Derek Walsh

3.0k total citations · 1 hit paper
49 papers, 2.2k citations indexed

About

Derek Walsh is a scholar working on Molecular Biology, Epidemiology and Virology. According to data from OpenAlex, Derek Walsh has authored 49 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 16 papers in Epidemiology and 11 papers in Virology. Recurrent topics in Derek Walsh's work include Herpesvirus Infections and Treatments (13 papers), RNA and protein synthesis mechanisms (12 papers) and Cytomegalovirus and herpesvirus research (11 papers). Derek Walsh is often cited by papers focused on Herpesvirus Infections and Treatments (13 papers), RNA and protein synthesis mechanisms (12 papers) and Cytomegalovirus and herpesvirus research (11 papers). Derek Walsh collaborates with scholars based in United States, Ireland and United Kingdom. Derek Walsh's co-authors include Ian Mohr, Mojgan H. Naghavi, Vladimir Jovasevic, Eric Jan, Cesar A. Perez, Yosef Sabo, Carolina Arias, Viacheslav Malikov, Scott G. Morham and Denis Barry and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Derek Walsh

47 papers receiving 2.2k citations

Hit Papers

Viral subversion of the host protein synthesis machinery 2011 2026 2016 2021 2011 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
Derek Walsh United States 25 1.1k 647 435 421 394 49 2.2k
Alessia Ruggieri Germany 27 1.1k 1.0× 519 0.8× 329 0.8× 546 1.3× 670 1.7× 46 2.5k
Iván Ventoso Spain 19 982 0.9× 265 0.4× 190 0.4× 493 1.2× 389 1.0× 33 1.7k
Eran Bacharach Israel 27 1.2k 1.1× 392 0.6× 363 0.8× 918 2.2× 534 1.4× 63 2.7k
Richard Peluso United States 27 1.2k 1.1× 936 1.4× 349 0.8× 192 0.5× 478 1.2× 38 2.7k
Andrew J. Mouland Canada 38 2.4k 2.2× 370 0.6× 1.4k 3.2× 573 1.4× 766 1.9× 90 3.5k
Sibylle Schleich Germany 24 720 0.7× 502 0.8× 663 1.5× 225 0.5× 253 0.6× 29 1.8k
Katinka Döhner Germany 22 625 0.6× 1.0k 1.6× 212 0.5× 534 1.3× 223 0.6× 37 1.9k
Jean‐Luc Darlix France 22 1.0k 1.0× 284 0.4× 912 2.1× 463 1.1× 435 1.1× 30 1.8k
Yohei Yamauchi Japan 28 867 0.8× 916 1.4× 122 0.3× 510 1.2× 312 0.8× 57 2.0k
Gavin S. Wilkie United Kingdom 28 1.4k 1.3× 820 1.3× 125 0.3× 358 0.9× 274 0.7× 55 2.7k

Countries citing papers authored by Derek Walsh

Since Specialization
Citations

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

Fields of papers citing papers by Derek Walsh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Derek Walsh

This figure shows the co-authorship network connecting the top 25 collaborators of Derek Walsh. A scholar is included among the top collaborators of Derek Walsh 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 Derek Walsh. Derek Walsh 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.
Walsh, Derek, et al.. (2025). Cytomegalovirus disrupts Lamin A/C to control microtubule-mediated nuclear movement and cell migration. Proceedings of the National Academy of Sciences. 122(48). e2507831122–e2507831122.
2.
3.
Park, Chorong, et al.. (2025). Distinct non-canonical translation initiation modes arise for specific host and viral mRNAs during poxvirus-induced shutoff. Nature Microbiology. 10(6). 1535–1549. 1 indexed citations
4.
Walsh, Derek. (2024). Primal FEAR protects against infection. Nature Microbiology. 9(4). 886–888. 1 indexed citations
5.
Chakrabarty, Ram Prosad, et al.. (2023). The poxvirus F17 protein counteracts mitochondrially orchestrated antiviral responses. Nature Communications. 14(1). 7889–7889. 12 indexed citations
6.
Park, Chorong & Derek Walsh. (2022). Ribosomes in poxvirus infection. Current Opinion in Virology. 56. 101256–101256. 6 indexed citations
7.
Zaichick, Sofia, Ewa Bomba-Warczak, Vladimir Jovasevic, et al.. (2021). Herpesviruses assimilate kinesin to produce motorized viral particles. Nature. 599(7886). 662–666. 36 indexed citations
8.
Banerjee, Avik, Masatoshi Nukui, Kevin Kruse, et al.. (2018). The HCMV Assembly Compartment Is a Dynamic Golgi-Derived MTOC that Controls Nuclear Rotation and Virus Spread. Developmental Cell. 45(1). 83–100.e7. 64 indexed citations
9.
Li, Hua, et al.. (2018). Poxviruses Evade Cytosolic Sensing through Disruption of an mTORC1-mTORC2 Regulatory Circuit. Cell. 174(5). 1143–1157.e17. 79 indexed citations
10.
Walsh, Derek & Mojgan H. Naghavi. (2018). Exploitation of Cytoskeletal Networks during Early Viral Infection. Trends in Microbiology. 27(1). 39–50. 73 indexed citations
11.
Chai, Qingqing, Vladimir Jovasevic, Viacheslav Malikov, et al.. (2017). HIV-1 counteracts an innate restriction by amyloid precursor protein resulting in neurodegeneration. Nature Communications. 8(1). 1522–1522. 47 indexed citations
12.
Malikov, Viacheslav, Vladimir Jovasevic, Bianca Schulte, et al.. (2015). HIV-1 capsids bind and exploit the kinesin-1 adaptor FEZ1 for inward movement to the nucleus. Nature Communications. 6(1). 6660–6660. 107 indexed citations
13.
Walsh, Derek & Ian Mohr. (2014). Coupling 40S ribosome recruitment to modification of a cap-binding initiation factor by eIF3 subunit e. Genes & Development. 28(8). 835–840. 33 indexed citations
14.
Sabo, Yosef, Derek Walsh, Denis Barry, et al.. (2013). HIV-1 Induces the Formation of Stable Microtubules to Enhance Early Infection. Cell Host & Microbe. 14(5). 535–546. 118 indexed citations
15.
Henry, Michael, et al.. (2012). Recruitment of host translation initiation factor eIF4G by the Vaccinia Virus ssDNA-binding protein I3. Virology. 425(1). 11–22. 21 indexed citations
16.
Brown, Craig, Scott G. Morham, Derek Walsh, & Mojgan H. Naghavi. (2011). Focal Adhesion Proteins Talin-1 and Vinculin Negatively Affect Paxillin Phosphorylation and Limit Retroviral Infection. Journal of Molecular Biology. 410(5). 761–777. 32 indexed citations
17.
Arias, Carolina, Derek Walsh, Jack W. Harbell, Angus C. Wilson, & Ian Mohr. (2009). Activation of Host Translational Control Pathways by a Viral Developmental Switch. PLoS Pathogens. 5(3). e1000334–e1000334. 58 indexed citations
18.
Walsh, Derek & Ian Mohr. (2006). Assembly of an active translation initiation factor complex by a viral protein. Genes & Development. 20(4). 461–472. 71 indexed citations
19.
Walsh, Derek & Ian Mohr. (2004). Phosphorylation of eIF4E by Mnk-1 enhances HSV-1 translation and replication in quiescent cells. Genes & Development. 18(6). 660–672. 160 indexed citations
20.
Walsh, Derek, et al.. (2003). Increased levels of the translation initiation factor eIF4E in differentiating epithelial lung tumor cell lines. Differentiation. 71(2). 126–134. 17 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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