Anne E. Willis

15.5k total citations · 4 hit papers
158 papers, 11.3k citations indexed

About

Anne E. Willis is a scholar working on Molecular Biology, Oncology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Anne E. Willis has authored 158 papers receiving a total of 11.3k indexed citations (citations by other indexed papers that have themselves been cited), including 128 papers in Molecular Biology, 23 papers in Oncology and 22 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Anne E. Willis's work include RNA and protein synthesis mechanisms (68 papers), RNA Research and Splicing (57 papers) and RNA modifications and cancer (39 papers). Anne E. Willis is often cited by papers focused on RNA and protein synthesis mechanisms (68 papers), RNA Research and Splicing (57 papers) and RNA modifications and cancer (39 papers). Anne E. Willis collaborates with scholars based in United Kingdom, United States and Italy. Anne E. Willis's co-authors include Martin Bushell, Keith A. Spriggs, Mark Stoneley, Sally A. Mitchell, Becky M. Pickering, Mark J. Coldwell, Richard N. Perham, John Le Quesne, Tomas Lindahl and Giovanna R. Mallucci and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Anne E. Willis

155 papers receiving 11.2k citations

Hit Papers

Translational Regulation ... 2010 2026 2015 2020 2010 2012 2013 2023 100 200 300 400 500

Author Peers

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

Author Last Decade Papers Cites
Anne E. Willis 8.9k 1.5k 1.1k 1.1k 926 158 11.3k
Sylvain Meloche 7.3k 0.8× 1.3k 0.8× 1.2k 1.1× 1.1k 1.0× 1.9k 2.1× 151 10.6k
Todd Evans 9.0k 1.0× 721 0.5× 717 0.6× 1.2k 1.1× 784 0.8× 161 11.7k
Lorenzo Silengo 5.6k 0.6× 832 0.5× 565 0.5× 2.0k 1.8× 895 1.0× 145 9.1k
Ye‐Guang Chen 8.8k 1.0× 1.4k 0.9× 387 0.3× 1.3k 1.2× 2.2k 2.4× 178 12.2k
Angela Bachi 7.4k 0.8× 983 0.6× 281 0.2× 1.1k 1.0× 1.1k 1.1× 200 11.2k
Raija Sormunen 5.3k 0.6× 1.7k 1.1× 300 0.3× 1.0k 0.9× 891 1.0× 177 9.0k
James F. Collawn 4.0k 0.5× 1.1k 0.7× 367 0.3× 1.7k 1.5× 406 0.4× 144 7.6k
Fiorella Altruda 5.1k 0.6× 577 0.4× 628 0.6× 1.7k 1.5× 822 0.9× 156 9.0k
Gordon Campbell 3.9k 0.4× 1.2k 0.8× 1.6k 1.4× 1.1k 1.0× 587 0.6× 162 11.0k
Masafumi Tsujimoto 6.8k 0.8× 1.1k 0.7× 366 0.3× 1.0k 0.9× 2.1k 2.2× 191 11.0k

Countries citing papers authored by Anne E. Willis

Since Specialization
Citations

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

Fields of papers citing papers by Anne E. Willis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne E. Willis. 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 Anne E. Willis. The network helps show where Anne E. Willis may publish in the future.

