Patrick W.K. Lee

7.9k total citations · 1 hit paper
91 papers, 6.5k citations indexed

About

Patrick W.K. Lee is a scholar working on Genetics, Infectious Diseases and Molecular Biology. According to data from OpenAlex, Patrick W.K. Lee has authored 91 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Genetics, 48 papers in Infectious Diseases and 31 papers in Molecular Biology. Recurrent topics in Patrick W.K. Lee's work include Virus-based gene therapy research (52 papers), Viral gastroenteritis research and epidemiology (48 papers) and Cancer Research and Treatments (20 papers). Patrick W.K. Lee is often cited by papers focused on Virus-based gene therapy research (52 papers), Viral gastroenteritis research and epidemiology (48 papers) and Cancer Research and Treatments (20 papers). Patrick W.K. Lee collaborates with scholars based in Canada, United States and Portugal. Patrick W.K. Lee's co-authors include Paola Marcato, James E. Strong, Matthew Coffey, Shashi Gujar, Kara L. Norman, Carman A. Giacomantonio, Cheryl A. Dean, Peter Forsyth, Wolfgang K. Joklik and Edward C. Hayes and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Patrick W.K. Lee

91 papers receiving 6.3k citations

Hit Papers

Reovirus Therapy of Tumor... 1998 2026 2007 2016 1998 200 400 600

Author Peers

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

Author Last Decade Papers Cites
Patrick W.K. Lee 3.3k 2.6k 2.3k 2.2k 834 91 6.5k
J. Ignacio Casal 1.4k 0.4× 3.9k 1.5× 1.2k 0.5× 1.4k 0.6× 684 0.8× 167 7.4k
Philip E. Branton 3.7k 1.1× 5.1k 1.9× 710 0.3× 2.2k 1.0× 315 0.4× 120 7.2k
L R Gooding 2.9k 0.9× 3.0k 1.1× 893 0.4× 1.4k 0.7× 204 0.2× 86 6.2k
Riccardo Cortese 2.0k 0.6× 5.7k 2.2× 960 0.4× 849 0.4× 382 0.5× 144 11.1k
Jan E. Carette 1.7k 0.5× 5.4k 2.0× 2.0k 0.9× 668 0.3× 177 0.2× 109 8.9k
Andrew J. Dorner 885 0.3× 3.1k 1.2× 704 0.3× 904 0.4× 251 0.3× 87 7.3k
Lindsey Moffat 2.2k 0.7× 4.9k 1.9× 396 0.2× 1.0k 0.5× 295 0.4× 10 7.7k
Amos Panet 1.3k 0.4× 2.9k 1.1× 927 0.4× 664 0.3× 156 0.2× 175 5.7k
Zong Sheng Guo 2.5k 0.8× 2.1k 0.8× 376 0.2× 2.6k 1.2× 563 0.7× 78 4.8k
Nancy C. Reich 1.1k 0.3× 3.5k 1.3× 789 0.3× 3.9k 1.8× 302 0.4× 93 7.7k

Countries citing papers authored by Patrick W.K. Lee

Since Specialization
Citations

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

Fields of papers citing papers by Patrick W.K. Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick W.K. Lee. 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 Patrick W.K. Lee. The network helps show where Patrick W.K. Lee may publish in the future.

