Martha E. Trujillo

8.3k total citations · 2 hit papers
108 papers, 5.7k citations indexed

About

Martha E. Trujillo is a scholar working on Molecular Biology, Plant Science and Ecology. According to data from OpenAlex, Martha E. Trujillo has authored 108 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Molecular Biology, 44 papers in Plant Science and 32 papers in Ecology. Recurrent topics in Martha E. Trujillo's work include Genomics and Phylogenetic Studies (65 papers), Microbial Community Ecology and Physiology (31 papers) and Legume Nitrogen Fixing Symbiosis (23 papers). Martha E. Trujillo is often cited by papers focused on Genomics and Phylogenetic Studies (65 papers), Microbial Community Ecology and Physiology (31 papers) and Legume Nitrogen Fixing Symbiosis (23 papers). Martha E. Trujillo collaborates with scholars based in Spain, United Kingdom and Germany. Martha E. Trujillo's co-authors include Aharon Oren, Milton S. da Costa, Jongsik Chun, Eustoquio Martı́nez-Molina, António Ventosa, Sofie E. De Meyer, Alejandro P. Rooney, Hana Yi, David R. Arahal and Henrik Christensen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and The Science of The Total Environment.

In The Last Decade

Martha E. Trujillo

108 papers receiving 5.6k citations

Hit Papers

Proposed minimal standards for the use of genome data for... 2018 2026 2020 2023 2018 2024 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martha E. Trujillo Spain 36 3.6k 2.1k 2.1k 812 612 108 5.7k
Yong‐Joon Cho South Korea 23 4.4k 1.2× 1.3k 0.6× 2.6k 1.2× 727 0.9× 489 0.8× 99 6.3k
Kihyun Lee South Korea 9 4.0k 1.1× 1.2k 0.6× 2.4k 1.2× 659 0.8× 428 0.7× 21 5.2k
Soon-Wo Kwon South Korea 36 3.0k 0.8× 1.8k 0.8× 1.8k 0.9× 325 0.4× 573 0.9× 253 4.7k
Rüdiger Pukall Germany 35 3.2k 0.9× 792 0.4× 2.0k 1.0× 670 0.8× 275 0.4× 74 4.7k
Seok-Hwan Yoon South Korea 11 3.5k 1.0× 941 0.4× 2.1k 1.0× 394 0.5× 306 0.5× 17 4.4k
USHA PREMACHANDRAN United States 10 4.2k 1.1× 947 0.4× 2.6k 1.2× 545 0.7× 416 0.7× 10 4.8k
David R. Arahal Spain 30 4.0k 1.1× 880 0.4× 2.8k 1.3× 302 0.4× 312 0.5× 116 5.3k
Kyung Sook Bae South Korea 37 2.5k 0.7× 942 0.4× 1.5k 0.7× 494 0.6× 323 0.5× 131 3.9k
M. Mesbah Egypt 7 4.0k 1.1× 947 0.4× 2.5k 1.2× 457 0.6× 407 0.7× 12 4.5k
Jung‐Sook Lee South Korea 33 2.6k 0.7× 940 0.4× 1.5k 0.7× 301 0.4× 267 0.4× 259 4.1k

Countries citing papers authored by Martha E. Trujillo

Since Specialization
Citations

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

Fields of papers citing papers by Martha E. Trujillo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martha E. Trujillo. 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 Martha E. Trujillo. The network helps show where Martha E. Trujillo may publish in the future.

