Lawrence W. Kummer

1.4k total citations
28 papers, 1.1k citations indexed

About

Lawrence W. Kummer is a scholar working on Genetics, Immunology and Pharmacology. According to data from OpenAlex, Lawrence W. Kummer has authored 28 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 7 papers in Immunology and 6 papers in Pharmacology. Recurrent topics in Lawrence W. Kummer's work include Yersinia bacterium, plague, ectoparasites research (13 papers), Pharmacological Effects of Natural Compounds (5 papers) and Immune Cell Function and Interaction (4 papers). Lawrence W. Kummer is often cited by papers focused on Yersinia bacterium, plague, ectoparasites research (13 papers), Pharmacological Effects of Natural Compounds (5 papers) and Immune Cell Function and Interaction (4 papers). Lawrence W. Kummer collaborates with scholars based in United States, Canada and United Kingdom. Lawrence W. Kummer's co-authors include Frank M. Szaba, Stephen T. Smiley, Michelle A. Parent, Lawrence L. Johnson, Jr‐Shiuan Lin, Isis Kanevsky, Markus Mohrs, Kiera N. Berggren, Georgia Perona‐Wright and Katja Mohrs and has published in prestigious journals such as The Journal of Immunology, Infection and Immunity and Cell Host & Microbe.

In The Last Decade

Lawrence W. Kummer

26 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lawrence W. Kummer United States 19 442 407 287 212 206 28 1.1k
K Varkila Finland 11 137 0.3× 811 2.0× 443 1.5× 92 0.4× 348 1.7× 17 1.7k
P Ahvonen Finland 14 536 1.2× 213 0.5× 123 0.4× 77 0.4× 363 1.8× 27 1.4k
Hidehito Kato Japan 22 163 0.4× 555 1.4× 295 1.0× 32 0.2× 184 0.9× 50 1.3k
E. Nancy Miller United Kingdom 23 164 0.4× 368 0.9× 196 0.7× 227 1.1× 733 3.6× 29 1.5k
Adrian V. S. Hill United Kingdom 8 96 0.2× 608 1.5× 246 0.9× 100 0.5× 346 1.7× 8 1.4k
Jessica Carrière France 13 116 0.3× 219 0.5× 409 1.4× 103 0.5× 221 1.1× 37 1.0k
James E. Estep United States 19 325 0.7× 146 0.4× 688 2.4× 76 0.4× 202 1.0× 22 1.2k
Mercedes Domínguez Spain 21 109 0.2× 232 0.6× 280 1.0× 113 0.5× 687 3.3× 83 1.4k
Masashi Emoto Japan 25 76 0.2× 1.4k 3.4× 206 0.7× 53 0.3× 264 1.3× 69 1.9k
Sten Winblad Sweden 20 459 1.0× 121 0.3× 158 0.6× 63 0.3× 114 0.6× 56 1.1k

Countries citing papers authored by Lawrence W. Kummer

Since Specialization
Citations

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

Fields of papers citing papers by Lawrence W. Kummer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lawrence W. Kummer. 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 Lawrence W. Kummer. The network helps show where Lawrence W. Kummer may publish in the future.

