Alan L. Rothman

19.3k total citations · 4 hit papers
208 papers, 15.1k citations indexed

About

Alan L. Rothman is a scholar working on Public Health, Environmental and Occupational Health, Infectious Diseases and Immunology. According to data from OpenAlex, Alan L. Rothman has authored 208 papers receiving a total of 15.1k indexed citations (citations by other indexed papers that have themselves been cited), including 173 papers in Public Health, Environmental and Occupational Health, 152 papers in Infectious Diseases and 25 papers in Immunology. Recurrent topics in Alan L. Rothman's work include Mosquito-borne diseases and control (171 papers), Viral Infections and Vectors (143 papers) and Malaria Research and Control (79 papers). Alan L. Rothman is often cited by papers focused on Mosquito-borne diseases and control (171 papers), Viral Infections and Vectors (143 papers) and Malaria Research and Control (79 papers). Alan L. Rothman collaborates with scholars based in United States, Thailand and United Kingdom. Alan L. Rothman's co-authors include Francis A. Ennis, Sharone Green, Siripen Kalayanarooj, Ananda Nisalak, David W. Vaughn, Daniel H. Libraty, Saroj Suntayakorn, Anuja Mathew, Suchitra Nimmannitya and Timothy P. Endy and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Alan L. Rothman

202 papers receiving 14.6k citations

Hit Papers

Dengue Viremia Titer, Antibody Response Pattern, and Viru... 1997 2026 2006 2016 2000 2011 2002 1997 400 800 1.2k

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Alan L. Rothman United States 66 12.1k 10.7k 1.7k 1.4k 1.2k 208 15.1k
Eng Eong Ooi Singapore 62 6.6k 0.5× 7.9k 0.7× 1.7k 1.0× 1.6k 1.1× 454 0.4× 264 12.7k
David W. Vaughn United States 66 11.6k 1.0× 11.2k 1.0× 839 0.5× 1.8k 1.2× 537 0.4× 166 14.7k
Eva Harris United States 83 18.0k 1.5× 14.6k 1.4× 1.8k 1.1× 2.7k 1.9× 1.2k 1.0× 329 22.2k
Scott B. Halstead United States 73 17.4k 1.4× 14.3k 1.3× 931 0.6× 2.0k 1.4× 985 0.8× 223 20.3k
María G. Guzmán Cuba 49 10.1k 0.8× 7.9k 0.7× 512 0.3× 1.1k 0.7× 581 0.5× 221 11.8k
Ananda Nisalak Thailand 68 14.4k 1.2× 12.1k 1.1× 644 0.4× 1.3k 0.9× 559 0.4× 181 16.2k
Sharone Green United States 45 7.2k 0.6× 6.1k 0.6× 823 0.5× 656 0.5× 573 0.5× 79 8.3k
Aravinda M. de Silva United States 43 5.3k 0.4× 7.3k 0.7× 1.1k 0.7× 860 0.6× 325 0.3× 114 9.3k
Francis A. Ennis United States 63 6.5k 0.5× 7.3k 0.7× 3.5k 2.1× 3.6k 2.5× 2.0k 1.6× 203 13.1k
Ernest A. Gould United Kingdom 64 9.5k 0.8× 9.1k 0.9× 544 0.3× 1.7k 1.1× 677 0.5× 202 13.4k

Countries citing papers authored by Alan L. Rothman

Since Specialization
Citations

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

Fields of papers citing papers by Alan L. Rothman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alan L. Rothman. 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 Alan L. Rothman. The network helps show where Alan L. Rothman may publish in the future.