Co-authorship network of co-authors of Patrick W.K. Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick W.K. Lee. A scholar is included among the top collaborators of Patrick W.K. Lee 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 Patrick W.K. Lee. Patrick W.K. Lee 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.
Ahn, Dae‐Gyun, Tanveer Sharif, Kenneth Chisholm, et al.. (2015). Ras transformation results in cleavage of reticulon protein Nogo-B that is associated with impairment of IFN response. Cell Cycle. 14(14). 2301–2310. 11 indexed citations
2.
Marcato, Paola, Cheryl A. Dean, Rong‐Zong Liu, et al.. (2014). Aldehyde dehydrogenase 1A3 influences breast cancer progression via differential retinoic acid signaling. Molecular Oncology. 9(1). 17–31. 105 indexed citations
3.
Gujar, Shashi & Patrick W.K. Lee. (2014). Oncolytic Virus-Mediated Reversal of Impaired Tumor Antigen Presentation. Frontiers in Oncology. 4. 77–77. 52 indexed citations
4.
Marcato, Paola, Cheryl A. Dean, Carman A. Giacomantonio, & Patrick W.K. Lee. (2011). Aldehyde dehydrogenase: Its role as a cancer stem cell marker comes down to the specific isoform. Cell Cycle. 10(9). 1378–1384. 412 indexed citations
5.
Shmulevitz, Maya, et al.. (2010). Oncogenic Ras Promotes Reovirus Spread by Suppressing IFN-β Production through Negative Regulation of RIG-I Signaling. Cancer Research. 70(12). 4912–4921. 79 indexed citations
6.
Gujar, Shashi, Paola Marcato, Da Pan, & Patrick W.K. Lee. (2010). Reovirus Virotherapy Overrides Tumor Antigen Presentation Evasion and Promotes Protective Antitumor Immunity. Molecular Cancer Therapeutics. 9(11). 2924–2933. 99 indexed citations
7.
Leidal, Andrew M., et al.. (2009). p21Cip1/WAF1mediates cyclin B1 degradation in response to DNA damage. Cell Cycle. 8(2). 253–256. 65 indexed citations
8.
Hill, Richard, Andrew M. Leidal, Patrícia A. Madureira, et al.. (2008). Chromium-mediated apoptosis: Involvement of DNA-dependent protein kinase (DNA-PK) and differential induction of p53 target genes. DNA repair. 7(9). 1484–1499. 26 indexed citations
9.
Hill, Richard, Andrew M. Leidal, Patrícia A. Madureira, et al.. (2007). Hypersensitivity to chromium-induced DNA damage correlates with constitutive deregulation of upstream p53 kinases in p21−/− HCT116 colon cancer cells. DNA repair. 7(2). 239–252. 20 indexed citations
10.
Egan, Catherine, et al.. (2005). Acquired resistance to reoviral oncolysis. Cancer Research. 65. 797–797. 1 indexed citations
11.
Norman, Kara L. & Patrick W.K. Lee. (2005). Not all viruses are bad guys: the case for reovirus in cancer therapy. Drug Discovery Today. 10(12). 847–855. 51 indexed citations
12.
Shmulevitz, Maya, Paola Marcato, & Patrick W.K. Lee. (2005). Unshackling the links between reovirus oncolysis, Ras signaling, translational control and cancer. Oncogene. 24(52). 7720–7728. 85 indexed citations
13.
Farassati, Faris, An-Dao Yang, & Patrick W.K. Lee. (2001). Oncogenes in Ras signalling pathway dictate host-cell permissiveness to herpes simplex virus 1. Nature Cell Biology. 3(8). 745–750. 191 indexed citations
14.
Norman, Kara L. & Patrick W.K. Lee. (2000). Reovirus as a novel oncolytic agent. Journal of Clinical Investigation. 105(8). 1035–1038. 93 indexed citations
15.
Coffey, Matthew, et al.. (1998). Active Participation of Hsp90 in the Biogenesis of the Trimeric Reovirus Cell Attachment Protein ς1. Journal of Biological Chemistry. 273(24). 15227–15233. 19 indexed citations
16.
Duncan, Roy & Patrick W.K. Lee. (1994). Localization of Two Protease-Sensitive Regions Separating Distinct Domains in the Reovirus Cell-Attachment Protein σ1. Virology. 203(1). 149–152. 17 indexed citations
17.
Duncan, Roy, James E. Strong, Gustavo Leone, et al.. (1991). Conformational and functional analysis of the C-terminal globular head of the reovirus cell attachment protein. Virology. 182(2). 810–819. 34 indexed citations
18.
Choi, Anthony H.-C., Ralph W. Paul, & Patrick W.K. Lee. (1990). Reovirus binds to multiple plasma membrane proteins of mouse L fibroblasts. Virology. 178(1). 316–320. 38 indexed citations
19.
Mah, David, et al.. (1990). The N-terminal quarter of reovirus cell attachment protein σ1 possesses intrinsic virion-anchoring function. Virology. 179(1). 95–103. 37 indexed citations
20.
Paul, Ralph W., Anthony H.-C. Choi, & Patrick W.K. Lee. (1989). The α-anomeric form of sialic acid is the minimal receptor determinant recognized by reovirus. Virology. 172(1). 382–385. 99 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026