Thomas Preiß

15.1k total citations · 3 hit papers
110 papers, 10.0k citations indexed

About

Thomas Preiß is a scholar working on Molecular Biology, Cancer Research and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Thomas Preiß has authored 110 papers receiving a total of 10.0k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Molecular Biology, 22 papers in Cancer Research and 10 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Thomas Preiß's work include RNA Research and Splicing (64 papers), RNA modifications and cancer (54 papers) and RNA and protein synthesis mechanisms (51 papers). Thomas Preiß is often cited by papers focused on RNA Research and Splicing (64 papers), RNA modifications and cancer (54 papers) and RNA and protein synthesis mechanisms (51 papers). Thomas Preiß collaborates with scholars based in Australia, Germany and United States. Thomas Preiß's co-authors include Matthias W. Hentze, Alfredo Castelló, David T. Humphreys, Thomas Schwarzl, Traude H. Beilharz, Bernd Fischer, Tennille Sibbritt, Nikolay E. Shirokikh, David I. K. Martin and Rastislav Horos and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Thomas Preiß

110 papers receiving 9.9k citations

Hit Papers

Insights into RNA Biology from an Atlas of Mammalian mRNA... 2012 2026 2016 2021 2012 2018 2012 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Preiß Australia 47 9.0k 2.8k 514 486 431 110 10.0k
Pavel Ivanov United States 46 9.1k 1.0× 1.9k 0.7× 333 0.6× 306 0.6× 486 1.1× 107 10.2k
Björn Schwanhäußer Germany 8 7.5k 0.8× 2.9k 1.1× 353 0.7× 135 0.3× 717 1.7× 8 9.4k
Christopher W. J. Smith United Kingdom 44 6.9k 0.8× 843 0.3× 333 0.6× 805 1.7× 334 0.8× 93 7.9k
Tamás Kiss Hungary 44 7.3k 0.8× 1.5k 0.5× 965 1.9× 167 0.3× 272 0.6× 94 8.3k
David R. Corey United States 56 10.2k 1.1× 2.8k 1.0× 280 0.5× 193 0.4× 523 1.2× 172 11.8k
Michael F. Lin United States 12 5.0k 0.6× 3.5k 1.2× 312 0.6× 106 0.2× 293 0.7× 13 6.3k
Tetsuro Hirose Japan 51 7.6k 0.8× 3.5k 1.3× 469 0.9× 88 0.2× 310 0.7× 153 8.9k
Giuseppe Biamonti Italy 47 5.5k 0.6× 688 0.2× 457 0.9× 287 0.6× 263 0.6× 114 6.3k
Guohong Li China 42 6.4k 0.7× 669 0.2× 784 1.5× 217 0.4× 421 1.0× 129 7.4k
Anthony K. L. Leung United States 40 5.6k 0.6× 1.4k 0.5× 362 0.7× 246 0.5× 866 2.0× 81 7.3k

