Ralph C. Budd

8.4k total citations
116 papers, 6.9k citations indexed

About

Ralph C. Budd is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Ralph C. Budd has authored 116 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Immunology, 44 papers in Molecular Biology and 18 papers in Oncology. Recurrent topics in Ralph C. Budd's work include T-cell and B-cell Immunology (52 papers), Immune Cell Function and Interaction (46 papers) and Cell death mechanisms and regulation (29 papers). Ralph C. Budd is often cited by papers focused on T-cell and B-cell Immunology (52 papers), Immune Cell Function and Interaction (46 papers) and Cell death mechanisms and regulation (29 papers). Ralph C. Budd collaborates with scholars based in United States, Switzerland and United Kingdom. Ralph C. Budd's co-authors include H. Robson MacDonald, Jürg Tschopp, Takao Kataoka, Rawleigh Howe, Jennifer Q. Russell, Karen A. Fortner, Norman J. Kennedy, J C Cerottini, Claude Bron and Burton E. Sobel and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Ralph C. Budd

116 papers receiving 6.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ralph C. Budd United States 43 4.1k 3.0k 975 734 694 116 6.9k
Naoto Itoh Japan 26 3.5k 0.8× 4.2k 1.4× 1.1k 1.2× 801 1.1× 938 1.4× 50 7.9k
Cosima T. Baldari Italy 47 3.4k 0.8× 3.6k 1.2× 972 1.0× 451 0.6× 524 0.8× 228 7.8k
P H Krammer Germany 30 3.8k 0.9× 3.0k 1.0× 958 1.0× 677 0.9× 881 1.3× 38 6.5k
Kohsuke Imai Japan 40 2.4k 0.6× 3.3k 1.1× 1.0k 1.1× 760 1.0× 781 1.1× 232 6.6k
S.G. Hymowitz United States 40 3.0k 0.7× 4.7k 1.5× 1.6k 1.6× 1.1k 1.5× 718 1.0× 50 7.6k
Akio Matsuzawa Japan 25 3.7k 0.9× 2.4k 0.8× 1.6k 1.6× 455 0.6× 632 0.9× 146 6.2k
Nils Holler Switzerland 20 3.9k 0.9× 5.0k 1.6× 1.1k 1.2× 1.5k 2.1× 917 1.3× 20 8.3k
Kenji Kishihara Japan 35 6.0k 1.5× 2.1k 0.7× 1.4k 1.4× 559 0.8× 853 1.2× 97 8.4k
Laura DeForge United States 33 2.5k 0.6× 3.2k 1.1× 1.1k 1.2× 789 1.1× 877 1.3× 54 5.8k
Gerrit Koopman Netherlands 27 2.9k 0.7× 3.0k 1.0× 868 0.9× 354 0.5× 606 0.9× 98 7.0k

Countries citing papers authored by Ralph C. Budd

Since Specialization
Citations

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

Fields of papers citing papers by Ralph C. Budd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ralph C. Budd

