Tillmann Pape

3.7k total citations
34 papers, 2.8k citations indexed

About

Tillmann Pape is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Tillmann Pape has authored 34 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 15 papers in Genetics and 5 papers in Ecology. Recurrent topics in Tillmann Pape's work include RNA and protein synthesis mechanisms (20 papers), Bacterial Genetics and Biotechnology (14 papers) and RNA modifications and cancer (11 papers). Tillmann Pape is often cited by papers focused on RNA and protein synthesis mechanisms (20 papers), Bacterial Genetics and Biotechnology (14 papers) and RNA modifications and cancer (11 papers). Tillmann Pape collaborates with scholars based in United Kingdom, Germany and Denmark. Tillmann Pape's co-authors include Marin van Heel, Marina V. Rodnina, Ardan Patwardhan, Elena V. Orlova, Rishi Matadeen, Brent Gowen, Wolfgang Wintermeyer, Holger Stark, Dana Cohen and Michael Schätz and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Tillmann Pape

33 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tillmann Pape United Kingdom 27 2.3k 702 284 239 213 34 2.8k
Christos Gatsogiannis Germany 27 1.6k 0.7× 275 0.4× 341 1.2× 207 0.9× 243 1.1× 50 2.7k
Stanley D. Dunn Canada 38 3.8k 1.7× 347 0.5× 290 1.0× 293 1.2× 105 0.5× 89 4.4k
Billy K. Poon United States 16 2.7k 1.2× 379 0.5× 369 1.3× 833 3.5× 279 1.3× 31 3.7k
Christiane Schaffitzel United Kingdom 38 3.9k 1.7× 849 1.2× 74 0.3× 194 0.8× 445 2.1× 90 4.7k
Arne Moeller Germany 23 1.4k 0.6× 210 0.3× 335 1.2× 156 0.7× 95 0.4× 59 2.3k
Shashi Bhushan Singapore 28 2.0k 0.9× 332 0.5× 89 0.3× 135 0.6× 163 0.8× 59 2.4k
Keren Lasker United States 24 2.5k 1.1× 380 0.5× 432 1.5× 639 2.7× 143 0.7× 37 3.1k
Thomas Becker Germany 35 4.2k 1.8× 727 1.0× 198 0.7× 162 0.7× 296 1.4× 62 5.0k
Philippe Ringler Switzerland 27 1.5k 0.7× 478 0.7× 100 0.4× 257 1.1× 257 1.2× 57 2.8k
А.A. Коростелев United States 32 3.4k 1.5× 775 1.1× 148 0.5× 263 1.1× 294 1.4× 60 3.9k

