Rita C. Guedes

3.1k total citations
114 papers, 2.5k citations indexed

About

Rita C. Guedes is a scholar working on Molecular Biology, Organic Chemistry and Oncology. According to data from OpenAlex, Rita C. Guedes has authored 114 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 41 papers in Organic Chemistry and 18 papers in Oncology. Recurrent topics in Rita C. Guedes's work include Computational Drug Discovery Methods (15 papers), Free Radicals and Antioxidants (12 papers) and Protease and Inhibitor Mechanisms (8 papers). Rita C. Guedes is often cited by papers focused on Computational Drug Discovery Methods (15 papers), Free Radicals and Antioxidants (12 papers) and Protease and Inhibitor Mechanisms (8 papers). Rita C. Guedes collaborates with scholars based in Portugal, United States and United Kingdom. Rita C. Guedes's co-authors include Rui Moreira, Benedito J. Costa Cabral, José A. Martinho Simões, Leif A. Eriksson, M. Matilde Marques, Daniel J. V. A. dos Santos, P. Cabral do Couto, Lídia Gonçalves, Philip J. Rosenthal and Jiří Gut and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Chemical Physics and The Journal of Physical Chemistry B.

In The Last Decade

Rita C. Guedes

113 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rita C. Guedes Portugal 32 974 816 279 261 248 114 2.5k
Gregory J. Tawa United States 28 697 0.7× 958 1.2× 150 0.5× 388 1.5× 47 0.2× 62 2.4k
Richard A. Bryce United Kingdom 29 678 0.7× 1.2k 1.4× 119 0.4× 264 1.0× 62 0.3× 143 2.4k
Julian E. Fuchs Austria 32 687 0.7× 1.4k 1.7× 274 1.0× 74 0.3× 100 0.4× 92 2.5k
Peng Zou United States 32 560 0.6× 997 1.2× 221 0.8× 374 1.4× 60 0.2× 94 3.5k
Yixiang Cao United States 14 687 0.7× 1.5k 1.9× 233 0.8× 453 1.7× 57 0.2× 23 3.1k
Charles H. Reynolds United States 33 1.0k 1.1× 1.9k 2.3× 355 1.3× 263 1.0× 191 0.8× 88 4.2k
A. M. Mulichak United States 29 766 0.8× 1.3k 1.6× 182 0.7× 133 0.5× 175 0.7× 107 2.8k
Ralf Thoma Switzerland 23 329 0.3× 1.3k 1.6× 297 1.1× 59 0.2× 174 0.7× 33 2.3k
Miguel Machuqueiro Portugal 29 630 0.6× 1.8k 2.2× 332 1.2× 309 1.2× 152 0.6× 100 2.9k
Zhijian Xu China 31 772 0.8× 1.6k 2.0× 287 1.0× 132 0.5× 195 0.8× 209 3.5k

Countries citing papers authored by Rita C. Guedes

Since Specialization
Citations

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

Fields of papers citing papers by Rita C. Guedes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rita C. Guedes. 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 Rita C. Guedes. The network helps show where Rita C. Guedes may publish in the future.

