Michaela Serpi

1.2k total citations
43 papers, 872 citations indexed

About

Michaela Serpi is a scholar working on Molecular Biology, Infectious Diseases and Organic Chemistry. According to data from OpenAlex, Michaela Serpi has authored 43 papers receiving a total of 872 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 20 papers in Infectious Diseases and 10 papers in Organic Chemistry. Recurrent topics in Michaela Serpi's work include Biochemical and Molecular Research (20 papers), HIV/AIDS drug development and treatment (19 papers) and Chronic Lymphocytic Leukemia Research (5 papers). Michaela Serpi is often cited by papers focused on Biochemical and Molecular Research (20 papers), HIV/AIDS drug development and treatment (19 papers) and Chronic Lymphocytic Leukemia Research (5 papers). Michaela Serpi collaborates with scholars based in United Kingdom, United States and Italy. Michaela Serpi's co-authors include Fabrizio Pertusati, Christopher McGuigan, Valentina Ferrari, Magdalena Ślusarczyk, Maura Marinozzi, Charles E. McKenna, B. A. Kashemirov, Karolina Madela, Larryn W. Peterson and Essam Ghazaly and has published in prestigious journals such as Chemical Reviews, Cancer Research and Nature Protocols.

In The Last Decade

Michaela Serpi

41 papers receiving 862 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michaela Serpi United Kingdom 17 444 380 329 157 46 43 872
Fabrizio Pertusati United Kingdom 15 348 0.8× 419 1.1× 250 0.8× 131 0.8× 32 0.7× 38 844
Shalini Bansal United States 14 440 1.0× 224 0.6× 654 2.0× 609 3.9× 47 1.0× 29 1.4k
Helena Mertlíková‐Kaiserová Czechia 18 361 0.8× 211 0.6× 120 0.4× 86 0.5× 114 2.5× 61 827
Kamal N. Tiwari United States 14 519 1.2× 396 1.0× 213 0.6× 114 0.7× 40 0.9× 32 800
Lenka Poštová Slavětínská Czechia 18 435 1.0× 418 1.1× 224 0.7× 144 0.9× 38 0.8× 71 891
Christophe Mathé France 16 578 1.3× 424 1.1× 507 1.5× 203 1.3× 33 0.7× 71 1.1k
Linda L. Wotring United States 22 632 1.4× 684 1.8× 233 0.7× 223 1.4× 131 2.8× 69 1.5k
Krystyna Lesiak United States 23 865 1.9× 304 0.8× 315 1.0× 179 1.1× 76 1.7× 67 1.3k
Tokumi Maruyama Japan 15 424 1.0× 356 0.9× 198 0.6× 126 0.8× 23 0.5× 79 713
Thomas I. Kalman United States 16 523 1.2× 278 0.7× 168 0.5× 94 0.6× 114 2.5× 67 797

Countries citing papers authored by Michaela Serpi

Since Specialization
Citations

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

Fields of papers citing papers by Michaela Serpi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michaela Serpi

