Nahum Sonenberg

124.2k total citations · 43 hit papers
673 papers, 97.8k citations indexed

About

Nahum Sonenberg is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Immunology. According to data from OpenAlex, Nahum Sonenberg has authored 673 papers receiving a total of 97.8k indexed citations (citations by other indexed papers that have themselves been cited), including 570 papers in Molecular Biology, 122 papers in Cardiology and Cardiovascular Medicine and 62 papers in Immunology. Recurrent topics in Nahum Sonenberg's work include RNA and protein synthesis mechanisms (269 papers), RNA Research and Splicing (218 papers) and PI3K/AKT/mTOR signaling in cancer (154 papers). Nahum Sonenberg is often cited by papers focused on RNA and protein synthesis mechanisms (269 papers), RNA Research and Splicing (218 papers) and PI3K/AKT/mTOR signaling in cancer (154 papers). Nahum Sonenberg collaborates with scholars based in Canada, United States and United Kingdom. Nahum Sonenberg's co-authors include Anne‐Claude Gingras, Witold Filipowicz, Nissim Hay, Jerry Pelletier, Brian Raught, Alan G. Hinnebusch, Marc R. Fabian, Suvendra N. Bhattacharyya, Yuri V. Svitkin and Arnim Pause and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Nahum Sonenberg

664 papers receiving 96.2k citations

Hit Papers

Mechanisms of post-transc... 1982 2026 1996 2011 2008 2004 2010 2009 1999 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
Nahum Sonenberg 77.5k 12.8k 10.2k 9.1k 8.7k 673 97.8k
Peter Carmeliet 53.1k 0.7× 27.4k 2.1× 5.8k 0.6× 11.7k 1.3× 5.4k 0.6× 729 100.0k
Eric N. Olson 109.1k 1.4× 24.0k 1.9× 20.7k 2.0× 6.8k 0.7× 15.5k 1.8× 761 135.3k
George D. Yancopoulos 55.1k 0.7× 11.9k 0.9× 6.8k 0.7× 16.0k 1.8× 6.1k 0.7× 430 103.1k
Josef Penninger 40.9k 0.5× 7.5k 0.6× 8.0k 0.8× 18.0k 2.0× 3.9k 0.5× 582 78.3k
Harvey F. Lodish 49.1k 0.6× 11.2k 0.9× 3.9k 0.4× 8.7k 1.0× 6.7k 0.8× 646 82.0k
John C. Reed 73.3k 0.9× 12.2k 1.0× 2.6k 0.3× 20.4k 2.2× 6.1k 0.7× 799 107.5k
Simon C. Watkins 28.3k 0.4× 5.3k 0.4× 3.9k 0.4× 12.9k 1.4× 4.6k 0.5× 788 59.2k
Christopher K. Glass 61.4k 0.8× 12.2k 1.0× 2.4k 0.2× 19.3k 2.1× 17.9k 2.1× 375 96.6k
Steven P. Gygi 88.4k 1.1× 11.7k 0.9× 2.4k 0.2× 7.9k 0.9× 7.6k 0.9× 695 121.5k
Paul Tempst 62.1k 0.8× 7.6k 0.6× 1.6k 0.2× 9.0k 1.0× 6.6k 0.8× 320 80.8k

Countries citing papers authored by Nahum Sonenberg

Since Specialization
Citations

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

Fields of papers citing papers by Nahum Sonenberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nahum Sonenberg

