Alga Zuccaro

8.5k total citations · 1 hit paper
58 papers, 4.5k citations indexed

About

Alga Zuccaro is a scholar working on Plant Science, Cell Biology and Molecular Biology. According to data from OpenAlex, Alga Zuccaro has authored 58 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Plant Science, 21 papers in Cell Biology and 8 papers in Molecular Biology. Recurrent topics in Alga Zuccaro's work include Plant-Microbe Interactions and Immunity (38 papers), Mycorrhizal Fungi and Plant Interactions (22 papers) and Plant Pathogens and Fungal Diseases (21 papers). Alga Zuccaro is often cited by papers focused on Plant-Microbe Interactions and Immunity (38 papers), Mycorrhizal Fungi and Plant Interactions (22 papers) and Plant Pathogens and Fungal Diseases (21 papers). Alga Zuccaro collaborates with scholars based in Germany, United Kingdom and France. Alga Zuccaro's co-authors include Gregor Langen, Karl‐Heinz Kogel, Urs Lahrmann, Daniel Lanver, Stefanie Reißmann, Gabriel Schweizer, Shigeyuki TANAKA, Liang Liang, Libera Lo Presti and Marie Tollot and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and The Plant Cell.

In The Last Decade

Alga Zuccaro

54 papers receiving 4.4k citations

Hit Papers

Fungal Effectors and Plant Susceptibility 2015 2026 2018 2022 2015 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alga Zuccaro Germany 35 3.7k 1.4k 970 560 466 58 4.5k
Pablo R. Hardoim Netherlands 13 3.2k 0.9× 1.0k 0.7× 988 1.0× 391 0.7× 328 0.7× 15 3.9k
Suha Jabaji Canada 33 2.8k 0.8× 749 0.5× 780 0.8× 362 0.6× 321 0.7× 105 3.6k
Paul Bayman Puerto Rico 32 2.6k 0.7× 1.7k 1.2× 784 0.8× 1.4k 2.5× 557 1.2× 80 3.9k
Joan M. Henson United States 22 2.3k 0.6× 1.4k 1.0× 749 0.8× 678 1.2× 421 0.9× 41 3.2k
T. S. Suryanarayanan India 32 1.6k 0.4× 1.7k 1.3× 475 0.5× 764 1.4× 966 2.1× 86 2.8k
Zamir K. Punja Canada 39 4.8k 1.3× 1.8k 1.4× 2.0k 2.0× 357 0.6× 275 0.6× 213 5.7k
Laila P. Partida‐Martínez Mexico 26 2.1k 0.6× 784 0.6× 842 0.9× 361 0.6× 688 1.5× 41 3.2k
KD Hyde Thailand 36 3.4k 0.9× 3.7k 2.7× 1.1k 1.1× 1.1k 1.9× 912 2.0× 139 4.5k
Itthayakorn Promputtha Thailand 25 2.4k 0.6× 2.2k 1.6× 706 0.7× 629 1.1× 565 1.2× 97 2.9k
Gonzalo Platas Spain 33 1.5k 0.4× 1.5k 1.1× 875 0.9× 603 1.1× 1.0k 2.2× 83 3.1k

Countries citing papers authored by Alga Zuccaro

Since Specialization
Citations

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

Fields of papers citing papers by Alga Zuccaro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alga Zuccaro

