Ping Zhu

8.5k total citations · 3 hit papers
93 papers, 4.9k citations indexed

About

Ping Zhu is a scholar working on Molecular Biology, Infectious Diseases and Virology. According to data from OpenAlex, Ping Zhu has authored 93 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 16 papers in Infectious Diseases and 13 papers in Virology. Recurrent topics in Ping Zhu's work include HIV Research and Treatment (13 papers), RNA modifications and cancer (12 papers) and Genomics and Chromatin Dynamics (11 papers). Ping Zhu is often cited by papers focused on HIV Research and Treatment (13 papers), RNA modifications and cancer (12 papers) and Genomics and Chromatin Dynamics (11 papers). Ping Zhu collaborates with scholars based in China, United States and Italy. Ping Zhu's co-authors include Kenneth H. Roux, Kenneth A. Taylor, Jun Liu, Elena Chertova, Guohong Li, Julian W. Bess, Jeffrey D. Lifson, Henry Grisé, Dennis R. Burton and Gilad Ofek and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Ping Zhu

85 papers receiving 4.8k citations

Hit Papers

Antibody Domain Exchange Is an Immunological Solution to ... 2003 2026 2010 2018 2003 2006 2014 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Antibody Domain Exchange Is an Immunological Solution to Carbohydrate Cluster Recognition
    2003 632 citations D.A. Calarese, Christopher N. Scanlan et al. Science profile →
  2. Distribution and three-dimensional structure of AIDS virus envelope spikes
    2006 596 citations Ping Zhu, Kenneth H. Roux et al. profile →
  3. Cryo-EM Study of the Chromatin Fiber Reveals a Double Helix Twisted by Tetranucleosomal Units
    2014 468 citations Feng Song, Ping Chen et al. Science profile →

Peers

Ping Zhu
José L. Nieva Spain
Dmitry Lyumkis United States
Natalia de Val United States
Debra M. Eckert United States
Erik A. Whitehorn United States
Ursula Dietrich Germany
William R. Schief United States
Elena Chertova United States
Fredric S. Cohen United States
Owen Pornillos United States
José L. Nieva Spain
Ping Zhu
Citations per year, relative to Ping Zhu Ping Zhu (= 1×) peers José L. Nieva

Countries citing papers authored by Ping Zhu

Since Specialization
Citations

This map shows the geographic impact of Ping Zhu'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 Ping Zhu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ping Zhu more than expected).

Fields of papers citing papers by Ping Zhu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ping Zhu. 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 Ping Zhu. The network helps show where Ping Zhu may publish in the future.

Co-authorship network of co-authors of Ping Zhu

This figure shows the co-authorship network connecting the top 25 collaborators of Ping Zhu. A scholar is included among the top collaborators of Ping Zhu 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 Ping Zhu. Ping Zhu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Zhu, Ping, Mengyuan Wang, Chang Liu, et al.. (2024). Recognition mechanism of split T-2 toxin aptamer coupled with reliable dual-mode detection in peanut and beer. Food Bioscience. 60. 104268–104268. 5 indexed citations
2.
Zeng, Wenfeng, Xiuli Wei, Kai Song, et al.. (2023). Stable IL‐2 Nano‐Assembly for Improved Anti‐Tumor Effect. Advanced Therapeutics. 7(3). 1 indexed citations
3.
Huang, Li, Haizhen Long, Zengqi Wen, et al.. (2023). Structural insight into H4K20 methylation on H2A.Z-nucleosome by SUV420H1. Molecular Cell. 83(16). 2884–2895.e7. 9 indexed citations
4.
Zhang, Hui, Hongjia Li, Fa Zhang, & Ping Zhu. (2023). A strategy combining denoising and cryo-EM single particle analysis. Briefings in Bioinformatics. 24(3). 1 indexed citations
5.
Zhang, Haonan, Yan Li, Yanan Liu, et al.. (2023). A method for restoring signals and revealing individual macromolecule states in cryo-ET, REST. Nature Communications. 14(1). 2937–2937. 11 indexed citations
6.
Ye, Hua, Mengyuan Wang, Xi Yu, et al.. (2023). Molecular Docking Insight into the Label-Free Fluorescence Aptasensor for Ochratoxin A Detection. Molecules. 28(12). 4841–4841. 3 indexed citations
7.
Li, Yan, et al.. (2023). Cryo-ET study from in vitro to in vivo revealed a general folding mode of chromatin with two-start helical architecture. Cell Reports. 42(9). 113134–113134. 10 indexed citations
8.
Li, Hongjia, Hui Zhang, Xiaohua Wan, et al.. (2022). Noise-Transfer2Clean: denoising cryo-EM images based on noise modeling and transfer. Bioinformatics. 38(7). 2022–2029. 18 indexed citations
9.
Bao, Keyan, et al.. (2022). In situ structures of polymerase complex of mammalian reovirus illuminate RdRp activation and transcription regulation. Proceedings of the National Academy of Sciences. 119(50). e2203054119–e2203054119. 6 indexed citations
10.
11.
Guan, Hongxin, Ting Yu, Abdullah F. U. H. Saeed, et al.. (2020). Cryo-EM structures of the human PA200 and PA200-20S complex reveal regulation of proteasome gate opening and two PA200 apertures. PLoS Biology. 18(3). e3000654–e3000654. 29 indexed citations
12.
Finci, Lorenzo I., Xiaofeng Zhang, Xiuliang Huang, et al.. (2018). The cryo-EM structure of the SF3b spliceosome complex bound to a splicing modulator reveals a pre-mRNA substrate competitive mechanism of action. Genes & Development. 32(3-4). 309–320. 91 indexed citations
13.
Song, Feng, Ping Chen, Dapeng Sun, et al.. (2014). Cryo-EM Study of the Chromatin Fiber Reveals a Double Helix Twisted by Tetranucleosomal Units. Science. 344(6182). 376–380. 468 indexed citations breakdown →
14.
Cheng, Lingpeng, Xiaoxing Huang, Xiaomin Li, et al.. (2014). Cryo-EM structures of two bovine adenovirus type 3 intermediates. Virology. 450-451. 174–181. 26 indexed citations
15.
Jiao, Lianying, Songying Ouyang, Neil Shaw, et al.. (2014). Mechanism of the Rpn13-induced activation of Uch37. Protein & Cell. 5(8). 616–630. 28 indexed citations
16.
Yang, Lifei, Yufeng Song, Xiaomin Li, et al.. (2012). HIV-1 Virus-Like Particles Produced by Stably Transfected Drosophila S2 Cells: a Desirable Vaccine Component. Journal of Virology. 86(14). 7662–7676. 37 indexed citations
17.
18.
Crooks, Emma T., Penny L. Moore, Michael Franti, et al.. (2007). A comparative immunogenicity study of HIV-1 virus-like particles bearing various forms of envelope proteins, particles bearing no envelope and soluble monomeric gp120. Virology. 366(2). 245–262. 106 indexed citations
19.
Løset, Geir Åge, Kenneth H. Roux, Ping Zhu, Terje E. Michaelsen, & Inger Sandlie. (2004). Differential Segmental Flexibility and Reach Dictate the Antigen Binding Mode of Chimeric IgD and IgM: Implications for the Function of the B Cell Receptor. The Journal of Immunology. 172(5). 2925–2934. 40 indexed citations
20.
Calarese, D.A., Christopher N. Scanlan, Michael B. Zwick, et al.. (2003). Antibody Domain Exchange Is an Immunological Solution to Carbohydrate Cluster Recognition. Science. 300(5628). 2065–2071. 632 indexed citations breakdown →

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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