Fernando Martínez‐Checa

1.8k total citations
42 papers, 1.3k citations indexed

About

Fernando Martínez‐Checa is a scholar working on Molecular Biology, Ecology and Pollution. According to data from OpenAlex, Fernando Martínez‐Checa has authored 42 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 26 papers in Ecology and 8 papers in Pollution. Recurrent topics in Fernando Martínez‐Checa's work include Microbial Community Ecology and Physiology (25 papers), Genomics and Phylogenetic Studies (23 papers) and Enzyme Production and Characterization (7 papers). Fernando Martínez‐Checa is often cited by papers focused on Microbial Community Ecology and Physiology (25 papers), Genomics and Phylogenetic Studies (23 papers) and Enzyme Production and Characterization (7 papers). Fernando Martínez‐Checa collaborates with scholars based in Spain, Netherlands and Austria. Fernando Martínez‐Checa's co-authors include Emilia Quesada, Victoria Béjar, Inmaculada Llamas, Carmen María González-Domenech, M. José Martínez-Cánovas, Ana del Moral, Concepción Calvo, Inmaculada Sampedro, David J. Castro and Soledad Arias and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Science of The Total Environment and Bioresource Technology.

In The Last Decade

Fernando Martínez‐Checa

42 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fernando Martínez‐Checa Spain 21 709 577 322 227 219 42 1.3k
Gejiao Wang China 23 816 1.2× 536 0.9× 436 1.4× 193 0.9× 171 0.8× 89 1.6k
Srinivasan Krishnamurthi India 21 668 0.9× 480 0.8× 253 0.8× 135 0.6× 133 0.6× 67 1.2k
Luciana Albuquerque Portugal 21 820 1.2× 731 1.3× 135 0.4× 149 0.7× 143 0.7× 55 1.3k
Inmaculada Llamas Spain 28 1.3k 1.8× 720 1.2× 669 2.1× 253 1.1× 445 2.0× 67 2.3k
Carsten Strömpl Germany 17 846 1.2× 436 0.8× 171 0.5× 162 0.7× 146 0.7× 24 1.3k
Leonid N. Ten South Korea 26 1.4k 1.9× 647 1.1× 581 1.8× 154 0.7× 161 0.7× 140 1.8k
Shih-Yao Lin Taiwan 23 891 1.3× 662 1.1× 402 1.2× 118 0.5× 114 0.5× 102 1.3k
Nimaichand Salam China 22 1.2k 1.6× 767 1.3× 527 1.6× 97 0.4× 260 1.2× 106 1.9k
Hyun Mi Jin South Korea 19 757 1.1× 582 1.0× 112 0.3× 299 1.3× 116 0.5× 53 1.2k
Govind Kumar India 22 499 0.7× 354 0.6× 469 1.5× 305 1.3× 137 0.6× 39 1.4k

Countries citing papers authored by Fernando Martínez‐Checa

Since Specialization
Citations

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

Fields of papers citing papers by Fernando Martínez‐Checa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fernando Martínez‐Checa. 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 Fernando Martínez‐Checa. The network helps show where Fernando Martínez‐Checa may publish in the future.