This figure shows the co-authorship network connecting the top 25 collaborators of Alga Zuccaro. A scholar is included among the top collaborators of Alga Zuccaro 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 Alga Zuccaro. Alga Zuccaro 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
3.
Llamas, Ernesto, et al.. (2024). Root cap cell corpse clearance limits microbial colonization in Arabidopsis thaliana. eLife. 13. 1 indexed citations
4.
Miyauchi, Shingo, Stefan Cord‐Landwehr, Daniel G. Peterson, et al.. (2024). Transcriptomics reveal a mechanism of niche defense: two beneficial root endophytes deploy an antimicrobial GH18CBM5 chitinase to protect their hosts. New Phytologist. 244(3). 980–996. 6 indexed citations
5.
Pistorio, Valéria, María Asunción Campanero‐Rhodes, Rocco Di Girolamo, et al.. (2024). Structure and properties of the exopolysaccharide isolated from Flavobacterium sp. Root935. Carbohydrate Polymers. 343. 122433–122433. 7 indexed citations
6.
Llamas, Ernesto, et al.. (2024). Root cap cell corpse clearance limits microbial colonization in Arabidopsis thaliana. eLife. 13. 3 indexed citations
7.
Porzel, Andrea, Hidayat Hussain, Ulschan Bathe, et al.. (2024). Hordedane diterpenoid phytoalexins restrict Fusarium graminearum infection but enhance Bipolaris sorokiniana colonization of barley roots. Molecular Plant. 17(8). 1307–1327. 5 indexed citations
8.
Wanke, Alan, Stephan Wawra, Balakumaran Chandrasekar, et al.. (2023). A GH81-type β-glucan-binding protein enhances colonization by mutualistic fungi in barley. Current Biology. 33(23). 5071–5084.e7. 14 indexed citations
9.
Llamas, Ernesto, Hyun Ju Lee, M. Victoria Barja, et al.. (2021). The intrinsic chaperone network of Arabidopsis stem cells confers protection against proteotoxic stress. Aging Cell. 20(8). e13446–e13446. 11 indexed citations
10.
Miyauchi, Shingo, Rubén Garrido‐Oter, Gregor Langen, et al.. (2021). The fungal root endophyte Serendipita vermifera displays inter-kingdom synergistic beneficial effects with the microbiota in Arabidopsis thaliana and barley. The ISME Journal. 16(3). 876–889. 41 indexed citations
11.
Harris, Jeanne M., Kathryn M. Jones, Dong Wang, & Alga Zuccaro. (2021). Focus on How Plants Engage With Beneficial Microorganisms While at the Same Time Restricting Pathogens. Molecular Plant-Microbe Interactions. 34(5). 461–461.
12.
Sánchez‐Vallet, Andrea, Hui Tian, Luis Rodríguez‐Moreno, et al.. (2020). A secreted LysM effector protects fungal hyphae through chitin-dependent homodimer polymerization. PLoS Pathogens. 16(6). e1008652–e1008652. 53 indexed citations
13.
Hilbert, Magdalena, Shadab Nizam, Hanna Rövenich, et al.. (2020). A secreted fungal histidine‐ and alanine‐rich protein regulates metal ion homeostasis and oxidative stress. New Phytologist. 227(4). 1174–1188. 37 indexed citations
14.
Nizam, Shadab, Xiaoyu Qiang, Stephan Wawra, et al.. (2019). Serendipita indica E5′ NT modulates extracellular nucleotide levels in the plant apoplast and affects fungal colonization. EMBO Reports. 20(2). 62 indexed citations
15.
Zuccaro, Alga, et al.. (2016). Dissecting endophytic lifestyle along the parasitism/mutualism continuum in Arabidopsis. Current Opinion in Microbiology. 32. 103–112. 88 indexed citations
16.
Rövenich, Hanna, Alga Zuccaro, & Bart P. H. J. Thomma. (2016). Convergent evolution of filamentous microbes towards evasion of glycan‐triggered immunity. New Phytologist. 212(4). 896–901. 50 indexed citations
17.
Zuccaro, Alga, et al.. (2015). β-glucan: Crucial component of the fungal cell wall and elusive MAMP in plants. Fungal Genetics and Biology. 90. 53–60. 232 indexed citations
18.
Lahrmann, Urs & Alga Zuccaro. (2012). Opprimo ergo sum—Evasion and Suppression in the Root Endophytic Fungus Piriformospora indica. Molecular Plant-Microbe Interactions. 25(6). 727–737. 56 indexed citations
19.
Roth, Andreas, Alga Zuccaro, Susanne Kneip, & Petra Dersch. (2007). Characterization of a new inducible promoter for protein expression in Aspergillus niger, using a green fluorescent protein reporter system. Journal of Biotechnology. 131(2). S256–S257. 1 indexed citations
20.
Bach, Stéphane, Marc Blondel, Anne Cueff, et al.. (2004). Cytotoxicity of diatom-derived oxylipins in organisms belonging to different phyla. Journal of Experimental Biology. 207(17). 2935–2946. 80 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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