Stefan L. Ameres

6.7k total citations · 1 hit paper
40 papers, 4.5k citations indexed

About

Stefan L. Ameres is a scholar working on Molecular Biology, Cancer Research and Immunology. According to data from OpenAlex, Stefan L. Ameres has authored 40 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 18 papers in Cancer Research and 2 papers in Immunology. Recurrent topics in Stefan L. Ameres's work include RNA modifications and cancer (25 papers), RNA Research and Splicing (20 papers) and MicroRNA in disease regulation (16 papers). Stefan L. Ameres is often cited by papers focused on RNA modifications and cancer (25 papers), RNA Research and Splicing (20 papers) and MicroRNA in disease regulation (16 papers). Stefan L. Ameres collaborates with scholars based in Austria, United States and United Kingdom. Stefan L. Ameres's co-authors include Phillip D. Zamore, Javier Martı̂nez, Renée Schroeder, Veronika A. Herzog, Jui‐Hung Hung, Zhiping Weng, Brian Reichholf, Jia Xu, Stephanie Kueng and Tobias Neumann and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Stefan L. Ameres

40 papers receiving 4.4k citations

Hit Papers

Diversifying microRNA sequence and function 2013 2026 2017 2021 2013 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefan L. Ameres Austria 23 3.9k 1.9k 515 308 228 40 4.5k
Charles E. Vejnar United States 23 3.0k 0.8× 1.1k 0.6× 274 0.5× 416 1.4× 242 1.1× 33 3.6k
Łukasz Jaśkiewicz Switzerland 15 2.8k 0.7× 1.5k 0.8× 378 0.7× 185 0.6× 200 0.9× 32 3.2k
Sihem Cheloufi United States 16 4.0k 1.0× 2.1k 1.1× 502 1.0× 251 0.8× 293 1.3× 24 4.5k
Alena Shkumatava France 19 3.2k 0.8× 1.6k 0.8× 381 0.7× 416 1.4× 162 0.7× 29 3.7k
Ligang Wu China 28 3.9k 1.0× 2.2k 1.1× 394 0.8× 274 0.9× 321 1.4× 75 4.7k
Michael Basson United States 8 3.7k 1.0× 3.0k 1.5× 451 0.9× 223 0.7× 250 1.1× 16 4.9k
Eilon Sharon Israel 17 3.2k 0.8× 1.6k 0.8× 316 0.6× 429 1.4× 265 1.2× 22 3.8k
Shobha Vasudevan United States 20 3.8k 1.0× 2.8k 1.4× 194 0.4× 274 0.9× 319 1.4× 32 4.6k
Martin J. Simard Canada 29 3.7k 1.0× 1.9k 1.0× 725 1.4× 185 0.6× 306 1.3× 59 4.6k
Oliver H. Tam United States 13 2.4k 0.6× 895 0.5× 740 1.4× 270 0.9× 129 0.6× 20 2.7k

Countries citing papers authored by Stefan L. Ameres

Since Specialization
Citations

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

Fields of papers citing papers by Stefan L. Ameres

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stefan L. Ameres. 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 Stefan L. Ameres. The network helps show where Stefan L. Ameres may publish in the future.