Co-authorship network of co-authors of Fernando Martínez‐Checa

This figure shows the co-authorship network connecting the top 25 collaborators of Fernando Martínez‐Checa. A scholar is included among the top collaborators of Fernando Martínez‐Checa 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 Fernando Martínez‐Checa. Fernando Martínez‐Checa 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.
Martínez‐Checa, Fernando, et al.. (2025). Pseudomonas halotolerans sp. nov., a halotolerant biocontrol agent with plant-growth properties. Frontiers in Plant Science. 16. 1605131–1605131. 1 indexed citations
2.
Roca, Amalia, et al.. (2024). Potential of the quorum‐quenching and plant‐growth promoting halotolerant Bacillus toyonensis AA1EC1 as biocontrol agent. Microbial Biotechnology. 17(3). e14420–e14420. 17 indexed citations
3.
Moral, Ana del, et al.. (2023). Microbial composition of Saharan dust plumes deposited as red rain in Granada (Southern Spain). The Science of The Total Environment. 913. 169745–169745. 5 indexed citations
4.
Ramos, Ventura Castillo, et al.. (2022). ZIF-8 and Its Magnetic Functionalization as Vehicle for the Transport and Release of Ciprofloxacin. Pharmaceutics. 14(11). 2546–2546. 22 indexed citations
5.
Rodríguez, Miguel, et al.. (2022). Peribacillus castrilensis sp. nov.: A Plant-Growth-Promoting and Biocontrol Species Isolated From a River Otter in Castril, Granada, Southern Spain. Frontiers in Plant Science. 13. 896728–896728. 12 indexed citations
6.
7.
Toral, Laura, Miguel Rodríguez, Fernando Martínez‐Checa, et al.. (2021). Identification of Volatile Organic Compounds in Extremophilic Bacteria and Their Effective Use in Biocontrol of Postharvest Fungal Phytopathogens. Frontiers in Microbiology. 12. 773092–773092. 41 indexed citations
8.
Martínez‐Checa, Fernando, et al.. (2021). Cambios en los perfiles laborales en la República Dominicana como resultado de la pandemia. SHILAP Revista de lepidopterología. 46(2). 31–45. 2 indexed citations
9.
Castro, David J., et al.. (2020). Biological Control of Verticillium Wilt on Olive Trees by the Salt-Tolerant Strain Bacillus velezensis XT1. Microorganisms. 8(7). 1080–1080. 29 indexed citations
10.
Castro, David J., et al.. (2018). Study of Bacterial Community Composition and Correlation of Environmental Variables in Rambla Salada, a Hypersaline Environment in South-Eastern Spain. Frontiers in Microbiology. 9. 1377–1377. 19 indexed citations
11.
12.
González-Domenech, Carmen María, Fernando Martínez‐Checa, Victoria Béjar, & Emilia Quesada. (2010). Denitrification as an important taxonomic marker within the genus Halomonas. Systematic and Applied Microbiology. 33(2). 85–93. 48 indexed citations
13.
González-Domenech, Carmen María, Fernando Martínez‐Checa, Emilia Quesada, & Victoria Béjar. (2008). Halomonas cerina sp. nov., a moderately halophilic, denitrifying, exopolysaccharide-producing bacterium. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 58(4). 803–809. 103 indexed citations
14.
Sorlózano, Antonio, et al.. (2006). Activity of tigecycline against clinical isolates of Staphylococcus aureus and extended-spectrum β-lactamase-producing Escherichia coli in Granada, Spain. International Journal of Antimicrobial Agents. 28(6). 532–536. 17 indexed citations
15.
Llamas, Inmaculada, et al.. (2006). Halomonas maura is a physiologically versatile bacterium of both ecological and biotechnological interest. Antonie van Leeuwenhoek. 89(3-4). 395–403. 54 indexed citations
16.
Argandoña, Montserrat, et al.. (2006). A membrane-bound nitrate reductase encoded by the narGHJI operon is responsible for anaerobic respiration in Halomonas maura. Extremophiles. 10(5). 411–419. 15 indexed citations
17.
Martínez‐Checa, Fernando, et al.. (2006). Characteristics of bioemulsifier V2-7 synthesized in culture media added of hydrocarbons: Chemical composition, emulsifying activity and rheological properties. Bioresource Technology. 98(16). 3130–3135. 56 indexed citations
18.
Martínez‐Checa, Fernando, Emilia Quesada, M. José Martínez-Cánovas, Inmaculada Llamas, & Victoria Béjar. (2005). Palleronia marisminoris gen. nov., sp. nov., a moderately halophilic, exopolysaccharide-producing bacterium belonging to the ‘Alphaproteobacteria’, isolated from a saline soil. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 55(6). 2525–2530. 35 indexed citations
19.
Llamas, Inmaculada, et al.. (2005). epsABCJ genes are involved in the biosynthesis of the exopolysaccharide mauran produced by Halomonas maura. Microbiology. 151(9). 2841–2851. 18 indexed citations
20.
Martínez-Cánovas, M. José, Emilia Quesada, Fernando Martínez‐Checa, Ana del Moral, & Victoria Béjar. (2004). Salipiger mucescens gen. nov., sp. nov., a moderately halophilic, exopolysaccharide-producing bacterium isolated from hypersaline soil, belonging to the α-Proteobacteria. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 54(5). 1735–1740. 60 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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