William J. Karpus

7.2k total citations
73 papers, 6.1k citations indexed

About

William J. Karpus is a scholar working on Immunology, Oncology and Rheumatology. According to data from OpenAlex, William J. Karpus has authored 73 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Immunology, 34 papers in Oncology and 19 papers in Rheumatology. Recurrent topics in William J. Karpus's work include T-cell and B-cell Immunology (33 papers), Chemokine receptors and signaling (24 papers) and Systemic Lupus Erythematosus Research (19 papers). William J. Karpus is often cited by papers focused on T-cell and B-cell Immunology (33 papers), Chemokine receptors and signaling (24 papers) and Systemic Lupus Erythematosus Research (19 papers). William J. Karpus collaborates with scholars based in United States, France and Belgium. William J. Karpus's co-authors include Stephen D. Miller, Kevin J. Kennedy, Nicholas W. Lukacs, Richard M. Ransohoff, Brian T. Fife, Robert H. Swanborg, Steven L. Kunkel, Adam Elhofy, William A. Kuziel and Biao Hu and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and The Journal of Experimental Medicine.

In The Last Decade

William J. Karpus

73 papers receiving 6.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William J. Karpus United States 39 3.8k 1.9k 1.1k 1.0k 929 73 6.1k
Vincent K. Tuohy United States 46 4.3k 1.1× 1.7k 0.9× 1.2k 1.1× 1.6k 1.5× 1.5k 1.6× 116 7.5k
Avraham Ben‐Nun Israel 42 4.7k 1.2× 891 0.5× 777 0.7× 1.8k 1.7× 1.2k 1.3× 112 7.0k
Abdolmohamad Rostami United States 51 5.5k 1.4× 1.6k 0.8× 1.3k 1.1× 2.0k 1.9× 1.9k 2.1× 185 9.4k
Piet Stinissen Belgium 48 3.5k 0.9× 881 0.5× 971 0.9× 1.9k 1.8× 1.4k 1.5× 162 6.7k
Mireia Sospedra Switzerland 33 2.8k 0.7× 943 0.5× 642 0.6× 1.7k 1.6× 1.1k 1.2× 74 5.0k
Eva Tolosa Germany 36 2.5k 0.7× 788 0.4× 1.3k 1.2× 534 0.5× 1.5k 1.6× 98 5.5k
Sachiko Miyake Japan 56 5.8k 1.5× 1.4k 0.7× 494 0.4× 1.3k 1.2× 3.1k 3.4× 152 10.0k
D. E. McFarlin United States 34 3.0k 0.8× 720 0.4× 522 0.5× 1.3k 1.2× 1.3k 1.4× 79 5.1k
Maria Wiekowski United States 34 4.3k 1.1× 1.8k 0.9× 275 0.2× 754 0.7× 1.3k 1.4× 52 7.0k
Dale E. McFarlin United States 34 3.2k 0.8× 712 0.4× 354 0.3× 1.8k 1.7× 1.0k 1.1× 84 5.6k

Countries citing papers authored by William J. Karpus

Since Specialization
Citations

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

Fields of papers citing papers by William J. Karpus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William J. Karpus. 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 William J. Karpus. The network helps show where William J. Karpus may publish in the future.

