J. Sjef Verbeek

10.6k total citations · 1 hit paper
129 papers, 7.9k citations indexed

About

J. Sjef Verbeek is a scholar working on Immunology, Radiology, Nuclear Medicine and Imaging and Molecular Biology. According to data from OpenAlex, J. Sjef Verbeek has authored 129 papers receiving a total of 7.9k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Immunology, 75 papers in Radiology, Nuclear Medicine and Imaging and 44 papers in Molecular Biology. Recurrent topics in J. Sjef Verbeek's work include Monoclonal and Polyclonal Antibodies Research (74 papers), T-cell and B-cell Immunology (41 papers) and Glycosylation and Glycoproteins Research (24 papers). J. Sjef Verbeek is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (74 papers), T-cell and B-cell Immunology (41 papers) and Glycosylation and Glycoproteins Research (24 papers). J. Sjef Verbeek collaborates with scholars based in Netherlands, United States and United Kingdom. J. Sjef Verbeek's co-authors include Frans M.A. Hofhuis, J. Engelbert Gessner, Jan G. J. van de Winkel, Ferry Ossendorp, Reinhold Schmidt, Takashi Saito, Wouter L. W. Hazenbos, P J Capel, Ingmar Heijnen and Dirk Meyer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

J. Sjef Verbeek

129 papers receiving 7.8k citations

Hit Papers

Arthritis Critically Dependent on Innate Immune System Pl... 2002 2026 2010 2018 2002 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Sjef Verbeek Netherlands 52 4.8k 2.8k 2.5k 844 739 129 7.9k
Silvia Bolland United States 42 5.6k 1.2× 2.1k 0.8× 2.7k 1.1× 745 0.9× 410 0.6× 80 8.2k
David C. Wraith United Kingdom 52 6.2k 1.3× 1.3k 0.5× 1.6k 0.7× 1.1k 1.3× 744 1.0× 166 9.4k
Jérry Y. Niederkorn United States 60 4.5k 0.9× 3.3k 1.2× 2.6k 1.0× 884 1.0× 836 1.1× 295 12.2k
Marie Kosco‐Vilbois Switzerland 50 5.8k 1.2× 1.0k 0.4× 2.1k 0.8× 1.4k 1.6× 614 0.8× 142 8.9k
Daisuke Kitamura Japan 47 6.4k 1.3× 979 0.4× 3.2k 1.3× 1.3k 1.5× 639 0.9× 148 9.8k
Iqbal S. Grewal United States 56 7.7k 1.6× 1.3k 0.5× 2.0k 0.8× 2.3k 2.8× 690 0.9× 125 10.8k
Robert A. Eisenberg United States 50 6.6k 1.4× 2.7k 1.0× 2.1k 0.8× 853 1.0× 549 0.7× 180 9.6k
Timo K. van den Berg Netherlands 57 6.0k 1.2× 909 0.3× 3.1k 1.2× 1.1k 1.3× 669 0.9× 157 10.7k
G. J. Thorbecke United States 46 4.7k 1.0× 1.2k 0.4× 1.7k 0.7× 977 1.2× 643 0.9× 268 7.9k
Thierry Defrance France 42 4.6k 1.0× 742 0.3× 1.3k 0.5× 962 1.1× 433 0.6× 85 6.7k

Countries citing papers authored by J. Sjef Verbeek

Since Specialization
Citations

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

Fields of papers citing papers by J. Sjef Verbeek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. Sjef Verbeek. 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 J. Sjef Verbeek. The network helps show where J. Sjef Verbeek may publish in the future.