Co-authorship network of co-authors of Rita C. Guedes

This figure shows the co-authorship network connecting the top 25 collaborators of Rita C. Guedes. A scholar is included among the top collaborators of Rita C. Guedes 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 Rita C. Guedes. Rita C. Guedes 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.
Florindo, Helena F., et al.. (2025). Structural insights and clinical advances in small-molecule inhibitors targeting TGF-β receptor I. PubMed. 33(1). 200945–200945. 4 indexed citations
2.
3.
Guedes, Rita C., et al.. (2024). Inferring molecular inhibition potency with AlphaFold predicted structures. Scientific Reports. 14(1). 8252–8252. 3 indexed citations
4.
Carvalho, Andreia Neves, Ana S. Ressurreição, Adriana O. Santos, et al.. (2023). New Scaffolds of Proteasome Inhibitors: Boosting Anticancer Potential by Exploiting the Synergy of In Silico and In Vitro Methodologies. Pharmaceuticals. 16(8). 1096–1096. 3 indexed citations
5.
Pais, Teresa F., Nádia Duarte, Rita Neres, et al.. (2022). Brain endothelial STING1 activation by Plasmodium -sequestered heme promotes cerebral malaria via type I IFN response. Proceedings of the National Academy of Sciences. 119(36). e2206327119–e2206327119. 22 indexed citations
6.
Aniceto, Natália, Vanda Marques, Joana D. Amaral, et al.. (2022). Harnessing Protein-Ligand Interaction Fingerprints to Predict New Scaffolds of RIPK1 Inhibitors. Molecules. 27(15). 4718–4718. 2 indexed citations
7.
Marques, Vanda, Marta B. Afonso, Dean G. Brown, et al.. (2020). Phenotypic high-throughput screening platform identifies novel chemotypes for necroptosis inhibition. Cell Death Discovery. 6(1). 6–6. 16 indexed citations
8.
Aniceto, Natália, et al.. (2019). Chemical Patterns of Proteasome Inhibitors: Lessons Learned from Two Decades of Drug Design. International Journal of Molecular Sciences. 20(21). 5326–5326. 12 indexed citations
9.
Guedes, Rita C., M. Fátima Cabral, Judite Costa, et al.. (2019). Pyridine-Containing Macrocycles Display MMP-2/9 Inhibitory Activity and Distinct Effects on Migration and Invasion of 2D and 3D Breast Cancer Models. International Journal of Molecular Sciences. 20(20). 5109–5109. 4 indexed citations
10.
Ribeiro, Nádia, Adelino M. Galvão, Clara S. B. Gomes, et al.. (2019). Naphthoylhydrazones: coordination to metal ions and biological screening. New Journal of Chemistry. 43(45). 17801–17818. 15 indexed citations
11.
12.
António, João P. M., Lídia Gonçalves, Rita C. Guedes, Rui Moreira, & Pedro M. P. Góis. (2018). Diazaborines as New Inhibitors of Human Neutrophil Elastase. ACS Omega. 3(7). 7418–7423. 44 indexed citations
13.
Martins, M. Rosário, Elisabete P. Carreiro, Óscar López, et al.. (2018). In silico, NMR and pharmacological evaluation of an hydroxyoxindole cholinesterase inhibitor. Bioorganic & Medicinal Chemistry. 27(2). 354–363. 13 indexed citations
14.
Gonçalves, Lídia, Rita C. Guedes, Stefan Hofbauer, et al.. (2016). Clickable 4‐Oxo‐β‐lactam‐Based Selective Probing for Human Neutrophil Elastase Related Proteomes. ChemMedChem. 11(18). 2037–2042. 25 indexed citations
15.
Rodrigues, Tiago, Ana S. Ressurreição, Filipa P. da Cruz, et al.. (2013). Flavones as isosteres of 4(1H)-quinolones: Discovery of ligand efficient and dual stage antimalarial lead compounds. European Journal of Medicinal Chemistry. 69. 872–880. 16 indexed citations
16.
Montalbano, Francesco, Pedro M. S. D. Cal, Lídia Gonçalves, et al.. (2013). Discovery of new heterocycles with activity against human neutrophile elastase based on a boron promoted one-pot assembly reaction. Organic & Biomolecular Chemistry. 11(27). 4465–4465. 32 indexed citations
17.
Mugumbate, Grace, Ana S. Newton, Philip J. Rosenthal, et al.. (2013). Novel anti-Plasmodial hits identified by virtual screening of the ZINC database. Journal of Computer-Aided Molecular Design. 27(10). 859–871. 18 indexed citations
18.
Lavrado, João, Ghislain G. Cabal, Miguel Prudêncio, et al.. (2011). Incorporation of Basic Side Chains into Cryptolepine Scaffold: Structure−Antimalarial Activity Relationships and Mechanistic Studies. Journal of Medicinal Chemistry. 54(3). 734–750. 59 indexed citations
19.
Guedes, Rita C., et al.. (2008). Azetidine-2,4-diones (4-Oxo-β-lactams) as Scaffolds for Designing Elastase Inhibitors. Journal of Medicinal Chemistry. 51(6). 1783–1790. 30 indexed citations
20.
Coutinho, Kaline, Rita C. Guedes, Benedito J. Costa Cabral, & Sylvio Canuto. (2003). Electronic polarization of liquid water: converged Monte Carlo-quantum mechanics results for the multipole moments. Chemical Physics Letters. 369(3-4). 345–353. 61 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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