Mário Soberón

14.5k total citations · 3 hit papers
205 papers, 9.6k citations indexed

About

Mário Soberón is a scholar working on Molecular Biology, Insect Science and Plant Science. According to data from OpenAlex, Mário Soberón has authored 205 papers receiving a total of 9.6k indexed citations (citations by other indexed papers that have themselves been cited), including 180 papers in Molecular Biology, 149 papers in Insect Science and 86 papers in Plant Science. Recurrent topics in Mário Soberón's work include Insect Resistance and Genetics (169 papers), Insect and Pesticide Research (115 papers) and Entomopathogenic Microorganisms in Pest Control (82 papers). Mário Soberón is often cited by papers focused on Insect Resistance and Genetics (169 papers), Insect and Pesticide Research (115 papers) and Entomopathogenic Microorganisms in Pest Control (82 papers). Mário Soberón collaborates with scholars based in Mexico, China and United States. Mário Soberón's co-authors include Alejandra Bravo, Sarjeet S. Gill, Isabel Gómez, Liliana Pardo‐López, Supaporn Likitvivatanavong, Jorge Sánchez, Carlos Muñóz-Garay, Juan Miranda‐Ríos, Luisa Elena Fernández and Helena Porta and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Mário Soberón

201 papers receiving 9.3k citations

Hit Papers

Mode of action of Bacillus thuringiensis Cry and Cyt toxi... 2006 2026 2012 2019 2006 2011 2012 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
Mário Soberón Mexico 50 8.7k 6.8k 3.9k 373 277 205 9.6k
Alejandra Bravo Mexico 56 10.1k 1.2× 8.4k 1.2× 4.5k 1.1× 415 1.1× 223 0.8× 235 11.0k
Jeroen Van Rie Belgium 35 6.9k 0.8× 5.5k 0.8× 3.6k 0.9× 71 0.2× 216 0.8× 55 7.5k
Raymond J. St. Leger United States 64 6.1k 0.7× 8.8k 1.3× 4.8k 1.2× 169 0.5× 1.5k 5.5× 143 11.3k
Michael J. Adang United States 50 5.7k 0.7× 4.3k 0.6× 2.8k 0.7× 173 0.5× 167 0.6× 101 6.1k
Magdy M. Mahfouz Saudi Arabia 50 6.3k 0.7× 961 0.1× 4.2k 1.1× 243 0.7× 544 2.0× 105 7.6k
Walter R. Terra Brazil 49 4.7k 0.5× 4.9k 0.7× 2.0k 0.5× 436 1.2× 1.1k 3.9× 208 7.9k
Ruud A. de Maagd Netherlands 39 4.0k 0.5× 1.9k 0.3× 3.3k 0.8× 50 0.1× 181 0.7× 98 5.4k
Dwayne D. Hegedus Canada 40 2.7k 0.3× 1.4k 0.2× 2.9k 0.7× 114 0.3× 308 1.1× 136 5.1k
Karl Gordon Australia 38 2.7k 0.3× 1.9k 0.3× 2.0k 0.5× 113 0.3× 469 1.7× 97 4.3k
Henryk Czosnek Israel 48 1.9k 0.2× 3.8k 0.6× 6.1k 1.6× 179 0.5× 338 1.2× 142 7.7k

