Christoph Garbers

9.4k total citations · 3 hit papers
118 papers, 6.4k citations indexed

About

Christoph Garbers is a scholar working on Oncology, Immunology and Molecular Biology. According to data from OpenAlex, Christoph Garbers has authored 118 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Oncology, 71 papers in Immunology and 31 papers in Molecular Biology. Recurrent topics in Christoph Garbers's work include Cytokine Signaling Pathways and Interactions (68 papers), Toxin Mechanisms and Immunotoxins (24 papers) and Monoclonal and Polyclonal Antibodies Research (16 papers). Christoph Garbers is often cited by papers focused on Cytokine Signaling Pathways and Interactions (68 papers), Toxin Mechanisms and Immunotoxins (24 papers) and Monoclonal and Polyclonal Antibodies Research (16 papers). Christoph Garbers collaborates with scholars based in Germany, United Kingdom and Australia. Christoph Garbers's co-authors include Stefan Rose‐John, Jürgen Scheller, Juliane Lokau, Samadhi Aparicio-Siegmund, Athena Chalaris, Janina Wolf, Joachim Grötzinger, Sylvia Heink, Thomas Korn and Björn Rabe and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Nature reviews. Immunology.

In The Last Decade

Christoph Garbers

115 papers receiving 6.4k citations

Hit Papers

Interleukin-6 and its receptors: A highly regulated and d... 2014 2026 2018 2022 2014 2018 2023 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christoph Garbers Germany 40 2.8k 2.7k 1.9k 662 604 118 6.4k
Bo Tang China 31 1.9k 0.7× 2.4k 0.9× 2.5k 1.3× 828 1.3× 521 0.9× 114 6.5k
Ursula Fearon Ireland 54 3.0k 1.1× 1.3k 0.5× 2.7k 1.5× 1.0k 1.5× 504 0.8× 166 8.4k
Kamran Ghoreschi Germany 44 4.4k 1.6× 2.0k 0.7× 1.7k 0.9× 389 0.6× 599 1.0× 143 8.2k
Brendan J. Jenkins Australia 43 3.8k 1.4× 4.0k 1.5× 2.8k 1.5× 1.2k 1.9× 644 1.1× 113 8.6k
Akihiro Kimura Japan 32 3.6k 1.3× 1.3k 0.5× 1.7k 0.9× 537 0.8× 514 0.9× 57 6.5k
Andrea Modesti Italy 43 2.4k 0.9× 1.9k 0.7× 2.4k 1.3× 564 0.9× 560 0.9× 203 6.8k
Hideo Yasukawa Japan 40 3.4k 1.2× 3.8k 1.4× 2.4k 1.3× 1.0k 1.6× 896 1.5× 77 8.4k
Norihiro Nishimoto Japan 46 3.9k 1.4× 3.4k 1.3× 2.2k 1.2× 684 1.0× 852 1.4× 132 11.0k
Maureen R. Horton United States 42 3.1k 1.1× 960 0.4× 2.3k 1.3× 700 1.1× 607 1.0× 91 7.3k
Fons A. J. van de Loo Netherlands 51 2.9k 1.0× 1.7k 0.6× 3.2k 1.7× 1.2k 1.8× 305 0.5× 148 8.6k

Countries citing papers authored by Christoph Garbers

Since Specialization
Citations

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

Fields of papers citing papers by Christoph Garbers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christoph Garbers

