Hen‐Ming Wu

11.8k total citations · 5 hit papers
64 papers, 8.8k citations indexed

About

Hen‐Ming Wu is a scholar working on Molecular Biology, Plant Science and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Hen‐Ming Wu has authored 64 papers receiving a total of 8.8k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 53 papers in Plant Science and 7 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Hen‐Ming Wu's work include Plant Reproductive Biology (53 papers), Plant Molecular Biology Research (44 papers) and Photosynthetic Processes and Mechanisms (20 papers). Hen‐Ming Wu is often cited by papers focused on Plant Reproductive Biology (53 papers), Plant Molecular Biology Research (44 papers) and Photosynthetic Processes and Mechanisms (20 papers). Hen‐Ming Wu collaborates with scholars based in United States, China and United Kingdom. Hen‐Ming Wu's co-authors include Alice Y. Cheung, Donald M. Crothers, Hyeon‐Sook Koo, Hong Wang, Qiaohong Duan, Daniel Kita, Chao Li, Lizhen Tao, Cândida Nibau and Ming‐Che Liu and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Hen‐Ming Wu

62 papers receiving 8.6k citations

Hit Papers

The locus of sequence-directed and protein-induced DNA be... 1984 2026 1998 2012 1984 1986 2018 2010 2021 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hen‐Ming Wu United States 43 7.4k 5.8k 820 731 422 64 8.8k
Wayne L. Gerlach Australia 39 4.2k 0.6× 3.9k 0.7× 426 0.5× 788 1.1× 171 0.4× 66 6.8k
Twan Rutten Germany 41 2.6k 0.4× 3.2k 0.6× 326 0.4× 476 0.7× 344 0.8× 128 4.5k
Daphne Preuss United States 43 6.1k 0.8× 5.1k 0.9× 1.2k 1.5× 448 0.6× 934 2.2× 75 7.5k
Jim Haseloff United Kingdom 48 6.5k 0.9× 6.1k 1.0× 241 0.3× 579 0.8× 502 1.2× 101 9.7k
Christian Dumas France 43 4.2k 0.6× 3.1k 0.5× 736 0.9× 310 0.4× 203 0.5× 148 5.5k
Bruce McClure United States 37 4.7k 0.6× 3.9k 0.7× 2.3k 2.8× 423 0.6× 118 0.3× 69 5.5k
Robert F. Whittier Japan 20 3.7k 0.5× 3.0k 0.5× 328 0.4× 709 1.0× 205 0.5× 26 4.9k
Yijun Qi China 54 5.7k 0.8× 9.3k 1.6× 189 0.2× 530 0.7× 158 0.4× 98 11.3k
Etsuko Katoh Japan 32 2.7k 0.4× 3.3k 0.6× 212 0.3× 627 0.9× 159 0.4× 86 4.9k
Takeshi Mizuno Japan 45 5.2k 0.7× 3.8k 0.6× 103 0.1× 1.7k 2.4× 241 0.6× 152 7.2k

Countries citing papers authored by Hen‐Ming Wu

Since Specialization
Citations

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

Fields of papers citing papers by Hen‐Ming Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hen‐Ming Wu. 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 Hen‐Ming Wu. The network helps show where Hen‐Ming Wu may publish in the future.

