Sara Sattin

1.6k total citations
36 papers, 1.2k citations indexed

About

Sara Sattin is a scholar working on Molecular Biology, Organic Chemistry and Immunology. According to data from OpenAlex, Sara Sattin has authored 36 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 14 papers in Organic Chemistry and 8 papers in Immunology. Recurrent topics in Sara Sattin's work include Glycosylation and Glycoproteins Research (13 papers), Carbohydrate Chemistry and Synthesis (9 papers) and Immunotherapy and Immune Responses (7 papers). Sara Sattin is often cited by papers focused on Glycosylation and Glycoproteins Research (13 papers), Carbohydrate Chemistry and Synthesis (9 papers) and Immunotherapy and Immune Responses (7 papers). Sara Sattin collaborates with scholars based in Italy, France and Spain. Sara Sattin's co-authors include Anna Bernardi, Franck Fieschi, Eduardo C. Escudero‐Adán, Marta Martínez‐Belmonte, Javier de Mendoza, Michel Thépaut, Javier Rojo, Giorgio Colombo, Rafaël Delgado and Elisabetta Moroni and has published in prestigious journals such as Journal of the American Chemical Society, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Sara Sattin

36 papers receiving 1.2k citations

Peers

Sara Sattin
Daniel P. Becker United States
Agnes L. Tan Singapore
Brad E. Sleebs Australia
William E. Harte United States
I.W. McNae United Kingdom
Tetsuo Uno United States
Daniel Obrecht Switzerland
Ryan P. Murelli United States
Daniel P. Becker United States
Sara Sattin
Citations per year, relative to Sara Sattin Sara Sattin (= 1×) peers Daniel P. Becker

Countries citing papers authored by Sara Sattin

Since Specialization
Citations

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

Fields of papers citing papers by Sara Sattin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Sattin

This figure shows the co-authorship network connecting the top 25 collaborators of Sara Sattin. A scholar is included among the top collaborators of Sara Sattin 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 Sara Sattin. Sara Sattin 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.
Civera, Monica, Sara Sattin, Oscar Francesconi, et al.. (2023). Tumor Carbohydrate Associated Antigen Analogs as Potential Binders for Siglec‐7. European Journal of Organic Chemistry. 26(40). 6 indexed citations
2.
Lorenzi, Roberto, Amanda Marchini, Luca Campone, et al.. (2023). Novel self-assembling cyclic peptides with reversible supramolecular nanostructures. Materials Chemistry Frontiers. 7(17). 3680–3692. 3 indexed citations
3.
Papi, Francesco, Cristina Nativi, Antonio Molinaro, et al.. (2022). Conformationally Constrained Sialyl Analogues as New Potential Binders of h‐CD22. ChemBioChem. 23(10). e202200076–e202200076. 6 indexed citations
4.
Thépaut, Michel, Joanna Luczkowiak, Corinne Vivès, et al.. (2021). DC/L-SIGN recognition of spike glycoprotein promotes SARS-CoV-2 trans-infection and can be inhibited by a glycomimetic antagonist. PLoS Pathogens. 17(5). e1009576–e1009576. 134 indexed citations
5.
Cassiano, Chiara, Elva Morretta, Matteo Costantini, et al.. (2021). Analysis of Hsp90 allosteric modulators interactome reveals a potential dual action mode involving mitochondrial MDH2. Bioorganic Chemistry. 115. 105258–105258. 2 indexed citations
6.
Civera, Monica & Sara Sattin. (2021). Homology Model of a Catalytically Competent Bifunctional Rel Protein. Frontiers in Molecular Biosciences. 8. 628596–628596. 3 indexed citations
7.
Montefiori, Marco, Monica Civera, Sara Sattin, et al.. (2020). Behavior of glycolylated sialoglycans in the binding pockets of murine and human CD22. iScience. 24(1). 101998–101998. 11 indexed citations
8.
Thépaut, Michel, Aline Le Roy, Sara Sattin, et al.. (2019). Enhancing Potency and Selectivity of a DC‐SIGN Glycomimetic Ligand by Fragment‐Based Design: Structural Basis. Chemistry - A European Journal. 25(64). 14659–14668. 27 indexed citations
9.
D’Annessa, Ilda, Sara Sattin, Jiahui Tao, et al.. (2017). Design of Allosteric Stimulators of the Hsp90 ATPase as New Anticancer Leads. Chemistry - A European Journal. 23(22). 5188–5192. 35 indexed citations
10.
Bagdány, Miklós, Guido Veit, Ryosuke Fukuda, et al.. (2017). Chaperones rescue the energetic landscape of mutant CFTR at single molecule and in cell. Nature Communications. 8(1). 398–398. 53 indexed citations
11.
Vasile, Francesca, Sara Sattin, Corinne Vivès, et al.. (2017). Facile access to pseudo-thio-1,2-dimannoside, a new glycomimetic DC-SIGN antagonist. Bioorganic & Medicinal Chemistry. 25(19). 5142–5147. 10 indexed citations
12.
Sattin, Sara, Matteo Panza, Francesca Vasile, et al.. (2016). Synthesis of Functionalized 2‐(4‐Hydroxyphenyl)‐3‐methylbenzofuran Allosteric Modulators of Hsp90 Activity. European Journal of Organic Chemistry. 2016(20). 3349–3364. 17 indexed citations
13.
Mauro, Nicolò, Paolo Ferruti, Elisabetta Ranucci, et al.. (2016). Linear biocompatible glyco-polyamidoamines as dual action mode virus infection inhibitors with potential as broad-spectrum microbicides for sexually transmitted diseases. Scientific Reports. 6(1). 33393–33393. 12 indexed citations
14.
Moroni, Elisabetta, Sara Sattin, Jiahui Tao, et al.. (2016). Molecular Dynamics Simulations Reveal the Mechanisms of Allosteric Activation of Hsp90 by Designed Ligands. Scientific Reports. 6(1). 23830–23830. 69 indexed citations
15.
Sattin, Sara & Anna Bernardi. (2016). Glycoconjugates and Glycomimetics as Microbial Anti-Adhesives. Trends in biotechnology. 34(6). 483–495. 62 indexed citations
16.
Sattin, Sara, Jiahui Tao, Elisabetta Moroni, et al.. (2015). Activation of Hsp90 Enzymatic Activity and Conformational Dynamics through Rationally Designed Allosteric Ligands. Chemistry - A European Journal. 21(39). 13598–13608. 60 indexed citations
17.
Morelli, Laura, Anna Bernardi, & Sara Sattin. (2014). Synthesis of potential allosteric modulators of Hsp90 by chemical glycosylation of Eupomatenoid-6. Carbohydrate Research. 390. 33–41. 11 indexed citations
18.
Sattin, Sara, et al.. (2012). Giant regular polyhedra from calixarene carboxylates and uranyl. Nature Communications. 3(1). 785–785. 192 indexed citations
19.
Obermajer, Nataša, Sara Sattin, Cinzia Colombo, et al.. (2010). Design, synthesis and activity evaluation of mannose-based DC-SIGN antagonists. Molecular Diversity. 15(2). 347–360. 26 indexed citations
20.
Reina, José J., Sara Sattin, Silvia Mari, et al.. (2007). 1,2‐Mannobioside Mimic: Synthesis, DC‐SIGN Interaction by NMR and Docking, and Antiviral Activity. ChemMedChem. 2(7). 1030–1036. 65 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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