Jonathan P. Butchar

7.1k total citations
58 papers, 2.3k citations indexed

About

Jonathan P. Butchar is a scholar working on Molecular Biology, Immunology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Jonathan P. Butchar has authored 58 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 29 papers in Immunology and 16 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Jonathan P. Butchar's work include Monoclonal and Polyclonal Antibodies Research (16 papers), Immune Cell Function and Interaction (14 papers) and Chronic Lymphocytic Leukemia Research (12 papers). Jonathan P. Butchar is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (16 papers), Immune Cell Function and Interaction (14 papers) and Chronic Lymphocytic Leukemia Research (12 papers). Jonathan P. Butchar collaborates with scholars based in United States, China and United Kingdom. Jonathan P. Butchar's co-authors include Susheela Tridandapani, Thomas Cremer, Kishore V. L. Parsa, Clay B. Marsh, Murugesan V. S. Rajaram, William E. Carson, Xiaokui Mo, Amal O. Amer, Michael A. Caligiuri and John S. Gunn and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Blood.

In The Last Decade

Jonathan P. Butchar

57 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jonathan P. Butchar United States	28	1.1k	1.0k	424	289	278	58	2.3k
Ileana Quinto Italy	26	1.1k 1.0×	688 0.7×	422 1.0×	140 0.5×	429 1.5×	78	2.1k
Rachel M. Gerstein United States	32	1.5k 1.4×	2.3k 2.3×	528 1.2×	353 1.2×	242 0.9×	61	4.0k
Gaëtan Jégo France	28	1.6k 1.5×	1.9k 1.8×	685 1.6×	247 0.9×	231 0.8×	53	3.8k
Annaiah Cariappa United States	24	958 0.9×	2.4k 2.4×	344 0.8×	139 0.5×	360 1.3×	34	3.3k
Joëlle Wiels France	32	1.6k 1.5×	1.1k 1.1×	687 1.6×	153 0.5×	133 0.5×	91	3.3k
Andrew L. Snow United States	28	747 0.7×	1.4k 1.3×	901 2.1×	89 0.3×	385 1.4×	63	2.5k
Pierre Garrone France	21	602 0.6×	2.6k 2.5×	581 1.4×	111 0.4×	191 0.7×	34	3.6k
Ryo Goitsuka Japan	28	996 0.9×	1.3k 1.3×	321 0.8×	164 0.6×	178 0.6×	97	2.6k
Shinya Suzu Japan	30	909 0.8×	1.3k 1.3×	646 1.5×	146 0.5×	186 0.7×	96	2.7k
Jhagvaral Hasbold Australia	24	786 0.7×	2.3k 2.2×	335 0.8×	119 0.4×	171 0.6×	29	3.0k

Countries citing papers authored by Jonathan P. Butchar

Since Specialization

Citations

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

Fields of papers citing papers by Jonathan P. Butchar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jonathan P. Butchar. 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 Jonathan P. Butchar. The network helps show where Jonathan P. Butchar may publish in the future.

Co-authorship network of co-authors of Jonathan P. Butchar

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

All Works

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20 of 20 papers shown

Santhanam, Ramasamy, Frank Robledo‐Avila, Juan de Dios Ruiz‐Rosado, et al.. (2024). NOD2 activation enhances macrophage Fcγ receptor function and may increase the efficacy of antibody therapy. Frontiers in Immunology. 15. 1409333–1409333. 2 indexed citations

Kumar, Krishan, Deepak Kanojia, David J. Bentrem, et al.. (2023). Targeting BET Proteins Decreases Hyaluronidase-1 in Pancreatic Cancer. Cells. 12(11). 1490–1490. 7 indexed citations

Santhanam, Ramasamy, Huiqing Fang, Krishan Kumar, et al.. (2023). Inhibition of BET Proteins Regulates Fcγ Receptor Function and Reduces Inflammation in Rheumatoid Arthritis. International Journal of Molecular Sciences. 24(8). 7623–7623. 10 indexed citations

McMichael, Elizabeth L., Brenda F. Reader, Huiqing Fang, et al.. (2016). Interferon-γ Promotes Antibody-mediated Fratricide of Acute Myeloid Leukemia Cells. Journal of Biological Chemistry. 291(49). 25656–25666. 14 indexed citations

Gautam, Shalini, Brenda F. Reader, Li Ren, et al.. (2016). Reprogramming Nurse-like Cells with Interferon γ to Interrupt Chronic Lymphocytic Leukemia Cell Survival. Journal of Biological Chemistry. 291(27). 14356–14362. 18 indexed citations