This figure shows the co-authorship network connecting the top 25 collaborators of Ralph C. Budd. A scholar is included among the top collaborators of Ralph C. Budd 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 Ralph C. Budd. Ralph C. Budd 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.
Collins, Cheryl, et al.. (2023). Endobronchial ultrasound-guided transbronchial needle injection of cisplatin results in dynamic changes in the tumor immune microenvironment. Respiratory Medicine and Research. 84. 100994–100994. 3 indexed citations
2.
Collins, Cheryl, et al.. (2023). Regulation of Synovial γδ T Cell Ligand Expression by Mitochondrial Reactive Oxygen Species and Gasdermin-D. The Journal of Immunology. 210(1). 61–71. 1 indexed citations
3.
Budd, Ralph C., et al.. (2021). T Cell Homeostatic Proliferation Promotes a Redox State That Drives Metabolic and Epigenetic Upregulation of Inflammatory Pathways in Lupus. Antioxidants and Redox Signaling. 36(7-9). 410–422. 4 indexed citations
4.
Cushman, Mary, et al.. (2020). Thromboinflammation response to tocilizumab in COVID‐19. Research and Practice in Thrombosis and Haemostasis. 4(8). 1262–1268. 1 indexed citations
5.
Fortner, Karen A., Jeffrey P. Bond, James W. Austin, Jeremy M. Boss, & Ralph C. Budd. (2017). The molecular signature of murine T cell homeostatic proliferation reveals both inflammatory and immune inhibition patterns. Journal of Autoimmunity. 82. 47–61. 17 indexed citations
6.
Fortner, Karen A., et al.. (2014). IL-15 maintains T-cell survival via S-nitrosylation-mediated inhibition of caspase-3. Cell Death and Differentiation. 21(6). 904–914. 19 indexed citations
7.
Buskiewicz, Iwona A., Andreas Koenig, Sally A. Huber, & Ralph C. Budd. (2012). Caspase-8 and FLIP Regulate RIG-I/MDA5-induced Innate Immune Host Responses to Picornaviruses. Future Virology. 7(12). 1221–1236. 12 indexed citations
8.
Collins, Cheryl, et al.. (2008). Activation of γδ T Cells by Borrelia burgdorferi Is Indirect via a TLR- and Caspase-Dependent Pathway. The Journal of Immunology. 181(4). 2392–2398. 32 indexed citations
9.
Dienz, Oliver, Sheri M. Eaton, Troy Krahl, et al.. (2007). Accumulation of NFAT mediates IL-2 expression in memory, but not naïve, CD4 + T cells. Proceedings of the National Academy of Sciences. 104(17). 7175–7180. 50 indexed citations
10.
Taatjes, Douglas J., Burton E. Sobel, & Ralph C. Budd. (2007). Morphological and cytochemical determination of cell death by apoptosis. Histochemistry and Cell Biology. 129(1). 33–43. 179 indexed citations
11.
Budd, Ralph C., Edward J. Harley, Alexander Quarshie, et al.. (2006). A re‐appraisal of the normal cut‐off assignment for anticardiolipin IgM tests. Journal of Thrombosis and Haemostasis. 4(10). 2210–2214. 14 indexed citations
12.
Collins, Cheryl, et al.. (2005). Lyme Arthritis Synovial γδ T Cells Instruct Dendritic Cells via Fas Ligand. The Journal of Immunology. 175(9). 5656–5665. 36 indexed citations
13.
Fortner, Karen A. & Ralph C. Budd. (2005). The Death Receptor Fas (CD95/APO-1) Mediates the Deletion of T Lymphocytes Undergoing Homeostatic Proliferation. The Journal of Immunology. 175(7). 4374–4382. 38 indexed citations
14.
Dohrman, Austin, Takao Kataoka, Solange Cuenin, et al.. (2005). Cellular FLIP (Long Form) Regulates CD8+ T Cell Activation through Caspase-8-Dependent NF-κB Activation. The Journal of Immunology. 174(9). 5270–5278. 105 indexed citations
15.
Dohrman, Austin, Jennifer Q. Russell, Solange Cuenin, et al.. (2005). Cellular FLIP Long Form Augments Caspase Activity and Death of T Cells through Heterodimerization with and Activation of Caspase-8. The Journal of Immunology. 175(1). 311–318. 37 indexed citations
16.
Roessner, Karen, et al.. (2003). High Expression of Fas Ligand by Synovial Fluid-Derived γδ T Cells in Lyme Arthritis. The Journal of Immunology. 170(5). 2702–2710. 28 indexed citations
17.
Budd, Ralph C.. (2002). Death receptors couple to both cell proliferation and apoptosis. Journal of Clinical Investigation. 109(4). 437–442. 120 indexed citations
18.
Budd, Ralph C.. (2002). Death receptors couple to both cell proliferation and apoptosis. Journal of Clinical Investigation. 109(4). 437–442. 3 indexed citations
19.
Budd, Ralph C.. (2002). Death receptors couple to both cell proliferation and apoptosis. Journal of Clinical Investigation. 109(4). 437–442. 118 indexed citations
20.
Kennedy, Norman J., et al.. (2001). Liver Damage by Infiltrating CD8+ T Cells Is Fas Dependent. The Journal of Immunology. 167(11). 6654–6662. 35 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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