Santiago Gutiérrez

6.8k total citations
131 papers, 4.6k citations indexed

About

Santiago Gutiérrez is a scholar working on Plant Science, Molecular Biology and Pharmacology. According to data from OpenAlex, Santiago Gutiérrez has authored 131 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Plant Science, 68 papers in Molecular Biology and 48 papers in Pharmacology. Recurrent topics in Santiago Gutiérrez's work include Plant-Microbe Interactions and Immunity (48 papers), Microbial Natural Products and Biosynthesis (36 papers) and Fungal and yeast genetics research (31 papers). Santiago Gutiérrez is often cited by papers focused on Plant-Microbe Interactions and Immunity (48 papers), Microbial Natural Products and Biosynthesis (36 papers) and Fungal and yeast genetics research (31 papers). Santiago Gutiérrez collaborates with scholars based in Spain, United States and Brazil. Santiago Gutiérrez's co-authors include Juan F. Martı́n, Rosa E. Cardoza, Enrique Monte, Rosa Hermosa, Francisco Fierro, Javier Casqueiro, Begoña Díez, Francisco J. Fernández, Susan P. McCormick and Mónica G. Malmierca and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Santiago Gutiérrez

127 papers receiving 4.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Santiago Gutiérrez Spain 41 2.5k 2.3k 1.5k 901 522 131 4.6k
Eduardo A. Espeso Spain 40 2.5k 1.0× 3.5k 1.5× 1.4k 0.9× 1.4k 1.6× 352 0.7× 105 4.9k
Andy M. Bailey United Kingdom 40 1.7k 0.7× 2.1k 0.9× 2.0k 1.3× 625 0.7× 554 1.1× 138 4.5k
Jeffrey W. Cary United States 44 4.3k 1.7× 2.9k 1.2× 1.3k 0.9× 1.5k 1.6× 529 1.0× 136 5.7k
You‐Liang Peng China 41 4.8k 1.9× 2.8k 1.2× 758 0.5× 1.5k 1.7× 259 0.5× 177 6.3k
Ana M. Calvo United States 39 3.2k 1.3× 2.8k 1.2× 2.0k 1.3× 1.2k 1.4× 391 0.7× 74 5.0k
Jin Woo Bok United States 34 2.9k 1.2× 3.7k 1.6× 3.5k 2.3× 1.3k 1.4× 603 1.2× 56 6.5k
Liangcheng Du United States 39 1.4k 0.6× 2.6k 1.1× 2.2k 1.5× 527 0.6× 842 1.6× 110 4.5k
Gary A. Payne United States 45 5.9k 2.4× 2.6k 1.1× 1.2k 0.8× 2.2k 2.4× 476 0.9× 116 7.3k
John E. Linz United States 42 3.6k 1.4× 2.5k 1.1× 1.2k 0.8× 1.1k 1.2× 423 0.8× 110 5.3k
Thorsten Heinekamp Germany 40 1.6k 0.6× 2.3k 1.0× 1.4k 0.9× 566 0.6× 273 0.5× 83 4.5k

Countries citing papers authored by Santiago Gutiérrez

Since Specialization
Citations

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

Fields of papers citing papers by Santiago Gutiérrez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Santiago Gutiérrez

