Witold Filipowicz

36.2k total citations · 11 hit papers
162 papers, 28.9k citations indexed

About

Witold Filipowicz is a scholar working on Molecular Biology, Plant Science and Cancer Research. According to data from OpenAlex, Witold Filipowicz has authored 162 papers receiving a total of 28.9k indexed citations (citations by other indexed papers that have themselves been cited), including 141 papers in Molecular Biology, 42 papers in Plant Science and 37 papers in Cancer Research. Recurrent topics in Witold Filipowicz's work include RNA Research and Splicing (77 papers), RNA modifications and cancer (72 papers) and RNA and protein synthesis mechanisms (64 papers). Witold Filipowicz is often cited by papers focused on RNA Research and Splicing (77 papers), RNA modifications and cancer (72 papers) and RNA and protein synthesis mechanisms (64 papers). Witold Filipowicz collaborates with scholars based in Switzerland, United States and Poland. Witold Filipowicz's co-authors include Nahum Sonenberg, Suvendra N. Bhattacharyya, Jacek Król, Inga Loedige, Marc R. Fabian, Ramesh S. Pillai, Łukasz Jaśkiewicz, Gregory J. Goodall, Marina Chekulaeva and Tamás Kiss and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Witold Filipowicz

162 papers receiving 28.4k citations

Hit Papers

Mechanisms of post-transc... 2004 2026 2011 2018 2008 2010 2010 2005 2006 1000 2.0k 3.0k 4.0k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Witold Filipowicz 23.8k 14.4k 3.2k 1.9k 1.3k 162 28.9k
Victor Ambros 31.8k 1.3× 25.2k 1.8× 4.0k 1.3× 2.2k 1.2× 1.9k 1.5× 107 42.0k
Mihaela Zavolan 16.5k 0.7× 9.1k 0.6× 1.8k 0.6× 1.2k 0.6× 929 0.7× 141 19.7k
Joshua T. Mendell 26.4k 1.1× 20.3k 1.4× 3.3k 1.0× 2.3k 1.2× 1.9k 1.5× 90 34.4k
Sakari Kauppinen 14.1k 0.6× 12.2k 0.8× 1.3k 0.4× 1.1k 0.6× 634 0.5× 112 18.7k
V. Narry Kim 23.0k 1.0× 16.8k 1.2× 2.4k 0.7× 1.9k 1.0× 1.1k 0.9× 92 28.3k
Christopher B. Burge 33.4k 1.4× 16.7k 1.2× 3.4k 1.1× 2.1k 1.1× 2.4k 1.9× 119 39.7k
Scott M. Hammond 24.3k 1.0× 15.0k 1.0× 2.7k 0.9× 1.8k 0.9× 1.9k 1.5× 72 28.8k
Michael T. McManus 15.4k 0.6× 8.2k 0.6× 1.7k 0.6× 2.0k 1.1× 2.1k 1.7× 202 20.9k
Lee P. Lim 17.8k 0.7× 14.2k 1.0× 2.6k 0.8× 1.1k 0.6× 958 0.8× 47 21.6k
Sam Griffiths‐Jones 23.2k 1.0× 16.9k 1.2× 5.3k 1.7× 1.7k 0.9× 1.8k 1.4× 78 30.4k

Countries citing papers authored by Witold Filipowicz

Since Specialization
Citations

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

Fields of papers citing papers by Witold Filipowicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Witold Filipowicz

