Michael C. Abt

7.6k total citations · 5 hit papers
33 papers, 6.0k citations indexed

About

Michael C. Abt is a scholar working on Infectious Diseases, Molecular Biology and Immunology. According to data from OpenAlex, Michael C. Abt has authored 33 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Infectious Diseases, 15 papers in Molecular Biology and 14 papers in Immunology. Recurrent topics in Michael C. Abt's work include Clostridium difficile and Clostridium perfringens research (19 papers), Gut microbiota and health (15 papers) and IL-33, ST2, and ILC Pathways (7 papers). Michael C. Abt is often cited by papers focused on Clostridium difficile and Clostridium perfringens research (19 papers), Gut microbiota and health (15 papers) and IL-33, ST2, and ILC Pathways (7 papers). Michael C. Abt collaborates with scholars based in United States, Canada and Croatia. Michael C. Abt's co-authors include David Artis, Eric G. Pamer, E. John Wherry, Laurel A. Monticelli, Gregory F. Sonnenberg, Theresa Alenghat, Travis A. Doering, Jill Angelosanto, Brian J. Laidlaw and Peter T. McKenney and has published in prestigious journals such as Nature, Nature Medicine and Nature Communications.

In The Last Decade

Michael C. Abt

32 papers receiving 6.0k citations

Hit Papers

Innate lymphoid cells promote lung-tissue homeostasis aft... 2011 2026 2016 2021 2011 2011 2012 2012 2016 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael C. Abt United States 18 3.5k 1.8k 1.8k 1.3k 850 33 6.0k
Nicolas Bouladoux United States 35 4.8k 1.4× 2.2k 1.2× 772 0.4× 940 0.7× 849 1.0× 52 8.1k
Jérôme Viala France 22 3.7k 1.1× 1.7k 0.9× 1.4k 0.8× 636 0.5× 1.2k 1.5× 78 6.3k
Kenneth W. Beagley Australia 50 4.3k 1.2× 1.3k 0.7× 904 0.5× 720 0.5× 1.6k 1.8× 237 8.6k
Yun‐Gi Kim Japan 34 3.4k 1.0× 3.7k 2.0× 598 0.3× 1.2k 0.9× 1.3k 1.5× 73 7.3k
Phillip D. Smith United States 52 4.0k 1.1× 1.8k 1.0× 2.7k 1.5× 2.0k 1.5× 1.9k 2.2× 181 10.4k
Gregory F. Sonnenberg United States 38 7.8k 2.2× 2.3k 1.3× 4.0k 2.3× 1.1k 0.8× 1.2k 1.4× 68 11.1k
Jason A. Hall United States 19 5.5k 1.6× 2.3k 1.3× 601 0.3× 701 0.5× 675 0.8× 26 8.2k
Kohtaro Fujihashi United States 53 5.0k 1.4× 1.5k 0.8× 492 0.3× 1.3k 0.9× 1.5k 1.7× 169 8.3k
Marije Oosting Netherlands 38 3.1k 0.9× 2.8k 1.5× 469 0.3× 1.9k 1.5× 1.4k 1.6× 75 7.2k
Marcel R. de Zoete Netherlands 34 2.2k 0.6× 3.0k 1.6× 520 0.3× 930 0.7× 627 0.7× 50 5.6k

Countries citing papers authored by Michael C. Abt

Since Specialization
Citations

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

Fields of papers citing papers by Michael C. Abt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael C. Abt. 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 Michael C. Abt. The network helps show where Michael C. Abt may publish in the future.

