James F. Mohan

1.5k total citations
18 papers, 1.2k citations indexed

About

James F. Mohan is a scholar working on Immunology, Genetics and Surgery. According to data from OpenAlex, James F. Mohan has authored 18 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Immunology, 10 papers in Genetics and 5 papers in Surgery. Recurrent topics in James F. Mohan's work include Diabetes and associated disorders (10 papers), Immune Cell Function and Interaction (9 papers) and T-cell and B-cell Immunology (7 papers). James F. Mohan is often cited by papers focused on Diabetes and associated disorders (10 papers), Immune Cell Function and Interaction (9 papers) and T-cell and B-cell Immunology (7 papers). James F. Mohan collaborates with scholars based in United States and Switzerland. James F. Mohan's co-authors include Emil R. Unanue, Shirley J. Petzold, Boris Calderón, Diane Mathis, Christophe Benoıst, Ralph Weissleder, Jhoanne L. Bautista, James Scott‐Browne, Chyi‐Song Hsieh and Hyang‐Mi Lee and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

James F. Mohan

18 papers receiving 1.2k citations

Peers

James F. Mohan
Chiju Wei China
Annie Mirsoian United States
Seokho Kim South Korea
Uriel Barkai United States
Jane Sun Australia
Chiju Wei China
James F. Mohan
Citations per year, relative to James F. Mohan James F. Mohan (= 1×) peers Chiju Wei

Countries citing papers authored by James F. Mohan

Since Specialization
Citations

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

Fields of papers citing papers by James F. Mohan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James F. Mohan. 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 James F. Mohan. The network helps show where James F. Mohan may publish in the future.

Co-authorship network of co-authors of James F. Mohan

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

All Works

18 of 18 papers shown
1.
Panduro, Marisella, Ricard Masia, Andrew C. Lake, et al.. (2023). Abstract 5125: Depletion of CCR8+ tumor Treg cells with SRF114 or anti-CCR8 therapy promotes robust antitumor activity and reshapes the tumor microenvironment toward a more pro-inflammatory milieu. Cancer Research. 83(7_Supplement). 5125–5125. 1 indexed citations
2.
Haines, Robert R, Marisella Panduro, Vito J. Palombella, et al.. (2023). 1354 Anti-CCR8 antibody CHS-114 (SRF114) depletes tumor-infiltrating regulatory T cells in dissociated tumors from patients with head and neck squamous cell carcinoma. SHILAP Revista de lepidopterología. A1508–A1508. 1 indexed citations
3.
Haines, Robert, Marisella Panduro, Andrew C. Lake, et al.. (2022). 1338 SRF114, an afucosylated anti-CCR8 antibody, depletes intratumoral Treg cells and reduces tumor growth. Regular and Young Investigator Award Abstracts. A1389–A1389. 1 indexed citations
4.
Panduro, Marisella, Jing Hua, Vito J. Palombella, et al.. (2020). Abstract 4548: SRF813, a fully human monoclonal antibody targeting the inhibitory receptor CD112R, enhances immune cell activation and demonstrates preclinical in vivo anti-tumor activity. Cancer Research. 80(16_Supplement). 4548–4548. 2 indexed citations
5.
Syed, Ismail, James F. Mohan, Pedro M. Moraes‐Vieira, et al.. (2019). PAHSAs attenuate immune responses and promote β cell survival in autoimmune diabetic mice. Journal of Clinical Investigation. 129(9). 3717–3731. 61 indexed citations
6.
Mohan, James F., Rainer H. Köhler, Jonathan A. Hill, et al.. (2017). Imaging the emergence and natural progression of spontaneous autoimmune diabetes. Proceedings of the National Academy of Sciences. 114(37). E7776–E7785. 48 indexed citations
7.
Miller, Miles A., Ravi A. Chandra, Michael F. Cuccarese, et al.. (2017). Radiation therapy primes tumors for nanotherapeutic delivery via macrophage-mediated vascular bursts. Science Translational Medicine. 9(392). 184 indexed citations
8.
Yissachar, Nissan, Yan Zhou, W. Lloyd Ung, et al.. (2017). An Intestinal Organ Culture System Uncovers a Role for the Nervous System in Microbe-Immune Crosstalk. Cell. 168(6). 1135–1148.e12. 185 indexed citations
9.
Clardy, Susan M., James F. Mohan, Claudio Vinegoni, et al.. (2015). Rapid, high efficiency isolation of pancreatic ß-cells. Scientific Reports. 5(1). 13681–13681. 16 indexed citations
10.
Ferris, Stephen T., Javier A. Carrero, James F. Mohan, et al.. (2014). A Minor Subset of Batf3-Dependent Antigen-Presenting Cells in Islets of Langerhans Is Essential for the Development of Autoimmune Diabetes. Immunity. 41(4). 657–669. 115 indexed citations
11.
Mohan, James F., Boris Calderón, Mark S. Anderson, & Emil R. Unanue. (2013). Pathogenic CD4+ T cells recognizing an unstable peptide of insulin are directly recruited into islets bypassing local lymph nodes. The Journal of Experimental Medicine. 210(11). 2403–2414. 47 indexed citations
12.
Clardy, Susan M., Edmund J. Keliher, James F. Mohan, et al.. (2013). Fluorescent Exendin-4 Derivatives for Pancreatic β-Cell Analysis. Bioconjugate Chemistry. 25(1). 171–177. 34 indexed citations
13.
Mohan, James F. & Emil R. Unanue. (2012). Unconventional recognition of peptides by T cells and the implications for autoimmunity. Nature reviews. Immunology. 12(10). 721–728. 71 indexed citations
14.
Mohan, James F. & Emil R. Unanue. (2012). A novel pathway of presentation by class II-MHC molecules involving peptides or denatured proteins important in autoimmunity. Molecular Immunology. 55(2). 166–168. 19 indexed citations
15.
Lee, Hyang‐Mi, Jhoanne L. Bautista, James Scott‐Browne, James F. Mohan, & Chyi‐Song Hsieh. (2012). A Broad Range of Self-Reactivity Drives Thymic Regulatory T Cell Selection to Limit Responses to Self. Immunity. 37(3). 475–486. 143 indexed citations
16.
Mohan, James F. & Emil R. Unanue. (2012). Register shifting of an insulin peptide–MHC complex allows diabetogenic T cells to escape thymic deletion. Molecular Immunology. 51(1). 26–26. 4 indexed citations
17.
Mohan, James F., Shirley J. Petzold, & Emil R. Unanue. (2011). Register shifting of an insulin peptide–MHC complex allows diabetogenic T cells to escape thymic deletion. The Journal of Experimental Medicine. 208(12). 2375–2383. 115 indexed citations
18.
Mohan, James F., Matteo Levisetti, Boris Calderón, et al.. (2010). Unique autoreactive T cells recognize insulin peptides generated within the islets of Langerhans in autoimmune diabetes. Nature Immunology. 11(4). 350–354. 147 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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