Patrick R. Burkett

6.5k total citations · 3 hit papers
30 papers, 3.6k citations indexed

About

Patrick R. Burkett is a scholar working on Immunology, Surgery and Oncology. According to data from OpenAlex, Patrick R. Burkett has authored 30 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Immunology, 11 papers in Surgery and 7 papers in Oncology. Recurrent topics in Patrick R. Burkett's work include Immune Cell Function and Interaction (14 papers), T-cell and B-cell Immunology (12 papers) and Transplantation: Methods and Outcomes (6 papers). Patrick R. Burkett is often cited by papers focused on Immune Cell Function and Interaction (14 papers), T-cell and B-cell Immunology (12 papers) and Transplantation: Methods and Outcomes (6 papers). Patrick R. Burkett collaborates with scholars based in United States, Mexico and Canada. Patrick R. Burkett's co-authors include Averil Ma, Rima Koka, Vijay K. Kuchroo, David L. Boone, Marcia Chien, Sophia Chai, James P. Lodolce, Gerd Meyer zu Hörste, Faye Chan and Chen Zhu 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

Patrick R. Burkett

30 papers receiving 3.6k citations

Hit Papers

Treg Cells Expressing the Coinhibitory Molecule TIGI... 2006 2026 2012 2019 2014 2006 2018 200 400 600

Peers

Patrick R. Burkett
Long Gu United States
Greg Elson Switzerland
Lynn Williams United Kingdom
Erin E. West United States
Long Gu United States
Patrick R. Burkett
Citations per year, relative to Patrick R. Burkett Patrick R. Burkett (= 1×) peers Long Gu

Countries citing papers authored by Patrick R. Burkett

Since Specialization
Citations

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

Fields of papers citing papers by Patrick R. Burkett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick R. Burkett. 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 Patrick R. Burkett. The network helps show where Patrick R. Burkett may publish in the future.

