Thomas S. Kupper

26.2k total citations · 8 hit papers
246 papers, 19.3k citations indexed

About

Thomas S. Kupper is a scholar working on Immunology, Dermatology and Immunology and Allergy. According to data from OpenAlex, Thomas S. Kupper has authored 246 papers receiving a total of 19.3k indexed citations (citations by other indexed papers that have themselves been cited), including 158 papers in Immunology, 91 papers in Dermatology and 44 papers in Immunology and Allergy. Recurrent topics in Thomas S. Kupper's work include Immunotherapy and Immune Responses (80 papers), T-cell and B-cell Immunology (70 papers) and Cutaneous lymphoproliferative disorders research (52 papers). Thomas S. Kupper is often cited by papers focused on Immunotherapy and Immune Responses (80 papers), T-cell and B-cell Immunology (70 papers) and Cutaneous lymphoproliferative disorders research (52 papers). Thomas S. Kupper collaborates with scholars based in United States, Germany and Japan. Thomas S. Kupper's co-authors include Rachael A. Clark, Robert C. Fuhlbrigge, Chang Ook Park, Hitoshi Mizutani, Caroline Robert, Luzheng Liu, Rei Watanabe, Xiaodong Jiang, Richard Groves and Ifor R. Williams and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Thomas S. Kupper

242 papers receiving 18.9k citations

Hit Papers

Identification of cells i... 1989 2026 2001 2013 2008 1989 2012 2006 2004 250 500 750 1000

Author Peers

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

Author Last Decade Papers Cites
Thomas S. Kupper 11.2k 5.2k 3.8k 3.7k 2.5k 246 19.3k
Brian J. Nickoloff 9.1k 0.8× 5.6k 1.1× 4.4k 1.2× 5.3k 1.4× 1.3k 0.5× 239 19.0k
Enno Christophers 10.1k 0.9× 6.0k 1.1× 2.5k 0.7× 3.7k 1.0× 2.0k 0.8× 362 18.9k
Georg Stingl 9.5k 0.8× 4.2k 0.8× 2.2k 0.6× 2.5k 0.7× 3.2k 1.3× 331 17.8k
Bernhard Homey 11.4k 1.0× 6.7k 1.3× 6.6k 1.8× 4.4k 1.2× 3.9k 1.6× 263 23.1k
Thomas Ruzicka 6.2k 0.6× 11.9k 2.3× 3.3k 0.9× 5.7k 1.5× 3.7k 1.5× 672 26.2k
Frank O. Nestlé 18.4k 1.6× 7.2k 1.4× 4.7k 1.3× 5.0k 1.3× 889 0.4× 202 24.1k
Lars E. French 7.3k 0.7× 5.2k 1.0× 4.4k 1.2× 6.7k 1.8× 701 0.3× 482 21.2k
Raif S. Geha 19.4k 1.7× 4.3k 0.8× 2.7k 0.7× 5.3k 1.4× 6.5k 2.6× 501 31.8k
Atul K. Bhan 9.1k 0.8× 1.4k 0.3× 3.0k 0.8× 3.2k 0.9× 1.6k 0.6× 235 19.5k
Gerold Schuler 25.1k 2.2× 2.2k 0.4× 7.7k 2.0× 7.8k 2.1× 1.8k 0.7× 355 33.0k