Suarez‐Kelly, Lorena P., Amanda R. Campbell, Ambika Bumb, et al.. (2016). Fluorescent nanodiamonds engage innate immune effector cells: A potential vehicle for targeted anti-tumor immunotherapy. Nanomedicine Nanotechnology Biology and Medicine. 13(3). 909–920. 31 indexed citations

Ren, Li, Huiqing Fang, Xiaokui Mo, et al.. (2015). Toll-like Receptor 4 Ligands Down-regulate Fcγ Receptor IIb (FcγRIIb) via MARCH3 Protein-mediated Ubiquitination. Journal of Biological Chemistry. 291(8). 3895–3904. 16 indexed citations

Ren, Li, Huiqing Fang, Shalini Gautam, et al.. (2015). Analysis of the Effects of the Bruton's tyrosine kinase (Btk) Inhibitor Ibrutinib on Monocyte Fcγ Receptor (FcγR) Function. Journal of Biological Chemistry. 291(6). 3043–3052. 54 indexed citations

Tridandapani, Susheela, et al.. (2014). Monocyte/macrophage inflammatory response pathways to combat Francisella infection: possible therapeutic targets?. Frontiers in Cellular and Infection Microbiology. 4. 18–18. 10 indexed citations

10.

Shah, Prexy, Payal Mehta, Julie M. Roda, et al.. (2013). Fcγ Receptor-induced Soluble Vascular Endothelial Growth Factor Receptor-1 (VEGFR-1) Production Inhibits Angiogenesis and Enhances Efficacy of Anti-tumor Antibodies. Journal of Biological Chemistry. 288(37). 26800–26809. 11 indexed citations

11.

Shah, Prexy, Thomas Cremer, Mikhail A. Gavrilin, et al.. (2012). Analysis of Human Bronchial Epithelial Cell Proinflammatory Response to Burkholderia cenocepacia Infection. Journal of Biological Chemistry. 288(6). 3691–3695. 21 indexed citations

12.

Cremer, Thomas, Prexy Shah, Hemal H. Patel, et al.. (2012). MiR-155 Induction by Microbes/Microbial Ligands Requires NF-κB-Dependent de novo Protein Synthesis. Frontiers in Cellular and Infection Microbiology. 2. 73–73. 26 indexed citations

13.

Mehta, Payal, Anne‐Sophie Wavreille, Rachel Marsh, et al.. (2011). LyGDI, a Novel SHIP-Interacting Protein, Is a Negative Regulator of FcγR-Mediated Phagocytosis. PLoS ONE. 6(6). e21175–e21175. 10 indexed citations

14.

Yu, Jianhua, Takeki Mitsui, Wei Min, et al.. (2011). NKp46 identifies an NKT cell subset susceptible to leukemic transformation in mouse and human. Journal of Clinical Investigation. 121(4). 1456–1470. 58 indexed citations

15.

Cremer, Thomas, Jonathan P. Butchar, & Susheela Tridandapani. (2011). Francisella Subverts Innate Immune Signaling: Focus On PI3K/Akt. Frontiers in Microbiology. 5. 13–13. 22 indexed citations

16.

Cremer, Thomas, Amal O. Amer, Susheela Tridandapani, & Jonathan P. Butchar. (2009). Francisella tularensisregulates autophagy-related host cell signaling pathways. Autophagy. 5(1). 125–128. 35 indexed citations

17.

Akhter, Anwari, Mikhail A. Gavrilin, Dominique H. Limoli, et al.. (2009). Caspase-7 Activation by the Nlrc4/Ipaf Inflammasome Restricts Legionella pneumophila Infection. PLoS Pathogens. 5(4). e1000361–e1000361. 157 indexed citations

18.

Butchar, Jonathan P., Thomas Cremer, Corey D. Clay, et al.. (2008). Microarray Analysis of Human Monocytes Infected with Francisella tularensis Identifies New Targets of Host Response Subversion. PLoS ONE. 3(8). e2924–e2924. 100 indexed citations

19.

Parsa, Kishore V. L., Jonathan P. Butchar, Murugesan V. S. Rajaram, Thomas Cremer, & Susheela Tridandapani. (2008). The tyrosine kinase Syk promotes phagocytosis of Francisella through the activation of Erk. Molecular Immunology. 45(10). 3012–3021. 45 indexed citations

20.

Rajaram, Murugesan V. S., Latha P. Ganesan, Kishore V. L. Parsa, et al.. (2006). Akt/Protein Kinase B Modulates Macrophage Inflammatory Response to Francisella Infection and Confers a Survival Advantage in Mice. The Journal of Immunology. 177(9). 6317–6324. 96 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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