This figure shows the co-authorship network connecting the top 25 collaborators of Christoph Garbers. A scholar is included among the top collaborators of Christoph Garbers 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 Christoph Garbers. Christoph Garbers 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.
Kopfnagel, Verena, Franziska Rademacher, Juliane Lokau, et al.. (2025). RNase 7 and Th cytokines synergistically increase the secretion of interleukin-6 from keratinocytes. Scientific Reports. 15(1). 19396–19396.
2.
Düsterhöft, Stefan, et al.. (2025). Investigating plasticity within the interleukin-6 family with AlphaFold-Multimer. Computational and Structural Biotechnology Journal. 27. 946–959.
3.
Dolla, Guillaume, Sarah Nicolas, Alexandre Bourgeois, et al.. (2024). Ectodomain shedding of PLA2R1 is mediated by the metalloproteases ADAM10 and ADAM17. Journal of Biological Chemistry. 300(7). 107480–107480. 5 indexed citations
4.
Garbers, Christoph, et al.. (2024). The role of interleukin-6 classic and trans-signaling and interleukin-11 classic signaling in gastric cancer cells. Współczesna Onkologia. 28(2). 105–113. 2 indexed citations
5.
Garbers, Christoph, Jana Dietrich, Danny Jonigk, et al.. (2024). The metalloproteinase ADAM10 sheds angiotensin‐converting enzyme (ACE) from the pulmonary endothelium as a soluble, functionally active convertase. The FASEB Journal. 38(19). e70105–e70105. 7 indexed citations
6.
Lokau, Juliane, Christoph Garbers, Kristina Behnke, et al.. (2024). Interleukin‐11 receptor is an alternative α‐receptor for interleukin‐6 and the chimeric cytokine IC 7. FEBS Journal. 292(3). 523–536. 4 indexed citations
7.
Lokau, Juliane, et al.. (2023). The soluble IL‐2 receptor α/CD25 as a modulator of IL‐2 function. Immunology. 171(3). 377–387. 16 indexed citations
8.
Garbers, Christoph, et al.. (2022). The collectrin‐like part of the SARS‐CoV‐1 and ‐2 receptor ACE2 is shed by the metalloproteinases ADAM10 and ADAM17. The FASEB Journal. 36(3). e22234–e22234. 24 indexed citations
9.
Kasper, Philipp, Christina Vohlen, Ruth Janoschek, et al.. (2021). Brain-Restricted Inhibition of IL-6 Trans-Signaling Mildly Affects Metabolic Consequences of Maternal Obesity in Male Offspring. Nutrients. 13(11). 3735–3735. 3 indexed citations
10.
Düsterhöft, Stefan, Petr Kašpárek, Shixin Liu, et al.. (2021). The iRhom homology domain is indispensable for ADAM17-mediated TNFα and EGF receptor ligand release. Cellular and Molecular Life Sciences. 78(11). 5015–5040. 13 indexed citations
11.
Agthe, Maria, et al.. (2021). Interleukin‐11 (IL‐11) receptor cleavage by the rhomboid protease RHBDL2 induces IL‐11 trans‐signaling. The FASEB Journal. 35(3). e21380–e21380. 29 indexed citations
12.
Martínez‐Fábregas, Jonathan, Stephan Wilmes, Luopin Wang, et al.. (2019). Kinetics of cytokine receptor trafficking determine signaling and functional selectivity. eLife. 8. 31 indexed citations
13.
Aparicio-Siegmund, Samadhi, Yvonne Garbers, Charlotte M. Flynn, et al.. (2019). The IL-6-neutralizing sIL-6R-sgp130 buffer system is disturbed in patients with type 2 diabetes. American Journal of Physiology-Endocrinology and Metabolism. 317(2). E411–E420. 40 indexed citations
14.
Lokau, Juliane, Maria Agthe, Charlotte M. Flynn, & Christoph Garbers. (2017). Proteolytic control of Interleukin-11 and Interleukin-6 biology. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1864(11). 2105–2117. 40 indexed citations
15.
Ruwanpura, Saleela M., Louise McLeod, Lovisa Dousha, et al.. (2016). Therapeutic Targeting of the IL-6 Trans-Signaling/Mechanistic Target of Rapamycin Complex 1 Axis in Pulmonary Emphysema. American Journal of Respiratory and Critical Care Medicine. 194(12). 1494–1505. 39 indexed citations
16.
Schumacher, Neele, Janina Wolf, Jeanette Schwarz, et al.. (2015). Shedding of Endogenous Interleukin-6 Receptor (IL-6R) Is Governed by A Disintegrin and Metalloproteinase (ADAM) Proteases while a Full-length IL-6R Isoform Localizes to Circulating Microvesicles. Journal of Biological Chemistry. 290(43). 26059–26071. 116 indexed citations
17.
Garbers, Christoph, Janina Wolf, Ahmad Trad, et al.. (2014). Alternative Intronic Polyadenylation Generates the Interleukin-6 Trans-signaling Inhibitor sgp130-E10. Journal of Biological Chemistry. 289(32). 22140–22150. 30 indexed citations
18.
Effenberger, Timo, Kareen Bartsch, Christoph Garbers, et al.. (2014). Senescence‐associated release of transmembrane proteins involves proteolytic processing by ADAM17 and microvesicle shedding. The FASEB Journal. 28(11). 4847–4856. 47 indexed citations
19.
Aurich, Matthias, Samadhi Aparicio-Siegmund, Doreen M. Floß, et al.. (2014). The Amino Acid Exchange R28E in Ciliary Neurotrophic Factor (CNTF) Abrogates Interleukin-6 Receptor-dependent but Retains CNTF Receptor-dependent Signaling via Glycoprotein 130 (gp130)/Leukemia Inhibitory Factor Receptor (LIFR). Journal of Biological Chemistry. 289(26). 18442–18450. 24 indexed citations
20.
Dewitz, Christin, Katja Möller‐Hackbarth, Ahmad Trad, et al.. (2013). Soluble T cell immunoglobulin and mucin domain (TIM)-1 and -4 generated by A Disintegrin And Metalloprotease (ADAM)-10 and -17 bind to phosphatidylserine. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1843(2). 275–287. 32 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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