This figure shows the co-authorship network connecting the top 25 collaborators of Witold Filipowicz. A scholar is included among the top collaborators of Witold Filipowicz 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 Witold Filipowicz. Witold Filipowicz 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.
Calviello, Lorenzo, Srivats Venkataramanan, Emanuel Wyler, et al.. (2021). DDX3 depletion represses translation of mRNAs with complex 5′ UTRs. Nucleic Acids Research. 49(9). 5336–5350. 71 indexed citations
2.
Filipowicz, Witold & Nahum Sonenberg. (2015). The long unfinished march towards understanding microRNA-mediated repression. RNA. 21(4). 519–524. 19 indexed citations
3.
Busskamp, Volker, Jacek Król, Tamás Szikra, et al.. (2014). miRNAs 182 and 183 Are Necessary to Maintain Adult Cone Photoreceptor Outer Segments and Visual Function. Neuron. 83(3). 586–600. 110 indexed citations
4.
Doyle, Michael, Lukas Badertscher, Łukasz Jaśkiewicz, et al.. (2013). The double-stranded RNA binding domain of human Dicer functions as a nuclear localization signal. RNA. 19(9). 1238–1252. 74 indexed citations
5.
Król, Jacek, Volker Busskamp, Michael Stadler, et al.. (2010). Characterizing Light-Regulated Retinal MicroRNAs Reveals Rapid Turnover as a Common Property of Neuronal MicroRNAs. Cell. 141(4). 618–631. 391 indexed citations
6.
Chekulaeva, Marina, Witold Filipowicz, & Roy Parker. (2009). Multiple independent domains of dGW182 function in miRNA-mediated repression in Drosophila. RNA. 15(5). 794–803. 61 indexed citations
7.
Bhattacharyya, Sankar, et al.. (2009). Importance of the C-terminal domain of the human GW182 protein TNRC6C for translational repression. RNA. 15(5). 781–793. 109 indexed citations
8.
Sinnreich, Magdalena Filipowicz, Edward J. Oakeley, François H.T. Duong, et al.. (2008). Interferon signaling and treatment outcome in chronic hepatitis C. Proceedings of the National Academy of Sciences. 105(19). 7034–7039. 520 indexed citations breakdown →
9.
Sinnreich, Magdalena Filipowicz, Verena Christen, François H.T. Duong, et al.. (2008). 9 INTERFERON REGULATED GENE EXPRESSION IN THE LIVER DETERMINES RESPONSE TO TREATMENT IN CHRONIC HEPATITIS C. Journal of Hepatology. 48. S6–S6. 1 indexed citations
10.
Mathonnet, Géraldine, Marc R. Fabian, Yuri V. Svitkin, et al.. (2007). MicroRNA Inhibition of Translation Initiation in Vitro by Targeting the Cap-Binding Complex eIF4F. Science. 317(5845). 1764–1767. 403 indexed citations
11.
Kotaja, Noora, Suvendra N. Bhattacharyya, Łukasz Jaśkiewicz, et al.. (2006). The chromatoid body of male germ cells: Similarity with processing bodies and presence of Dicer and microRNA pathway components. Proceedings of the National Academy of Sciences. 103(8). 2647–2652. 283 indexed citations
12.
Bhattacharyya, Suvendra N., et al.. (2006). Relief of microRNA-Mediated Translational Repression in Human Cells Subjected to Stress. Cell. 125(6). 1111–1124. 1033 indexed citations breakdown →
13.
Haase, Astrid D., Łukasz Jaśkiewicz, Haidi Zhang, et al.. (2005). TRBP, a regulator of cellular PKR and HIV‐1 virus expression, interacts with Dicer and functions in RNA silencing. EMBO Reports. 6(10). 961–967. 517 indexed citations breakdown →
14.
Pillai, Ramesh S., Suvendra N. Bhattacharyya, Nicolas Cougot, et al.. (2005). Inhibition of Translational Initiation by Let-7 MicroRNA in Human Cells. Science. 309(5740). 1573–1576. 1077 indexed citations breakdown →
15.
Filipowicz, Witold. (2005). RNAi: The Nuts and Bolts of the RISC Machine. Cell. 122(1). 17–20. 391 indexed citations
16.
Jaśkiewicz, Łukasz, et al.. (2005). ATP modulates siRNA interactions with an endogenous human Dicer complex. RNA. 11(11). 1719–1724. 17 indexed citations
17.
Pillai, Ramesh S., et al.. (2004). Tethering of human Ago proteins to mRNA mimics the miRNA-mediated repression of protein synthesis. RNA. 10(10). 1518–1525. 297 indexed citations
18.
Lambermon, Mark H. L., et al.. (2002). UBA1 and UBA2, Two Proteins That Interact with UBP1, a Multifunctional Effector of Pre-mRNA Maturation in Plants. Molecular and Cellular Biology. 22(12). 4346–4357. 68 indexed citations
19.
Dragon, François, Vanda Pogačić, & Witold Filipowicz. (2000). In Vitro Assembly of Human H/ACA Small Nucleolar RNPs Reveals Unique Features of U17 and Telomerase RNAs. Molecular and Cellular Biology. 20(9). 3037–3048. 138 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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