This figure shows the co-authorship network connecting the top 25 collaborators of Michaela Serpi. A scholar is included among the top collaborators of Michaela Serpi 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 Michaela Serpi. Michaela Serpi 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.
Serpi, Michaela, et al.. (2024). Design, synthesis and biological evaluation of aryloxy thiophosphoramidate triesters of anticancer nucleoside analogues. Bioorganic & Medicinal Chemistry. 103. 117696–117696. 1 indexed citations
4.
Vittorio, Serena, et al.. (2023). Improved Antibacterial Activity of 1,3,4-Oxadiazole-Based Compounds That Restrict Staphylococcus aureus Growth Independent of LtaS Function. ACS Infectious Diseases. 9(11). 2141–2159. 5 indexed citations
5.
Serpi, Michaela, Fabrizio Pertusati, Serena Vittorio, et al.. (2023). Synthesis, molecular docking and antibacterial activity of an oxadiazole-based lipoteichoic acid inhibitor and its metabolites. Journal of Molecular Structure. 1278. 134977–134977. 7 indexed citations
6.
Serpi, Michaela, Valentina Ferrari, Christopher McGuigan, Essam Ghazaly, & Chris Pepper. (2022). Synthesis and Characterization of NUC-7738, an Aryloxy Phosphoramidate of 3′-Deoxyadenosine, as a Potential Anticancer Agent. Journal of Medicinal Chemistry. 65(23). 15789–15804. 13 indexed citations
7.
Ślusarczyk, Magdalena, Michaela Serpi, Essam Ghazaly, et al.. (2021). Single Diastereomers of the Clinical Anticancer ProTide Agents NUC-1031 and NUC-3373 Preferentially Target Cancer Stem CellsIn Vitro. Journal of Medicinal Chemistry. 64(12). 8179–8193. 17 indexed citations
8.
Serpi, Michaela, et al.. (2018). Expedient synthesis and biological evaluation of alkenyl acyclic nucleoside phosphonate prodrugs. Bioorganic & Medicinal Chemistry. 26(12). 3596–3609. 6 indexed citations
9.
McGuigan, Christopher, Michaela Serpi, Magdalena Ślusarczyk, et al.. (2016). Anti‐flavivirus Activity of Different Tritylated Pyrimidine and Purine Nucleoside Analogues. ChemistryOpen. 5(3). 227–235. 19 indexed citations
10.
Ferrari, Valentina, Michaela Serpi, Christopher McGuigan, & Fabrizio Pertusati. (2015). ChemoselectiveN-Deacetylation of Protected Nucleosides and Nucleotides Promoted by Schwartz's Reagent. Nucleosides Nucleotides & Nucleic Acids. 34(11). 799–814. 5 indexed citations
11.
McGuigan, Christopher, Marco Derudas, Sahar Kandil, et al.. (2014). ProTides of N-(3-(5-(2′-deoxyuridine))prop-2-ynyl)octanamide as potential anti-tubercular and anti-viral agents. Bioorganic & Medicinal Chemistry. 22(9). 2816–2824. 30 indexed citations
12.
Hamon, Nadège, Magdalena Ślusarczyk, Michaela Serpi, Jan Balzarini, & Christopher McGuigan. (2014). Synthesis and biological evaluation of phosphoramidate prodrugs of two analogues of 2-deoxy-d-ribose-1-phosphate directed to the discovery of two carbasugars as new potential anti-HIV leads. Bioorganic & Medicinal Chemistry. 23(4). 829–838. 9 indexed citations
13.
McGuigan, Christopher, Marco Derudas, Nadège Hamon, et al.. (2013). Design, synthesis and biological evaluation of phosphorodiamidate prodrugs of antiviral and anticancer nucleosides. European Journal of Medicinal Chemistry. 70. 326–340. 25 indexed citations
14.
Peterson, Larryn W., et al.. (2010). Serine Side Chain-Linked Peptidomimetic Conjugates of Cyclic HPMPC and HPMPA: Synthesis and Interaction with hPEPT1. Molecular Pharmaceutics. 7(6). 2349–2361. 23 indexed citations
15.
Hammond, Victoria J., Christopher P. Thomas, Keri A. Tallman, et al.. (2010). Quantitative assays for esterified oxylipins generated by immune cells. Nature Protocols. 5(12). 1919–1931. 47 indexed citations
16.
Sala‐Rabanal, Monica, Larryn W. Peterson, Michaela Serpi, et al.. (2009). Interactions Between the Human Oligopeptide Transporter, hPepT1 and Serine Side-chain-linked Cidofovir Prodrugs. Antiviral Research. 82(2). A53–A54. 1 indexed citations
17.
19.
Pellicciari, Roberto, Maura Marinozzi, Antonio Macchiarulo, et al.. (2007). Synthesis, Molecular Modeling Studies, and Preliminary Pharmacological Characterization of All Possible 2-(2‘-Sulfonocyclopropyl)glycine Stereoisomers as Conformationally ConstrainedL-Homocysteic Acid Analogs. Journal of Medicinal Chemistry. 50(19). 4630–4641. 16 indexed citations
20.
Amori, Laura, Michaela Serpi, Maura Marinozzi, et al.. (2005). Synthesis and preliminary biological evaluation of (2S,1′R,2′S)- and (2S,1′S,2′R)-2-(2′-phosphonocyclopropyl)glycines, two novel conformationally constrained l-AP4 analogues. Bioorganic & Medicinal Chemistry Letters. 16(1). 196–199. 17 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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