Co-authorship network of co-authors of Hen‐Ming Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Hen‐Ming Wu. A scholar is included among the top collaborators of Hen‐Ming Wu 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 Hen‐Ming Wu. Hen‐Ming Wu 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.
Zhang, Xiaojing, Hao Jiang, Yaqin Li, et al.. (2025). RLCKs phosphorylate RopGEFs to control auxin-dependent Arabidopsis development. Nature Plants. 11(10). 2130–2144.
2.
Chaudhary, Ajeet, Yu‐Chun Hsiao, Fang‐Ling Yeh, et al.. (2025). FERONIA signaling maintains cell wall integrity during brassinosteroid-induced cell expansion in Arabidopsis. Molecular Plant. 18(4). 603–618. 5 indexed citations
4.
Liu, Ming‐Che, Fang‐Ling Yeh, K.J. Simpson, et al.. (2023). Extracellular pectin-RALF phase separation mediates FERONIA global signaling function. Cell. 187(2). 312–330.e22. 79 indexed citations
5.
Cheung, Alice Y., Qiaohong Duan, Chao Li, Ming‐Che Liu, & Hen‐Ming Wu. (2022). Pollen–pistil interactions: It takes two to tangle but a molecular cast of many to deliver. Current Opinion in Plant Biology. 69. 102279–102279. 30 indexed citations
6.
Liu, Chen, Yu Xiao, Chao Peng, et al.. (2021). Pollen PCP-B peptides unlock a stigma peptide–receptor kinase gating mechanism for pollination. Science. 372(6538). 171–175. 154 indexed citations breakdown →
7.
He, Yang, Dong Wang, Li Guo, et al.. (2021). Malectin/Malectin-like domain-containing proteins: A repertoire of cell surface molecules with broad functional potential. SHILAP Revista de lepidopterología. 7. 100056–100056. 35 indexed citations
8.
Duan, Qiaohong, Ming‐Che Liu, Daniel Kita, et al.. (2020). FERONIA controls pectin- and nitric oxide-mediated male–female interaction. Nature. 579(7800). 561–566. 154 indexed citations
9.
Liu, Yuting, Daniel Kita, Jiabao Huang, et al.. (2017). RopGEF1 Plays a Critical Role in Polar Auxin Transport in Early Development. PLANT PHYSIOLOGY. 175(1). 157–171. 32 indexed citations
10.
García-Valencia, Liliana E., et al.. (2017). SIPP, a Novel Mitochondrial Phosphate Carrier, Mediates in Self-Incompatibility. PLANT PHYSIOLOGY. 175(3). 1105–1120. 22 indexed citations
11.
Li, Chao, Hen‐Ming Wu, & Alice Y. Cheung. (2016). FERONIA and Her Pals: Functions and Mechanisms. PLANT PHYSIOLOGY. 171(4). 2379–2392. 129 indexed citations
12.
Duan, Qiaohong, et al.. (2014). Reactive oxygen species mediate pollen tube rupture to release sperm for fertilization in Arabidopsis. Nature Communications. 5(1). 3129–3129. 276 indexed citations
13.
Cheung, Alice Y., et al.. (2014). Glycosylphosphatidylinositol Anchoring: Control through Modification. PLANT PHYSIOLOGY. 166(2). 748–750. 18 indexed citations
14.
Nibau, Cândida, et al.. (2013). The Arabidopsis small GTPase AtRAC7/ROP9 is a modulator of auxin and abscisic acid signalling. Journal of Experimental Botany. 64(11). 3425–3437. 27 indexed citations
15.
Hernández-Barrera, Alejandra, Carmen Quinto, Eric A. Johnson, et al.. (2013). Using Hyper as a Molecular Probe to Visualize Hydrogen Peroxide in Living Plant Cells. Methods in enzymology on CD-ROM/Methods in enzymology. 527. 275–290. 28 indexed citations
16.
Duan, Qiaohong, Daniel Kita, Chao Li, Alice Y. Cheung, & Hen‐Ming Wu. (2010). FERONIA receptor-like kinase regulates RHO GTPase signaling of root hair development. Proceedings of the National Academy of Sciences. 107(41). 17821–17826. 491 indexed citations breakdown →
17.
Moreno, Nuno, Erwan Michard, Jorge Carneiro, et al.. (2008). Exclusion of a Proton ATPase from the Apical Membrane Is Associated with Cell Polarity and Tip Growth in Nicotiana tabacum Pollen Tubes. The Plant Cell. 20(3). 614–634. 99 indexed citations
18.
Cheung, Alice Y., Qiaohong Duan, Barend H. J. de Graaf, et al.. (2008). The Dynamic Pollen Tube Cytoskeleton: Live Cell Studies Using Actin-Binding and Microtubule-Binding Reporter Proteins. Molecular Plant. 1(4). 686–702. 93 indexed citations
19.
Cheung, Alice Y. & Hen‐Ming Wu. (2004). Overexpression of an Arabidopsis Formin Stimulates Supernumerary Actin Cable Formation from Pollen Tube Cell Membrane[W]. The Plant Cell. 16(1). 257–269. 180 indexed citations
20.
Wu, Hen‐Ming, et al.. (2000). Programmed cell death in plant reproduction. Plant Molecular Biology. 44(3). 267–281. 233 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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