Countries citing papers authored by Mário Soberón

Since Specialization
Citations

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

Fields of papers citing papers by Mário Soberón

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mário Soberón

This figure shows the co-authorship network connecting the top 25 collaborators of Mário Soberón. A scholar is included among the top collaborators of Mário Soberón 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 Mário Soberón. Mário Soberón 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.
Xu, Jikai, Xudong Li, Pengfei Zhu, et al.. (2025). Evolutionary selection of trimethoprim-resistant dfrA genes in lytic phages affects phage and host fitness during infection. Science Advances. 11(39). eadt4817–eadt4817. 1 indexed citations
2.
Soberón, Mário & Alejandra Bravo. (2025). The Future of Bt Proteins: From Pore Formation and Insect Resistance to the Next Generation of Pest Control. Toxins. 17(11). 522–522.
3.
Lu, Xiao-Ming, Li Chen, Ziwei Zhao, et al.. (2025). Two novel trimethoprim resistance genes, dfra50 and dfra51 , identified in phage-plasmids. Antimicrobial Agents and Chemotherapy. 69(7). e0169524–e0169524.
4.
Huang, Guoqiang, Zhonglin Liu, Feng Chen, et al.. (2024). Silencing Ditylenchus destructor cathepsin L-like cysteine protease has negative pleiotropic effect on nematode ontogenesis. Scientific Reports. 14(1). 10030–10030. 3 indexed citations
5.
Pacheco, Sabino, et al.. (2023). Structural changes upon membrane insertion of the insecticidal pore-forming toxins produced by Bacillus thuringiensis. Frontiers in Insect Science. 3. 1188891–1188891. 15 indexed citations
6.
Pacheco, Sabino, Isabel Gómez, Mário Soberón, & Alejandra Bravo. (2022). A major conformational change of N‐terminal helices of Bacillus thuringiensis Cry1Ab insecticidal protein is necessary for membrane insertion and toxicity. FEBS Journal. 290(10). 2692–2705. 9 indexed citations
7.
Guo, Zhaojiang, Shi Kang, Qingjun Wu, et al.. (2021). The regulation landscape of MAPK signaling cascade for thwarting Bacillus thuringiensis infection in an insect host. PLoS Pathogens. 17(9). e1009917–e1009917. 55 indexed citations
8.
Zhang, Fengjuan, et al.. (2020). Systemic mitochondrial disruption is a key event in the toxicity of bacterial pore‐forming toxins to Caenorhabditis elegans . Environmental Microbiology. 23(9). 4896–4907. 6 indexed citations
9.
Quan, Yudong, et al.. (2018). Characterization of the Cry1Ah resistance in Asian corn Borer and its cross-resistance to other Bacillus thuringiensis toxins. Scientific Reports. 8(1). 234–234. 30 indexed citations
10.
Grande, Ricardo, Jorge Sánchez, Bruce E. Tabashnik, et al.. (2018). The C-terminal protoxin region of Bacillus thuringiensis Cry1Ab toxin has a functional role in binding to GPI-anchored receptors in the insect midgut. Journal of Biological Chemistry. 293(52). 20263–20272. 30 indexed citations
11.
Soberón, Mário, et al.. (2017). Cell lines as models for the study of Cry toxins from Bacillus thuringiensis. Insect Biochemistry and Molecular Biology. 93. 66–78. 13 indexed citations
12.
Wang, Zeyu, Yuxiao Liu, Gemei Liang, et al.. (2016). Identification of ABCC2 as a binding protein of Cry1Ac on brush border membrane vesicles fromHelicoverpa armigeraby an improved pull‐down assay. MicrobiologyOpen. 5(4). 659–669. 31 indexed citations
13.
Muñóz-Garay, Carlos, Liliana Pardo‐López, Nuria Jiménez-Juárez, et al.. (2009). Characterization of the mechanism of action of the genetically modified Cry1AbMod toxin that is active against Cry1Ab-resistant insects. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1788(10). 2229–2237. 40 indexed citations
14.
Ibarra, Jorge E., Enrique Galindo, José Antonio Ortega Carrillo, et al.. (2006). Los microorganismos en el control biológico de insectos y fitopatógenos. 48(2). 113–120. 5 indexed citations
15.
Pardo‐López, Liliana, Isabel Gómez, Carlos Muñóz-Garay, et al.. (2006). Structural and functional analysis of the pre-pore and membrane-inserted pore of Cry1Ab toxin. Journal of Invertebrate Pathology. 92(3). 172–177. 20 indexed citations
16.
Miranda‐Ríos, Juan, et al.. (2001). A conserved RNA structure ( thi box) is involved in regulation of thiamin biosynthetic gene expression in bacteria. Proceedings of the National Academy of Sciences. 98(17). 9736–9741. 185 indexed citations
17.
Romero, David, et al.. (2000). Expression pattern of Rhizobium etli ccmIEFH genes involved in c-type cytochrome maturation. Gene. 250(1-2). 149–157. 4 indexed citations
18.
Girard, Lourdes, et al.. (2000). Differential Regulation of fixN-Reiterated Genes in Rhizobium etli by a Novel fixL—fixK Cascade. Molecular Plant-Microbe Interactions. 13(12). 1283–1292. 59 indexed citations
19.
Yurgel, Svetlana N., et al.. (1998). Isolation ofSinorhizobium melilotiTn5mutants with altered cytochrome terminal oxidase expression and improved symbiotic performance. FEMS Microbiology Letters. 165(1). 167–173. 17 indexed citations
20.
Soberón, Mário & Alicia González. (1987). Physiological Role of Glutaminase Activity in Saccharomyces cerevisiae. Microbiology. 133(1). 1–8. 33 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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