Peter Cherepanov

16.3k total citations · 3 hit papers
107 papers, 10.1k citations indexed

About

Peter Cherepanov is a scholar working on Molecular Biology, Virology and Infectious Diseases. According to data from OpenAlex, Peter Cherepanov has authored 107 papers receiving a total of 10.1k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 70 papers in Virology and 63 papers in Infectious Diseases. Recurrent topics in Peter Cherepanov's work include HIV Research and Treatment (70 papers), HIV/AIDS drug development and treatment (55 papers) and Biochemical and Molecular Research (34 papers). Peter Cherepanov is often cited by papers focused on HIV Research and Treatment (70 papers), HIV/AIDS drug development and treatment (55 papers) and Biochemical and Molecular Research (34 papers). Peter Cherepanov collaborates with scholars based in United Kingdom, United States and Belgium. Peter Cherepanov's co-authors include Alan Engelman, Wilfried Wackernagel, S. Hare, Goedele N. Maertens, Zeger Debyser, Erik De Clercq, Saumya Gupta, Eugene Valkov, Yves Engelborghs and Shaila Rahman and has published in prestigious journals such as Nature, Science and Chemical Reviews.

In The Last Decade

Peter Cherepanov

105 papers receiving 10.0k citations

Hit Papers

Gene disruption in Escherichia coli: TcR and KmR cassette... 1995 2026 2005 2015 1995 2002 2010 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter Cherepanov United Kingdom 53 6.5k 5.3k 5.0k 2.2k 1.3k 107 10.1k
Andréa Dessen France 47 3.9k 0.6× 1.3k 0.2× 2.3k 0.5× 1.6k 0.7× 1.5k 1.1× 119 8.2k
Alan Engelman United States 74 10.6k 1.6× 11.8k 2.2× 9.7k 1.9× 1.9k 0.9× 2.5k 1.9× 202 16.9k
Ian M. Jones United Kingdom 51 3.3k 0.5× 2.5k 0.5× 1.7k 0.3× 1.1k 0.5× 1.7k 1.3× 177 8.1k
Robert Craigie United States 51 7.5k 1.2× 6.0k 1.1× 5.8k 1.2× 1.5k 0.7× 1.1k 0.8× 93 10.5k
Marc Girard France 46 3.0k 0.5× 2.7k 0.5× 3.0k 0.6× 824 0.4× 1.8k 1.4× 215 8.2k
Anna Marie Skalka United States 44 3.7k 0.6× 2.7k 0.5× 2.7k 0.5× 1.0k 0.5× 732 0.6× 103 5.6k
Theodore C. Pierson United States 66 2.8k 0.4× 6.2k 1.2× 10.9k 2.2× 621 0.3× 3.1k 2.3× 125 16.8k
Bernard Ehresmann France 51 8.6k 1.3× 2.9k 0.6× 1.7k 0.3× 1.5k 0.7× 378 0.3× 174 9.6k
Dennis E. Hruby United States 53 3.4k 0.5× 4.5k 0.8× 889 0.2× 1.7k 0.8× 3.6k 2.7× 212 7.7k
Ronald Swanstrom United States 62 4.1k 0.6× 6.9k 1.3× 5.0k 1.0× 1.2k 0.5× 2.2k 1.7× 185 11.5k

Countries citing papers authored by Peter Cherepanov

Since Specialization
Citations

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

Fields of papers citing papers by Peter Cherepanov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Cherepanov

