Ziguo Zhang

8.0k total citations · 1 hit paper
65 papers, 6.2k citations indexed

About

Ziguo Zhang is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Ziguo Zhang has authored 65 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 34 papers in Cell Biology and 26 papers in Plant Science. Recurrent topics in Ziguo Zhang's work include Microtubule and mitosis dynamics (29 papers), Ubiquitin and proteasome pathways (17 papers) and Plant-Microbe Interactions and Immunity (13 papers). Ziguo Zhang is often cited by papers focused on Microtubule and mitosis dynamics (29 papers), Ubiquitin and proteasome pathways (17 papers) and Plant-Microbe Interactions and Immunity (13 papers). Ziguo Zhang collaborates with scholars based in United Kingdom, China and United States. Ziguo Zhang's co-authors include Hans Thordal‐Christensen, David B. Collinge, Yangdou Wei, David Barford, Jing Yang, Leifu Chang, Kiran Kulkarni, Sarah J. Gurr, Eric H. Kong and Stephen H. McLaughlin and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Ziguo Zhang

64 papers receiving 6.1k citations

Hit Papers

Subcellular localization of H2O2 in plants. H2O2 accumula... 1997 2026 2006 2016 1997 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ziguo Zhang United Kingdom 34 3.8k 3.3k 1.9k 322 271 65 6.2k
Mark J. Banfield United Kingdom 46 4.1k 1.1× 2.6k 0.8× 734 0.4× 213 0.7× 250 0.9× 112 6.2k
Miguel Á. Peñalva Spain 55 2.2k 0.6× 5.8k 1.8× 2.8k 1.5× 164 0.5× 648 2.4× 127 7.7k
Stephen A. Osmani United States 40 1.4k 0.4× 5.7k 1.7× 3.2k 1.7× 317 1.0× 237 0.9× 100 6.4k
Robert Dudler Switzerland 41 3.3k 0.9× 2.7k 0.8× 370 0.2× 409 1.3× 225 0.8× 81 5.1k
Enrico Schleiff Germany 57 3.0k 0.8× 7.5k 2.2× 364 0.2× 182 0.6× 455 1.7× 203 8.7k
Claudio Scazzocchio France 46 2.5k 0.7× 6.1k 1.8× 954 0.5× 135 0.4× 818 3.0× 182 7.4k
Scott C. Peck United States 40 5.9k 1.6× 3.8k 1.1× 513 0.3× 109 0.3× 100 0.4× 76 7.6k
Jean T. Greenberg United States 45 6.9k 1.8× 3.7k 1.1× 594 0.3× 71 0.2× 496 1.8× 76 8.9k
E. Schönbrunn United States 42 1.0k 0.3× 3.8k 1.1× 802 0.4× 736 2.3× 294 1.1× 96 5.4k
Kiminori Toyooka Japan 44 4.5k 1.2× 4.1k 1.2× 727 0.4× 81 0.3× 149 0.5× 139 7.0k

Countries citing papers authored by Ziguo Zhang

Since Specialization
Citations

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

Fields of papers citing papers by Ziguo Zhang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ziguo Zhang