Countries citing papers authored by Thomas Preiß

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Preiß

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Preiß

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Preiß. A scholar is included among the top collaborators of Thomas Preiß 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 Preiß. Thomas Preiß 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.
Völkers, Mirko, Thomas Preiß, & Matthias W. Hentze. (2024). RNA-binding proteins in cardiovascular biology and disease: the beat goes on. Nature Reviews Cardiology. 21(6). 361–378. 21 indexed citations
2.
Guarnacci, Marco & Thomas Preiß. (2024). Theje ne sais quoiof 5-methylcytosine in messenger RNA. RNA. 30(5). 560–569. 2 indexed citations
3.
Guarnacci, Marco, Peihong Zhang, Madhu M. Kanchi, et al.. (2024). Substrate diversity of NSUN enzymes and links of 5-methylcytosine to mRNA translation and turnover. Life Science Alliance. 7(9). e202402613–e202402613. 8 indexed citations
4.
Horváth, Attila, Shafi Mahmud, Alice Cleynen, et al.. (2024). Comprehensive translational profiling and STE AI uncover rapid control of protein biosynthesis during cell stress. Nucleic Acids Research. 52(13). 7925–7946. 1 indexed citations
5.
Wagner, Susan, Jonathan Bohlen, Anna Herrmannová, et al.. (2022). Selective footprinting of 40S and 80S ribosome subpopulations (Sel-TCP-seq) to study translation and its control. Nature Protocols. 17(10). 2139–2187. 11 indexed citations
6.
Pountney, Dean L., et al.. (2021). The Effect of Oxidized Dopamine on the Structure and Molecular Chaperone Function of the Small Heat-Shock Proteins, αB-Crystallin and Hsp27. International Journal of Molecular Sciences. 22(7). 3700–3700. 8 indexed citations
7.
Ragan, Chikako, Gregory J. Goodall, Nikolay E. Shirokikh, & Thomas Preiß. (2019). Insights into the biogenesis and potential functions of exonic circular RNA. Scientific Reports. 9(1). 2048–2048. 108 indexed citations
8.
Preiß, Thomas, et al.. (2019). Control of Translation at the Initiation Phase During Glucose Starvation in Yeast. International Journal of Molecular Sciences. 20(16). 4043–4043. 25 indexed citations
9.
Shirokikh, Nikolay E., et al.. (2019). Migration of Small Ribosomal Subunits on the 5′ Untranslated Regions of Capped Messenger RNA. International Journal of Molecular Sciences. 20(18). 4464–4464. 13 indexed citations
10.
Shirokikh, Nikolay E. & Thomas Preiß. (2018). Translation initiation by cap‐dependent ribosome recruitment: Recent insights and open questions. Wiley Interdisciplinary Reviews - RNA. 9(4). e1473–e1473. 104 indexed citations
11.
Shirokikh, Nikolay E., Stuart K. Archer, Traude H. Beilharz, David Powell, & Thomas Preiß. (2017). Translation complex profile sequencing to study the in vivo dynamics of mRNA–ribosome interactions during translation initiation, elongation and termination. Nature Protocols. 12(4). 697–731. 39 indexed citations
12.
David, Rakesh, Alice Burgess, Brian J. Parker, et al.. (2017). Transcriptome-Wide Mapping of RNA 5-Methylcytosine in Arabidopsis mRNAs and Noncoding RNAs. The Plant Cell. 29(3). 445–460. 181 indexed citations
13.
Patel, Hardip R., David T. Humphreys, M. Evers, et al.. (2016). Role of miRNAs and alternative mRNA 3′-end cleavage and polyadenylation of their mRNA targets in cardiomyocyte hypertrophy. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1859(5). 744–756. 18 indexed citations
14.
Reichel, Marlene, Yalin Liao, Mandy Rettel, et al.. (2016). In Planta Determination of the mRNA-Binding Proteome of Arabidopsis Etiolated Seedlings. The Plant Cell. 28(10). 2435–2452. 138 indexed citations
15.
Srivastava, Monika, Nadia J. Kershaw, Vicki Athanasopoulos, et al.. (2015). Roquin binds microRNA-146a and Argonaute2 to regulate microRNA homeostasis. Nature Communications. 6(1). 6253–6253. 60 indexed citations
16.
Olesen, Morten S., Bo Liang, Anders Peter Larsen, et al.. (2013). TASK-1 potassium channel mutations in atrial fibrillation. European Heart Journal. 34(suppl 1). 3411–3411. 2 indexed citations
17.
Li, Cheryl C. Y., Jennifer E. Cropley, Mark J. Cowley, et al.. (2011). A Sustained Dietary Change Increases Epigenetic Variation in Isogenic Mice. PLoS Genetics. 7(4). e1001380–e1001380. 58 indexed citations
18.
Hentze, Matthias W., Fátima Gebauer, & Thomas Preiß. (2007). Cis-regulatory sequences and trans-acting factors in translation control. Cold Spring Harbor Monograph Archive. 48. 269–295. 22 indexed citations
19.
Westman, Belinda J., Janusz Stȩpiński, Remigiusz Worch, et al.. (2005). The antiviral drug ribavirin does not mimic the 7-methylguanosine moiety of the mRNA cap structure in vitro. RNA. 11(10). 1505–1513. 35 indexed citations
20.
Hemmings-Mieszczak, Maja, Thomas Höhn, & Thomas Preiß. (2000). Termination and Peptide Release at the Upstream Open Reading Frame Are Required for Downstream Translation on Synthetic Shunt-Competent mRNA Leaders. Molecular and Cellular Biology. 20(17). 6212–6223. 22 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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