Co-authorship network of co-authors of Alan L. Rothman

This figure shows the co-authorship network connecting the top 25 collaborators of Alan L. Rothman. A scholar is included among the top collaborators of Alan L. Rothman 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 Alan L. Rothman. Alan L. Rothman 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.
Ashraf, Usama, Saborni Chakraborty, Nathan C. Lo, et al.. (2025). Afucosylation of anti-dengue IgG is associated with enhanced susceptibility to dengue virus infection postvaccination. Science Translational Medicine. 17(817). eadx7231–eadx7231. 1 indexed citations
2.
Mathew, Anuja, Henrik Salje, David A. Sousa, et al.. (2024). Protective Role of NS1-Specific Antibodies in the Immune Response to Dengue Virus Through Antibody-Dependent Cellular Cytotoxicity. The Journal of Infectious Diseases. 230(5). 1147–1156. 7 indexed citations
3.
O’Driscoll, Megan, Darunee Buddhari, Angkana T. Huang, et al.. (2023). Maternally derived antibody titer dynamics and risk of hospitalized infant dengue disease. Proceedings of the National Academy of Sciences. 120(41). e2308221120–e2308221120. 15 indexed citations
4.
Fung, Christian, Tao Li, Simon Pollett, et al.. (2021). Effect of low-passage number on dengue consensus genomes and intra-host variant frequencies. Journal of General Virology. 102(3). 4 indexed citations
5.
Morrison, Amy C., William H. Elson, Helvio Astete, et al.. (2021). The impact of dengue illness on social distancing and caregiving behavior. PLoS neglected tropical diseases. 15(7). e0009614–e0009614. 2 indexed citations
6.
Elson, William H., Amy C. Morrison, Erik J. Groessl, et al.. (2020). Measuring health related quality of life for dengue patients in Iquitos, Peru. PLoS neglected tropical diseases. 14(7). e0008477–e0008477. 6 indexed citations
7.
Adam, Awadalkareem, Marcia Woda, Sonia Kounlavouth, et al.. (2018). Multiplexed FluoroSpot for the Analysis of Dengue Virus– and Zika Virus–Specific and Cross-Reactive Memory B Cells. The Journal of Immunology. 201(12). 3804–3814. 17 indexed citations
8.
Moulton, Steven L., Jane Mulligan, Anon Srikiatkhachorn, et al.. (2016). State-of-the-art monitoring in treatment of dengue shock syndrome: a case series. Journal of Medical Case Reports. 10(1). 233–233. 20 indexed citations
9.
Barbier, Vincent, et al.. (2016). Dengue virus induces mitochondrial elongation through impairment of Drp1-triggered mitochondrial fission. Virology. 500. 149–160. 82 indexed citations
10.
Mathew, Anuja, William R. Marshall, Girish J. Kotwal, et al.. (2008). Robust Intrapulmonary CD8 T Cell Responses and Protection with an Attenuated N1L Deleted Vaccinia Virus. PLoS ONE. 3(10). e3323–e3323. 13 indexed citations
11.
Laoprasopwattana, Kamolwish, Daniel H. Libraty, Timothy P. Endy, et al.. (2007). Antibody‐Dependent Cellular Cytotoxicity Mediated by Plasma Obtained before Secondary Dengue Virus Infections: Potential Involvement in Early Control of Viral Replication. The Journal of Infectious Diseases. 195(8). 1108–1116. 52 indexed citations
12.
Bashyam, Hema, Sharone Green, & Alan L. Rothman. (2006). Dengue Virus-Reactive CD8+ T Cells Display Quantitative and Qualitative Differences in Their Response to Variant Epitopes of Heterologous Viral Serotypes. The Journal of Immunology. 176(5). 2817–2824. 111 indexed citations
13.
Rothman, Alan L., et al.. (2005). Altered Cytokine Responses of Dengue-Specific CD4+ T Cells to Heterologous Serotypes. The Journal of Immunology. 175(4). 2676–2683. 155 indexed citations
14.
Mathew, Anuja, Masanori Terajima, Kim West, et al.. (2005). Identification of Murine Poxvirus-Specific CD8+ CTL Epitopes with Distinct Functional Profiles. The Journal of Immunology. 174(4). 2212–2219. 40 indexed citations
15.
Pichyangkul, Sathit, Timothy P. Endy, Siripen Kalayanarooj, et al.. (2003). A Blunted Blood Plasmacytoid Dendritic Cell Response to an Acute Systemic Viral Infection Is Associated with Increased Disease Severity. The Journal of Immunology. 171(10). 5571–5578. 94 indexed citations
16.
Terajima, Masanori, John Cruz, Elizabeth D. Kilpatrick, et al.. (2003). Quantitation of CD8+ T Cell Responses to Newly Identified HLA-A*0201–restricted T Cell Epitopes Conserved Among Vaccinia and Variola (Smallpox) Viruses. The Journal of Experimental Medicine. 197(7). 927–932. 97 indexed citations
17.
Green, Sharone, David W. Vaughn, Siripen Kalayanarooj, et al.. (2002). T Cell Responses to an HLA-B*07-Restricted Epitope on the Dengue NS3 Protein Correlate with Disease Severity. The Journal of Immunology. 168(11). 5959–5965. 120 indexed citations
18.
Mathew, Anuja, et al.. (1996). Dominant recognition by human CD8+ cytotoxic T lymphocytes of dengue virus nonstructural proteins NS3 and NS1.2a.. Journal of Clinical Investigation. 98(7). 1684–1691. 101 indexed citations
19.
Kurane, I, Alan L. Rothman, Susan J. Gagnon, et al.. (1994). Immunopathologic mechanisms of dengue hemorrhagic fever and dengue shock syndrome. PubMed. 9. 59–64. 85 indexed citations
20.
Eckels, Kenneth H., D R Dubois, P L Summers, et al.. (1994). Immunization of Monkeys with Baculovirus-Dengue Type-4 Recombinants Containing Envelope and Nonstructural Proteins: Evidence of Priming and Partial Protection. American Journal of Tropical Medicine and Hygiene. 50(4). 472–478. 38 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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