Eduardo A. Espeso

6.5k total citations · 1 hit paper
105 papers, 4.9k citations indexed

About

Eduardo A. Espeso is a scholar working on Molecular Biology, Plant Science and Pharmacology. According to data from OpenAlex, Eduardo A. Espeso has authored 105 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Molecular Biology, 52 papers in Plant Science and 36 papers in Pharmacology. Recurrent topics in Eduardo A. Espeso's work include Fungal and yeast genetics research (71 papers), Plant Pathogens and Fungal Diseases (22 papers) and Fungal Biology and Applications (21 papers). Eduardo A. Espeso is often cited by papers focused on Fungal and yeast genetics research (71 papers), Plant Pathogens and Fungal Diseases (22 papers) and Fungal Biology and Applications (21 papers). Eduardo A. Espeso collaborates with scholars based in Spain, United States and United Kingdom. Eduardo A. Espeso's co-authors include Miguel Á. Peñalva, Herbert N. Arst, Joan Tilburn, Oier Etxebeste, Unai Ugalde, Aitor Garzia, Lidia Araújo‐Bazán, Margarita Orejas, Sovan Sarkar and Ana M. Calvo and has published in prestigious journals such as Journal of Biological Chemistry, Genes & Development and The EMBO Journal.

In The Last Decade

Eduardo A. Espeso

103 papers receiving 4.8k citations

Hit Papers

The Aspergillus PacC zinc... 1995 2026 2005 2015 1995 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eduardo A. Espeso Spain 40 3.5k 2.5k 1.4k 1.4k 414 105 4.9k
Ana M. Calvo United States 39 2.8k 0.8× 3.2k 1.3× 1.2k 0.9× 2.0k 1.4× 311 0.8× 74 5.0k
Santiago Gutiérrez Spain 41 2.3k 0.7× 2.5k 1.0× 901 0.6× 1.5k 1.1× 138 0.3× 131 4.6k
John E. Hamer United States 35 4.4k 1.3× 4.3k 1.7× 2.3k 1.6× 1.4k 1.0× 214 0.5× 55 6.2k
Stephen J. Free United States 26 2.0k 0.6× 1.7k 0.7× 740 0.5× 548 0.4× 351 0.8× 71 3.4k
Özgür Bayram Germany 30 2.3k 0.7× 1.9k 0.8× 703 0.5× 1.3k 0.9× 262 0.6× 61 3.3k
Michael Bölker Germany 38 3.5k 1.0× 2.1k 0.9× 869 0.6× 816 0.6× 143 0.3× 76 4.5k
B. Gillian Turgeon United States 46 3.6k 1.0× 5.5k 2.2× 3.1k 2.2× 1.6k 1.2× 277 0.7× 112 7.6k
William E. Timberlake United States 50 5.6k 1.6× 3.6k 1.5× 1.7k 1.1× 2.5k 1.8× 492 1.2× 111 7.5k
Oliver Valerius Germany 34 2.5k 0.7× 1.6k 0.7× 777 0.5× 793 0.6× 189 0.5× 99 3.6k
Joan Tilburn United Kingdom 25 2.2k 0.6× 1.1k 0.5× 751 0.5× 730 0.5× 278 0.7× 32 3.1k

Countries citing papers authored by Eduardo A. Espeso

Since Specialization
Citations

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

Fields of papers citing papers by Eduardo A. Espeso

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eduardo A. Espeso. 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 Eduardo A. Espeso. The network helps show where Eduardo A. Espeso may publish in the future.