Co-authorship network of co-authors of Lawrence W. Kummer

This figure shows the co-authorship network connecting the top 25 collaborators of Lawrence W. Kummer. A scholar is included among the top collaborators of Lawrence W. Kummer 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 Lawrence W. Kummer. Lawrence W. Kummer 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.
Muraoka, Wayne T., Qingqing Xia, Sergey A. Shein, et al.. (2020). Campylobacter infection promotes IFNγ-dependent intestinal pathology via ILC3 to ILC1 conversion. Mucosal Immunology. 14(3). 703–716. 16 indexed citations
2.
Szaba, Frank M., Stephen T. Smiley, András Gruber, et al.. (2020). Fibrin Facilitates Both Innate and T Cell-Mediated Defense against Yersinia pestis. UNC Libraries.
3.
4.
Smiley, Stephen T., Frank M. Szaba, Lawrence W. Kummer, Debra K. Duso, & Jr‐Shiuan Lin. (2019). Yersinia pestis Pla Protein Thwarts T Cell Defense against Plague. Infection and Immunity. 87(5). 4 indexed citations
5.
Szaba, Frank M., Michael Tighe, Lawrence W. Kummer, et al.. (2018). Zika virus infection in immunocompetent pregnant mice causes fetal damage and placental pathology in the absence of fetal infection. PLoS Pathogens. 14(4). e1006994–e1006994. 69 indexed citations
6.
Lin, Jr‐Shiuan, Katja Mohrs, Frank M. Szaba, et al.. (2018). Virtual memory CD8 T cells expanded by helminth infection confer broad protection against bacterial infection. Mucosal Immunology. 12(1). 258–264. 29 indexed citations
7.
Szaba, Frank M., Lawrence W. Kummer, Debra K. Duso, et al.. (2014). TNFα and IFNγ but Not Perforin Are Critical for CD8 T Cell-Mediated Protection against Pulmonary Yersinia pestis Infection. PLoS Pathogens. 10(5). e1004142–e1004142. 31 indexed citations
8.
Luo, Deyan, Jr‐Shiuan Lin, Michelle A. Parent, et al.. (2013). Fibrin Facilitates Both Innate and T Cell–Mediated Defense against Yersinia pestis. The Journal of Immunology. 190(8). 4149–4161. 26 indexed citations
9.
Freeman, Michael L., Kathleen G. Lanzer, Alan D. Roberts, et al.. (2012). Gammaherpesvirus latency induces antibody-associated thrombocytopenia in mice. Journal of Autoimmunity. 42. 71–79. 11 indexed citations
10.
Lanthier, Paula A., Gail E. Huston, Amy Moquin, et al.. (2011). Live attenuated influenza vaccine (LAIV) impacts innate and adaptive immune responses. Vaccine. 29(44). 7849–7856. 52 indexed citations
11.
Luo, Deyan, Frank M. Szaba, Lawrence W. Kummer, et al.. (2011). Factor XI-Deficient Mice Display Reduced Inflammation, Coagulopathy, and Bacterial Growth during Listeriosis. Infection and Immunity. 80(1). 91–99. 28 indexed citations
12.
13.
Lin, Jr‐Shiuan, Frank M. Szaba, Lawrence W. Kummer, Brett A. Chromy, & Stephen T. Smiley. (2011). Yersinia pestis YopE Contains a Dominant CD8 T Cell Epitope that Confers Protection in a Mouse Model of Pneumonic Plague. The Journal of Immunology. 187(2). 897–904. 36 indexed citations
14.
Couper, Kevin N., Paula A. Lanthier, Georgia Perona‐Wright, et al.. (2009). Anti-CD25 Antibody-Mediated Depletion of Effector T Cell Populations Enhances Susceptibility of Mice to Acute but Not Chronic Toxoplasma gondii Infection. The Journal of Immunology. 182(7). 3985–3994. 66 indexed citations
15.
Perona‐Wright, Georgia, Katja Mohrs, Frank M. Szaba, et al.. (2009). Systemic but Not Local Infections Elicit Immunosuppressive IL-10 Production by Natural Killer Cells. Cell Host & Microbe. 6(6). 503–512. 154 indexed citations
16.
Kummer, Lawrence W., Frank M. Szaba, Michelle A. Parent, et al.. (2008). Antibodies and cytokines independently protect against pneumonic plague. Vaccine. 26(52). 6901–6907. 43 indexed citations
17.
18.
Szaba, Frank M., et al.. (2006). In situ assays demonstrate that interferon‐gamma suppresses infection‐stimulated hepatic fibrin deposition by promoting fibrinolysis. Journal of Thrombosis and Haemostasis. 4(7). 1580–1587. 12 indexed citations
19.
Kanevsky, Isis, Frank M. Szaba, Kiera N. Berggren, et al.. (2005). Infection-Stimulated Fibrin Deposition Controls Hemorrhage and Limits Hepatic Bacterial Growth during Listeriosis. Infection and Immunity. 73(7). 3888–3895. 56 indexed citations
20.
Parent, Michelle A., Kiera N. Berggren, Lawrence W. Kummer, et al.. (2005). Cell-Mediated Protection against PulmonaryYersinia pestisInfection. Infection and Immunity. 73(11). 7304–7310. 117 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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