Co-authorship network of co-authors of J. Sjef Verbeek

This figure shows the co-authorship network connecting the top 25 collaborators of J. Sjef Verbeek. A scholar is included among the top collaborators of J. Sjef Verbeek 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 J. Sjef Verbeek. J. Sjef Verbeek 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.
Braster, Rens, Marijn Bögels, Manfred Wuhrer, et al.. (2021). Afucosylated IgG Targets FcγRIV for Enhanced Tumor Therapy in Mice. Cancers. 13(10). 2372–2372. 7 indexed citations
2.
Brouwers, Conny, Margot M. Linssen, Marcel Camps, et al.. (2020). Immunogenicity of rat-neu+ mouse mammary tumours determines the T cell-dependent therapeutic efficacy of anti-neu monoclonal antibody treatment. Scientific Reports. 10(1). 3933–3933. 5 indexed citations
3.
Yu, Xiaojie, H.T. Claude Chan, Christine A. Penfold, et al.. (2020). Isotype Switching Converts Anti-CD40 Antagonism to Agonism to Elicit Potent Antitumor Activity. Cancer Cell. 37(6). 850–866.e7. 48 indexed citations
4.
Koelink, Pim J., Felicia M. Bloemendaal, Bofeng Li, et al.. (2019). Anti-TNF therapy in IBD exerts its therapeutic effect through macrophage IL-10 signalling. Gut. 69(6). 1053–1063. 164 indexed citations
5.
Breukel, Cor, Jill Claassens, Conny Brouwers, et al.. (2018). High FcγR Expression on Intratumoral Macrophages Enhances Tumor-Targeting Antibody Therapy. The Journal of Immunology. 201(12). 3741–3749. 7 indexed citations
6.
Altıntaş, Işıl, Marjolein Sluijter, Sandra Verploegen, et al.. (2018). CD3-Bispecific Antibody Therapy Turns Solid Tumors into Inflammatory Sites but Does Not Install Protective Memory. Molecular Cancer Therapeutics. 18(2). 312–322. 61 indexed citations
7.
Bloemendaal, Felicia M., Alon D. Levin, Manon E. Wildenberg, et al.. (2017). Anti–Tumor Necrosis Factor With a Glyco-Engineered Fc-Region Has Increased Efficacy in Mice With Colitis. Gastroenterology. 153(5). 1351–1362.e4. 27 indexed citations
8.
Bieren, Julia Esser‐von, Ilaria Mosconi, Romain Guiet, et al.. (2013). Antibodies Trap Tissue Migrating Helminth Larvae and Prevent Tissue Damage by Driving IL-4Rα-Independent Alternative Differentiation of Macrophages. PLoS Pathogens. 9(11). e1003771–e1003771. 88 indexed citations
9.
Beers, Stephen A., Ruth R. French, H.T. Claude Chan, et al.. (2010). Antigenic modulation limits the efficacy of anti-CD20 antibodies: implications for antibody selection. Blood. 115(25). 5191–5201. 241 indexed citations
10.
Mittal, Rahul, Sunil K. Sukumaran, M. Madan Babu, et al.. (2010). Fcγ Receptor I Alpha Chain (CD64) Expression in Macrophages Is Critical for the Onset of Meningitis by Escherichia coli K1. PLoS Pathogens. 6(11). e1001203–e1001203. 34 indexed citations
11.
Bergthaler, Andreas, Lukas Flatz, Admar Verschoor, et al.. (2009). Correction: Impaired Antibody Response Causes Persistence of Prototypic T Cell–Contained Virus. PLoS Biology. 7(8). 14 indexed citations
12.
Otten, Marielle A., Tom W.L. Groeneveld, Roelof Flierman, et al.. (2009). Both Complement and IgG Fc Receptors Are Required for Development of Attenuated Antiglomerular Basement Membrane Nephritis in Mice. The Journal of Immunology. 183(6). 3980–3988. 37 indexed citations
13.
Ding, Jin, Tingting Zhou, Huasong Zeng, et al.. (2008). Hyperacute Rejection by Anti-Gal IgG1, IgG2a, and IgG2b Is Dependent on Complement and Fc-γ Receptors. The Journal of Immunology. 180(1). 261–268. 22 indexed citations
14.
Baudino, Lucie, Falk Nimmerjahn, Yasuro Shinohara, et al.. (2008). Impact of a Three Amino Acid Deletion in the CH2 Domain of Murine IgG1 on Fc-Associated Effector Functions. The Journal of Immunology. 181(6). 4107–4112. 14 indexed citations
15.
Bos, Rinke, Suzanne van Duikeren, Thorbald van Hall, et al.. (2007). Characterization of Antigen-Specific Immune Responses Induced by Canarypox Virus Vaccines. The Journal of Immunology. 179(9). 6115–6122. 19 indexed citations
16.
Rodriguez, Wilfredo, Carolyn Mold, Milena Kataranovski, et al.. (2007). C-Reactive Protein-Mediated Suppression of Nephrotoxic Nephritis: Role of Macrophages, Complement, and Fcγ Receptors. The Journal of Immunology. 178(1). 530–538. 51 indexed citations
17.
Schuurhuis, Danita H., Nadine van Montfoort, Andreea Ioan‐Facsinay, et al.. (2006). Immune Complex-Loaded Dendritic Cells Are Superior to Soluble Immune Complexes as Antitumor Vaccine. The Journal of Immunology. 176(8). 4573–4580. 97 indexed citations
18.
Saeland, Eiríkur, Gestur Vidarsson, Jeanette H.W. Leusen, et al.. (2003). Central Role of Complement in Passive Protection by Human IgG1 and IgG2 Anti-pneumococcal Antibodies in Mice. The Journal of Immunology. 170(12). 6158–6164. 65 indexed citations
19.
Ji, Hong, Koichiro Ohmura, Umar Mahmood, et al.. (2002). Arthritis Critically Dependent on Innate Immune System Players. Immunity. 16(2). 157–168. 563 indexed citations breakdown →
20.
Baumann, Ulrich, Jörg Köhl, Thomas Tschernig, et al.. (2000). A Codominant Role of FcγRI/III and C5aR in the Reverse Arthus Reaction. The Journal of Immunology. 164(2). 1065–1070. 98 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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