Bruno E. Correia

10.6k total citations · 8 hit papers
91 papers, 4.7k citations indexed

About

Bruno E. Correia is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Oncology. According to data from OpenAlex, Bruno E. Correia has authored 91 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 19 papers in Radiology, Nuclear Medicine and Imaging and 15 papers in Oncology. Recurrent topics in Bruno E. Correia's work include Protein Structure and Dynamics (23 papers), Monoclonal and Polyclonal Antibodies Research (19 papers) and RNA and protein synthesis mechanisms (15 papers). Bruno E. Correia is often cited by papers focused on Protein Structure and Dynamics (23 papers), Monoclonal and Polyclonal Antibodies Research (19 papers) and RNA and protein synthesis mechanisms (15 papers). Bruno E. Correia collaborates with scholars based in Switzerland, United States and Portugal. Bruno E. Correia's co-authors include Benjamin F. Cravatt, Stefano Forli, Keriann M. Backus, Michael M. Bronstein, Pablo Gaínza, Freyr Sverrisson, Kenneth M. Lum, Emanuele Rodolà, Federico Monti and Davide Boscaini and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Bruno E. Correia

85 papers receiving 4.6k citations

Hit Papers

Proteome-wide covalent ligand discovery in native biologi... 2016 2026 2019 2022 2016 2019 2022 2024 2024 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bruno E. Correia Switzerland 33 3.4k 886 697 569 497 91 4.7k
Dmitri Beglov United States 30 5.1k 1.5× 460 0.5× 877 1.3× 557 1.0× 1.2k 2.4× 51 6.9k
Nir London Israel 31 3.0k 0.9× 534 0.6× 480 0.7× 602 1.1× 666 1.3× 65 3.8k
Adrian Whitty United States 40 4.2k 1.2× 1.4k 1.6× 882 1.3× 1.1k 1.9× 1.0k 2.1× 78 6.9k
Enrico O. Purisima Canada 36 3.3k 1.0× 376 0.4× 341 0.5× 597 1.0× 541 1.1× 113 4.7k
Masoud Vedadi Canada 49 7.9k 2.4× 558 0.6× 277 0.4× 968 1.7× 375 0.8× 141 9.7k
Kam Y. J. Zhang Japan 40 4.9k 1.4× 878 1.0× 231 0.3× 684 1.2× 905 1.8× 152 6.3k
Ji-Hu Zhang United States 13 4.0k 1.2× 401 0.5× 306 0.4× 663 1.2× 521 1.0× 19 6.3k
Romelia Salomón–Ferrer United States 11 3.7k 1.1× 495 0.6× 242 0.3× 311 0.5× 690 1.4× 17 5.3k
Milton T. Stubbs Germany 41 3.4k 1.0× 598 0.7× 216 0.3× 607 1.1× 424 0.9× 117 5.6k
Orly Dym Israel 36 4.1k 1.2× 407 0.5× 437 0.6× 293 0.5× 297 0.6× 76 5.4k

Countries citing papers authored by Bruno E. Correia

Since Specialization
Citations

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

Fields of papers citing papers by Bruno E. Correia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruno E. Correia

