M. Suresh

10.2k total citations · 2 hit papers
103 papers, 7.2k citations indexed

About

M. Suresh is a scholar working on Immunology, Infectious Diseases and Epidemiology. According to data from OpenAlex, M. Suresh has authored 103 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Immunology, 17 papers in Infectious Diseases and 16 papers in Epidemiology. Recurrent topics in M. Suresh's work include Immune Cell Function and Interaction (49 papers), T-cell and B-cell Immunology (48 papers) and Immunotherapy and Immune Responses (40 papers). M. Suresh is often cited by papers focused on Immune Cell Function and Interaction (49 papers), T-cell and B-cell Immunology (48 papers) and Immunotherapy and Immune Responses (40 papers). M. Suresh collaborates with scholars based in United States, Japan and United Kingdom. M. Suresh's co-authors include Rafi Ahmed, John D. Altman, Kaja Murali‐Krishna, David Sourdive, Allan Zajac, Joseph N. Blattman, Jill E. Slansky, Joseph D. Miller, Eui Ho Kim and Erin H. Plisch and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

M. Suresh

101 papers receiving 7.1k citations

Hit Papers

Counting Antigen-Specific CD8 T Cells: A Reevaluation of ... 1998 2026 2007 2016 1998 1998 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
M. Suresh United States 38 5.2k 1.6k 1.2k 1.1k 1.0k 103 7.2k
Allan Randrup Thomsen Denmark 43 4.4k 0.8× 1.6k 1.0× 1.0k 0.9× 1.2k 1.1× 940 0.9× 178 6.6k
Allan Zajac United States 38 6.8k 1.3× 1.5k 1.0× 1.6k 1.4× 914 0.8× 898 0.9× 66 8.4k
Jan Pravsgaard Christensen Denmark 42 3.9k 0.7× 1.6k 1.0× 1.6k 1.3× 814 0.8× 1.2k 1.1× 149 6.3k
Vaiva Vezys United States 39 7.7k 1.5× 1.2k 0.8× 1.5k 1.3× 776 0.7× 1.2k 1.2× 73 9.2k
Hubertus Hochrein Germany 39 8.1k 1.5× 1.4k 0.9× 944 0.8× 811 0.8× 2.4k 2.3× 73 10.5k
Andreas Wack United Kingdom 43 5.3k 1.0× 2.5k 1.6× 740 0.6× 1.9k 1.8× 1.9k 1.8× 82 8.4k
Andrea Cerutti United States 52 6.2k 1.2× 1.2k 0.8× 904 0.8× 1.0k 1.0× 2.3k 2.3× 125 10.0k
Nicholas M. Valiante United States 34 7.1k 1.4× 1.5k 0.9× 993 0.8× 720 0.7× 1.5k 1.5× 50 9.3k
David G. Brooks United States 48 4.6k 0.9× 1.4k 0.9× 1.6k 1.3× 1.2k 1.1× 2.3k 2.2× 120 8.4k
Anne Krug Germany 44 6.8k 1.3× 1.5k 0.9× 853 0.7× 1.3k 1.2× 1.9k 1.8× 80 9.3k

Countries citing papers authored by M. Suresh

Since Specialization
Citations

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

Fields of papers citing papers by M. Suresh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Suresh. 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 M. Suresh. The network helps show where M. Suresh may publish in the future.

