Douglas S. Kwon

13.3k total citations · 2 hit papers
82 papers, 6.3k citations indexed

About

Douglas S. Kwon is a scholar working on Virology, Immunology and Epidemiology. According to data from OpenAlex, Douglas S. Kwon has authored 82 papers receiving a total of 6.3k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Virology, 34 papers in Immunology and 31 papers in Epidemiology. Recurrent topics in Douglas S. Kwon's work include HIV Research and Treatment (35 papers), Immune Cell Function and Interaction (24 papers) and Reproductive tract infections research (23 papers). Douglas S. Kwon is often cited by papers focused on HIV Research and Treatment (35 papers), Immune Cell Function and Interaction (24 papers) and Reproductive tract infections research (23 papers). Douglas S. Kwon collaborates with scholars based in United States, Germany and South Africa. Douglas S. Kwon's co-authors include Dan R. Littman, Vineet N. KewalRamani, Jeena Middel, Gerard C.F. van Duijnhoven, Ruurd Torensma, Yvette van Kooyk, Hans S.L.M. Nottet, Sandra J. van Vliet, Carl G. Figdor and Teunis B. H. Geijtenbeek and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Douglas S. Kwon

79 papers receiving 6.2k citations

Hit Papers

DC-SIGN, a Dendritic Cell–Specific HIV-1-Binding Protein ... 2000 2026 2008 2017 2000 2015 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Douglas S. Kwon United States 33 3.1k 2.5k 1.6k 1.5k 1.3k 82 6.3k
Mary E. Klotman United States 48 2.1k 0.7× 2.1k 0.9× 1.9k 1.2× 1.6k 1.0× 2.3k 1.8× 131 7.3k
Gregory T. Spear United States 41 2.0k 0.6× 1.6k 0.6× 1.1k 0.6× 1.6k 1.0× 1.0k 0.8× 124 5.0k
Herman F. Staats United States 39 3.2k 1.0× 961 0.4× 1.2k 0.8× 1.1k 0.7× 970 0.7× 109 5.5k
Myra O. McClure United Kingdom 44 1.3k 0.4× 2.5k 1.0× 1.6k 1.0× 1.8k 1.2× 2.1k 1.6× 172 6.8k
Otto O. Yang United States 42 3.2k 1.0× 3.2k 1.3× 1.4k 0.9× 1.1k 0.7× 1.3k 1.0× 182 6.6k
Christopher J. Miller United States 52 4.2k 1.3× 5.3k 2.2× 1.4k 0.9× 2.7k 1.8× 2.9k 2.2× 188 9.1k
Nichole R. Klatt United States 35 2.0k 0.6× 2.6k 1.1× 1.1k 0.6× 1.3k 0.8× 1.7k 1.3× 109 5.1k
Charles R. Wira United States 57 6.6k 2.1× 1.1k 0.4× 944 0.6× 1.6k 1.1× 931 0.7× 204 9.9k
Karin Loré Sweden 42 3.7k 1.2× 1.5k 0.6× 1.3k 0.8× 1.0k 0.7× 1.2k 0.9× 108 5.8k
Melissa Pope United States 41 4.4k 1.4× 3.4k 1.4× 965 0.6× 1.1k 0.8× 1.1k 0.9× 80 6.4k

Countries citing papers authored by Douglas S. Kwon

Since Specialization
Citations

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

Fields of papers citing papers by Douglas S. Kwon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Douglas S. Kwon. 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 Douglas S. Kwon. The network helps show where Douglas S. Kwon may publish in the future.

