David De Vleesschauwer

5.8k total citations
45 papers, 3.8k citations indexed

About

David De Vleesschauwer is a scholar working on Plant Science, Molecular Biology and Cell Biology. According to data from OpenAlex, David De Vleesschauwer has authored 45 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Plant Science, 8 papers in Molecular Biology and 4 papers in Cell Biology. Recurrent topics in David De Vleesschauwer's work include Plant-Microbe Interactions and Immunity (32 papers), Plant Parasitism and Resistance (12 papers) and Plant Stress Responses and Tolerance (10 papers). David De Vleesschauwer is often cited by papers focused on Plant-Microbe Interactions and Immunity (32 papers), Plant Parasitism and Resistance (12 papers) and Plant Stress Responses and Tolerance (10 papers). David De Vleesschauwer collaborates with scholars based in Belgium, United States and Japan. David De Vleesschauwer's co-authors include Monica Höfte, Godelieve Gheysen, Jonas Van Bockhaven, Bob Asselbergh, Jing Xu, Tina Kyndt, Kamrun Nahar, Hamed Soren Seifi, Pamela C. Ronald and Mohammad Djavaheri and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and PLANT PHYSIOLOGY.

In The Last Decade

David De Vleesschauwer

45 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David De Vleesschauwer Belgium 32 3.5k 908 387 334 176 45 3.8k
Heqiang Huo United States 27 1.8k 0.5× 982 1.1× 90 0.2× 71 0.2× 99 0.6× 79 2.3k
Michael Riemann Germany 29 2.2k 0.6× 867 1.0× 197 0.5× 575 1.7× 20 0.1× 62 2.6k
Jude W. Grosser United States 37 3.7k 1.0× 2.6k 2.8× 437 1.1× 304 0.9× 19 0.1× 183 4.4k
Christine Rustérucci France 15 2.5k 0.7× 1.5k 1.7× 143 0.4× 283 0.8× 13 0.1× 21 3.2k
Jeong Sheop Shin South Korea 31 2.5k 0.7× 1.8k 2.0× 144 0.4× 98 0.3× 23 0.1× 103 3.3k
Victoria Pastor Spain 27 2.9k 0.8× 895 1.0× 270 0.7× 411 1.2× 8 0.0× 54 3.4k
Kenneth L. Korth United States 23 1.6k 0.5× 1.2k 1.3× 109 0.3× 572 1.7× 14 0.1× 40 2.5k
Sung Chul Lee South Korea 38 5.2k 1.5× 2.4k 2.6× 200 0.5× 160 0.5× 12 0.1× 132 5.8k
Yong Hwa Cheong South Korea 32 4.9k 1.4× 2.8k 3.1× 158 0.4× 122 0.4× 14 0.1× 60 5.6k
Weimin Fang China 30 2.2k 0.6× 1.4k 1.5× 146 0.4× 150 0.4× 9 0.1× 133 2.6k

Countries citing papers authored by David De Vleesschauwer

Since Specialization
Citations

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

Fields of papers citing papers by David De Vleesschauwer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David De Vleesschauwer. 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 David De Vleesschauwer. The network helps show where David De Vleesschauwer may publish in the future.

