Samuel M. Behar

15.6k total citations · 2 hit papers
127 papers, 11.8k citations indexed

About

Samuel M. Behar is a scholar working on Immunology, Infectious Diseases and Epidemiology. According to data from OpenAlex, Samuel M. Behar has authored 127 papers receiving a total of 11.8k indexed citations (citations by other indexed papers that have themselves been cited), including 101 papers in Immunology, 61 papers in Infectious Diseases and 34 papers in Epidemiology. Recurrent topics in Samuel M. Behar's work include Tuberculosis Research and Epidemiology (59 papers), Immune Cell Function and Interaction (57 papers) and T-cell and B-cell Immunology (44 papers). Samuel M. Behar is often cited by papers focused on Tuberculosis Research and Epidemiology (59 papers), Immune Cell Function and Interaction (57 papers) and T-cell and B-cell Immunology (44 papers). Samuel M. Behar collaborates with scholars based in United States, Portugal and United Kingdom. Samuel M. Behar's co-authors include Michael B. Brenner, Steven A. Porcelli, Heinz G. Remold, Maziar Divangahi, Joshua S. Woodworth, Markus Sköld, Cláudio Nunes-Alves, Alissa A. Chackerian, Evan Beckman and Pushpa Jayaraman and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Samuel M. Behar

124 papers receiving 11.7k citations

Hit Papers

Recognition of a lipid antigen by CD1-restricted αβ+ T cells 1994 2026 2004 2015 1994 2006 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Samuel M. Behar United States 59 7.8k 5.0k 3.8k 2.3k 1.1k 127 11.8k
Thomas J. Scriba South Africa 50 5.2k 0.7× 5.6k 1.1× 3.5k 0.9× 1.9k 0.8× 617 0.6× 206 9.2k
W. Henry Boom United States 62 5.2k 0.7× 6.9k 1.4× 5.3k 1.4× 2.1k 0.9× 636 0.6× 213 11.1k
J. Ernst United States 53 4.2k 0.5× 5.7k 1.1× 4.1k 1.1× 2.6k 1.1× 745 0.7× 136 10.1k
Mark R. Alderson United States 56 7.4k 0.9× 2.3k 0.5× 3.3k 0.9× 2.9k 1.3× 1.6k 1.5× 115 12.0k
Peter A. Sieling United States 45 5.3k 0.7× 2.2k 0.4× 2.5k 0.6× 1.7k 0.7× 763 0.7× 84 8.9k
Carl G. Feng Australia 49 5.5k 0.7× 3.2k 0.6× 3.0k 0.8× 1.5k 0.6× 857 0.8× 100 8.7k
Shabaana A. Khader United States 49 6.0k 0.8× 4.5k 0.9× 3.6k 0.9× 1.8k 0.8× 928 0.8× 117 10.1k
John Chan United States 52 4.6k 0.6× 7.4k 1.5× 5.8k 1.5× 2.0k 0.9× 1.4k 1.3× 122 12.6k
Stefan Ehlers Germany 54 3.3k 0.4× 3.7k 0.7× 3.4k 0.9× 2.4k 1.0× 817 0.7× 146 8.8k
Heinz G. Remold United States 49 4.3k 0.6× 3.5k 0.7× 2.9k 0.8× 2.3k 1.0× 695 0.6× 118 8.8k

Countries citing papers authored by Samuel M. Behar

Since Specialization
Citations

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

Fields of papers citing papers by Samuel M. Behar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samuel M. Behar