Co-authorship network of co-authors of Martha E. Trujillo

This figure shows the co-authorship network connecting the top 25 collaborators of Martha E. Trujillo. A scholar is included among the top collaborators of Martha E. Trujillo 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 Martha E. Trujillo. Martha E. Trujillo 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.
Patrick, Sheila, Laura Filkins, Markus Göker, et al.. (2025). ‘What’s in a name? Fit-for-purpose bacterial nomenclature’: meeting report. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 75(7). 3 indexed citations
2.
Ortúzar, Maite, et al.. (2024). Unraveling the dynamic interplay of microbial communities associated to Lupinus angustifolius in response to environmental and cultivation conditions. The Science of The Total Environment. 946. 174277–174277. 6 indexed citations
3.
Heo, Young Mok, Seunghyun Kang, Seyoung Mun, et al.. (2023). Dermatobacter hominis gen. nov., sp. nov., a new member of the family Iamiaceae, revealed the potential utilisation of skin-derived metabolites. Antonie van Leeuwenhoek. 116(11). 1139–1150. 2 indexed citations
4.
Riesco, Raúl, Maite Ortúzar, J M Fernández-Abalos, & Martha E. Trujillo. (2022). Deciphering Genomes: Genetic Signatures of Plant-Associated Micromonospora. Frontiers in Plant Science. 13. 872356–872356. 6 indexed citations
5.
Ortúzar, Maite, Martha E. Trujillo, Brenda Román‐Ponce, & Lorena Carro. (2020). Micromonospora metallophores: A plant growth promotion trait useful for bacterial-assisted phytoremediation?. The Science of The Total Environment. 739. 139850–139850. 26 indexed citations
6.
Abdulla, Hesham, et al.. (2019). An integrated bioaugmentation/electrocoagulation concept for olive mill wastewater management and the reuse in irrigation of biofuel plants: a pilot study. Environmental Science and Pollution Research. 26(16). 15803–15815. 9 indexed citations
7.
Carro, Lorena, Imen Nouioui, Vartul Sangal, et al.. (2018). Genome-based classification of micromonosporae with a focus on their biotechnological and ecological potential. Scientific Reports. 8(1). 525–525. 83 indexed citations
8.
Castro, Jean Franco, Imen Nouioui, Vartul Sangal, et al.. (2018). Geodermatophilus chilensis sp. nov., from soil of the Yungay core-region of the Atacama Desert, Chile. Systematic and Applied Microbiology. 41(5). 427–436. 22 indexed citations
9.
Carro, Lorena, Raúl Riesco, Cathrin Spröer, & Martha E. Trujillo. (2016). Micromonospora luteifusca sp. nov. isolated from cultivated Pisum sativum. Systematic and Applied Microbiology. 39(4). 237–242. 18 indexed citations
10.
Trujillo, Martha E., Rodrigo Bacigalupe, Petar Pujić, et al.. (2014). Genome Features of the Endophytic Actinobacterium Micromonospora lupini Strain Lupac 08: On the Process of Adaptation to an Endophytic Life Style?. PLoS ONE. 9(9). e108522–e108522. 57 indexed citations
11.
Martínez‐Hidalgo, Pilar, Purificación Galindo‐Villardón, Martha E. Trujillo, José M. Igual, & Eustoquio Martı́nez-Molina. (2014). Micromonospora from nitrogen fixing nodules of alfalfa (Medicago sativa L.). A new promising Plant Probiotic Bacteria.. Scientific Reports. 4(1). 6389–6389. 54 indexed citations
12.
Sánchez‐Juanes, Fernando, Laura Ferreira, Ángel Valverde, et al.. (2013). MALDI-TOF mass spectrometry as a tool for differentiation of Bradyrhizobium species: Application to the identification of Lupinus nodulating strains. Systematic and Applied Microbiology. 36(8). 565–571. 15 indexed citations
13.
Carro, Lorena, Cathrin Spröer, Pilar Alonso, & Martha E. Trujillo. (2012). Diversity of Micromonospora strains isolated from nitrogen fixing nodules and rhizosphere of Pisum sativum analyzed by multilocus sequence analysis. Systematic and Applied Microbiology. 35(2). 73–80. 57 indexed citations
14.
Sutcliffe, Iain C., Martha E. Trujillo, & Michael Goodfellow. (2011). A call to arms for systematists: revitalising the purpose and practises underpinning the description of novel microbial taxa. Antonie van Leeuwenhoek. 101(1). 13–20. 57 indexed citations
15.
Trujillo, Martha E., et al.. (2010). The genus Micromonospora is widespread in legume root nodules: the example of Lupinus angustifolius. The ISME Journal. 4(10). 1265–1281. 121 indexed citations
16.
Velázquez, Encarna, José Luis Rodríguez-Arias Palomo, Raúl Rivas, et al.. (2010). Analysis of core genes supports the reclassification of strains Agrobacterium radiobacter K84 and Agrobacterium tumefaciens AKE10 into the species Rhizobium rhizogenes. Systematic and Applied Microbiology. 33(5). 247–251. 43 indexed citations
17.
Carro, Lorena, et al.. (2010). Auraticoccus monumenti gen. nov., sp. nov., an actinomycete isolated from a deteriorated sandstone monument. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 61(5). 1098–1103. 8 indexed citations
18.
Quintana, Erika T., Martha E. Trujillo, & Michael Goodfellow. (2003). Actinomadura mexicana sp. nov. and Actinomadura meyerii sp. nov., Two Novel Soil Sporoactinomycetes. Systematic and Applied Microbiology. 26(4). 511–517. 15 indexed citations
19.
Trujillo, Martha E. & Michael Goodfellow. (2003). Numerical phenetic classification of clinically significant aerobic sporoactinomycetes and related organisms. Antonie van Leeuwenhoek. 84(1). 39–68. 33 indexed citations
20.
Chun, Jongsik, Mohamed E. Hamid, Martha E. Trujillo, et al.. (1993). Rapid identification of streptomycetes by artificial neural network analysis of pyrolysis mass spectra. FEMS Microbiology Letters. 114(1). 115–119. 15 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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