Beatrix Suess

5.0k total citations
115 papers, 3.9k citations indexed

About

Beatrix Suess is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Beatrix Suess has authored 115 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 108 papers in Molecular Biology, 16 papers in Genetics and 10 papers in Cancer Research. Recurrent topics in Beatrix Suess's work include RNA and protein synthesis mechanisms (84 papers), Advanced biosensing and bioanalysis techniques (46 papers) and RNA modifications and cancer (32 papers). Beatrix Suess is often cited by papers focused on RNA and protein synthesis mechanisms (84 papers), Advanced biosensing and bioanalysis techniques (46 papers) and RNA modifications and cancer (32 papers). Beatrix Suess collaborates with scholars based in Germany, Sweden and United Kingdom. Beatrix Suess's co-authors include Julia E. Weigand, Florian Groher, Christian Berens, Marc Vogel, Dieter Steinhilber, Jens Wöhnert, Amit Arora, Elke Duchardt‐Ferner, Manuel Grez and Martin Rudolph and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Beatrix Suess

111 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Beatrix Suess Germany 38 3.4k 635 275 265 209 115 3.9k
M.P. Coles Germany 29 2.6k 0.8× 522 0.8× 64 0.2× 387 1.5× 185 0.9× 66 3.3k
Nathan W. Luedtke Switzerland 36 3.1k 0.9× 198 0.3× 183 0.7× 378 1.4× 147 0.7× 92 3.7k
Tomasz Heyduk United States 36 3.1k 0.9× 1.3k 2.0× 319 1.2× 355 1.3× 680 3.3× 87 3.7k
Ming‐Qun Xu United States 35 4.1k 1.2× 422 0.7× 148 0.5× 236 0.9× 451 2.2× 69 4.6k
Jörg S. Hartig Germany 34 3.9k 1.1× 446 0.7× 422 1.5× 301 1.1× 248 1.2× 114 4.3k
Christian Heinis Switzerland 37 4.3k 1.3× 92 0.1× 241 0.9× 257 1.0× 171 0.8× 99 5.5k
Marjeta Urh United States 24 3.0k 0.9× 280 0.4× 225 0.8× 210 0.8× 123 0.6× 51 3.8k
Chang C. Liu United States 23 2.7k 0.8× 500 0.8× 173 0.6× 156 0.6× 153 0.7× 49 3.2k
Kensaku Sakamoto Japan 36 3.8k 1.1× 655 1.0× 99 0.4× 209 0.8× 201 1.0× 101 4.2k
Jean‐Jacques Toulmé France 39 4.5k 1.3× 322 0.5× 320 1.2× 168 0.6× 379 1.8× 156 5.1k

Countries citing papers authored by Beatrix Suess

Since Specialization
Citations

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

Fields of papers citing papers by Beatrix Suess

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beatrix Suess

This figure shows the co-authorship network connecting the top 25 collaborators of Beatrix Suess. A scholar is included among the top collaborators of Beatrix Suess 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 Beatrix Suess. Beatrix Suess 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.
Steinhilber, Dieter, et al.. (2025). Control of ALOX5 expression in monocytic cells using a synthetic riboswitch. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1870(7). 159671–159671. 1 indexed citations
3.
Wang, Tianhe, et al.. (2025). Beyond the niche - unlocking the full potential of synthetic riboswitches. Nature Communications. 16(1). 9897–9897.
4.
Duchardt‐Ferner, Elke, et al.. (2025). Structural basis for ligand recognition in the tobramycin riboswitch. Nucleic Acids Research. 53(16).
5.
Martinez, Andres W., et al.. (2025). Triple SELEX approach for the selection of a highly specific RNA aptamer binding homoeriodictyol. Biological Chemistry. 406(8-9). 349–362.
6.
Suess, Beatrix, et al.. (2023). Tapping the potential of synthetic riboswitches: reviewing the versatility of the tetracycline aptamer. RNA Biology. 20(1). 457–468. 9 indexed citations
7.
Duchardt‐Ferner, Elke, et al.. (2023). Development of a novel tobramycin dependent riboswitch. Nucleic Acids Research. 51(20). 11375–11385. 10 indexed citations
8.
Vogel, Marc, Bettina Appel, Julia E. Weigand, et al.. (2023). Magnesium Ion-Driven Folding and Conformational Switching Kinetics of Tetracycline Binding Aptamer: Implications for in vivo Riboswitch Engineering. Journal of Molecular Biology. 435(20). 168253–168253. 5 indexed citations
10.
Vogel, Marc, et al.. (2020). Inducible nuclear import by TetR aptamer-controlled 3′ splice site selection. RNA. 27(2). 234–241. 3 indexed citations
11.
Ohuchi, Shoji & Beatrix Suess. (2017). Altered stoichiometry of an evolved RNA aptamer. RNA. 24(4). 480–485. 2 indexed citations
12.
Kaushik, Monu, et al.. (2015). Dynamic nuclear polarization of nucleic acid with endogenously bound manganese. Journal of Biomolecular NMR. 63(1). 97–109. 54 indexed citations
13.
Duchardt‐Ferner, Elke, Florian Groher, Julia E. Weigand, et al.. (2014). Building a stable RNA U-turn with a protonated cytidine. RNA. 20(8). 1163–1172. 22 indexed citations
14.
Suess, Beatrix, et al.. (2011). Selection of tetracycline inducible self-cleaving ribozymes as synthetic devices for gene regulation in yeast. Molecular BioSystems. 7(8). 2419–2427. 66 indexed citations
15.
Weigand, Julia E., et al.. (2011). Conformational dynamics of the tetracycline-binding aptamer. Nucleic Acids Research. 40(4). 1807–1817. 46 indexed citations
16.
Mayer, Günter, Marcus Klotzsche, Michael Blind, et al.. (2009). An RNA Aptamer that Induces Transcription. Chemistry & Biology. 16(2). 173–180. 47 indexed citations
17.
Weigand, Julia E., et al.. (2007). Screening for engineered neomycin riboswitches that control translation initiation. RNA. 14(1). 89–97. 173 indexed citations
18.
Weigand, Julia E. & Beatrix Suess. (2007). Tetracycline aptamer-controlled regulation of pre-mRNA splicing in yeast. Nucleic Acids Research. 35(12). 4179–4185. 102 indexed citations
19.
Fink, Barbara, et al.. (2005). Molecular analysis of a synthetic tetracycline-binding riboswitch. RNA. 11(4). 503–511. 58 indexed citations
20.
Berthelot, Karine, et al.. (2003). Tetracycline‐aptamer‐mediated translational regulation in yeast. Molecular Microbiology. 49(6). 1627–1637. 93 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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