Co-authorship network of co-authors of Patrick R. Burkett

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick R. Burkett. A scholar is included among the top collaborators of Patrick R. Burkett 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 Patrick R. Burkett. Patrick R. Burkett 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.
Rojas, Joselyn, María Laucho-Contreras, Xiaoyun Wang, et al.. (2023). CC16 augmentation reduces exaggerated COPD-like disease in Cc16-deficient mice. JCI Insight. 8(6). 8 indexed citations
2.
Pawlak, Mathias, David DeTomaso, Alexandra Schnell, et al.. (2022). Induction of a colitogenic phenotype in Th1-like cells depends on interleukin-23 receptor signaling. Immunity. 55(9). 1663–1679.e6. 27 indexed citations
3.
Courtwright, Andrew, Anil J. Trindade, Patrick R. Burkett, et al.. (2019). Hyaluronan and LYVE-1 and allograft function in lung transplantation recipients. Scientific Reports. 9(1). 9003–9003. 6 indexed citations
4.
Wallrapp, Antonia, Patrick R. Burkett, Samantha J. Riesenfeld, et al.. (2019). Calcitonin Gene-Related Peptide Negatively Regulates Alarmin-Driven Type 2 Innate Lymphoid Cell Responses. Immunity. 51(4). 709–723.e6. 175 indexed citations
5.
Rojas, Joselyn, Xiaoyun Wang, Jennifer L. Tipper, et al.. (2018). Matrix metalloproteinase-9 deficiency protects mice from severe influenza A viral infection. JCI Insight. 3(24). 40 indexed citations
6.
Baral, Pankaj, Benjamin D. Umans, Lu Li, et al.. (2018). Nociceptor sensory neurons suppress neutrophil and γδ T cell responses in bacterial lung infections and lethal pneumonia. Nature Medicine. 24(4). 417–426. 290 indexed citations breakdown →
7.
Burkett, Patrick R., Phillip C. Camp, Miguel Divo, et al.. (2017). Comparison of extracorporeal photopheresis and alemtuzumab for the treatment of chronic lung allograft dysfunction. The Journal of Heart and Lung Transplantation. 37(3). 340–348. 27 indexed citations
8.
Courtwright, Andrew, Patrick R. Burkett, Miguel Divo, et al.. (2017). Posttransplant Lymphoproliferative Disorders in Epstein-Barr Virus Donor Positive/Recipient Negative Lung Transplant Recipients. The Annals of Thoracic Surgery. 105(2). 441–447. 8 indexed citations
9.
Courtwright, Andrew, Anne L. Fuhlbrigge, Miguel Divo, et al.. (2016). Predictors and outcomes of unplanned early rehospitalization in the first year following lung transplantation. Clinical Transplantation. 30(9). 1053–1058. 8 indexed citations
10.
Jacob, Samuel, Andrew Courtwright, Souheil El‐Chemaly, et al.. (2015). Donor-acquired fat embolism syndrome after lung transplantation. European Journal of Cardio-Thoracic Surgery. 49(5). 1344–1347. 12 indexed citations
11.
Krishnamoorthy, Nandini, Patrick R. Burkett, Jesmond Dalli, et al.. (2014). Cutting Edge: Maresin-1 Engages Regulatory T Cells To Limit Type 2 Innate Lymphoid Cell Activation and Promote Resolution of Lung Inflammation. The Journal of Immunology. 194(3). 863–867. 155 indexed citations
12.
Joller, Nicole, Ester Lozano, Patrick R. Burkett, et al.. (2014). Treg Cells Expressing the Coinhibitory Molecule TIGIT Selectively Inhibit Proinflammatory Th1 and Th17 Cell Responses. Immunity. 40(4). 569–581. 714 indexed citations breakdown →
13.
Chang, Jihoon, Patrick R. Burkett, Christopher M. Borges, et al.. (2013). MyD88 is essential to sustain mTOR activation necessary to promote T helper 17 cell proliferation by linking IL-1 and IL-23 signaling. Proceedings of the National Academy of Sciences. 110(6). 2270–2275. 66 indexed citations
14.
Burkett, Patrick R., Rima Koka, Marcia Chien, et al.. (2004). Coordinate Expression and Trans Presentation of Interleukin (IL)-15Rα and IL-15 Supports Natural Killer Cell and Memory CD8+ T Cell Homeostasis. The Journal of Experimental Medicine. 200(7). 825–834. 313 indexed citations
15.
Burkett, Patrick R., Rima Koka, Marcia Chien, David L. Boone, & Averil Ma. (2004). Generation, Maintenance, and Function of Memory T Cells. Advances in immunology. 83. 191–231. 4 indexed citations
16.
Koka, Rima, Patrick R. Burkett, Marcia Chien, et al.. (2003). Interleukin (IL)-15Rα–deficient Natural Killer Cells Survive in Normal but Not IL-15Rα–deficient Mice. The Journal of Experimental Medicine. 197(8). 977–984. 208 indexed citations
17.
Lodolce, James P., Patrick R. Burkett, Rima Koka, David L. Boone, & Averil Ma. (2002). Regulation of lymphoid homeostasis by interleukin-15. Cytokine & Growth Factor Reviews. 13(6). 429–439. 88 indexed citations
18.
Boone, David L., et al.. (2002). Recent Advances in Understanding NF-κB Regulation. Inflammatory Bowel Diseases. 8(3). 201–212. 43 indexed citations
19.
Lodolce, James P., Patrick R. Burkett, Rima Koka, et al.. (2002). Interleukin-15 and the regulation of lymphoid homeostasis. Molecular Immunology. 39(9). 537–544. 55 indexed citations
20.
Lodolce, James P., Patrick R. Burkett, David L. Boone, Marcia Chien, & Averil Ma. (2001). T Cell–Independent Interleukin 15rα Signals Are Required for Bystander Proliferation. The Journal of Experimental Medicine. 194(8). 1187–1194. 151 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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