Robert Tampé

21.4k total citations · 3 hit papers
317 papers, 16.9k citations indexed

About

Robert Tampé is a scholar working on Molecular Biology, Immunology and Oncology. According to data from OpenAlex, Robert Tampé has authored 317 papers receiving a total of 16.9k indexed citations (citations by other indexed papers that have themselves been cited), including 206 papers in Molecular Biology, 93 papers in Immunology and 87 papers in Oncology. Recurrent topics in Robert Tampé's work include RNA Interference and Gene Delivery (71 papers), Drug Transport and Resistance Mechanisms (69 papers) and Immunotherapy and Immune Responses (68 papers). Robert Tampé is often cited by papers focused on RNA Interference and Gene Delivery (71 papers), Drug Transport and Resistance Mechanisms (69 papers) and Immunotherapy and Immune Responses (68 papers). Robert Tampé collaborates with scholars based in Germany, United States and Netherlands. Robert Tampé's co-authors include Rupert Abele, Christoph Thomas, Ulrich Rant, Ruoshan Wei, Peter Van Endert, Stephan Uebel, Lutz Schmitt, Ralph Wieneke, Jacob Piehler and Peter Cresswell and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Robert Tampé

314 papers receiving 16.6k citations

Hit Papers

A viral inhibitor of pept... 1995 2026 2005 2015 1995 2012 2020 100 200 300 400 500

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Robert Tampé 8.8k 5.5k 3.8k 2.0k 1.9k 317 16.9k
Dimiter S. Dimitrov 7.1k 0.8× 6.4k 1.2× 3.2k 0.8× 3.2k 1.6× 1.7k 0.9× 364 20.7k
Charles S. Craik 10.6k 1.2× 2.2k 0.4× 3.4k 0.9× 2.0k 1.0× 545 0.3× 344 19.6k
David G. Myszka 9.1k 1.0× 1.8k 0.3× 938 0.2× 781 0.4× 1.7k 0.9× 133 13.2k
Stephen B. H. Kent 22.2k 2.5× 1.6k 0.3× 3.4k 0.9× 1.7k 0.8× 934 0.5× 261 29.0k
Matthew Bogyo 12.0k 1.4× 2.9k 0.5× 4.7k 1.2× 2.7k 1.4× 1.5k 0.8× 300 21.5k
Arup K. Chakraborty 5.2k 0.6× 4.3k 0.8× 1.0k 0.3× 471 0.2× 737 0.4× 189 12.3k
Yifan Cheng 16.6k 1.9× 1.3k 0.2× 1.2k 0.3× 1.3k 0.7× 940 0.5× 213 25.5k
Jeffrey Shabanowitz 22.6k 2.6× 7.7k 1.4× 2.9k 0.8× 934 0.5× 791 0.4× 323 34.8k
Jacob Piehler 5.6k 0.6× 2.4k 0.4× 1.8k 0.5× 437 0.2× 1.7k 0.9× 212 10.5k
John J. Rossi 24.5k 2.8× 2.9k 0.5× 1.7k 0.4× 1.4k 0.7× 1.7k 0.9× 415 29.6k

Countries citing papers authored by Robert Tampé

Since Specialization
Citations

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

Fields of papers citing papers by Robert Tampé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Tampé

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Tampé. A scholar is included among the top collaborators of Robert Tampé 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 Robert Tampé. Robert Tampé 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.
Neumann, Piotr, Lukas Sušac, Stefano Da Vela, et al.. (2024). Structural and functional insights into tRNA recognition by human tRNA guanine transglycosylase. Structure. 32(3). 316–327.e5. 8 indexed citations
2.
Tampé, Robert, et al.. (2024). Interdomain communication in a homodimeric ABC transporter. Journal of Biological Chemistry. 300(7). 107440–107440. 1 indexed citations
3.
Winter, Christian, Claire Battin, Ben de Wet, et al.. (2024). Dual role of the peptide-loading complex as proofreader and limiter of MHC-I presentation. Proceedings of the National Academy of Sciences. 121(22). e2321600121–e2321600121. 6 indexed citations
4.
Tampé, Robert, et al.. (2023). Design principles for engineering light-controlled antibodies. Trends in biotechnology. 41(12). 1501–1517. 1 indexed citations
5.
Dietz, Marina S., Ulrike Müller, Julian Weghuber, et al.. (2022). Dynamic in Situ Confinement Triggers Ligand-Free Neuropeptide Receptor Signaling. Nano Letters. 22(20). 8363–8371. 4 indexed citations
6.
Zhu, Rong, Mateusz Sikora, Miriam Klausberger, et al.. (2022). Force-tuned avidity of spike variant-ACE2 interactions viewed on the single-molecule level. Nature Communications. 13(1). 7926–7926. 25 indexed citations
7.
Winter, Christian, et al.. (2022). Structure of an MHC I–tapasin–ERp57 editing complex defines chaperone promiscuity. Nature Communications. 13(1). 5383–5383. 23 indexed citations
8.
Winter, Christian, Lukas Sušac, Nicole Zitzmann, et al.. (2022). Molecular basis of MHC I quality control in the peptide loading complex. Nature Communications. 13(1). 4701–4701. 32 indexed citations
9.
Els‐Heindl, Sylvia, et al.. (2021). Photoinduced receptor confinement drives ligand-independent GPCR signaling. Science. 371(6536). 15 indexed citations
11.
Winter, Christian, et al.. (2021). Light-guided intrabodies for on-demand in situ target recognition in human cells. Chemical Science. 12(16). 5787–5795. 15 indexed citations
12.
Rudolph, Michael, et al.. (2020). Thermodynamic Basis for Conformational Coupling in an ATP-Binding Cassette Exporter. The Journal of Physical Chemistry Letters. 11(19). 7946–7953. 11 indexed citations
13.
Gatterdam, Karl, et al.. (2020). Ultrafast in-gel detection by fluorescent super-chelator probes with HisQuick-PAGE. Communications Biology. 3(1). 138–138. 5 indexed citations
14.
Dorey, Adam, Yongzheng Xing, Jonathan R. Burns, et al.. (2019). Synthetic protein-conductive membrane nanopores built with DNA. Nature Communications. 10(1). 5018–5018. 85 indexed citations
15.
Döring, Marius, H. Blees, Nicole Koller, et al.. (2019). Modulation of TAP-dependent antigen compartmentalization during human monocyte-to-DC differentiation. Blood Advances. 3(6). 839–850. 16 indexed citations
16.
Thomas, Christoph & Robert Tampé. (2017). Structure of the TAPBPR–MHC I complex defines the mechanism of peptide loading and editing. Science. 358(6366). 1060–1064. 96 indexed citations
17.
Heuer, André, Milan Gerovac, Christian Schmidt, et al.. (2017). Structure of the 40S–ABCE1 post-splitting complex in ribosome recycling and translation initiation. Nature Structural & Molecular Biology. 24(5). 453–460. 62 indexed citations
18.
Noll, A., Christoph Thomas, Ahmad Reza Mehdipour, et al.. (2017). Crystal structure and mechanistic basis of a functional homolog of the antigen transporter TAP. Proceedings of the National Academy of Sciences. 114(4). E438–E447. 64 indexed citations
19.
Karas, Michael, et al.. (2006). Mechanism of Substrate Sensing and Signal Transmission within an ABC Transporter. Journal of Biological Chemistry. 282(6). 3871–3880. 38 indexed citations
20.
Ackerman, Anne L., et al.. (2003). Early phagosomes in dendritic cells form a cellular compartment sufficient for cross presentation of exogenous antigens. Proceedings of the National Academy of Sciences. 100(22). 12889–12894. 296 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026