Countries citing papers authored by Thomas S. Kupper

Since Specialization
Citations

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

Fields of papers citing papers by Thomas S. Kupper

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas S. Kupper

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas S. Kupper. A scholar is included among the top collaborators of Thomas S. Kupper 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 Thomas S. Kupper. Thomas S. Kupper 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.
Jfri, Abdulhadi, César A. Virgen, Marianne Tawa, et al.. (2023). Prevalence and implications of mogamulizumab-induced immune-related adverse events in mycosis fungoides/Sézary syndrome; a single-center experience. Journal of the American Academy of Dermatology. 89(5). 1044–1047. 3 indexed citations
2.
Virgen, César A., Jeffrey A. Sparks, Anju Nohria, et al.. (2023). Mogamulizumab-Associated Myositis With and Without Myasthenia Gravis and/or Myocarditis in Patients With T-Cell Lymphoma. The Oncologist. 28(8). e694–e698. 3 indexed citations
3.
Tian, Tian, Serena Lofftus, Youdong Pan, et al.. (2020). IL1α Antagonizes IL1β and Promotes Adaptive Immune Rejection of Malignant Tumors. Cancer Immunology Research. 8(5). 660–671. 18 indexed citations
4.
O’Malley, John T., Adèle de Masson, Elizabeth L. Lowry, et al.. (2019). Radiotherapy Eradicates Malignant T Cells and Is Associated with Improved Survival in Early-Stage Mycosis Fungoides. Clinical Cancer Research. 26(2). 408–418. 17 indexed citations
5.
Masson, Adèle de, John T. O’Malley, Christopher P. Elco, et al.. (2018). High-throughput sequencing of the T cell receptor β gene identifies aggressive early-stage mycosis fungoides. Science Translational Medicine. 10(440). 81 indexed citations
6.
Jain, Salvia, Abigail Washington, Rebecca Karp Leaf, et al.. (2017). Decitabine Priming Enhances Mucin 1 Inhibition Mediated Disruption of Redox Homeostasis in Cutaneous T-Cell Lymphoma. Molecular Cancer Therapeutics. 16(10). 2304–2314. 10 indexed citations
7.
Jain, Salvia, Dina Stroopinsky, Yin Li, et al.. (2015). Mucin 1 is a potential therapeutic target in cutaneous T-cell lymphoma. Blood. 126(3). 354–362. 28 indexed citations
8.
Litvinov, Ivan V., Elena Netchiporouk, Linda Moreau, et al.. (2015). The Use of Transcriptional Profiling to Improve Personalized Diagnosis and Management of Cutaneous T-cell Lymphoma (CTCL). Clinical Cancer Research. 21(12). 2820–2829. 66 indexed citations
9.
Litvinov, Ivan V., Yuanshen Huang, Kevin Pehr, et al.. (2014). Ectopic Expression of Cancer–Testis Antigens in Cutaneous T-cell Lymphoma Patients. Clinical Cancer Research. 20(14). 3799–3808. 37 indexed citations
10.
Schlapbach, Christoph, Ahmed Gehad, Chao Yang, et al.. (2014). Human T H 9 Cells Are Skin-Tropic and Have Autocrine and Paracrine Proinflammatory Capacity. Science Translational Medicine. 6(219). 219ra8–219ra8. 163 indexed citations
11.
Martin, Jennifer & Thomas S. Kupper. (2012). Infektionsrisiken junger Freiwilliger bei internationalen Sozialprojekten von Non-Governmental Organizations. RWTH Publications (RWTH Aachen). 1 indexed citations
12.
Chang, De-Kuan, Jianhua Sui, Shusheng Geng, et al.. (2012). Humanization of an Anti-CCR4 Antibody That Kills Cutaneous T-Cell Lymphoma Cells and Abrogates Suppression by T-Regulatory Cells. Molecular Cancer Therapeutics. 11(11). 2451–2461. 60 indexed citations
13.
Kupper, Thomas S., et al.. (2011). Benjamin-Handbuch. J.B. Metzler eBooks. 1 indexed citations
14.
Frank, Natasha Y., Tobias Schatton, Soo‐Jeong Kim, et al.. (2011). VEGFR-1 Expressed by Malignant Melanoma-Initiating Cells Is Required for Tumor Growth. Cancer Research. 71(4). 1474–1485. 133 indexed citations
15.
Litvinov, Ivan V., David A. Jones, Denis Sasseville, & Thomas S. Kupper. (2010). Transcriptional Profiles Predict Disease Outcome in Patients with Cutaneous T-Cell Lymphoma. Clinical Cancer Research. 16(7). 2106–2114. 53 indexed citations
16.
Clark, Rachael A., Susan S. Huang, George F. Murphy, et al.. (2008). Human squamous cell carcinomas evade the immune response by down-regulation of vascular E-selectin and recruitment of regulatory T cells. The Journal of Experimental Medicine. 205(10). 2221–2234. 170 indexed citations
17.
Weishaupt, Carsten, et al.. (2007). T-Cell Distribution and Adhesion Receptor Expression in Metastatic Melanoma. Clinical Cancer Research. 13(9). 2549–2556. 60 indexed citations
18.
Clark, Rachael A. & Thomas S. Kupper. (2006). IL-15 and dermal fibroblasts induce proliferation of natural regulatory T cells isolated from human skin. Blood. 109(1). 194–202. 144 indexed citations
19.
Yamanaka, Keiichi, et al.. (2005). Decreased T-Cell Receptor Excision Circles in Cutaneous T-Cell Lymphoma. Clinical Cancer Research. 11(16). 5748–5755. 26 indexed citations
20.
Kupper, Thomas S. & Douglas R. Green. (1984). Immunoregulation after thermal injury: sequential appearance of I-J+, Ly-1 T suppressor inducer cells and Ly-2 T suppressor effector cells following thermal trauma in mice.. The Journal of Immunology. 133(6). 3047–3053. 32 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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