Alexander Borodavka

1.3k total citations
27 papers, 791 citations indexed

About

Alexander Borodavka is a scholar working on Infectious Diseases, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Alexander Borodavka has authored 27 papers receiving a total of 791 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Infectious Diseases, 13 papers in Molecular Biology and 10 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Alexander Borodavka's work include Viral gastroenteritis research and epidemiology (19 papers), Viral Infections and Immunology Research (10 papers) and Animal Virus Infections Studies (9 papers). Alexander Borodavka is often cited by papers focused on Viral gastroenteritis research and epidemiology (19 papers), Viral Infections and Immunology Research (10 papers) and Animal Virus Infections Studies (9 papers). Alexander Borodavka collaborates with scholars based in United Kingdom, United States and Germany. Alexander Borodavka's co-authors include Roman Tůma, Peter G. Stockley, Ulrich Desselberger, Guido Papa, Eric C. Dykeman, Don C. Lamb, Julia Acker, John T. Patton, Waldemar Schrimpf and Óscar R. Burrone and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Alexander Borodavka

25 papers receiving 781 citations

Peers

Alexander Borodavka
Diane L. Farsetta United States
Nerea Irigoyen United Kingdom
Tijana Ivanovic United States
Jibo Hou China
Mason Lai United States
Alexander Borodavka
Citations per year, relative to Alexander Borodavka Alexander Borodavka (= 1×) peers Sangita Venkataraman

Countries citing papers authored by Alexander Borodavka

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Borodavka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Borodavka

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Borodavka. A scholar is included among the top collaborators of Alexander Borodavka 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 Alexander Borodavka. Alexander Borodavka 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.
Acker, Julia, et al.. (2024). Phase separation and viral factories: unveiling the physical processes supporting RNA packaging in dsRNA viruses. Biochemical Society Transactions. 52(5). 2101–2112. 4 indexed citations
2.
Styles, Christine T., Jie Zhou, Katie E. Flight, et al.. (2023). Propylene glycol inactivates respiratory viruses and prevents airborne transmission. EMBO Molecular Medicine. 15(12). e17932–e17932. 5 indexed citations
3.
Brown, Heather M., et al.. (2023). Flexibility of the Rotavirus NSP2 C-Terminal Region Supports Factory Formation via Liquid-Liquid Phase Separation. Journal of Virology. 97(2). e0003923–e0003923. 15 indexed citations
4.
Mojzeš, Peter, Tomáš Bílý, Zdeněk Franta, et al.. (2023). Shedding light on reovirus assembly—Multimodal imaging of viral factories. Advances in virus research. 116. 173–213. 2 indexed citations
5.
Šneideris, Tomas, Nadia A. Erkamp, Hannes Ausserwӧger, et al.. (2023). Targeting nucleic acid phase transitions as a mechanism of action for antimicrobial peptides. Nature Communications. 14(1). 7170–7170. 28 indexed citations
6.
Strauss, Sebastian, Julia Acker, Guido Papa, et al.. (2023). Principles of RNA recruitment to viral ribonucleoprotein condensates in a segmented dsRNA virus. eLife. 12. 10 indexed citations
7.
Knight, Michael L., et al.. (2022). Rotavirus RNA chaperone mediates global transcriptome-wide increase in RNA backbone flexibility. Nucleic Acids Research. 50(17). 10078–10092. 6 indexed citations
8.
Arter, William E., Runzhang Qi, Nadia A. Erkamp, et al.. (2022). Biomolecular condensate phase diagrams with a combinatorial microdroplet platform. Nature Communications. 13(1). 53 indexed citations
9.
Sharp, Colin, Wenfang Tan, Joanne M. Stevens, et al.. (2022). Using Species a Rotavirus Reverse Genetics to Engineer Chimeric Viruses Expressing SARS-CoV-2 Spike Epitopes. Journal of Virology. 96(14). e0048822–e0048822. 11 indexed citations
10.
Bravo, Jack P. K., Julia Acker, Chen Davidovich, et al.. (2021). Structural basis of rotavirus RNA chaperone displacement and RNA annealing. Proceedings of the National Academy of Sciences. 118(41). 21 indexed citations
11.
Caddy, Sarah, Guido Papa, Alexander Borodavka, & Ulrich Desselberger. (2021). Rotavirus research: 2014–2020. Virus Research. 304. 198499–198499. 33 indexed citations
12.
Geiger, Florian, Julia Acker, Guido Papa, et al.. (2021). Liquid–liquid phase separation underpins the formation of replication factories in rotaviruses. The EMBO Journal. 40(21). e107711–e107711. 76 indexed citations
13.
Papa, Guido, Francesca Arnoldi, Elisabeth M. Schraner, et al.. (2019). Recombinant Rotaviruses Rescued by Reverse Genetics Reveal the Role of NSP5 Hyperphosphorylation in the Assembly of Viral Factories. Journal of Virology. 94(1). 40 indexed citations
14.
Borodavka, Alexander, Ulrich Desselberger, & John T. Patton. (2018). Genome packaging in multi-segmented dsRNA viruses: distinct mechanisms with similar outcomes. Current Opinion in Virology. 33. 106–112. 52 indexed citations
15.
Bravo, Jack P. K., Alexander Borodavka, Anders Barth, et al.. (2018). Stability of local secondary structure determines selectivity of viral RNA chaperones. Nucleic Acids Research. 46(15). 7924–7937. 22 indexed citations
16.
Borodavka, Alexander, Eric C. Dykeman, Waldemar Schrimpf, & Don C. Lamb. (2017). Protein-mediated RNA folding governs sequence-specific interactions between rotavirus genome segments. eLife. 6. 58 indexed citations
17.
Borodavka, Alexander, et al.. (2016). Sizes of Long RNA Molecules Are Determined by the Branching Patterns of Their Secondary Structures. Biophysical Journal. 111(10). 2077–2085. 40 indexed citations
18.
Borodavka, Alexander, James R. Ault, Peter G. Stockley, & Roman Tůma. (2015). Evidence that avian reovirus σNS is an RNA chaperone: implications for genome segment assortment. Nucleic Acids Research. 43(14). 7044–7057. 24 indexed citations
19.
Borodavka, Alexander, Roman Tůma, & Peter G. Stockley. (2013). A two-stage mechanism of viral RNA compaction revealed by single molecule fluorescence. RNA Biology. 10(4). 481–489. 34 indexed citations
20.
Stockley, Peter G., Reidun Twarock, Saskia E. Bakker, et al.. (2013). Packaging signals in single-stranded RNA viruses: nature’s alternative to a purely electrostatic assembly mechanism. Journal of Biological Physics. 39(2). 277–287. 80 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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