Co-authorship network of co-authors of William J. Karpus

This figure shows the co-authorship network connecting the top 25 collaborators of William J. Karpus. A scholar is included among the top collaborators of William J. Karpus 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 William J. Karpus. William J. Karpus 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.
Hsu, Martin, Aditya Rayasam, Julie A. Kijak, et al.. (2019). Neuroinflammation-induced lymphangiogenesis near the cribriform plate contributes to drainage of CNS-derived antigens and immune cells. Nature Communications. 10(1). 229–229. 151 indexed citations
2.
Shahrara, Shiva, Sarah R. Pickens, Arthur M. Mandelin, et al.. (2010). IL-17–Mediated Monocyte Migration Occurs Partially through CC Chemokine Ligand 2/Monocyte Chemoattractant Protein-1 Induction. The Journal of Immunology. 184(8). 4479–4487. 120 indexed citations
3.
Bennett, Jami, Adam Elhofy, Israel Charo, et al.. (2007). CCR2 Regulates Development of Theiler's Murine Encephalomyelitis Virus-Induced Demyelinating Disease. Viral Immunology. 20(1). 19–33. 22 indexed citations
4.
DePaolo, R. William, et al.. (2004). CCR5 Regulates High Dose Oral Tolerance by Modulating CC Chemokine Ligand 2 Levels in the GALT. The Journal of Immunology. 173(1). 314–320. 8 indexed citations
5.
DePaolo, R. William, Barrett J. Rollins, William A. Kuziel, & William J. Karpus. (2003). CC Chemokine Ligand 2 and Its Receptor Regulate Mucosal Production of IL-12 and TGF-β in High Dose Oral Tolerance. The Journal of Immunology. 171(7). 3560–3567. 18 indexed citations
6.
Karpus, William J.. (2001). Chemokines and central nervous system disorders. Journal of NeuroVirology. 7(6). 493–500. 24 indexed citations
7.
Fife, Brian T., Mary Paniagua, Nicholas W. Lukacs, Steven L. Kunkel, & William J. Karpus. (2001). Selective CC chemokine receptor expression by central nervous system‐infiltrating encephalitogenic T cells during experimental autoimmune encephalomyelitis. Journal of Neuroscience Research. 66(4). 705–714. 43 indexed citations
8.
Kennedy, Kevin J. & William J. Karpus. (1999). Role of Chemokines in the Regulation of Th1/Th2 and Autoimmune Encephalomyelitis. Journal of Clinical Immunology. 19(5). 273–279. 39 indexed citations
9.
Karpus, William J., Kevin J. Kennedy, Brian T. Fife, & Linda M. Hoffman. (1999). Chemokine Regulation of Immune-mediated Demyelinating Disease. ILAR Journal. 40(4). 183–189. 3 indexed citations
10.
Hoffman, Lisa & William J. Karpus. (1998). Chemokine regulation of CNS T-cell infiltration in experimental autoimmune encephalomyelitis. Research in Immunology. 149(9). 790–794. 7 indexed citations
11.
Karpus, William J. & Richard M. Ransohoff. (1998). Chemokine regulation of experimental autoimmune encephalomyelitis: temporal and spatial expression patterns govern disease pathogenesis.. PubMed. 161(6). 2667–71. 190 indexed citations
12.
Karpus, William J., et al.. (1997). Differential CC chemokine-induced enhancement of T helper cell cytokine production. The Journal of Immunology. 158(9). 4129–4136. 363 indexed citations
13.
14.
Karpus, William J., et al.. (1996). Inhibition of relapsing experimental autoimmune encephalomyelitis in SJL mice by feeding the immunodominant PLP139-151 peptide. Journal of Neuroscience Research. 45(4). 410–423. 46 indexed citations
15.
Karpus, William J. & Nicholas W. Lukacs. (1996). The Role of Chemokines in Oral Tolerance.. Annals of the New York Academy of Sciences. 778(1). 133–144. 23 indexed citations
16.
17.
Stevens, David B., et al.. (1992). Studies of Vβ8 T cell receptor peptide treatment in experimental autoimmune encephalomyelitis. Journal of Neuroimmunology. 37(1-2). 123–129. 33 indexed citations
18.
Karpus, William J. & Robert H. Swanborg. (1991). Protection against experimental autoimmune encephalomyelitis requires both CD4+ T suppressor cells and myelin basic protein-primed B cells. Journal of Neuroimmunology. 33(2). 173–177. 27 indexed citations
19.
20.
Karpus, William J. & Robert H. Swanborg. (1989). CD4+ suppressor cells differentially affect the production of IFN-gamma by effector cells of experimental autoimmune encephalomyelitis.. The Journal of Immunology. 143(11). 3492–3497. 64 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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