Egon Ogris

4.6k total citations · 1 hit paper
50 papers, 3.6k citations indexed

About

Egon Ogris is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Egon Ogris has authored 50 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 13 papers in Oncology and 12 papers in Cell Biology. Recurrent topics in Egon Ogris's work include Polyomavirus and related diseases (8 papers), Fungal and yeast genetics research (7 papers) and Virus-based gene therapy research (6 papers). Egon Ogris is often cited by papers focused on Polyomavirus and related diseases (8 papers), Fungal and yeast genetics research (7 papers) and Virus-based gene therapy research (6 papers). Egon Ogris collaborates with scholars based in Austria, United States and Germany. Egon Ogris's co-authors include Ingrid Mudrak, Estelle Sontag, David C. Pallas, Charles L. White, Stefan Schüchner, Viyada Nunbhakdi‐Craig, Erhard Wintersberger, Sascha Martens, Claudine Kraft and Julia Romanov and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Egon Ogris

50 papers receiving 3.6k citations

Hit Papers

Mechanism and functions of membrane binding by the Atg5–A... 2012 2026 2016 2021 2012 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Egon Ogris Austria 28 2.6k 893 565 402 401 50 3.6k
Nicholas A. Morrice United Kingdom 36 3.3k 1.3× 653 0.7× 657 1.2× 316 0.8× 335 0.8× 64 4.2k
Marcus B. Smolka United States 36 3.1k 1.2× 968 1.1× 469 0.8× 311 0.8× 312 0.8× 82 4.1k
Toshiaki Suzuki Japan 27 2.6k 1.0× 1.0k 1.2× 571 1.0× 460 1.1× 746 1.9× 69 4.3k
Thomas Baumruker Austria 40 4.9k 1.9× 1.0k 1.2× 569 1.0× 734 1.8× 251 0.6× 75 6.6k
Martin Steger Germany 17 1.8k 0.7× 782 0.9× 408 0.7× 517 1.3× 217 0.5× 24 3.0k
William F. Matter United States 14 3.1k 1.2× 542 0.6× 689 1.2× 372 0.9× 255 0.6× 19 4.5k
Monique Beullens Belgium 47 4.9k 1.9× 1.3k 1.5× 521 0.9× 407 1.0× 220 0.5× 104 6.0k
Matthew Jarpe United States 27 4.0k 1.6× 530 0.6× 1.1k 1.9× 595 1.5× 219 0.5× 47 5.5k
Hilary McLauchlan United Kingdom 13 3.2k 1.3× 821 0.9× 775 1.4× 441 1.1× 209 0.5× 16 4.6k
Arthur Edelman United States 19 3.6k 1.4× 544 0.6× 311 0.6× 539 1.3× 413 1.0× 25 4.4k

Countries citing papers authored by Egon Ogris

Since Specialization
Citations

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

Fields of papers citing papers by Egon Ogris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Egon Ogris

