Robert Buschauer

2.9k total citations · 1 hit paper
20 papers, 1.6k citations indexed

About

Robert Buschauer is a scholar working on Molecular Biology, Ecology and Genetics. According to data from OpenAlex, Robert Buschauer has authored 20 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 4 papers in Ecology and 3 papers in Genetics. Recurrent topics in Robert Buschauer's work include RNA and protein synthesis mechanisms (15 papers), RNA modifications and cancer (9 papers) and RNA Research and Splicing (9 papers). Robert Buschauer is often cited by papers focused on RNA and protein synthesis mechanisms (15 papers), RNA modifications and cancer (9 papers) and RNA Research and Splicing (9 papers). Robert Buschauer collaborates with scholars based in Germany, United States and Japan. Robert Buschauer's co-authors include Roland Beckmann, Otto Berninghausen, Thomas Becker, Jingdong Cheng, Hanna Kratzat, Matthias Thoms, Petr Těšina, Timur Mackens‐Kiani, Michael Ameismeier and Timo Denk and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Robert Buschauer

20 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Structural basis for translational shutdown and immune evasion by the Nsp1 protein of SARS-CoV-2

2020 549 citations Matthias Thoms, Robert Buschauer et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Robert Buschauer Germany	15	1.1k	454	190	172	147	20	1.6k
David Paul Germany	17	509 0.5×	709 1.6×	61 0.3×	194 1.1×	222 1.5×	22	2.0k
Matthias Thoms Germany	25	1.9k 1.8×	438 1.0×	61 0.3×	179 1.0×	67 0.5×	36	2.4k
Anja W. M. de Jong Netherlands	18	840 0.8×	590 1.3×	70 0.4×	156 0.9×	58 0.4×	37	1.5k
Franck Martin France	25	1.6k 1.5×	225 0.5×	76 0.4×	137 0.8×	65 0.4×	75	2.1k
Antoni G. Wrobel United Kingdom	17	669 0.6×	1.0k 2.3×	120 0.6×	190 1.1×	64 0.4×	25	1.6k
Melanie D. Ohi United States	27	1.1k 1.0×	268 0.6×	65 0.3×	453 2.6×	70 0.5×	59	2.1k
Irwin Jungreis United States	19	1.7k 1.5×	263 0.6×	110 0.6×	145 0.8×	30 0.2×	33	2.2k
Amanda J. Price United Kingdom	21	1.3k 1.2×	813 1.8×	203 1.1×	524 3.0×	41 0.3×	26	2.5k
Hanna Kratzat Germany	11	734 0.7×	414 0.9×	49 0.3×	142 0.8×	61 0.4×	12	1.1k
Kristina M. Herbert United States	14	888 0.8×	204 0.4×	107 0.6×	224 1.3×	36 0.2×	18	1.3k

Countries citing papers authored by Robert Buschauer

Since Specialization

Citations

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

Fields of papers citing papers by Robert Buschauer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Buschauer

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

All Works

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20 of 20 papers shown

Li, Xiang, Mengjiao Wang, Timo Denk, et al.. (2024). Structural basis for differential inhibition of eukaryotic ribosomes by tigecycline. Nature Communications. 15(1). 5481–5481. 7 indexed citations

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

Mitterer, Valentin, Matthias Thoms, Robert Buschauer, et al.. (2023). Concurrent remodelling of nucleolar 60S subunit precursors by the Rea1 ATPase and Spb4 RNA helicase. eLife. 12. 9 indexed citations

Těšina, Petr, Robert Buschauer, Matthias Thoms, et al.. (2023). Molecular basis of eIF5A-dependent CAT tailing in eukaryotic ribosome-associated quality control. Molecular Cell. 83(4). 607–621.e4. 25 indexed citations

Thoms, Matthias, Dirk Flemming, Henrik M. Hammarén, et al.. (2023). Structure of nascent 5S RNPs at the crossroad between ribosome assembly and MDM2–p53 pathways. Nature Structural & Molecular Biology. 30(8). 1119–1131. 19 indexed citations

Saito, Kazuki, Hanna Kratzat, Annabelle Campbell, et al.. (2022). Ribosome collisions induce mRNA cleavage and ribosome rescue in bacteria. Nature. 603(7901). 503–508. 58 indexed citations

Li, Sihan, Ken Ikeuchi, Robert Buschauer, et al.. (2022). Sensing of individual stalled 80S ribosomes by Fap1 for nonfunctional rRNA turnover. Molecular Cell. 82(18). 3424–3437.e8. 27 indexed citations

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

Lei, Jian, Yue Ma‐Lauer, Matthias Thoms, et al.. (2021). The SARS‐unique domain (SUD) of SARS‐CoV and SARS‐CoV‐2 interacts with human Paip1 to enhance viral RNA translation. The EMBO Journal. 40(11). e102277–e102277. 34 indexed citations

10.

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

11.

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

12.

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 →

13.

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

14.

Watanabe, Reika, Robert Buschauer, Jan Böhning, et al.. (2020). The In situ Structure of Parkinson's Disease-Linked LRRK2. Biophysical Journal. 118(3). 486a–486a. 15 indexed citations

15.

Watanabe, Reika, Robert Buschauer, Jan Böhning, et al.. (2020). The In Situ Structure of Parkinson’s Disease-Linked LRRK2. Cell. 182(6). 1508–1518.e16. 144 indexed citations

16.

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

17.

Těšina, Petr, Robert Buschauer, Jingdong Cheng, et al.. (2019). Molecular mechanism of translational stalling by inhibitory codon combinations and poly(A) tracts. The EMBO Journal. 39(3). e103365–e103365. 114 indexed citations

18.

Chaikeeratisak, Vorrapon, Katrina Nguyen, Kanika Khanna, et al.. (2017). Assembly of a nucleus-like structure during viral replication in bacteria. Science. 355(6321). 194–197. 171 indexed citations

19.

Villa, Elizabeth, Reika Watanabe, Robert Buschauer, et al.. (2017). Revealing the Native Molecular Architecture of the Nuclear Periphery using Cryo-Focused-Ion-Beam Milling, Light Microscopy and Electron Tomography. Microscopy and Microanalysis. 23(S1). 1248–1249. 1 indexed citations

20.

Kedrov, Alexej, Stephan Wickles, Álvaro H. Crevenna, et al.. (2016). Structural Dynamics of the YidC:Ribosome Complex during Membrane Protein Biogenesis. Cell Reports. 17(11). 2943–2954. 40 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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