Daisy W. Leung

6.3k total citations · 1 hit paper
101 papers, 4.4k citations indexed

About

Daisy W. Leung is a scholar working on Infectious Diseases, Immunology and Molecular Biology. According to data from OpenAlex, Daisy W. Leung has authored 101 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Infectious Diseases, 28 papers in Immunology and 25 papers in Molecular Biology. Recurrent topics in Daisy W. Leung's work include Viral Infections and Vectors (47 papers), Viral Infections and Outbreaks Research (47 papers) and Viral gastroenteritis research and epidemiology (19 papers). Daisy W. Leung is often cited by papers focused on Viral Infections and Vectors (47 papers), Viral Infections and Outbreaks Research (47 papers) and Viral gastroenteritis research and epidemiology (19 papers). Daisy W. Leung collaborates with scholars based in United States, United Kingdom and Canada. Daisy W. Leung's co-authors include Gaya K. Amarasinghe, Christopher F. Basler, Michael K. Rosen, Reed S. Shabman, Dominika Borek, Priya Luthra, Parameshwaran Ramanan, Kathleen C. Prins, Ernest M. Wright and Megan R. Edwards and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Daisy W. Leung

99 papers receiving 4.3k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Oxeiptosis, a ROS-induced caspase-independent apoptosis-like cell-death pathway

2017 338 citations Daisy W. Leung, Gaya K. Amarasinghe et al. profile →

Author Peers

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

Author						Papers	Cites
Daisy W. Leung	1.9k	1.4k	1.2k	849	258	101	4.4k
Salomé LeibundGut‐Landmann	1.5k 0.8×	1.2k 0.9×	3.4k 2.8×	1.6k 1.9×	445 1.7×	81	5.9k
Geanncarlo Lugo‐Villarino	1.0k 0.5×	1.5k 1.0×	1.6k 1.3×	684 0.8×	258 1.0×	48	3.7k
Oliver T. Keppler	1.5k 0.8×	2.3k 1.6×	2.0k 1.6×	1.3k 1.5×	379 1.5×	135	5.8k
Dorothy E. Lewis	953 0.5×	1.4k 1.0×	1.4k 1.2×	767 0.9×	523 2.0×	119	4.9k
Norbert Reiling	1.4k 0.7×	1.7k 1.3×	2.2k 1.8×	1.4k 1.6×	492 1.9×	99	5.3k
Sonja I. Gringhuis	1.0k 0.5×	2.1k 1.5×	3.7k 3.0×	1.0k 1.2×	390 1.5×	54	6.2k
Shigeo Yagi	1.2k 0.6×	1.1k 0.8×	502 0.4×	1.6k 1.9×	280 1.1×	96	4.6k
Maren von Köckritz‐Blickwede	1.1k 0.6×	1.5k 1.1×	3.0k 2.5×	597 0.7×	284 1.1×	136	5.3k
Huan-Yao Lei	2.7k 1.4×	1.2k 0.9×	1.3k 1.0×	996 1.2×	142 0.6×	89	6.3k
Emer P. Reeves	690 0.4×	1.8k 1.3×	2.1k 1.7×	525 0.6×	449 1.7×	107	5.6k

Countries citing papers authored by Daisy W. Leung

Since Specialization

Citations

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

Fields of papers citing papers by Daisy W. Leung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daisy W. Leung. 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 Daisy W. Leung. The network helps show where Daisy W. Leung may publish in the future.

Co-authorship network of co-authors of Daisy W. Leung

This figure shows the co-authorship network connecting the top 25 collaborators of Daisy W. Leung. A scholar is included among the top collaborators of Daisy W. Leung 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 Daisy W. Leung. Daisy W. Leung is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Carlson, Rebecca J., J. J. Patten, Brian Y. Soong, et al.. (2025). Single-cell image-based screens identify host regulators of Ebola virus infection dynamics. Nature Microbiology. 10(8). 1989–2002. 3 indexed citations

Wang, Ling, Sarah H. Stubbs, Caroline G. Williams, et al.. (2025). A protein-proximity screen reveals Ebola virus co-opts the mRNA decapping complex through the scaffold protein EDC4. Nature Communications. 16(1). 8485–8485.

Luthra, Priya, O. A. Vogel, Jyoti Batra, et al.. (2025). Ebola virus VP35 NNLNS motif modulates viral RNA synthesis and MIB2-mediated signaling. Proceedings of the National Academy of Sciences. 122(39). e2411961122–e2411961122.