This figure shows the co-authorship network connecting the top 25 collaborators of Ziguo Zhang. A scholar is included among the top collaborators of Ziguo Zhang 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 Ziguo Zhang. Ziguo Zhang 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
2.
Yu, C., Joe G. Greener, Jing Yang, et al.. (2025). Molecular mechanism of Mad2 conformational conversion promoted by the Mad2 ‐interaction motif of Cdc20. Protein Science. 34(4). e70099–e70099. 1 indexed citations
3.
Vázquez-Fernández, Ester, Jing Yang, Ziguo Zhang, et al.. (2024). A comparative study of the cryo-EM structures of Saccharomyces cerevisiae and human anaphase-promoting complex/cyclosome (APC/C). eLife. 13. 1 indexed citations
4.
Yatskevich, Stanislau, Jing Yang, Dom Bellini, Ziguo Zhang, & David Barford. (2024). Structure of the human outer kinetochore KMN network complex. Nature Structural & Molecular Biology. 31(6). 874–883. 17 indexed citations
5.
Yang, Jing, Ziguo Zhang, Leifu Chang, et al.. (2024). Cryo-EM structures of apo-APC/C and APC/CCDH1:EMI1 complexes provide insights into APC/C regulation. Nature Communications. 15(1). 10074–10074. 2 indexed citations
6.
Vázquez-Fernández, Ester, Jing Yang, Ziguo Zhang, et al.. (2024). A comparative study of the cryo-EM structures of Saccharomyces cerevisiae and human anaphase-promoting complex/cyclosome (APC/C). eLife. 13. 1 indexed citations
7.
Muir, Kyle, Christopher Batters, Tom Dendooven, et al.. (2023). Structural mechanism of outer kinetochore Dam1-Ndc80 complex assembly on microtubules. Science. 382(6675). 1184–1190. 13 indexed citations
8.
Dendooven, Tom, Ziguo Zhang, Jing Yang, et al.. (2023). Cryo-EM structure of the complete inner kinetochore of the budding yeast point centromere. Science Advances. 9(30). eadg7480–eadg7480. 24 indexed citations
9.
Yatskevich, Stanislau, Kyle Muir, Dom Bellini, et al.. (2022). Structure of the human inner kinetochore bound to a centromeric CENP-A nucleosome. Science. 376(6595). 844–852. 72 indexed citations
10.
Gabel, C., Zhuang Li, Ziguo Zhang, et al.. (2022). Molecular architecture of the augmin complex. Nature Communications. 13(1). 5449–5449. 15 indexed citations
11.
Naydenova, Katerina, Kyle Muir, Long-Fei Wu, et al.. (2021). Structure of the SARS-CoV-2 RNA-dependent RNA polymerase in the presence of favipiravir-RTP. Proceedings of the National Academy of Sciences. 118(7). 142 indexed citations
12.
Yatskevich, Stanislau, Claudio Alfieri, Thomas Tischer, et al.. (2021). Molecular mechanisms of APC/C release from spindle assembly checkpoint inhibition by APC/C SUMOylation. Cell Reports. 34(13). 108929–108929. 15 indexed citations
13.
Zhang, Ziguo, Dom Bellini, & David Barford. (2020). Crystal structure of the Cenp-HIKHead-TW sub-module of the inner kinetochore CCAN complex. Nucleic Acids Research. 48(19). 11172–11184. 13 indexed citations
14.
Chang, Leifu, Jing Yang, Andreas Boland, et al.. (2020). Structure of the DOCK2−ELMO1 complex provides insights into regulation of the auto-inhibited state. Nature Communications. 11(1). 3464–3464. 42 indexed citations
15.
Wang, Yibin, Ní Hóng, Ziguo Zhang, et al.. (2019). First Report of Apple Rubbery Wood Virus 2 Infecting Pear (Pyrus spp.) in China. Plant Disease. 103(12). 3293–3293. 9 indexed citations
16.
Yan, Kaige, Ziguo Zhang, Jing Yang, Stephen H. McLaughlin, & David Barford. (2018). Architecture of the CBF3–centromere complex of the budding yeast kinetochore. Nature Structural & Molecular Biology. 25(12). 1103–1110. 18 indexed citations
17.
Alfieri, Claudio, Leifu Chang, Ziguo Zhang, et al.. (2016). Molecular basis of APC/C regulation by the spindle assembly checkpoint. Nature. 536(7617). 431–436. 168 indexed citations
18.
Chao, William Chong Hang, Kiran Kulkarni, Ziguo Zhang, Eric H. Kong, & David Barford. (2012). Structure of the mitotic checkpoint complex. Nature. 484(7393). 208–213. 242 indexed citations
19.
Yang, Jing, Ziguo Zhang, S. Mark Roe, Christopher J. Marshall, & David Barford. (2009). Activation of Rho GTPases by DOCK Exchange Factors Is Mediated by a Nucleotide Sensor. Science. 325(5946). 1398–1402. 99 indexed citations
20.
Zhang, Ziguo, et al.. (2001). The barley powdery mildew protein kinase C gene, pkc 1 and pkc ‐like gene, are differentially expressed during morphogenesis. Molecular Plant Pathology. 2(6). 327–337. 11 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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