This figure shows the co-authorship network connecting the top 25 collaborators of Nahum Sonenberg. A scholar is included among the top collaborators of Nahum Sonenberg 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 Nahum Sonenberg. Nahum Sonenberg 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.
Choi, Jung‐Hyun, Jun Luo, Niaz Mahmood, et al.. (2024). The 4EHP-mediated translational repression of cGAS impedes the host immune response against DNA viruses. Proceedings of the National Academy of Sciences. 121(48). e2413018121–e2413018121. 1 indexed citations
2.
Mahmood, Niaz, Jung‐Hyun Choi, Sean W. Dooling, et al.. (2024). The ISR downstream target ATF4 represses long-term memory in a cell type–specific manner. Proceedings of the National Academy of Sciences. 121(31). e2407472121–e2407472121. 5 indexed citations
3.
Wiebe, Shane, Jung‐Hyun Choi, Niaz Mahmood, et al.. (2024). Dysregulating mTORC1-4E-BP2 signaling in GABAergic interneurons impairs hippocampus-dependent learning and memory. Learning & Memory. 31(10-11). a054018–a054018. 2 indexed citations
4.
García, Alejandra, Yuri V. Svitkin, David Cantú de León, et al.. (2021). High-risk human papillomavirus-18 uses an mRNA sequence to synthesize oncoprotein E6 in tumors. Proceedings of the National Academy of Sciences. 118(41). 9 indexed citations
5.
Pearl, Dana, Sakie Katsumura, Mehdi Amiri, et al.. (2020). 4E-BP–Dependent Translational Control of Irf8 Mediates Adipose Tissue Macrophage Inflammatory Response. The Journal of Immunology. 204(9). 2392–2400. 13 indexed citations
6.
Dawson, Jennifer E., Alaji Bah, Zhenfu Zhang, et al.. (2020). Non-cooperative 4E-BP2 folding with exchange between eIF4E-binding and binding-incompatible states tunes cap-dependent translation inhibition. Nature Communications. 11(1). 3146–3146. 19 indexed citations
7.
Muller, David C., Théo Goullet de Rugy, Rémi Samain, et al.. (2019). eIF4A inhibition circumvents uncontrolled DNA replication mediated by 4E-BP1 loss in pancreatic cancer. JCI Insight. 4(21). 25 indexed citations
8.
Liu, Dong, Adam Stowie, Nuria de Zavalía, et al.. (2018). mTOR signaling in VIP neurons regulates circadian clock synchrony and olfaction. Proceedings of the National Academy of Sciences. 115(14). E3296–E3304. 39 indexed citations
9.
Ding, Mei, Theodorus van der Kwast, Ravi N. Vellanki, et al.. (2018). The mTOR Targets 4E-BP1/2 Restrain Tumor Growth and Promote Hypoxia Tolerance in PTEN-driven Prostate Cancer. Molecular Cancer Research. 16(4). 682–695. 22 indexed citations
10.
Ratcliffe, Colin D.H., Nadeem Siddiqui, Paula P. Coelho, et al.. (2018). HGF-induced migration depends on the PI(3,4,5)P3-binding microexon-spliced variant of the Arf6 exchange factor cytohesin-1. The Journal of Cell Biology. 218(1). 285–298. 21 indexed citations
11.
Chapat, Clément, Seyed Mehdi Jafarnejad, Edna Matta‐Camacho, et al.. (2017). Cap-binding protein 4EHP effects translation silencing by microRNAs. Proceedings of the National Academy of Sciences. 114(21). 5425–5430. 79 indexed citations
12.
Alain, Tommy, Masahiro Morita, Bruno D. Fonseca, et al.. (2012). eIF4E/4E-BP Ratio Predicts the Efficacy of mTOR Targeted Therapies. Cancer Research. 72(24). 6468–6476. 120 indexed citations
13.
Furic, Luc, Liwei Rong, Ola Larsson, et al.. (2010). eIF4E phosphorylation promotes tumorigenesis and is associated with prostate cancer progression. Proceedings of the National Academy of Sciences. 107(32). 14134–14139. 398 indexed citations
14.
Dowling, Ryan J.O., Ivan Topisirović, Tommy Alain, et al.. (2010). mTORC1-Mediated Cell Proliferation, But Not Cell Growth, Controlled by the 4E-BPs. Science. 328(5982). 1172–1176. 549 indexed citations breakdown →
15.
Yanagiya, Akiko, et al.. (2008). Requirement of RNA Binding of Mammalian Eukaryotic Translation Initiation Factor 4GI (eIF4GI) for Efficient Interaction of eIF4E with the mRNA Cap. Molecular and Cellular Biology. 29(6). 1661–1669. 88 indexed citations
16.
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
17.
Zakikhani, Mahvash, Ryan J.O. Dowling, I. George Fantus, Nahum Sonenberg, & Michaël Pollak. (2006). Metformin Is an AMP Kinase–Dependent Growth Inhibitor for Breast Cancer Cells. Cancer Research. 66(21). 10269–10273. 881 indexed citations breakdown →
18.
Matthews, James, Lisa Lindqvist, Olivia Novac, et al.. (2005). Stimulation of mammalian translation initiation factor eIF4A activity by a small molecule inhibitor of eukaryotic translation. Proceedings of the National Academy of Sciences. 102(30). 10460–10465. 180 indexed citations
19.
Nikolcheva, Tania, Stéphane Pyronnet, Nahum Sonenberg, et al.. (2002). A translational rheostat for RFLAT-1 regulates RANTES expression in T lymphocytes. Journal of Clinical Investigation. 110(1). 119–126. 43 indexed citations
20.
Gradi, Alessandra, Hiroaki Imataka, Yuri V. Svitkin, et al.. (1998). A Novel Functional Human Eukaryotic Translation Initiation Factor 4G. Molecular and Cellular Biology. 18(1). 334–342. 251 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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