This figure shows the co-authorship network connecting the top 25 collaborators of Samuel M. Behar. A scholar is included among the top collaborators of Samuel M. Behar 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 Samuel M. Behar. Samuel M. Behar 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.
Mortensen, Rasmus, Cecilia S. Lindestam Arlehamn, Rhea N. Coler, et al.. (2025). T cell–macrophage interactions in tuberculosis: What we've got here is failure to communicate. Journal of Internal Medicine. 299(1). 44–65.
2.
Lai, Rocky, et al.. (2023). Key advances in vaccine development for tuberculosis—success and challenges. npj Vaccines. 8(1). 158–158. 30 indexed citations
3.
Baer, Christina E., et al.. (2023). High Bacillary Burden and the ESX-1 Type VII Secretion System Promote MHC Class I Presentation by Mycobacterium tuberculosis–Infected Macrophages to CD8 T Cells. The Journal of Immunology. 210(10). 1531–1542. 10 indexed citations
4.
Lai, Rocky, Cecilia S. Lindestam Arlehamn, Gillian Beamer, et al.. (2023). Host genetic background is a barrier to broadly effective vaccine–mediated protection against tuberculosis. Journal of Clinical Investigation. 133(13). 24 indexed citations
5.
Sutiwisesak, Rujapak, Nathan Hicks, Kenan C. Murphy, et al.. (2020). A natural polymorphism of Mycobacterium tuberculosis in the esxH gene disrupts immunodomination by the TB10.4-specific CD8 T cell response. PLoS Pathogens. 16(10). e1009000–e1009000. 21 indexed citations
6.
Smith, Clare M., Megan K. Proulx, Rocky Lai, et al.. (2019). Functionally Overlapping Variants Control Tuberculosis Susceptibility in Collaborative Cross Mice. mBio. 10(6). 30 indexed citations
7.
Sutiwisesak, Rujapak, Yu‐Jung Lu, Fiona Raso, et al.. (2018). Mycobacterium tuberculosis-specific CD4+ and CD8+ T cells differ in their capacity to recognize infected macrophages. PLoS Pathogens. 14(5). e1007060–e1007060. 78 indexed citations
8.
Carpenter, Stephen M., et al.. (2017). Vaccine-elicited memory CD4+ T cell expansion is impaired in the lungs during tuberculosis. PLoS Pathogens. 13(11). e1006704–e1006704. 21 indexed citations
9.
Smith, Clare M., Megan K. Proulx, Andrew J. Olive, et al.. (2016). Tuberculosis Susceptibility and Vaccine Protection Are Independently Controlled by Host Genotype. mBio. 7(5). 131 indexed citations
10.
Martin, Constance J., et al.. (2013). Macrophages clean up: efferocytosis and microbial control. Current Opinion in Microbiology. 17. 17–23. 140 indexed citations
11.
Nandi, Bisweswar & Samuel M. Behar. (2011). Regulation of neutrophils by interferon-γ limits lung inflammation during tuberculosis infection. The Journal of Experimental Medicine. 208(11). 2251–2262. 283 indexed citations
12.
Layre, Emilie, Lindsay Sweet, Sun Hee Hong, et al.. (2011). A Comparative Lipidomics Platform for Chemotaxonomic Analysis of Mycobacterium tuberculosis. Chemistry & Biology. 18(12). 1537–1549. 141 indexed citations
13.
Jayaraman, Pushpa, Isabel Sada‐Ovalle, Ana C. Anderson, et al.. (2010). Tim3 binding to galectin-9 stimulates antimicrobial immunity. The Journal of Experimental Medicine. 207(11). 2343–2354. 165 indexed citations
14.
Sada‐Ovalle, Isabel, Markus Sköld, Tian Tian, Gurdyal S. Besra, & Samuel M. Behar. (2010). α-Galactosylceramide as a Therapeutic Agent for Pulmonary Mycobacterium tuberculosis Infection. American Journal of Respiratory and Critical Care Medicine. 182(6). 841–847. 48 indexed citations
15.
Chen, Minjian, Maziar Divangahi, Huixian Gan, et al.. (2008). Lipid mediators in innate immunity against tuberculosis: opposing roles of PGE2 and LXA4 in the induction of macrophage death. The Journal of Experimental Medicine. 205(12). 2791–2801. 280 indexed citations
16.
Ghosh, Shamik, Alissa A. Chackerian, Christina M. Parker, Christie M. Ballantyne, & Samuel M. Behar. (2006). The LFA-1 Adhesion Molecule Is Required for Protective Immunity during Pulmonary Mycobacterium tuberculosis Infection. The Journal of Immunology. 176(8). 4914–4922. 43 indexed citations
17.
Sköld, Markus, Xiaowei Xiong, Petr A. Illarionov, Gurdyal S. Besra, & Samuel M. Behar. (2005). Interplay of Cytokines and Microbial Signals in Regulation of CD1d Expression and NKT Cell Activation. The Journal of Immunology. 175(6). 3584–3593. 91 indexed citations
18.
Cernadas, Manuela, Masahiko Sugita, Nicole N. van der Wel, et al.. (2003). Lysosomal Localization of Murine CD1d Mediated by AP-3 Is Necessary for NK T Cell Development. The Journal of Immunology. 171(8). 4149–4155. 76 indexed citations
19.
Grant, Ethan, Evan Beckman, Samuel M. Behar, et al.. (2002). Fine Specificity of TCR Complementarity-Determining Region Residues and Lipid Antigen Hydrophilic Moieties in the Recognition of a CD1-Lipid Complex. The Journal of Immunology. 168(8). 3933–3940. 46 indexed citations
20.
Watts, Gerald F., Abdijapar Shamshiev, Gennaro De Libero, et al.. (2000). Molecular Recognition of Human CD1b Antigen Complexes: Evidence for a Common Pattern of Interaction with αβ TCRs. The Journal of Immunology. 165(8). 4494–4504. 45 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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