presence of Antibiotics is Effective Against Streptococcal Toxic-Shock-Like Syndrome (STSLS) Caused by Streptococcus suis. Frontiers in Cellular and Infection Microbiology. 5. 79–79. 26 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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