José Berenguer

4.8k total citations · 1 hit paper
148 papers, 3.6k citations indexed

About

José Berenguer is a scholar working on Molecular Biology, Ecology and Genetics. According to data from OpenAlex, José Berenguer has authored 148 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 109 papers in Molecular Biology, 35 papers in Ecology and 30 papers in Genetics. Recurrent topics in José Berenguer's work include Bacterial Genetics and Biotechnology (30 papers), Enzyme Structure and Function (25 papers) and Enzyme Catalysis and Immobilization (24 papers). José Berenguer is often cited by papers focused on Bacterial Genetics and Biotechnology (30 papers), Enzyme Structure and Function (25 papers) and Enzyme Catalysis and Immobilization (24 papers). José Berenguer collaborates with scholars based in Spain, Chile and United States. José Berenguer's co-authors include Felipe Cava, Miguel A. de Pedro, Aurélio Hidalgo, Luis Ángel Fernández, José M. Guisán, Javier Rocha‐Martín, Juan M. Bolívar, Íñigo Lasa, Alba Blesa and Roberto Fernández‐Lafuente and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

José Berenguer

144 papers receiving 3.5k citations

Hit Papers

DNA-guided DNA interference by a prokaryotic Argonaute 2014 2026 2018 2022 2014 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
José Berenguer Spain 32 2.7k 826 693 441 406 148 3.6k
Mitsuru Haruki Japan 31 1.7k 0.6× 439 0.5× 517 0.7× 515 1.2× 218 0.5× 82 2.7k
Abdul Matin United States 37 2.5k 0.9× 615 0.7× 1.3k 1.9× 502 1.1× 294 0.7× 118 4.6k
Tsukasa Ikeda Japan 34 2.3k 0.9× 462 0.6× 535 0.8× 388 0.9× 308 0.8× 126 4.0k
Sumió Shinoda Japan 42 2.2k 0.8× 578 0.7× 636 0.9× 386 0.9× 344 0.8× 296 6.5k
Haichun Gao China 37 2.1k 0.8× 953 1.2× 547 0.8× 337 0.8× 161 0.4× 134 4.1k
Alexa Price‐Whelan United States 28 2.6k 1.0× 640 0.8× 813 1.2× 163 0.4× 138 0.3× 39 3.7k
Richard J. Lewis United Kingdom 40 3.0k 1.1× 823 1.0× 1.5k 2.2× 523 1.2× 500 1.2× 86 4.5k
G. Dennis Sprott Canada 43 3.3k 1.2× 872 1.1× 343 0.5× 453 1.0× 159 0.4× 126 5.3k
Joan L. Slonczewski United States 34 2.7k 1.0× 675 0.8× 1.7k 2.5× 442 1.0× 477 1.2× 56 5.1k
Paul Blum United States 35 2.3k 0.9× 548 0.7× 765 1.1× 652 1.5× 477 1.2× 98 3.6k

Countries citing papers authored by José Berenguer

Since Specialization
Citations

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

Fields of papers citing papers by José Berenguer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of José Berenguer

