Kenneth A. Field

3.0k total citations
42 papers, 2.0k citations indexed

About

Kenneth A. Field is a scholar working on Ecology, Evolution, Behavior and Systematics, Infectious Diseases and Genetics. According to data from OpenAlex, Kenneth A. Field has authored 42 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Ecology, Evolution, Behavior and Systematics, 17 papers in Infectious Diseases and 10 papers in Genetics. Recurrent topics in Kenneth A. Field's work include Bat Biology and Ecology Studies (20 papers), Viral Infections and Vectors (16 papers) and Yersinia bacterium, plague, ectoparasites research (9 papers). Kenneth A. Field is often cited by papers focused on Bat Biology and Ecology Studies (20 papers), Viral Infections and Vectors (16 papers) and Yersinia bacterium, plague, ectoparasites research (9 papers). Kenneth A. Field collaborates with scholars based in United States, Finland and United Kingdom. Kenneth A. Field's co-authors include Barbara Baird, David Holowka, DeeAnn M. Reeder, Thomas M. Lilley, Joseph S. Johnson, Elizabeth J. Rogers, Sriram Krishnaswamy, K G Mann, Thomas S. Edgington and James H. Morrissey and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Immunology.

In The Last Decade

Kenneth A. Field

40 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kenneth A. Field United States 24 748 679 415 326 241 42 2.0k
Tsuyoshi Akagi Japan 24 688 0.9× 1.3k 1.9× 376 0.9× 137 0.4× 320 1.3× 50 2.6k
Dietmar Blohm Germany 25 556 0.7× 1.2k 1.8× 154 0.4× 80 0.2× 68 0.3× 42 2.3k
Astrid Murumägi Finland 23 416 0.6× 828 1.2× 343 0.8× 99 0.3× 93 0.4× 44 2.4k
Kurt Wollenberg United States 24 184 0.2× 784 1.2× 134 0.3× 133 0.4× 108 0.4× 49 2.0k
Kei‐ichi Kuma Japan 24 358 0.5× 1.2k 1.8× 122 0.3× 119 0.4× 197 0.8× 44 2.2k
José M. Almendral Spain 32 332 0.4× 1.8k 2.7× 368 0.9× 947 2.9× 141 0.6× 58 3.7k
Tomas Strandin Finland 21 257 0.3× 479 0.7× 238 0.6× 1.0k 3.2× 89 0.4× 54 1.9k
Ricardo Fujita Peru 24 322 0.4× 846 1.2× 75 0.2× 121 0.4× 166 0.7× 87 1.7k
Carmen W. van den Berg United Kingdom 31 745 1.0× 1.1k 1.7× 58 0.1× 79 0.2× 176 0.7× 79 2.7k
Jack Lenz United States 31 1.0k 1.4× 1.9k 2.9× 71 0.2× 142 0.4× 112 0.5× 64 3.4k

Countries citing papers authored by Kenneth A. Field

Since Specialization
Citations

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

Fields of papers citing papers by Kenneth A. Field

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kenneth A. Field. 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 Kenneth A. Field. The network helps show where Kenneth A. Field may publish in the future.

