Martijn Rep

18.3k total citations · 2 hit papers
112 papers, 10.5k citations indexed

About

Martijn Rep is a scholar working on Plant Science, Cell Biology and Molecular Biology. According to data from OpenAlex, Martijn Rep has authored 112 papers receiving a total of 10.5k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Plant Science, 78 papers in Cell Biology and 34 papers in Molecular Biology. Recurrent topics in Martijn Rep's work include Plant Pathogens and Fungal Diseases (75 papers), Plant-Microbe Interactions and Immunity (68 papers) and Mycorrhizal Fungi and Plant Interactions (27 papers). Martijn Rep is often cited by papers focused on Plant Pathogens and Fungal Diseases (75 papers), Plant-Microbe Interactions and Immunity (68 papers) and Mycorrhizal Fungi and Plant Interactions (27 papers). Martijn Rep collaborates with scholars based in Netherlands, United States and Germany. Martijn Rep's co-authors include Corné M. J. Pieterse, L.C. van Loon, Petra M. Houterman, Ben J. C. Cornelissen, Caroline B. Michielse, Frank L. W. Takken, H. Charlotte van der Does, Johan M. Thevelein, Stefan Hohmann and Leslie A. Grivell and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Martijn Rep

109 papers receiving 10.3k citations

Hit Papers

Significance of Inducible Defense-related Proteins in Inf... 2006 2026 2012 2019 2006 2009 500 1000 1.5k 2.0k 2.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martijn Rep Netherlands 53 8.2k 4.9k 3.7k 416 390 112 10.5k
Seogchan Kang United States 49 7.3k 0.9× 4.9k 1.0× 3.6k 1.0× 851 2.0× 331 0.8× 135 8.9k
Martin B. Dickman United States 51 7.2k 0.9× 2.1k 0.4× 3.7k 1.0× 479 1.2× 382 1.0× 116 9.2k
Pietro D. Spanu United Kingdom 37 5.7k 0.7× 2.4k 0.5× 2.4k 0.6× 540 1.3× 228 0.6× 90 7.2k
P.J.G.M. de Wit Netherlands 65 11.6k 1.4× 3.7k 0.8× 3.9k 1.1× 483 1.2× 522 1.3× 206 12.9k
David B. Collinge Denmark 46 7.8k 0.9× 1.8k 0.4× 3.8k 1.0× 366 0.9× 444 1.1× 104 9.5k
Barbara Valent United States 60 11.6k 1.4× 5.2k 1.1× 6.7k 1.8× 1.1k 2.6× 380 1.0× 118 13.6k
Karl‐Heinz Kogel Germany 59 10.2k 1.2× 2.8k 0.6× 3.4k 0.9× 572 1.4× 820 2.1× 164 11.8k
Ralph Hückelhoven Germany 46 7.7k 0.9× 2.1k 0.4× 2.8k 0.7× 307 0.7× 229 0.6× 146 8.9k
Zhensheng Kang China 62 12.3k 1.5× 2.4k 0.5× 5.2k 1.4× 345 0.8× 391 1.0× 466 13.5k
J. J. Rudd United Kingdom 34 5.7k 0.7× 2.3k 0.5× 2.4k 0.6× 370 0.9× 213 0.5× 61 6.4k