This figure shows the co-authorship network connecting the top 25 collaborators of José Berenguer. A scholar is included among the top collaborators of José Berenguer 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 José Berenguer. José Berenguer 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.
Yee, Brian A., et al.. (2020). TheThermus thermophilusDEAD-box protein Hera is a general RNA binding protein and plays a key role in tRNA metabolism. RNA. 26(11). 1557–1574. 4 indexed citations
2.
Rocha‐Martín, Javier, Pedro A. Sánchez‐Murcia, Fernando López‐Gallego, et al.. (2019). Functional Characterization and Structural Analysis of NADH Oxidase Mutants from Thermus thermophilus HB27: Role of Residues 166, 174, and 194 in the Catalytic Properties and Thermostability. Microorganisms. 7(11). 515–515. 4 indexed citations
3.
Hidalgo, Aurélio, et al.. (2019). A Modular Vector Toolkit with a Tailored Set of Thermosensors To Regulate Gene Expression in Thermus thermophilus. ACS Omega. 4(11). 14626–14632. 10 indexed citations
4.
Mencı́a, Mario, et al.. (2019). ICETh1 and ICETh2, two interdependent mobile genetic elements in Thermus thermophilus transjugation. Environmental Microbiology. 22(1). 158–169. 6 indexed citations
5.
Taboga, Oscar, et al.. (2018). A single mutation in cyclodextrin glycosyltransferase from Paenibacillus barengoltzii changes cyclodextrin and maltooligosaccharides production. Protein Engineering Design and Selection. 31(10). 399–407. 6 indexed citations
6.
Berenguer, José, et al.. (2017). Effects of diesel oil and environmental quality on the enzymatic activities of a tropical estuarine catfish and implications for contamination assessment. Ecotoxicology and Environmental contamination. 12(1). 103–111. 5 indexed citations
8.
Berenguer, José, et al.. (2015). Tubos de hueso de ave como implementos chamánicos en el Desierto de Atacama, Siglos XI-XV. Boletín del Museo Chileno de Arte Precolombino. 20(1). 51–72. 7 indexed citations
9.
Swarts, Daan C., Matthijs M. Jore, Edze R. Westra, et al.. (2014). DNA-guided DNA interference by a prokaryotic Argonaute. Nature. 507(7491). 258–261. 359 indexed citations breakdown →
10.
Schmidt, Marlen, et al.. (2012). Promiscuous enantioselective (−)-γ-lactamase activity in the Pseudomonas fluorescens esterase I. Organic & Biomolecular Chemistry. 10(17). 3388–3388. 24 indexed citations
11.
Rocha‐Martín, Javier, Juan M. Bolívar, Aurélio Hidalgo, et al.. (2011). Characterization and further stabilization of a new anti-prelog specific alcohol dehydrogenase from Thermus thermophilus HB27 for asymmetric reduction of carbonyl compounds. Bioresource Technology. 103(1). 343–350. 41 indexed citations
12.
Cava, Felipe, et al.. (2007). Control of the respiratory metabolism of Thermus thermophilus by the nitrate respiration conjugative element NCE. Molecular Microbiology. 64(3). 630–646. 30 indexed citations
13.
Martín‐Benito, Jaime, Juan J. Gómez‐Reino, Peter C. Stirling, et al.. (2007). Divergent Substrate-Binding Mechanisms Reveal an Evolutionary Specialization of Eukaryotic Prefoldin Compared to Its Archaeal Counterpart. Structure. 15(1). 101–110. 49 indexed citations
14.
Cava, Felipe, et al.. (2007). An activity-independent selection system of thermostable protein variants. Nature Methods. 4(11). 919–921. 27 indexed citations
15.
Laptenko, Oleg, Jookyung Lee, Marina Starodubtseva, et al.. (2006). pH‐dependent conformational switch activates the inhibitor of transcription elongation. The EMBO Journal. 25(10). 2131–2141. 53 indexed citations
16.
Nielsen, Axel E., et al.. (2006). El Qhapaqñan entre Atacama y Lípez. Intersecciones en antropología. 217–234. 9 indexed citations
17.
Ramírez‐Arcos, Sandra, Luis Ángel Fernández, & José Berenguer. (1998). A thermophilic nitrate reductase is responsible for the strain specific anaerobic growth of Thermus thermophilus HB8. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1396(2). 215–227. 69 indexed citations
18.
Fernández, Luis Ángel, Garbiñe Olabarrı́a, & José Berenguer. (1997). Surface proteins and a novel transcription factor regulate the expression of the S‐layer gene in Thermus thermophilus HB8. Molecular Microbiology. 24(1). 61–72. 28 indexed citations
19.
González, J., et al.. (1995). Measurement of inhibition zones in antibiotic residue analysis. Archiv für Lebensmittelhygiene. 46(6). 141–143. 1 indexed citations
20.
Plaimauer, Barbara, Beatrix Pfanzagl, José Berenguer, Miguel A. de Pedro, & Wolfgang Löffelhardt. (1991). Subcellular distribution of enzymes involved in the biosynthesis of cyanelle murein in the protist Cyanophora paradoxa. FEBS Letters. 284(2). 169–172. 11 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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