Co-authorship network of co-authors of M. Suresh

This figure shows the co-authorship network connecting the top 25 collaborators of M. Suresh. A scholar is included among the top collaborators of M. Suresh 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 M. Suresh. M. Suresh 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.
Kingstad-Bakke, Brock, Boyd L. Yount, Ryuta Uraki, et al.. (2023). Airway surveillance and lung viral control by memory T cells induced by COVID-19 mRNA vaccine. JCI Insight. 8(22). 12 indexed citations
2.
Denny, Michael F., Brock Kingstad-Bakke, Mandar Bawadekar, et al.. (2022). Peptidylarginine Deiminase 2 in Murine Antiviral and Autoimmune Antibody Responses. Journal of Immunology Research. 2022. 1–12. 2 indexed citations
3.
Dobson, Hannah E., Gregory C. Kujoth, Junfeng Huang, et al.. (2021). Structural basis of Blastomyces Endoglucanase-2 adjuvancy in anti-fungal and -viral immunity. PLoS Pathogens. 17(3). e1009324–e1009324. 9 indexed citations
4.
Kingstad-Bakke, Brock, Randall Toy, Woo‐Jong Lee, et al.. (2021). Polymeric Pathogen-Like Particles-Based Combination Adjuvants Elicit Potent Mucosal T Cell Immunity to Influenza A Virus. Frontiers in Immunology. 11. 559382–559382. 14 indexed citations
5.
Nanjappa, Som G., et al.. (2018). CBLB Constrains Inactivated Vaccine–Induced CD8+ T Cell Responses and Immunity against Lethal Fungal Pneumonia. The Journal of Immunology. 201(6). 1717–1726. 10 indexed citations
6.
Beems, Megan, et al.. (2018). Co-transfer of tumor-specific effector and memory CD8+ T cells enhances the efficacy of adoptive melanoma immunotherapy in a mouse model. Journal for ImmunoTherapy of Cancer. 6(1). 41–41. 10 indexed citations
7.
Shin, Hyun Mu, Varun N. Kapoor, Gwanghun Kim, et al.. (2017). Transient expression of ZBTB32 in anti-viral CD8+ T cells limits the magnitude of the effector response and the generation of memory. PLoS Pathogens. 13(8). e1006544–e1006544. 18 indexed citations
8.
Kim, Eui Ho, et al.. (2016). Mcl-1 regulates effector and memory CD8 T-cell differentiation during acute viral infection. Virology. 490. 75–82. 10 indexed citations
9.
Chandrasekhar, M, et al.. (2014). Combined effects of pranayama and suryanamaskar on dynamic spirometric values in normal young subject. National Journal of Physiology Pharmacy and Pharmacology. 5(2). 79–79. 3 indexed citations
10.
Das, Subash C., Jeremy F. Fuchs, M. Suresh, et al.. (2013). Deciphering the protective role of adaptive immunity to CHIKV/IRES a novel candidate vaccine against Chikungunya in the A129 mouse model. Vaccine. 31(33). 3353–3360. 69 indexed citations
11.
Walsh, Kevin B., John R. Teijaro, Peter R. Wilker, et al.. (2011). Suppression of cytokine storm with a sphingosine analog provides protection against pathogenic influenza virus. Proceedings of the National Academy of Sciences. 108(29). 12018–12023. 195 indexed citations
12.
Walsh, Kevin B., Peter R. Wilker, M. Suresh, et al.. (2011). Pathogenic H1N1 2009 influenza virus-induced pulmonary injury is suppressed by sphingosine analog-mediated inhibition of cytokine storm (49.3). The Journal of Immunology. 186(1_Supplement). 49.3–49.3. 1 indexed citations
13.
Russ, Andrew, Alexander L. Rakhmilevich, Christine M. Seroogy, et al.. (2011). Suppression of T-Cell Expansion by Melanoma is Exerted on Resting Cells. Annals of Surgical Oncology. 18(13). 3848–3857. 11 indexed citations
14.
Dharumadurai, Dhanasekaran, et al.. (2010). Diagnostic Value of Real Time PCR and Associated Bacterial and Fungal Infections in Female Genital Tuberculosis. Biomedical & Pharmacology Journal. 3(1). 73–79. 3 indexed citations
15.
Nakayama, Yumi, Shin‐Il Kim, Eui Ho Kim, et al.. (2009). C3 Promotes Expansion of CD8+ and CD4+ T Cells in a Listeria monocytogenes Infection. The Journal of Immunology. 183(5). 2921–2931. 33 indexed citations
16.
Nanjappa, Som G., Anju Singh, Erin H. Plisch, et al.. (2007). Cbl-b Regulates Antigen-Induced TCR Down-Regulation and IFN-γ Production by Effector CD8 T Cells without Affecting Functional Avidity. The Journal of Immunology. 179(11). 7233–7243. 38 indexed citations
17.
Tewari, Kavita, Yumi Nakayama, & M. Suresh. (2007). Role of Direct Effects of IFN-γ on T Cells in the Regulation of CD8 T Cell Homeostasis. The Journal of Immunology. 179(4). 2115–2125. 61 indexed citations
18.
Nakayama, Yumi, et al.. (2005). Role of Thymic Output in Regulating CD8 T-Cell Homeostasis during Acute and Chronic Viral Infection. Journal of Virology. 79(15). 9419–9429. 34 indexed citations
19.
Tewari, Kavita, Jonah B. Sacha, Xiaoyan Gao, & M. Suresh. (2004). Effect of Chronic Viral Infection on Epitope Selection, Cytokine Production, and Surface Phenotype of CD8 T Cells and the Role of IFN-γ Receptor in Immune Regulation. The Journal of Immunology. 172(3). 1491–1500. 26 indexed citations
20.
Suresh, M., Jason K. Whitmire, Laurie E. Harrington, et al.. (2001). Role of CD28-B7 Interactions in Generation and Maintenance of CD8 T Cell Memory. The Journal of Immunology. 167(10). 5565–5573. 165 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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