Thomas Becker

7.4k total citations · 2 hit papers
62 papers, 5.0k citations indexed

About

Thomas Becker is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Thomas Becker has authored 62 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Oncology. Recurrent topics in Thomas Becker's work include RNA and protein synthesis mechanisms (47 papers), RNA modifications and cancer (37 papers) and RNA Research and Splicing (14 papers). Thomas Becker is often cited by papers focused on RNA and protein synthesis mechanisms (47 papers), RNA modifications and cancer (37 papers) and RNA Research and Splicing (14 papers). Thomas Becker collaborates with scholars based in Germany, United States and France. Thomas Becker's co-authors include Roland Beckmann, Otto Berninghausen, Thorsten Mielke, Jingdong Cheng, Mario Halić, Jean‐Paul Armache, Robert Buschauer, Birgitta Beatrix, Petr Těšina and Martin Pool and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Thomas Becker

59 papers receiving 4.9k citations

Hit Papers

Structural basis for t... 2004 2026 2011 2018 2020 2004 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
Thomas Becker Germany 35 4.2k 727 466 434 386 62 5.0k
Kliment A. Verba United States 9 4.3k 1.0× 643 0.9× 531 1.1× 593 1.4× 350 0.9× 19 5.9k
Björn Forsberg Sweden 13 3.2k 0.8× 454 0.6× 390 0.8× 376 0.9× 516 1.3× 18 4.8k
Imre Berger United Kingdom 42 4.9k 1.2× 658 0.9× 644 1.4× 368 0.8× 203 0.5× 133 6.0k
Dari Kimanius United Kingdom 14 4.1k 1.0× 531 0.7× 527 1.1× 507 1.2× 275 0.7× 22 5.8k
Daniel Boehringer Switzerland 38 4.7k 1.1× 573 0.8× 148 0.3× 389 0.9× 273 0.7× 105 6.0k
Christiane Schaffitzel United Kingdom 38 3.9k 0.9× 849 1.2× 495 1.1× 352 0.8× 201 0.5× 90 4.7k
Nelly Panté Canada 40 5.1k 1.2× 703 1.0× 420 0.9× 668 1.5× 179 0.5× 84 6.3k
Yong Xiong United States 44 4.0k 0.9× 650 0.9× 730 1.6× 373 0.9× 495 1.3× 151 5.8k
Sua Myong United States 41 5.6k 1.3× 397 0.5× 173 0.4× 277 0.6× 261 0.7× 111 6.6k
Scott M. Stagg United States 31 3.2k 0.8× 681 0.9× 324 0.7× 928 2.1× 117 0.3× 75 4.8k

Countries citing papers authored by Thomas Becker

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Becker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Becker

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Becker. A scholar is included among the top collaborators of Thomas Becker 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 Thomas Becker. Thomas Becker 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.
Berninghausen, Otto, et al.. (2025). UFMylation orchestrates spatiotemporal coordination of RQC at the ER. Science Advances. 11(18). eadv0435–eadv0435. 3 indexed citations
2.
Saba, James A., Timo Denk, Eugene Park, et al.. (2025). ZAK activation at the collided ribosome. Nature. 649(8098). 1051–1060.
3.
Ikeuchi, Ken, Robert Buschauer, Jingdong Cheng, et al.. (2023). Molecular basis for recognition and deubiquitination of 40S ribosomes by Otu2. Nature Communications. 14(1). 2730–2730. 11 indexed citations
4.
Ahn, Minkoo, Tomasz Włodarski, Thomas Becker, et al.. (2022). Modulating co-translational protein folding by rational design and ribosome engineering. Nature Communications. 13(1). 4243–4243. 21 indexed citations
5.
Su, Ting, Renuka Kudva, Thomas Becker, et al.. (2021). Structural basis of l-tryptophan-dependent inhibition of release factor 2 by the TnaC arrest peptide. Nucleic Acids Research. 49(16). 9539–9547. 10 indexed citations
6.
Matsuo, Yoshitaka, Petr Těšina, Akinori Endo, et al.. (2020). RQT complex dissociates ribosomes collided on endogenous RQC substrate SDD1. Nature Structural & Molecular Biology. 27(4). 323–332. 105 indexed citations
7.
Kratzat, Hanna, Timur Mackens‐Kiani, Michael Ameismeier, et al.. (2020). A structural inventory of native ribosomal ABCE1‐43S pre‐initiation complexes. The EMBO Journal. 40(1). e105179–e105179. 39 indexed citations
8.
Buschauer, Robert, Yoshitaka Matsuo, Takato Sugiyama, et al.. (2020). The Ccr4-Not complex monitors the translating ribosome for codon optimality. Science. 368(6488). 171 indexed citations
9.
Thoms, Matthias, Robert Buschauer, Michael Ameismeier, et al.. (2020). Structural basis for translational shutdown and immune evasion by the Nsp1 protein of SARS-CoV-2. Science. 369(6508). 1249–1255. 549 indexed citations breakdown →
10.
Steinchen, Wieland, Birgitta Beatrix, Otto Berninghausen, et al.. (2020). Architecture of the active post‐translational Sec translocon. The EMBO Journal. 40(3). e105643–e105643. 32 indexed citations
11.
Buschauer, Robert, Timur Mackens‐Kiani, Hanna Kratzat, et al.. (2020). Structure and function of yeast Lso2 and human CCDC124 bound to hibernating ribosomes. PLoS Biology. 18(7). e3000780–e3000780. 68 indexed citations
12.
Těšina, Petr, Jingdong Cheng, Micheline Fromont‐Racine, et al.. (2019). Structure of the 80S ribosome–Xrn1 nuclease complex. Nature Structural & Molecular Biology. 26(4). 275–280. 60 indexed citations
13.
Ikeuchi, Ken, Petr Těšina, Yoshitaka Matsuo, et al.. (2019). Collided ribosomes form a unique structural interface to induce Hel2‐driven quality control pathways. The EMBO Journal. 38(5). 216 indexed citations
14.
Braunger, Katharina, Stefan Pfeffer, Shiteshu Shrimal, et al.. (2018). Structural basis for coupling protein transport and N-glycosylation at the mammalian endoplasmic reticulum. Science. 360(6385). 215–219. 161 indexed citations
15.
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
16.
Schmidt, Christian, Eva Kowalinski, Vivekanandan Shanmuganathan, et al.. (2016). The cryo-EM structure of a ribosome–Ski2-Ski3-Ski8 helicase complex. Science. 354(6318). 1431–1433. 86 indexed citations
17.
Schmidt, Christian, Thomas Becker, André Heuer, et al.. (2015). Structure of the hypusinylated eukaryotic translation factor eIF-5A bound to the ribosome. Nucleic Acids Research. 44(4). 1944–1951. 97 indexed citations
18.
Frauenfeld, Jens, James C. Gumbart, Eli O. van der Sluis, et al.. (2011). Cryo-EM structure of the ribosome–SecYE complex in the membrane environment. Nature Structural & Molecular Biology. 18(5). 614–621. 230 indexed citations
19.
Bhushan, Shashi, Agata L. Starosta, Thomas Becker, et al.. (2010). Structural Basis for Translational Stalling by Human Cytomegalovirus and Fungal Arginine Attenuator Peptide. Molecular Cell. 40(1). 138–146. 89 indexed citations
20.
Blau, Michael, Srinivas Mullapudi, Thomas Becker, et al.. (2005). ERj1p uses a universal ribosomal adaptor site to coordinate the 80S ribosome at the membrane. Nature Structural & Molecular Biology. 12(11). 1015–1016. 59 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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