Co-authorship network of co-authors of Stefan L. Ameres

This figure shows the co-authorship network connecting the top 25 collaborators of Stefan L. Ameres. A scholar is included among the top collaborators of Stefan L. Ameres 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 Stefan L. Ameres. Stefan L. Ameres 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.
Faraway, Rupert, Oscar G. Wilkins, Anob M. Chakrabarti, et al.. (2025). Collective homeostasis of condensation-prone proteins via their mRNAs. Nature. 647(8090). 798–808. 1 indexed citations
2.
Loubière, Vincent, Ramesh Yelagandula, Michaela Pagani, et al.. (2024). Proteome-scale tagging and functional screening in mammalian cells by ORFtag. Nature Methods. 21(9). 1668–1673. 4 indexed citations
3.
Popitsch, Niko, et al.. (2021). Transcriptome-Wide Profiling of RNA Stability. Methods in molecular biology. 2404. 311–330. 3 indexed citations
4.
Gasser, Catherina, Zsuzsanna Takács, Christoph C. H. Langer, et al.. (2020). Conformation of sister chromatids in the replicated human genome. Nature. 586(7827). 139–144. 66 indexed citations
5.
Herzog, Veronika A., Tobias Neumann, Katharina Gapp, et al.. (2019). Sequencing cell-type-specific transcriptomes with SLAM-ITseq. Nature Protocols. 14(8). 2261–2278. 16 indexed citations
6.
Reichholf, Brian, et al.. (2019). Time-Resolved Small RNA Sequencing Unravels the Molecular Principles of MicroRNA Homeostasis. Molecular Cell. 75(4). 756–768.e7. 114 indexed citations
7.
Herzog, Veronika A., et al.. (2019). Determining mRNA Stability by Metabolic RNA Labeling and Chemical Nucleoside Conversion. Methods in molecular biology. 2062. 169–189. 8 indexed citations
8.
Muhar, Matthias, Anja Ebert, Tobias Neumann, et al.. (2018). SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis. Science. 360(6390). 800–805. 237 indexed citations
9.
Herzog, Veronika A., Tobias Neumann, Katharina Gapp, et al.. (2018). SLAM-ITseq: Sequencing cell type-specific transcriptomes without cell sorting. Development. 145(13). 29 indexed citations
10.
Ameres, Stefan L., et al.. (2018). Structural basis for acceptor RNA substrate selectivity of the 3′ terminal uridylyl transferase Tailor. Nucleic Acids Research. 47(2). 1030–1042. 14 indexed citations
11.
Alberti, Chiara, et al.. (2018). Cell-type specific sequencing of microRNAs from complex animal tissues. Nature Methods. 15(4). 283–289. 64 indexed citations
12.
Herzog, Veronika A., Brian Reichholf, Tobias Neumann, et al.. (2017). Thiol-linked alkylation of RNA to assess expression dynamics. Nature Methods. 14(12). 1198–1204. 358 indexed citations
13.
Burkard, Thomas R., et al.. (2016). Molecular basis for cytoplasmic RNA surveillance by uridylation‐triggered decay in Drosophila. The EMBO Journal. 35(22). 2417–2434. 42 indexed citations
14.
Herzog, Veronika A. & Stefan L. Ameres. (2015). Approaching the Golden Fleece a Molecule at a Time: Biophysical Insights into Argonaute-Instructed Nucleic Acid Interactions. Molecular Cell. 59(1). 4–7. 8 indexed citations
15.
Bortolamiol-Bécet, Diane, Fuqu Hu, David Jee, et al.. (2015). Selective Suppression of the Splicing-Mediated MicroRNA Pathway by the Terminal Uridyltransferase Tailor. Molecular Cell. 59(2). 217–228. 53 indexed citations
16.
Han, Bo, Jui‐Hung Hung, Zhiping Weng, Phillip D. Zamore, & Stefan L. Ameres. (2011). The 3′-to-5′ Exoribonuclease Nibbler Shapes the 3′ Ends of MicroRNAs Bound to Drosophila Argonaute1. Current Biology. 21(22). 1878–1887. 132 indexed citations
17.
Ameres, Stefan L., Michael D. Horwich, Jui‐Hung Hung, et al.. (2010). Target RNA–Directed Trimming and Tailing of Small Silencing RNAs. Science. 328(5985). 1534–1539. 461 indexed citations
18.
Xie, Jun, Qing Xie, Hongwei Zhang, et al.. (2010). MicroRNA-regulated, Systemically Delivered rAAV9: A Step Closer to CNS-restricted Transgene Expression. Molecular Therapy. 19(3). 526–535. 133 indexed citations
19.
Tafer, Hakim, Stefan L. Ameres, Gregor Obernosterer, et al.. (2008). The impact of target site accessibility on the design of effective siRNAs. Nature Biotechnology. 26(5). 578–583. 226 indexed citations
20.
Ameres, Stefan L., et al.. (2006). Cleavage of the siRNA passenger strand during RISC assembly in human cells. EMBO Reports. 7(3). 314–320. 299 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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