Countries citing papers authored by Martijn Rep

Since Specialization
Citations

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

Fields of papers citing papers by Martijn Rep

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martijn Rep

This figure shows the co-authorship network connecting the top 25 collaborators of Martijn Rep. A scholar is included among the top collaborators of Martijn Rep 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 Martijn Rep. Martijn Rep 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
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Garrido, António, Bas Beerens, Ming Liang, et al.. (2025). The Tomato PR ‐5 Proteins PR ‐5x and NP24 Exert Antifungal Activity Against Fusarium oxysporum. Plant Pathology. 74(4). 1097–1113. 1 indexed citations
4.
Kramer, Gertjan, et al.. (2024). Tomato R-gene-mediated resistance against Fusarium wilt originates in roots and extends to shoots via xylem to limit pathogen colonization. Frontiers in Plant Science. 15. 1384431–1384431. 10 indexed citations
5.
Fokkens, Like, Corinne Audran, Yohann Petit, et al.. (2023). The neighbouring genes AvrLm10A and AvrLm10B are part of a large multigene family of cooperating effector genes conserved in Dothideomycetes and Sordariomycetes. Molecular Plant Pathology. 24(8). 914–931. 8 indexed citations
6.
Fokkens, Like & Martijn Rep. (2023). Population genomics reveals meiotic recombination in Fusarium oxysporum. Proceedings of the National Academy of Sciences. 120(30). e2309677120–e2309677120. 3 indexed citations
7.
Constantin, Maria E., Like Fokkens, Mara de Sain, Frank L. W. Takken, & Martijn Rep. (2021). Number of Candidate Effector Genes in Accessory Genomes Differentiates Pathogenic From Endophytic Fusarium oxysporum Strains. Frontiers in Plant Science. 12. 761740–761740. 24 indexed citations
8.
Constantin, Maria E., et al.. (2020). From laboratory to field: applying the Fo47 biocontrol strain in potato fields. European Journal of Plant Pathology. 158(3). 645–654. 5 indexed citations
9.
Kesten, Christopher, Francisco M. Gámez‐Arjona, Alexandra Menna, et al.. (2019). Pathogen‐induced pH changes regulate the growth‐defense balance in plants. The EMBO Journal. 38(24). e101822–e101822. 84 indexed citations
10.
Niño‐Sánchez, Jonatan, H. Charlotte van der Does, Peter van Dam, et al.. (2018). A SIX1 homolog in Fusarium oxysporum f.sp. cubense tropical race 4 contributes to virulence towards Cavendish banana. PLoS ONE. 13(10). e0205896–e0205896. 56 indexed citations
11.
Dam, Peter van & Martijn Rep. (2017). The Distribution of Miniature Impala Elements and SIX Genes in the Fusarium Genus is Suggestive of Horizontal Gene Transfer. Journal of Molecular Evolution. 85(1-2). 14–25. 36 indexed citations
12.
Gawehns, Fleur, Lisong Ma, Oskar Bruning, et al.. (2015). The effector repertoire of Fusarium oxysporum determines the tomato xylem proteome composition following infection. Frontiers in Plant Science. 6. 967–967. 58 indexed citations
13.
Beerens, Bas, et al.. (2015). Fluorescence Assisted Selection of Transformants (FAST): Using flow cytometry to select fungal transformants. Fungal Genetics and Biology. 76. 104–109. 9 indexed citations
14.
Schmidt, Sarah M., Petra M. Houterman, Ines Schreiver, et al.. (2013). MITEs in the promoters of effector genes allow prediction of novel virulence genes in Fusarium oxysporum. BMC Genomics. 14(1). 119–119. 164 indexed citations
15.
Lievens, Bart, Martijn Rep, & Bart P. H. J. Thomma. (2008). Recent developments in the molecular discrimination of formae speciales of Fusarium oxysporum. Pest Management Science. 64(8). 781–788. 145 indexed citations
16.
Rep, Martijn, H. Charlotte van der Does, Michiel Meijer, et al.. (2004). A small, cysteine‐rich protein secreted by Fusarium oxysporum during colonization of xylem vessels is required for I‐3‐mediated resistance in tomato. Molecular Microbiology. 53(5). 1373–1383. 304 indexed citations
17.
Rep, Martijn, Lukas Dekker, Jack H. Vossen, et al.. (2002). Mass Spectrometric Identification of Isoforms of PR Proteins in Xylem Sap of Fungus-Infected Tomato. PLANT PHYSIOLOGY. 130(2). 904–917. 174 indexed citations
18.
Koerkamp, Marian J.A. Groot, Martijn Rep, Harmen J. Bussemaker, et al.. (2002). Dissection of Transient Oxidative Stress Response inSaccharomyces cerevisiaeby Using DNA Microarrays. Molecular Biology of the Cell. 13(8). 2783–2794. 99 indexed citations
19.
Tamás, Markus J., Martijn Rep, Johan M. Thevelein, & Stefan Hohmann. (2000). Stimulation of the yeast high osmolarity glycerol (HOG) pathway: evidence for a signal generated by a change in turgor rather than by water stress. FEBS Letters. 472(1). 159–165. 83 indexed citations
20.
Guélin, Emmanuel, Martijn Rep, & Leslie A. Grivell. (1994). Yeast sequencing reports. Sequence of the AFG3 gene encoding a new member of the FtsH/Yme1/Tma subfamily of the AAA‐protein family. Yeast. 10(10). 1389–1394. 56 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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