Co-authorship network of co-authors of Anne E. Willis

This figure shows the co-authorship network connecting the top 25 collaborators of Anne E. Willis. A scholar is included among the top collaborators of Anne E. Willis 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 Anne E. Willis. Anne E. Willis 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.
Quintas, Ana, Robert F. Harvey, Gavin D. Garland, et al.. (2024). Eukaryotic initiation factor 4B is a multi-functional RNA binding protein that regulates histone mRNAs. Nucleic Acids Research. 52(19). 12039–12054. 5 indexed citations
2.
Monti, Mie, Leonardo Mancini, Charlotte Capitanchik, et al.. (2024). Interrogation of RNA-protein interaction dynamics in bacterial growth. Molecular Systems Biology. 20(5). 573–589. 2 indexed citations
3.
Screen, Michael, Louise S. Matheson, Andrew J.M. Howden, et al.. (2023). RNA helicase EIF4A1-mediated translation is essential for the GC response. Life Science Alliance. 7(2). e202302301–e202302301. 3 indexed citations
4.
Mulroney, Thomas E., Tuija Pöyry, Juan Carlos Yam‐Puc, et al.. (2023). N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting. Nature. 625(7993). 189–194. 116 indexed citations breakdown →
5.
Strader, Lucia C., Max V. Staller, Anne E. Willis, et al.. (2023). The complexity of transferring genetic information. Molecular Cell. 83(3). 320–323. 2 indexed citations
6.
Villanueva, Eneko, Tom Smith, Mariavittoria Pizzinga, et al.. (2023). System-wide analysis of RNA and protein subcellular localization dynamics. Nature Methods. 21(1). 60–71. 29 indexed citations
7.
Gerber, Pehuén Pereyra, Lidia M. Duncan, Edward JD Greenwood, et al.. (2022). A protease-activatable luminescent biosensor and reporter cell line for authentic SARS-CoV-2 infection. PLoS Pathogens. 18(2). e1010265–e1010265. 22 indexed citations
9.
Harvey, Robert F., Kenneth R. Pryde, Riccardo Serreli, et al.. (2020). Identification of a novel toxicophore in anti-cancer chemotherapeutics that targets mitochondrial respiratory complex I. eLife. 9. 15 indexed citations
10.
Mitchell, Louise, Kirsteen J. Campbell, Rachel A. Ridgway, et al.. (2019). Brf1 loss and not overexpression disrupts tissues homeostasis in the intestine, liver and pancreas. Cell Death and Differentiation. 26(12). 2535–2550. 6 indexed citations
11.
Marini, Alberto, Barak Rotblat, Thomas Sbarrato, et al.. (2018). TAp73 contributes to the oxidative stress response by regulating protein synthesis. Proceedings of the National Academy of Sciences. 115(24). 6219–6224. 27 indexed citations
12.
Sbarrato, Thomas, Ruth V. Spriggs, Lindsay A. Wilson, et al.. (2017). An improved analysis methodology for translational profiling by microarray. RNA. 23(11). 1601–1613. 2 indexed citations
13.
Delaunay, Sylvain, Francesca Rapino, Lars Tharun, et al.. (2016). Elp3 links tRNA modification to IRES-dependent translation of LEF1 to sustain metastasis in breast cancer. The Journal of Experimental Medicine. 213(11). 2503–2523. 131 indexed citations
14.
Meijer, Hedda A., Yi Wen Kong, Wei-Ting Lu, et al.. (2013). Translational Repression and eIF4A2 Activity Are Critical for MicroRNA-Mediated Gene Regulation. Science. 340(6128). 82–85. 252 indexed citations
15.
Roberts, Lisa O., Catherine L. Jopling, Richard J. Jackson, & Anne E. Willis. (2009). Chapter 9 Viral Strategies to Subvert the Mammalian Translation Machinery. Progress in molecular biology and translational science. 90. 313–367. 24 indexed citations
16.
Kong, Yi Wen, Ian G. Cannell, Cornelia H. de Moor, et al.. (2008). The mechanism of micro-RNA-mediated translation repression is determined by the promoter of the target gene. Proceedings of the National Academy of Sciences. 105(26). 8866–8871. 153 indexed citations
17.
Jopling, Catherine L., Keith A. Spriggs, Sally A. Mitchell, Mark Stoneley, & Anne E. Willis. (2004). L-Myc protein synthesis is initiated by internal ribosome entry. RNA. 10(2). 287–298. 44 indexed citations
18.
Mitchell, Sally A., Keith A. Spriggs, Mark J. Coldwell, Richard J. Jackson, & Anne E. Willis. (2003). The Apaf-1 Internal Ribosome Entry Segment Attains the Correct Structural Conformation for Function via Interactions with PTB and unr. Molecular Cell. 11(3). 757–771. 211 indexed citations
19.
Stoneley, Mark, Stephen A. Chappell, Catherine L. Jopling, et al.. (2000). c-Myc Protein Synthesis Is Initiated from the Internal Ribosome Entry Segment during Apoptosis. Molecular and Cellular Biology. 20(4). 1162–1169. 187 indexed citations
20.
Lehmann, Alan R., Anne E. Willis, Bernard C. Broughton, et al.. (1988). Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome.. PubMed. 48(22). 6343–7. 55 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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