Co-authorship network of co-authors of Kenneth A. Field

This figure shows the co-authorship network connecting the top 25 collaborators of Kenneth A. Field. A scholar is included among the top collaborators of Kenneth A. Field 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 Kenneth A. Field. Kenneth A. Field 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.
Field, Kenneth A., Tomáš Bartonička, Veronika N. Laine, et al.. (2025). Bat species tolerant and susceptible to fungal infection show transcriptomic differences in late hibernation and healing. Journal of Experimental Biology. 229(1).
2.
Blomberg, Anna S., et al.. (2024). A Palearctic view of a bat fungal disease. Conservation Biology. 39(1). e14265–e14265. 7 indexed citations
3.
Twort, Victoria, Veronika N. Laine, Kenneth A. Field, et al.. (2024). Signals of positive selection in genomes of palearctic Myotis-bats coexisting with a fungal pathogen. BMC Genomics. 25(1). 828–828.
4.
Chothe, Shubhada K., Santhamani Ramasamy, Abhinay Gontu, et al.. (2023). Little Brown Bats (Myotis lucifugus) Support the Binding of SARS-CoV-2 Spike and Are Likely Susceptible to SARS-CoV-2 Infection. Viruses. 15(5). 1103–1103. 2 indexed citations
5.
Pizzorno, Marie C., et al.. (2021). Transcriptomic Responses of the Honey Bee Brain to Infection with Deformed Wing Virus. Viruses. 13(2). 287–287. 18 indexed citations
6.
Field, Kenneth A., et al.. (2021). Heterothermy and antifungal responses in bats. Current Opinion in Microbiology. 62. 61–67. 7 indexed citations
7.
Lilley, Thomas M., Kenneth A. Field, DeeAnn M. Reeder, et al.. (2020). Genome-Wide Changes in Genetic Diversity in a Population of Myotis lucifugus Affected by White-Nose Syndrome. G3 Genes Genomes Genetics. 10(6). 2007–2020. 13 indexed citations
8.
Lilley, Thomas M., Jenni M. Prokkola, Anna S. Blomberg, et al.. (2019). Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis. Oecologia. 191(2). 295–309. 31 indexed citations
9.
Lilley, Thomas M., Riley F. Bernard, Emma V. Willcox, et al.. (2017). Molecular Detection of Candidatus Bartonella mayotimonensis in North American Bats. Vector-Borne and Zoonotic Diseases. 17(4). 243–246. 34 indexed citations
10.
Lilley, Thomas M., Joseph S. Johnson, Lasse Ruokolainen, et al.. (2016). White-nose syndrome survivors do not exhibit frequent arousals associated with Pseudogymnoascus destructans infection. Frontiers in Zoology. 13(1). 12–12. 52 indexed citations
11.
Reeder, DeeAnn M., Kenneth A. Field, & Matthew H. Slater. (2016). Balancing the Costs of Wildlife Research with the Benefits of Understanding a Panzootic Disease, White-Nose Syndrome. ILAR Journal. 56(3). 275–282. 11 indexed citations
12.
Field, Kenneth A., Joseph S. Johnson, Thomas M. Lilley, et al.. (2015). The White-Nose Syndrome Transcriptome: Activation of Anti-fungal Host Responses in Wing Tissue of Hibernating Little Brown Myotis. PLoS Pathogens. 11(10). e1005168–e1005168. 96 indexed citations
13.
Johnson, Joseph S., DeeAnn M. Reeder, Melissa B. Meierhofer, et al.. (2014). Host, Pathogen, and Environmental Characteristics Predict White-Nose Syndrome Mortality in Captive Little Brown Myotis (Myotis lucifugus). PLoS ONE. 9(11). e112502–e112502. 58 indexed citations
14.
Vokaer, B., Philippe Lemaître, Frédéric Lhomme, et al.. (2010). Critical Role of Regulatory T Cells in Th17-Mediated Minor Antigen-Disparate Rejection. The Journal of Immunology. 185(6). 3417–3425. 50 indexed citations
15.
McNab, Finlay W., Daniel G. Pellicci, Kenneth A. Field, et al.. (2007). Peripheral NK1.1− NKT Cells Are Mature and Functionally Distinct from Their Thymic Counterparts. The Journal of Immunology. 179(10). 6630–6637. 51 indexed citations
16.
McNab, Finlay W., Stuart P. Berzins, Daniel G. Pellicci, et al.. (2005). The Influence of CD1d in Postselection NKT Cell Maturation and Homeostasis. The Journal of Immunology. 175(6). 3762–3768. 92 indexed citations
17.
Vučković, Slavica, Kenneth A. Field, Devinder Gill, et al.. (2003). Monitoring dendritic cells in clinical practice using a new whole blood single-platform TruCOUNT assay. Journal of Immunological Methods. 284(1-2). 73–87. 69 indexed citations
18.
Field, Kenneth A., John Apgar, Elizabeth Hong‐Geller, et al.. (2000). Mutant RBL Mast Cells Defective in FcεRI Signaling and Lipid Raft Biosynthesis Are Reconstituted by Activated Rho-family GTPases. Molecular Biology of the Cell. 11(10). 3661–3673. 39 indexed citations
19.
Field, Kenneth A., David Holowka, & Barbara Baird. (1999). Structural Aspects of the Association of FcεRI with Detergent-resistant Membranes. Journal of Biological Chemistry. 274(3). 1753–1758. 93 indexed citations
20.
Ge, Mingtao, et al.. (1999). Electron Spin Resonance Characterization of Liquid Ordered Phase of Detergent-Resistant Membranes from RBL-2H3 Cells. Biophysical Journal. 77(2). 925–933. 101 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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