Co-authorship network of co-authors of Michael C. Abt

This figure shows the co-authorship network connecting the top 25 collaborators of Michael C. Abt. A scholar is included among the top collaborators of Michael C. Abt 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 Michael C. Abt. Michael C. Abt 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.
Denny, Joshua E., et al.. (2025). Therapeutic activation of IL-22-producing innate lymphoid cells enhances host defenses to Clostridioides difficile infection. Cell Reports. 44(4). 115438–115438. 1 indexed citations
2.
Denny, Joshua E., et al.. (2025). Standard mouse diets lead to differences in severity in infectious and non-infectious colitis. mBio. 16(4). e0330224–e0330224. 1 indexed citations
3.
Denny, Joshua E., Md. Zahidul Alam, Mohamad‐Gabriel Alameh, et al.. (2025). Clostridioides difficile toxin A and toxin B inhibit toxin-specific adaptive immune responses through glucosyltransferase-dependent activity. Mucosal Immunology. 18(6). 1271–1283.
5.
Alam, Md. Zahidul, et al.. (2023). Immunological consequences of microbiome-based therapeutics. Frontiers in Immunology. 13. 1046472–1046472. 15 indexed citations
6.
Alam, Md. Zahidul, et al.. (2023). IL10 producing regulatory T cells support fecal microbiota transplant (FMT)-mediated clearance of Clostridioides difficile Infection. The Journal of Immunology. 210(Supplement_1). 61.12–61.12. 1 indexed citations
7.
Abt, Michael C., et al.. (2023). Targeted activation of IL-22 producing innate lymphoid cells enhances host resistance against Clostridioides difficile infection. The Journal of Immunology. 210(Supplement_1). 241.15–241.15. 1 indexed citations
8.
Denny, Joshua E., et al.. (2021). Loss of Interleukin-10 (IL-10) Signaling Promotes IL-22-Dependent Host Defenses against Acute Clostridioides difficile Infection. Infection and Immunity. 89(5). 11 indexed citations
9.
Littmann, Eric R., Jung‐Jin Lee, Joshua E. Denny, et al.. (2021). Host immunity modulates the efficacy of microbiota transplantation for treatment of Clostridioides difficile infection. Nature Communications. 12(1). 755–755. 63 indexed citations
10.
Abt, Michael C., Brittany B. Lewis, Silvia Caballero, et al.. (2015). Innate Immune Defenses Mediated by Two ILC Subsets Are Critical for Protection against Acute Clostridium difficile Infection. Cell Host & Microbe. 18(1). 27–37. 227 indexed citations
11.
Lagor, William R., Robert C. Bauer, Alison Crawford, et al.. (2014). Genetic manipulation of the ApoF/Stat2 locus supports an important role for type I interferon signaling in atherosclerosis. Atherosclerosis. 233(1). 234–241. 20 indexed citations
12.
Abt, Michael C. & Eric G. Pamer. (2014). Commensal bacteria mediated defenses against pathogens. Current Opinion in Immunology. 29. 16–22. 122 indexed citations
13.
Laidlaw, Brian J., Vilma Decman, Mohammed A. Ali, et al.. (2013). Cooperativity Between CD8+ T Cells, Non-Neutralizing Antibodies, and Alveolar Macrophages Is Important for Heterosubtypic Influenza Virus Immunity. PLoS Pathogens. 9(3). e1003207–e1003207. 124 indexed citations
14.
Abt, Michael C. & David Artis. (2013). The dynamic influence of commensal bacteria on the immune response to pathogens. Current Opinion in Microbiology. 16(1). 4–9. 48 indexed citations
15.
Abt, Michael C., Lisa C. Osborne, Laurel A. Monticelli, et al.. (2012). Commensal Bacteria Calibrate the Activation Threshold of Innate Antiviral Immunity. Immunity. 37(1). 158–170. 789 indexed citations breakdown →
16.
Casey, Kerry A., Kathryn Fraser, Jason M. Schenkel, et al.. (2012). Antigen-Independent Differentiation and Maintenance of Effector-like Resident Memory T Cells in Tissues. The Journal of Immunology. 188(10). 4866–4875. 511 indexed citations breakdown →
17.
Monticelli, Laurel A., Gregory F. Sonnenberg, Michael C. Abt, et al.. (2011). Innate lymphoid cells promote lung-tissue homeostasis after infection with influenza virus. Nature Immunology. 12(11). 1045–1054. 1066 indexed citations breakdown →
18.
Abt, Michael C., et al.. (2009). The influence of commensal bacteria on anti-viral immunity (39.26). The Journal of Immunology. 182(Supplement_1). 39.26–39.26. 1 indexed citations
19.
Abt, Michael C. & David Artis. (2009). The intestinal microbiota in health and disease: the influence of microbial products on immune cell homeostasis. Current Opinion in Gastroenterology. 25(6). 496–502. 79 indexed citations
20.
Hill, David A., Christian Hoffmann, Michael C. Abt, et al.. (2009). Metagenomic analyses reveal antibiotic-induced temporal and spatial changes in intestinal microbiota with associated alterations in immune cell homeostasis. Mucosal Immunology. 3(2). 148–158. 335 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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