Co-authorship network of co-authors of Douglas S. Kwon

This figure shows the co-authorship network connecting the top 25 collaborators of Douglas S. Kwon. A scholar is included among the top collaborators of Douglas S. Kwon 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 Douglas S. Kwon. Douglas S. Kwon 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.
Jabbar, Karolina S., Sambhawa Priya, Jiawu Xu, et al.. (2025). Human immunodeficiency virus and antiretroviral therapies exert distinct influences across diverse gut microbiomes. Nature Microbiology. 10(11). 2720–2735.
2.
Foessleitner, Philipp, Marvin M. Goldenberg, M.R.V. Murthy, et al.. (2025). Association between changes in genital immune markers and vaginal microbiome transitions in bacterial vaginosis. Scientific Reports. 15(1). 3536–3536.
3.
Hussain, Fatima A., Caroline A. Werlang, Benjamin M. Woolston, et al.. (2024). Prevotella are major contributors of sialidases in the human vaginal microbiome. Proceedings of the National Academy of Sciences. 121(36). 16 indexed citations
4.
Symul, Laura, Pratheepa Jeganathan, Elizabeth K. Costello, et al.. (2023). Sub-communities of the vaginal microbiota in pregnant and non-pregnant women. Proceedings of the Royal Society B Biological Sciences. 290(2011). 20231461–20231461. 15 indexed citations
5.
Corleis, Björn, Constantine N. Tzouanas, Marc H. Wadsworth, et al.. (2023). Tobacco smoke exposure recruits inflammatory airspace monocytes that establish permissive lung niches for Mycobacterium tuberculosis. Science Translational Medicine. 15(725). eadg3451–eadg3451. 11 indexed citations
6.
Anahtar, Melis N., Jiawu Xu, Jeffrey M. Paer, et al.. (2021). Prediction of Antimicrobial Resistance in Clinical Enterococcus faecium Isolates Using a Rules-Based Analysis of Whole-Genome Sequences. Antimicrobial Agents and Chemotherapy. 66(1). e0119621–e0119621. 5 indexed citations
7.
Corleis, Björn, Amy K. Dickey, Abigail E. Schiff, et al.. (2021). Smoking and Human Immunodeficiency Virus 1 Infection Promote Retention of CD8+ T Cells in the Airway Mucosa. American Journal of Respiratory Cell and Molecular Biology. 65(5). 513–520. 12 indexed citations
8.
Hoang, Thuy, Kevin DeLong, Seth M. Bloom, et al.. (2020). The cervicovaginal mucus barrier to HIV-1 is diminished in bacterial vaginosis. PLoS Pathogens. 16(1). e1008236–e1008236. 52 indexed citations
9.
Bryson, Bryan D., Tracy R. Rosebrock, Fikadu Tafesse, et al.. (2019). Heterogeneous GM-CSF signaling in macrophages is associated with control of Mycobacterium tuberculosis. Nature Communications. 10(1). 2329–2329. 58 indexed citations
10.
McKinnon, Lyle R., Sharon L. Achilles, Catriona S. Bradshaw, et al.. (2019). The Evolving Facets of Bacterial Vaginosis: Implications for HIV Transmission. AIDS Research and Human Retroviruses. 35(3). 219–228. 193 indexed citations
11.
Olson, Gregory S., James M. Richter, John J. Garber, et al.. (2018). Increased frequency of systemic pro-inflammatory Vδ1+ γδ T cells in HIV elite controllers correlates with gut viral load. Scientific Reports. 8(1). 16471–16471. 21 indexed citations
12.
Shen, Shiqian, Grewo Lim, Zerong You, et al.. (2017). Gut microbiota is critical for the induction of chemotherapy-induced pain. Nature Neuroscience. 20(9). 1213–1216. 218 indexed citations
13.
Körner, Christian, Camille R. Simoneau, Philipp Schommers, et al.. (2017). HIV-1-Mediated Downmodulation of HLA-C Impacts Target Cell Recognition and Antiviral Activity of NK Cells. Cell Host & Microbe. 22(1). 111–119.e4. 30 indexed citations
14.
Corleis, Björn, Antonella Lisanti, Christian Körner, et al.. (2017). Early type I Interferon response induces upregulation of human β-defensin 1 during acute HIV-1 infection. PLoS ONE. 12(3). e0173161–e0173161. 11 indexed citations
15.
Liebenberg, Lenine J. P., Derseree Archary, Aida Sivro, & Douglas S. Kwon. (2017). Bugs, drugs, and HIV: the role of the vaginal microbiome in HIV risk and antiretroviral efficacy for HIV prevention. Genome Medicine. 9(1). 74–74. 8 indexed citations
16.
Riou, Catherine, Andreia Soares, Björn Corleis, et al.. (2016). HIV Skews the Lineage-Defining Transcriptional Profile of Mycobacterium tuberculosis–Specific CD4+ T Cells. The Journal of Immunology. 196(7). 3006–3018. 17 indexed citations
17.
Byrne, Elizabeth H., Melis N. Anahtar, Gregory S. Olson, et al.. (2014). Injectable Contraceptive Use Correlates with Increased HIV Target Cells at the Cervix in Young South African Women. AIDS Research and Human Retroviruses. 30(S1). A54–A55. 1 indexed citations
18.
Varadarajan, Navin, Douglas S. Kwon, Kenneth Law, et al.. (2012). Rapid, efficient functional characterization and recovery of HIV-specific human CD8 + T cells using microengraving. Proceedings of the National Academy of Sciences. 109(10). 3885–3890. 87 indexed citations
19.
Brockman, Mark A., Douglas S. Kwon, David F. Pavlik, et al.. (2009). IL-10 is up-regulated in multiple cell types during viremic HIV infection and reversibly inhibits virus-specific T cells. Blood. 114(2). 346–356. 225 indexed citations
20.
Kwon, Douglas S., Morris S. Jones, Craig B. Davis, et al.. (1998). The Amino Terminus of Human CCR5 Is Required for Its Function as a Receptor for Diverse Human and Simian Immunodeficiency Virus Envelope Glycoproteins. Virology. 248(2). 357–371. 59 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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