Countries citing papers authored by Tillmann Pape

Since Specialization
Citations

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

Fields of papers citing papers by Tillmann Pape

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tillmann Pape

This figure shows the co-authorship network connecting the top 25 collaborators of Tillmann Pape. A scholar is included among the top collaborators of Tillmann Pape 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 Tillmann Pape. Tillmann Pape 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.
2.
Sofos, Nicholas, et al.. (2024). Conformational landscape of the type V-K CRISPR-associated transposon integration assembly. Molecular Cell. 84(12). 2353–2367.e5. 6 indexed citations
3.
Mestre, Mario Rodríguez, Blanca López‐Méndez, Ivo A. Hendriks, et al.. (2024). Retron-Eco1 assembles NAD+-hydrolyzing filaments that provide immunity against bacteriophages. Molecular Cell. 84(11). 2185–2202.e12. 26 indexed citations
4.
Raj, Isha, et al.. (2023). Structural and mechanistic basis of substrate transport by the multidrug transporter MRP4. Structure. 31(11). 1407–1418.e6. 15 indexed citations
5.
Fuglsang, Anders, Tillmann Pape, Nicholas Sofos, et al.. (2021). Structure of the mini-RNA-guided endonuclease CRISPR-Cas12j3. Nature Communications. 12(1). 4476–4476. 35 indexed citations
6.
Sofos, Nicholas, Mingxia Feng, Stefano Stella, et al.. (2020). Structures of the Cmr-β Complex Reveal the Regulation of the Immunity Mechanism of Type III-B CRISPR-Cas. Molecular Cell. 79(5). 741–757.e7. 43 indexed citations
7.
Fusco, Giuliana, Tillmann Pape, Amberley D. Stephens, et al.. (2016). Structural basis of synaptic vesicle assembly promoted by α-synuclein. Nature Communications. 7(1). 12563–12563. 199 indexed citations
8.
Lossi, Nadine, Eleni Manoli, Andreas Förster, et al.. (2013). The HsiB1C1 (TssB-TssC) Complex of the Pseudomonas aeruginosa Type VI Secretion System Forms a Bacteriophage Tail Sheathlike Structure. Journal of Biological Chemistry. 288(11). 7536–7548. 67 indexed citations
9.
Pagliano, Cristina, Jon Nield, Francesco Marsano, et al.. (2013). Proteomic characterization and three-dimensional electron microscopy study of PSII–LHCII supercomplexes from higher plants. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1837(9). 1454–1462. 31 indexed citations
10.
Garnett, James A., Verónica I. Martínez-Santos, Zeus Saldaña‐Ahuactzi, et al.. (2012). Structural insights into the biogenesis and biofilm formation by the Escherichia coli common pilus. Proceedings of the National Academy of Sciences. 109(10). 3950–3955. 58 indexed citations
11.
Bose, Daniel, Tillmann Pape, Patricia C. Burrows, et al.. (2008). Organization of an Activator-Bound RNA Polymerase Holoenzyme. Molecular Cell. 32(3). 337–346. 62 indexed citations
12.
Wigneshweraraj, Sivaramesh, Daniel Bose, Patricia C. Burrows, et al.. (2008). Modus operandi of the bacterial RNA polymerase containing the σ54 promoter‐specificity factor. Molecular Microbiology. 68(3). 538–546. 97 indexed citations
13.
Costa, Alessandro, Tillmann Pape, Marin van Heel, et al.. (2006). Structural studies of the archaeal MCM complex in different functional states. Journal of Structural Biology. 156(1). 210–219. 44 indexed citations
14.
Pape, Tillmann, et al.. (2003). Hexameric ring structure of the full-length archaeal MCM protein complex. EMBO Reports. 4(11). 1079–1083. 40 indexed citations
15.
Pape, Tillmann, et al.. (2003). Hexameric ring structure of the full‐length archaeal MCM protein complex. EMBO Reports. 4(11). 1079–1083. 105 indexed citations
16.
Matadeen, Rishi, Петр В. Сергиев, Tillmann Pape, et al.. (2001). Direct localization by cryo-electron microscopy of secondary structural elements in Escherichia coli 23 S rRNA which differ from the corresponding regions in Haloarcula marismortui11Edited by D. E. Draper. Journal of Molecular Biology. 307(5). 1341–1349. 9 indexed citations
17.
Heel, Marin van, Brent Gowen, Rishi Matadeen, et al.. (2000). Single-particle electron cryo-microscopy: towards atomic resolution. Quarterly Reviews of Biophysics. 33(4). 307–369. 444 indexed citations
18.
Pape, Tillmann. (1999). Induced fit in initial selection and proofreading of aminoacyl-tRNA on the ribosome. The EMBO Journal. 18(13). 3800–3807. 263 indexed citations
19.
Pape, Tillmann. (1998). Complete kinetic mechanism of elongation factor Tu-dependent binding of aminoacyl-tRNA to the A site of the E.coli ribosome. The EMBO Journal. 17(24). 7490–7497. 305 indexed citations
20.
Rodnina, Marina V., et al.. (1995). Elongation factor Tu, a GTPase triggered by codon recognition on the ribosome: mechanism and GTP consumption. Biochemistry and Cell Biology. 73(11-12). 1221–1227. 29 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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