Ronald Derking

5.5k total citations · 1 hit paper
13 papers, 1.7k citations indexed

About

Ronald Derking is a scholar working on Virology, Radiology, Nuclear Medicine and Imaging and Molecular Biology. According to data from OpenAlex, Ronald Derking has authored 13 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Virology, 8 papers in Radiology, Nuclear Medicine and Imaging and 6 papers in Molecular Biology. Recurrent topics in Ronald Derking's work include HIV Research and Treatment (13 papers), Monoclonal and Polyclonal Antibodies Research (8 papers) and HIV/AIDS drug development and treatment (4 papers). Ronald Derking is often cited by papers focused on HIV Research and Treatment (13 papers), Monoclonal and Polyclonal Antibodies Research (8 papers) and HIV/AIDS drug development and treatment (4 papers). Ronald Derking collaborates with scholars based in Netherlands, United States and Canada. Ronald Derking's co-authors include Rogier W. Sanders, Ian A. Wilson, John P. Moore, Andrew B. Ward, Albert Cupo, Jean‐Philippe Julien, Per Johan Klasse, Anila Yasmeen, Helen J. Kim and Jacob Korzun and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Immunity.

In The Last Decade

Ronald Derking

13 papers receiving 1.7k citations

Hit Papers

A Next-Generation Cleaved, Soluble HIV-1 Env Trimer, BG50... 2013 2026 2017 2021 2013 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ronald Derking Netherlands 10 1.5k 687 669 661 463 13 1.7k
Javier Guenaga United States 21 1.3k 0.9× 741 1.1× 745 1.1× 546 0.8× 416 0.9× 40 1.7k
Anila Yasmeen United States 19 1.6k 1.1× 719 1.0× 849 1.3× 752 1.1× 533 1.2× 32 2.0k
Alba Torrents de la Peña United States 14 1.0k 0.7× 550 0.8× 613 0.9× 479 0.7× 391 0.8× 28 1.4k
Chih-chin Huang United States 10 1.4k 1.0× 742 1.1× 679 1.0× 602 0.9× 601 1.3× 10 1.8k
Joseph G. Jardine United States 11 827 0.6× 751 1.1× 707 1.1× 498 0.8× 652 1.4× 20 1.7k
Matthias Pauthner United States 14 1.0k 0.7× 622 0.9× 726 1.1× 445 0.7× 358 0.8× 24 1.5k
Rajesh P. Ringe India 20 930 0.6× 401 0.6× 512 0.8× 431 0.7× 364 0.8× 46 1.2k
Louise Scharf United States 16 1.3k 0.9× 1.2k 1.8× 586 0.9× 615 0.9× 433 0.9× 19 2.1k
Michael Golabek United States 8 966 0.7× 410 0.6× 518 0.8× 439 0.7× 287 0.6× 8 1.1k
Kelli Greene United States 11 1.5k 1.0× 799 1.2× 390 0.6× 391 0.6× 672 1.5× 17 1.7k

Countries citing papers authored by Ronald Derking

Since Specialization
Citations

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

Fields of papers citing papers by Ronald Derking

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ronald Derking

This figure shows the co-authorship network connecting the top 25 collaborators of Ronald Derking. A scholar is included among the top collaborators of Ronald Derking 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 Ronald Derking. Ronald Derking is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
Hossain, Md. Alamgir, Kara Anasti, Brian Watts, et al.. (2022). B cells expressing IgM B cell receptors of HIV-1 neutralizing antibodies discriminate antigen affinities by sensing binding association rates. Cell Reports. 39(13). 111021–111021. 3 indexed citations
2.
Li, Zeshi, Ronald Derking, Gerlof P. Bosman, et al.. (2022). Conjugation of a Toll‐Like Receptor Agonist to Glycans of an HIV Native‐Like Envelope Trimer Preserves Neutralization Epitopes. ChemBioChem. 23(16). e202200236–e202200236. 5 indexed citations
3.
Derking, Ronald & Rogier W. Sanders. (2021). Structure‐guided envelope trimer design in HIV‐1 vaccine development: a narrative review. Journal of the International AIDS Society. 24(S7). e25797–e25797. 27 indexed citations
4.
Lee, Jeong Hyun, Daniel P. Leaman, Arthur S. Kim, et al.. (2015). Antibodies to a conformational epitope on gp41 neutralize HIV-1 by destabilizing the Env spike. Nature Communications. 6(1). 8167–8167. 65 indexed citations
5.
Carrillo, Jorge, Maria Luisa Rodrı́guez de la Concepción, Sílvia Marfil, et al.. (2015). Gp120/CD4 Blocking Antibodies Are Frequently Elicited in ART-Naïve Chronically HIV-1 Infected Individuals. PLoS ONE. 10(3). e0120648–e0120648. 6 indexed citations
6.
Pugach, Pavel, Gabriel Ozorowski, Albert Cupo, et al.. (2015). A Native-Like SOSIP.664 Trimer Based on an HIV-1 Subtype B env Gene. Journal of Virology. 89(6). 3380–3395. 177 indexed citations
7.
Derking, Ronald, Gabriel Ozorowski, Kwinten Sliepen, et al.. (2015). Comprehensive Antigenic Map of a Cleaved Soluble HIV-1 Envelope Trimer. PLoS Pathogens. 11(3). e1004767–e1004767. 75 indexed citations
8.
Sluis, Renée M. van der, et al.. (2014). Interplay between viral Tat protein and c-Jun transcription factor in controlling LTR promoter activity in different human immunodeficiency virus type I subtypes. Journal of General Virology. 95(4). 968–979. 12 indexed citations
9.
Blattner, Claudia, Jeong Hyun Lee, Kwinten Sliepen, et al.. (2014). Structural Delineation of a Quaternary, Cleavage-Dependent Epitope at the gp41-gp120 Interface on Intact HIV-1 Env Trimers. Immunity. 40(5). 669–680. 249 indexed citations
10.
Yasmeen, Anila, Rajesh P. Ringe, Ronald Derking, et al.. (2014). Differential binding of neutralizing and non-neutralizing antibodies to native-like soluble HIV-1 Env trimers, uncleaved Env proteins, and monomeric subunits. Retrovirology. 11(1). 41–41. 114 indexed citations
11.
Sanders, Rogier W., Ronald Derking, Albert Cupo, et al.. (2013). A Next-Generation Cleaved, Soluble HIV-1 Env Trimer, BG505 SOSIP.664 gp140, Expresses Multiple Epitopes for Broadly Neutralizing but Not Non-Neutralizing Antibodies. PLoS Pathogens. 9(9). e1003618–e1003618. 629 indexed citations breakdown →
12.
Julien, Jean‐Philippe, Jeong Hyun Lee, Albert Cupo, et al.. (2013). Asymmetric recognition of the HIV-1 trimer by broadly neutralizing antibody PG9. Proceedings of the National Academy of Sciences. 110(11). 4351–4356. 192 indexed citations
13.
Ringe, Rajesh P., Rogier W. Sanders, Anila Yasmeen, et al.. (2013). Cleavage strongly influences whether soluble HIV-1 envelope glycoprotein trimers adopt a native-like conformation. Proceedings of the National Academy of Sciences. 110(45). 18256–18261. 134 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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