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Cherepanov. A scholar is included among the top collaborators of Peter Cherepanov 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 Peter Cherepanov. Peter Cherepanov 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.
Annamalai, Arun S., Franck Amblard, James R. Fuchs, et al.. (2024). The structural and mechanistic bases for the viral resistance to allosteric HIV-1 integrase inhibitor pirmitegravir. mBio. 15(11). e0046524–e0046524. 2 indexed citations
2.
Annamalai, Arun S., Nicola Cook, Valerie E. Pye, et al.. (2023). The Drug-Induced Interface That Drives HIV-1 Integrase Hypermultimerization and Loss of Function. mBio. 14(1). e0356022–e0356022. 5 indexed citations
3.
Oliveira, A. Sofia F., Annachiara Rosa, Christopher J. Arthur, et al.. (2023). Heme binding to the SARS-CoV-2 spike glycoprotein. Journal of Biological Chemistry. 299(8). 105014–105014. 12 indexed citations
4.
Garza-Garcı́a, Acely, Eugènia Almacellas, Stefano De Tito, et al.. (2023). ATG9B is a tissue-specific homotrimeric lipid scramblase that can compensate for ATG9A. Autophagy. 20(3). 557–576. 9 indexed citations
5.
Bonnard, Damien, Erwann Le Rouzic, Zhe Yu, et al.. (2023). Biological and Structural Analyses of New Potent Allosteric Inhibitors of HIV-1 Integrase. Antimicrobial Agents and Chemotherapy. 67(7). e0046223–e0046223. 5 indexed citations
6.
Ijaz, Samreen, Eleanor Parker, Elen Vink, et al.. (2022). Mapping of SARS-CoV-2 IgM and IgG in gingival crevicular fluid: Antibody dynamics and linkage to severity of COVID-19 in hospital inpatients. Journal of Infection. 85(2). 152–160. 2 indexed citations
7.
Ballandras-Colas, Allison, Dominika T. Gruszka, Parmit K. Singh, et al.. (2022). Multivalent interactions essential for lentiviral integrase function. Nature Communications. 13(1). 2416–2416. 10 indexed citations
8.
Zhao, Xue Zhi, Steven J. Smith, Allison Ballandras-Colas, et al.. (2021). Publisher Correction: Structural basis for the inhibition of HTLV-1 integration inferred from cryo-EM deltaretroviral intasome structures. Nature Communications. 12(1). 5927–5927. 1 indexed citations
9.
Zhao, Xue Zhi, Steven J. Smith, Allison Ballandras-Colas, et al.. (2021). Structural basis for the inhibition of HTLV-1 integration inferred from cryo-EM deltaretroviral intasome structures. Nature Communications. 12(1). 4996–4996. 10 indexed citations
10.
Davis, Christopher, Nicola Logan, Grace Tyson, et al.. (2021). Reduced neutralisation of the Delta (B.1.617.2) SARS-CoV-2 variant of concern following vaccination. PLoS Pathogens. 17(12). e1010022–e1010022. 117 indexed citations
11.
Maertens, Goedele N., Alan Engelman, & Peter Cherepanov. (2021). Structure and function of retroviral integrase. Nature Reviews Microbiology. 20(1). 20–34. 62 indexed citations
12.
Pye, Valerie E., Annachiara Rosa, Weston B. Struwe, et al.. (2020). A bipartite structural organization defines the SERINC family of HIV-1 restriction factors. Nature Structural & Molecular Biology. 27(1). 78–83. 41 indexed citations
13.
Pye, Valerie E., et al.. (2020). Cryo-EM structure of the deltaretroviral intasome in complex with the PP2A regulatory subunit B56γ. Nature Communications. 11(1). 5043–5043. 19 indexed citations
14.
Cook, Nicola, Wen Li, Dénes Berta, et al.. (2020). Structural basis of second-generation HIV integrase inhibitor action and viral resistance. Science. 367(6479). 806–810. 74 indexed citations
15.
Wilson, Marcus D., Ludovic Renault, Daniel P. Maskell, et al.. (2019). Retroviral integration into nucleosomes through DNA looping and sliding along the histone octamer. Nature Communications. 10(1). 4189–4189. 33 indexed citations
16.
Lesbats, Paul, Erik Serrao, Daniel P. Maskell, et al.. (2017). Structural basis for spumavirus GAG tethering to chromatin. Proceedings of the National Academy of Sciences. 114(21). 5509–5514. 43 indexed citations
17.
Maertens, Goedele N., Nicola Cook, Weifeng Wang, et al.. (2014). Structural basis for nuclear import of splicing factors by human Transportin 3. Proceedings of the National Academy of Sciences. 111(7). 2728–2733. 111 indexed citations
18.
Zaitseva, Lyubov, Peter Cherepanov, Lada Leyens, et al.. (2009). HIV-1 exploits importin 7 to maximize nuclear import of its DNA genome. Retrovirology. 6(1). 11–11. 80 indexed citations
19.
Cherepanov, Peter, A.L.B. Ambrosio, Shaila Rahman, Tom Ellenberger, & Alan Engelman. (2005). Structural basis for the recognition between HIV-1 integrase and transcriptional coactivator p75. Proceedings of the National Academy of Sciences. 102(48). 17308–17313. 325 indexed citations
20.
Hinnebusch, B. Joseph, et al.. (2002). Role of Yersinia Murine Toxin in Survival of Yersinia pestis in the Midgut of the Flea Vector. Science. 296(5568). 733–735. 232 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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