This figure shows the co-authorship network connecting the top 25 collaborators of Bruno E. Correia. A scholar is included among the top collaborators of Bruno E. Correia 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 Bruno E. Correia. Bruno E. Correia 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
2.
Igashov, Ilia, H. Stärk, Clément Vignac, et al.. (2024). Equivariant 3D-conditional diffusion model for molecular linker design. Nature Machine Intelligence. 6(4). 417–427. 70 indexed citations breakdown →
3.
Heid, Daniel, Michael Jendrusch, Sabine Aschenbrenner, et al.. (2024). A deep mutational scanning platform to characterize the fitness landscape of anti-CRISPR proteins. Nucleic Acids Research. 52(22). e103–e103.
4.
Pačesa, Martin, Casper A. Goverde, Prasun Kumar, et al.. (2024). An atlas of protein homo-oligomerization across domains of life. Cell. 187(4). 999–1010.e15. 56 indexed citations
5.
Vorobieva, Anastassia A., Ryo Tachibana, Roman P. Jakob, et al.. (2024). An evolved artificial radical cyclase enables the construction of bicyclic terpenoid scaffolds via an H-atom transfer pathway. Nature Chemistry. 16(10). 1656–1664. 12 indexed citations
6.
Aschenbrenner, Sabine, et al.. (2024). A modular toolbox for the optogenetic deactivation of transcription. Nucleic Acids Research. 53(3). 3 indexed citations
7.
Schneuing, Arne, Charles B. Harris, Yuanqi Du, et al.. (2024). Structure-based drug design with equivariant diffusion models. Nature Computational Science. 4(12). 899–909. 52 indexed citations breakdown →
8.
Sverrisson, Freyr, Mehmet Akdel, Jean Feydy, et al.. (2023). DiffMaSIF: Surface-based Protein-Protein Docking with Diffusion Models. SPIRE - Sciences Po Institutional REpository.
9.
Bonati, Lucia, Sailan Shui, Leo Scheller, et al.. (2023). Rational Design of Chemically Controlled Antibodies and Protein Therapeutics. ACS Chemical Biology. 18(6). 1259–1265. 11 indexed citations
10.
Shui, Sailan, Leo Scheller, & Bruno E. Correia. (2023). Protein-based bandpass filters for controlling cellular signaling with chemical inputs. Nature Chemical Biology. 20(5). 586–593. 8 indexed citations
11.
Scheck, Andreas, Stéphane Rosset, Michaël Defferrard, et al.. (2022). RosettaSurf—A surface-centric computational design approach. PLoS Computational Biology. 18(3). e1009178–e1009178. 4 indexed citations
12.
Yang, Che, Fabian Sesterhenn, Jaume Bonet, et al.. (2021). Bottom-up de novo design of functional proteins with complex structural features. Nature Chemical Biology. 17(4). 492–500. 62 indexed citations
13.
Gaínza, Pablo, Elise Gray-Gaillard, Elisabetta Cribioli, et al.. (2020). Author Correction: A computationally designed chimeric antigen receptor provides a small-molecule safety switch for T-cell therapy. Nature Biotechnology. 38(4). 503–503. 5 indexed citations
14.
Gaínza, Pablo, Elise Gray-Gaillard, Elisabetta Cribioli, et al.. (2020). A computationally designed chimeric antigen receptor provides a small-molecule safety switch for T-cell therapy. Nature Biotechnology. 38(4). 426–432. 103 indexed citations
15.
Harteveld, Zander, Carolin Schmelas, Julius Upmeier zu Belzen, et al.. (2020). Computational design of anti-CRISPR proteins with improved inhibition potency. Nature Chemical Biology. 16(7). 725–730. 15 indexed citations
16.
Hoffmann, Mareike D., Julius Upmeier zu Belzen, Zander Harteveld, et al.. (2020). Optogenetic control of Neisseria meningitidis Cas9 genome editing using an engineered, light-switchable anti-CRISPR protein. Nucleic Acids Research. 49(5). e29–e29. 33 indexed citations
17.
Bubeck, Felix, Mareike D. Hoffmann, Zander Harteveld, et al.. (2018). Engineered anti-CRISPR proteins for optogenetic control of CRISPR–Cas9. Nature Methods. 15(11). 924–927. 158 indexed citations
18.
Miranda, Marta Pires de, Chantal Beauchemin, Min Tan, et al.. (2017). Cross-species conservation of episome maintenance provides a basis for in vivo investigation of Kaposi's sarcoma herpesvirus LANA. PLoS Pathogens. 13(9). e1006555–e1006555. 13 indexed citations
19.
Correia, Bruno E., John Bates, Rebecca J. Loomis, et al.. (2015). Proof of principle for epitope-focused vaccine design. Protein Science. 24. 181–184. 6 indexed citations
20.
Niphakis, Micah J., Kenneth M. Lum, Armand B. Cognetta, et al.. (2015). A Global Map of Lipid-Binding Proteins and Their Ligandability in Cells. Cell. 161(7). 1668–1680. 178 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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