This figure shows the co-authorship network connecting the top 25 collaborators of Santiago Gutiérrez. A scholar is included among the top collaborators of Santiago Gutiérrez 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 Santiago Gutiérrez. Santiago Gutiérrez 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.
Rodríguez‐González, Álvaro, et al.. (2025). Biosolutions from Native Trichoderma Strains Against Grapevine Trunk Diseases. Agronomy. 15(8). 1901–1901. 1 indexed citations
2.
McCormick, Susan P., Rosa E. Cardoza, Karl E. Vermillion, et al.. (2024). The identification of a key gene highlights macrocyclic ring’s role in trichothecene toxicity. Applied Microbiology and Biotechnology. 108(1). 475–475. 1 indexed citations
3.
Cardoza, Rosa E., et al.. (2024). Biocontrol Potential of a Native Trichoderma Collection Against Fusarium oxysporum f. sp. cubense Subtropical Race 4. Agriculture. 14(11). 2016–2016. 2 indexed citations
4.
Mayo‐Prieto, Sara, et al.. (2023). Native Trichoderma Isolates from Soil and Rootstock to Fusarium spp. Control and Growth Promotion of Humulus lupulus L. Plantlets. Agriculture. 13(3). 720–720. 7 indexed citations
5.
6.
Cardoza, Rosa E., Susan P. McCormick, Sara Mayo‐Prieto, et al.. (2022). Effect of Farnesol in Trichoderma Physiology and in Fungal–Plant Interaction. Journal of Fungi. 8(12). 1266–1266. 5 indexed citations
7.
Mayo‐Prieto, Sara, et al.. (2022). Organic and Conventional Bean Pesticides in Development of Autochthonous Trichoderma Strains. Journal of Fungi. 8(6). 603–603. 7 indexed citations
8.
9.
Mayo‐Prieto, Sara, et al.. (2021). Influence of Fungicide Application and Vine Age on Trichoderma Diversity as Source of Biological Control Agents. Agronomy. 11(3). 446–446. 8 indexed citations
10.
Mayo‐Prieto, Sara, et al.. (2021). Volatile Organic Compound Chamber: A Novel Technology for Microbiological Volatile Interaction Assays. Journal of Fungi. 7(4). 248–248. 17 indexed citations
11.
Mayo‐Prieto, Sara, Álvaro Rodríguez‐González, Alicia Lorenzana de la Varga, Santiago Gutiérrez, & Pedro A. Casquero. (2020). Influence of Substrates in the Development of Bean and in Pathogenicity of Rhizoctonia solani JG Kühn. Agronomy. 10(5). 707–707. 8 indexed citations
12.
Mayo‐Prieto, Sara, et al.. (2020). Evaluation of substrates and additives to Trichoderma harzianum development by qPCR. Agronomy Journal. 112(4). 3188–3194. 4 indexed citations
13.
Mayo‐Prieto, Sara, Roberta Marra, Francesco Vinale, et al.. (2019). Effect of Trichoderma velutinum and Rhizoctonia solani on the Metabolome of Bean Plants (Phaseolus vulgaris L.). International Journal of Molecular Sciences. 20(3). 549–549. 33 indexed citations
14.
Rodríguez‐González, Álvaro, et al.. (2018). Investigations of Trichoderma spp. and Beauveria bassiana as biological control agent for Xylotrechus arvicola, a major insect pest in Spanish vineyards. Journal of Economic Entomology. 111(6). 2585–2591. 26 indexed citations
15.
Rodríguez‐González, Álvaro, Pedro A. Casquero, Sara Mayo‐Prieto, et al.. (2018). Effect of trichodiene production by Trichoderma harzianum on Acanthoscelides obtectus. Journal of Stored Products Research. 77. 231–239. 30 indexed citations
16.
McCormick, Susan P., Rosa E. Cardoza, Daren W. Brown, et al.. (2018). Effect of deletion of a trichothecene toxin regulatory gene on the secondary metabolism transcriptome of the saprotrophic fungus Trichoderma arundinaceum. Fungal Genetics and Biology. 119. 29–46. 26 indexed citations
17.
Moraga, Javier, et al.. (2018). Relevance of the deletion of the Tatri4 gene in the secondary metabolome of Trichoderma arundinaceum. Organic & Biomolecular Chemistry. 16(16). 2955–2965. 15 indexed citations
18.
19.
Hermosa, Rosa, Rosa E. Cardoza, Javier Moraga, et al.. (2011). Overexpression of the Trichoderma brevicompactum tri5 Gene: Effect on the Expression of the Trichodermin Biosynthetic Genes and on Tomato Seedlings. Toxins. 3(9). 1220–1232. 31 indexed citations
20.
Liu, Gang, et al.. (2001). Elicitation of Penicillin Biosynthesis by Alginate in Penicillium chrysogenum, Exerted on pcbAB, pcbC, and penDE Genes at the Transcriptional Level. Journal of Microbiology and Biotechnology. 11(5). 812–818. 14 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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