This figure shows the co-authorship network connecting the top 25 collaborators of Egon Ogris. A scholar is included among the top collaborators of Egon Ogris 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 Egon Ogris. Egon Ogris 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.
Hollenstein, David M., Natalie Romanov, Egon Ogris, et al.. (2022). PP2ARts1 antagonizes Rck2-mediated hyperosmotic stress signaling in yeast. Microbiological Research. 260. 127031–127031. 1 indexed citations
2.
Hochstoeger, Tobias, E. Pascal Malkemper, William D. Snider, et al.. (2021). The expression, localisation and interactome of pigeon CRY2. Scientific Reports. 11(1). 20293–20293. 8 indexed citations
3.
Schüchner, Stefan, Christian Behm, Ingrid Mudrak, & Egon Ogris. (2020). The Myc tag monoclonal antibody 9E10 displays highly variable epitope recognition dependent on neighboring sequence context. Science Signaling. 13(616). 21 indexed citations
4.
5.
Léonard, Daniel, Wei Huang, Sudeh Izadmehr, et al.. (2020). Selective PP2A Enhancement through Biased Heterotrimer Stabilization. Cell. 181(3). 688–701.e16. 116 indexed citations
6.
Itahana, Yoko, Masahiro Fukuda, H. Shawn Je, et al.. (2018). Ca 2+ -dependent demethylation of phosphatase PP2Ac promotes glucose deprivation–induced cell death independently of inhibiting glycolysis. Science Signaling. 11(512). 23 indexed citations
7.
Usui, Tatsuya, et al.. (2015). Protein Phosphatase Methyl-Esterase PME-1 Protects Protein Phosphatase 2A from Ubiquitin/Proteasome Degradation. PLoS ONE. 10(12). e0145226–e0145226. 31 indexed citations
8.
Romanov, Julia, Marta Walczak, Stefan Schüchner, et al.. (2012). Mechanism and functions of membrane binding by the Atg5–Atg12/Atg16 complex during autophagosome formation. The EMBO Journal. 31(22). 4304–4317. 371 indexed citations breakdown →
9.
Zuzuarregui, Aurora, Ilse Dohnal, Ingrid Mudrak, et al.. (2012). M-Track: detecting short-lived protein-protein interactions in vivo. Nature Methods. 9(6). 594–596. 27 indexed citations
10.
Sontag, Jean‐Marie, et al.. (2010). Regulation of protein phosphatase 2A methylation by LCMT1 and PME‐1 plays a critical role in differentiation of neuroblastoma cells. Journal of Neurochemistry. 115(6). 1455–1465. 47 indexed citations
11.
Riedel, Christian G., V.L. Katis, Yuki Katou, et al.. (2006). Protein phosphatase 2A protects centromeric sister chromatid cohesion during meiosis I. Nature. 441(7089). 53–61. 365 indexed citations
12.
Milojević, Tetyana, Veronika Reiterer, Eduard Stefan, et al.. (2005). The Ubiquitin-Specific Protease Usp4 Regulates the Cell Surface Level of the A2a Receptor. Molecular Pharmacology. 69(4). 1083–1094. 108 indexed citations
13.
Sontag, Estelle, Ampa Luangpirom, Christa L. Hladik, et al.. (2004). Altered Expression Levels of the Protein Phosphatase 2A ABαC Enzyme Are Associated with Alzheimer Disease Pathology. Journal of Neuropathology & Experimental Neurology. 63(4). 287–301. 205 indexed citations
14.
Sontag, Estelle, Christa L. Hladik, Lisa Montgomery, et al.. (2004). Downregulation of Protein Phosphatase 2A Carboxyl Methylation and Methyltransferase May Contribute to Alzheimer Disease Pathogenesis. Journal of Neuropathology & Experimental Neurology. 63(10). 1080–1091. 155 indexed citations
15.
Yeong, Foong May, Hans Hombauer, Kerstin S. Wendt, et al.. (2003). Identification of a Subunit of a Novel Kleisin-β/SMC Complex as a Potential Substrate of Protein Phosphatase 2A. Current Biology. 13(23). 2058–2064. 81 indexed citations
16.
Fellner, Thomas, et al.. (2003). A novel and essential mechanism determining specificity and activity of protein phosphatase 2A (PP2A) in vivo. Genes & Development. 17(17). 2138–2150. 87 indexed citations
17.
Wei, Huijun, Danita G. Ashby, Carlos S. Moreno, et al.. (2001). Carboxymethylation of the PP2A Catalytic Subunit in Saccharomyces cerevisiae Is Required for Efficient Interaction with the B-type Subunits Cdc55p and Rts1p. Journal of Biological Chemistry. 276(2). 1570–1577. 116 indexed citations
19.
Mudrak, Ingrid, Egon Ogris, Hans Rotheneder, & Erhard Wintersberger. (1994). Coordinated trans Activation of DNA Synthesis- and Precursor-Producing Enzymes by Polyomavirus Large T Antigen through Interaction with the Retinoblastoma Protein. Molecular and Cellular Biology. 14(3). 1886–1892. 18 indexed citations
20.
Sochor, Heinz, et al.. (1986). Infarct imaging with monoclonal antimyosin and 99m Tc-pyrophosphate (PYP). 25(4). 1 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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