Co-authorship network of co-authors of Eduardo A. Espeso

This figure shows the co-authorship network connecting the top 25 collaborators of Eduardo A. Espeso. A scholar is included among the top collaborators of Eduardo A. Espeso 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 Eduardo A. Espeso. Eduardo A. Espeso 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.
Melgarejo, P., et al.. (2025). Differences in Behavior During Early Nectarine Infection Among Main Monilinia spp. Causing Brown Rot. Phytopathology. 115(3). 269–280.
3.
Espeso, Eduardo A., et al.. (2023). A role for Penicillium rubens strain 212 xylanolytic system in biocontrol of Fusarium wilt disease in tomato plants. European Journal of Plant Pathology. 167(4). 621–635. 4 indexed citations
4.
Espeso, Eduardo A., et al.. (2023). Monilinia fructicola Response to White Light. Journal of Fungi. 9(10). 988–988. 4 indexed citations
5.
Espeso, Eduardo A., et al.. (2021). Light-Photoreceptors and Proteins Related to Monilinia laxa Photoresponses. Journal of Fungi. 7(1). 32–32. 9 indexed citations
8.
Etxebeste, Oier, et al.. (2019). Rewiring of transcriptional networks as a major event leading to the diversity of asexual multicellularity in fungi. Critical Reviews in Microbiology. 45(5-6). 548–563. 28 indexed citations
9.
Arst, Herbert N., et al.. (2016). Proteolytic activation of both components of the cation stress–responsive Slt pathway in Aspergillus nidulans. Molecular Biology of the Cell. 27(16). 2598–2612. 12 indexed citations
10.
Sebastián-Pérez, Víctor, Daniel I. Pérez, Carmen Gil, et al.. (2016). New applications for known drugs: Human glycogen synthase kinase 3 inhibitors as modulators of Aspergillus fumigatus growth. European Journal of Medicinal Chemistry. 116. 281–289. 11 indexed citations
11.
Espeso, Eduardo A.. (2015). The CRaZy Calcium Cycle. Advances in experimental medicine and biology. 892. 169–186. 24 indexed citations
12.
Etxebeste, Oier, et al.. (2013). Cytoplasmic Dynamics of the General Nuclear Import Machinery in Apically Growing Syncytial Cells. PLoS ONE. 8(12). e85076–e85076. 8 indexed citations
13.
Herrero‐García, Erika, et al.. (2011). 8-Carbon oxylipins inhibit germination and growth, and stimulate aerial conidiation in Aspergillus nidulans. Fungal Biology. 115(4-5). 393–400. 79 indexed citations
14.
Kwon, Nak‐Jung, Aitor Garzia, Eduardo A. Espeso, Unai Ugalde, & Jae‐Hyuk Yu. (2010). FlbC is a putative nuclear C2H2 transcription factor regulating development in Aspergillus nidulans. Molecular Microbiology. 77(5). 1203–1219. 130 indexed citations
15.
Espeso, Eduardo A., et al.. (2006). Aspergillus nidulans VeA subcellular localization is dependent on the importin α carrier and on light. Molecular Microbiology. 63(1). 242–255. 150 indexed citations
16.
Bernreiter, Andreas, Ana Ramón, Javier Fernández-Martı́nez, et al.. (2006). Nuclear Export of the Transcription Factor NirA Is a Regulatory Checkpoint for Nitrate Induction in Aspergillus nidulans. Molecular and Cellular Biology. 27(3). 791–802. 62 indexed citations
17.
Dı́ez, Eliecer, Eduardo A. Espeso, Teresa Suárez, et al.. (2002). Activation of the Aspergillus PacC zinc finger transcription factor requires two proteolytic steps. The EMBO Journal. 21(6). 1350–1359. 111 indexed citations
18.
Espeso, Eduardo A., et al.. (2001). Ambient pH Signaling Regulates Nuclear Localization of the Aspergillus nidulans PacC Transcription Factor. Molecular and Cellular Biology. 21(5). 1688–1699. 54 indexed citations
19.
Espeso, Eduardo A., et al.. (1995). Carbon regulation of penicillin biosynthesis inAspergillus nidulans: A minor effect of mutations increBandcreC. FEMS Microbiology Letters. 126(1). 63–67. 17 indexed citations
20.
Espeso, Eduardo A.. (1995). Carbon regulation of penicillin biosynthesis in Aspergillus nidulans: A minor effect of mutations in creB and creC. FEMS Microbiology Letters. 126(1). 63–67. 18 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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