Zhao, Junjie, Bojie Zhang, O. A. Vogel, et al.. (2025). The Biophysical Basis for Karyopherin-Dependent Ebola Virus VP24 Nuclear Transport. Viruses. 17(8). 1051–1051. 1 indexed citations

Singh, Srishti, Parismita Kalita, Charlotte Mason, et al.. (2025). Structure-guided engineering of CD112 receptor variants for optimized immunotherapy. Molecular Therapy. 33(8). 3590–3604. 1 indexed citations

Vogel, O. A., Jade K. Forwood, Daisy W. Leung, Gaya K. Amarasinghe, & Christopher F. Basler. (2023). Viral Targeting of Importin Alpha-Mediated Nuclear Import to Block Innate Immunity. Cells. 13(1). 71–71. 4 indexed citations

Wu, Chao, Nicole D. Wagner, Austin B. Moyle, et al.. (2023). Disruption of Ebola NP0VP35 Inclusion Body-like Structures reduce Viral Infection. Journal of Molecular Biology. 435(20). 168241–168241. 4 indexed citations

Qavi, Abraham J., Qisheng Jiang, M. Javad Aman, et al.. (2023). A Flexible, Quantitative Plasmonic-Fluor Lateral Flow Assay for the Rapid Detection of Orthoebolavirus zairense and Orthoebolavirus sudanense. ACS Infectious Diseases. 10(1). 57–63. 2 indexed citations

Wang, Lin, Amol C. Shetty, Megan R. Edwards, et al.. (2022). Multiple genetic paths including massive gene amplification allow Mycobacterium tuberculosis to overcome loss of ESX-3 secretion system substrates. Proceedings of the National Academy of Sciences. 119(8). 17 indexed citations

10.

Schwarz, Madeline M., David A. Price, Safder S. Ganaie, et al.. (2022). Oropouche orthobunyavirus infection is mediated by the cellular host factor Lrp1. Proceedings of the National Academy of Sciences. 119(33). e2204706119–e2204706119. 31 indexed citations

11.

Teyra, Joan, Shane Miersch, Lia Cardarelli, et al.. (2022). Development of Monoclonal Antibodies to Detect for SARS-CoV-2 Proteins. Journal of Molecular Biology. 434(10). 167583–167583. 4 indexed citations

12.

Mok, Chris Ka Pun, Carolyn A. Cohen, Samuel M. S. Cheng, et al.. (2021). Comparison of the immunogenicity of BNT162b2 and CoronaVac COVID ‐19 vaccines in Hong Kong. Respirology. 27(4). 301–310. 91 indexed citations

13.

Pei, Jingjing, Nicole D. Wagner, Dominika Borek, et al.. (2021). Structural basis for IFN antagonism by human respiratory syncytial virus nonstructural protein 2. Proceedings of the National Academy of Sciences. 118(10). 21 indexed citations

14.

Moncman, Carole L., et al.. (2021). Effect of clinical isolate or cleavage site mutations in the SARS-CoV-2 spike protein on protein stability, cleavage, and cell–cell fusion. Journal of Biological Chemistry. 297(1). 100902–100902. 20 indexed citations

15.

Batra, Jyoti, Hiroyuki Mori, Manu Anantpadma, et al.. (2021). Non‐canonical proline‐tyrosine interactions with multiple host proteins regulate Ebola virus infection. The EMBO Journal. 40(18). e105658–e105658. 12 indexed citations

16.

Binning, Jennifer M., Grigore Pintilie, Wah Chiu, et al.. (2021). Cryo-EM analysis of Ebola virus nucleocapsid-like assembly. STAR Protocols. 3(1). 101030–101030. 2 indexed citations

17.

Edwards, Megan R., Gai Liu, Julien Sourimant, et al.. (2020). Small Molecule Compounds That Inhibit Antioxidant Response Gene Expression in an Inducer-Dependent Manner. ACS Infectious Diseases. 6(3). 489–502. 1 indexed citations

18.

Edwards, Megan R., Hejun Liu, Reed S. Shabman, et al.. (2018). Conservation of Structure and Immune Antagonist Functions of Filoviral VP35 Homologs Present in Microbat Genomes. Cell Reports. 24(4). 861–872.e6. 15 indexed citations

19.

Luthra, Priya, Ekaterina Esaulova, Eugene Agapov, et al.. (2017). Structural basis for human respiratory syncytial virus NS1-mediated modulation of host responses. Nature Microbiology. 2(9). 17101–17101. 40 indexed citations

20.

Leung, Daisy W., Nathaniel D. Ginder, D. Bruce Fulton, et al.. (2009). Structure of the Ebola VP35 interferon inhibitory domain. Proceedings of the National Academy of Sciences. 106(2). 411–416. 127 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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