Co-authorship network of co-authors of David De Vleesschauwer

This figure shows the co-authorship network connecting the top 25 collaborators of David De Vleesschauwer. A scholar is included among the top collaborators of David De Vleesschauwer 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 David De Vleesschauwer. David De Vleesschauwer 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.
Gaillochet, Christophe, Vera Goossens, Andrzej Drozdzecki, et al.. (2023). Systematic optimization of Cas12a base editors in wheat and maize using the ITER platform. Genome biology. 24(1). 6–6. 38 indexed citations
2.
Scafaro, Andrew P., David De Vleesschauwer, Matthew A. Hannah, et al.. (2019). A single point mutation in the C-terminal extension of wheat Rubisco activase dramatically reduces ADP inhibition via enhanced ATP binding affinity. Journal of Biological Chemistry. 294(47). 17931–17940. 19 indexed citations
3.
Vleesschauwer, David De, et al.. (2018). The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice. Scientific Reports. 8(1). 3864–3864. 61 indexed citations
4.
Kyndt, Tina, Ashley Haeck, David De Vleesschauwer, et al.. (2017). Below-Ground Attack by the Root Knot Nematode Meloidogyne graminicola Predisposes Rice to Blast Disease. Molecular Plant-Microbe Interactions. 30(3). 255–266. 31 indexed citations
5.
Vleesschauwer, David De, et al.. (2016). The DELLA Protein SLR1 Integrates and Amplifies Salicylic Acid- and Jasmonic Acid-Dependent Innate Immunity in Rice. PLANT PHYSIOLOGY. 170(3). 1831–1847. 109 indexed citations
6.
Hosp, Fabian, Ines Lassowskat, Valeria Santoro, et al.. (2016). Lysine acetylation in mitochondria: From inventory to function. Mitochondrion. 33. 58–71. 67 indexed citations
7.
Ameye, Maarten, Kris Audenaert, Kathy Steppe, et al.. (2015). Priming of Wheat with the Green Leaf Volatile Z-3-Hexenyl Acetate Enhances Defense against Fusarium graminearum But Boosts Deoxynivalenol Production. PLANT PHYSIOLOGY. 167(4). 1671–1684. 108 indexed citations
8.
Ji, Hongli, Godelieve Gheysen, Chhana Ullah, et al.. (2015). The role of thionins in rice defence against root pathogens. Molecular Plant Pathology. 16(8). 870–881. 41 indexed citations
9.
Xu, Jing, Lian Zhou, Vittorio Venturi, et al.. (2015). Phytohormone-mediated interkingdom signaling shapes the outcome of rice-Xanthomonas oryzae pv. oryzae interactions. BMC Plant Biology. 15(1). 10–10. 33 indexed citations
10.
Bockhaven, Jonas Van, Kathy Steppe, Ingvar Bauweraerts, et al.. (2015). Primary metabolism plays a central role in moulding silicon‐inducible brown spot resistance in rice. Molecular Plant Pathology. 16(8). 811–824. 58 indexed citations
11.
Höfte, Monica, et al.. (2014). Connecting Growth and Defense: The Emerging Roles of Brassinosteroids and Gibberellins in Plant Innate Immunity. Molecular Plant. 7(6). 943–959. 206 indexed citations
12.
Seifi, Hamed Soren, David De Vleesschauwer, Aziz Aziz, & Monica Höfte. (2014). Modulating plant primary amino acid metabolism as a necrotrophic virulence strategy. Plant Signaling & Behavior. 9(2). e27995–e27995. 29 indexed citations
13.
Vleesschauwer, David De, Godelieve Gheysen, & Monica Höfte. (2013). Hormone defense networking in rice: tales from a different world. Trends in Plant Science. 18(10). 555–565. 208 indexed citations
14.
Sharma, Rita, David De Vleesschauwer, Manoj K. Sharma, & Pamela C. Ronald. (2013). Recent Advances in Dissecting Stress-Regulatory Crosstalk in Rice. Molecular Plant. 6(2). 250–260. 132 indexed citations
15.
Bockhaven, Jonas Van, David De Vleesschauwer, & Monica Höfte. (2012). Towards establishing broad-spectrum disease resistance in plants: silicon leads the way. Journal of Experimental Botany. 64(5). 1281–1293. 269 indexed citations
16.
González, Juan F., Giuliano Degrassi, Giulia Devescovi, et al.. (2012). A proteomic study of Xanthomonas oryzae pv. oryzae in rice xylem sap. Journal of Proteomics. 75(18). 5911–5919. 36 indexed citations
17.
Kyndt, Tina, Kamrun Nahar, Annelies Haegeman, et al.. (2011). Comparing systemic defence‐related gene expression changes upon migratory and sedentary nematode attack in rice. Plant Biology. 14(s1). 73–82. 74 indexed citations
18.
Izquierdo, Yovanny, et al.. (2011). Analysis of expressed sequence tags derived from a compatible Mycosphaerella fijiensis–banana interaction. Plant Cell Reports. 30(5). 913–928. 33 indexed citations
19.
Vleesschauwer, David De, Mohammad Djavaheri, Peter A. H. M. Bakker, & Monica Höfte. (2008). Pseudomonas fluorescens WCS374r-Induced Systemic Resistance in Rice against Magnaporthe oryzae Is Based on Pseudobactin-Mediated Priming for a Salicylic Acid-Repressible Multifaceted Defense Response. PLANT PHYSIOLOGY. 148(4). 1996–2012. 183 indexed citations
20.
Vleesschauwer, David De & Monica Höfte. (2005). Bacterial Determinants involved in Induced Systemic Resistance in Rice. Ghent University Academic Bibliography (Ghent University). 1 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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