Elizabeth A. Kosmacek

1.3k total citations
45 papers, 1.0k citations indexed

About

Elizabeth A. Kosmacek is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Cancer Research. According to data from OpenAlex, Elizabeth A. Kosmacek has authored 45 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 14 papers in Radiology, Nuclear Medicine and Imaging and 9 papers in Cancer Research. Recurrent topics in Elizabeth A. Kosmacek's work include Effects of Radiation Exposure (11 papers), Cancer-related Molecular Pathways (7 papers) and Cancer, Hypoxia, and Metabolism (7 papers). Elizabeth A. Kosmacek is often cited by papers focused on Effects of Radiation Exposure (11 papers), Cancer-related Molecular Pathways (7 papers) and Cancer, Hypoxia, and Metabolism (7 papers). Elizabeth A. Kosmacek collaborates with scholars based in United States, Latvia and China. Elizabeth A. Kosmacek's co-authors include Rebecca E. Oberley‐Deegan, Fiorenza Ianzini, Arpita Chatterjee, Jekaterina Ērenpreisa, Michael A. Mackey, Mārtiņš Kalējs, Mark S. Cragg, Qiang Tong, Tim Illidge and Paul J. Davis and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Cancer Research.

In The Last Decade

Elizabeth A. Kosmacek

43 papers receiving 995 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elizabeth A. Kosmacek United States 18 530 246 176 169 127 45 1.0k
Paula Cunnea United Kingdom 16 411 0.8× 157 0.6× 233 1.3× 125 0.7× 134 1.1× 38 968
Corinne Prévostel France 18 963 1.8× 167 0.7× 213 1.2× 187 1.1× 68 0.5× 31 1.3k
Sharmistha Chakraborty United States 23 891 1.7× 303 1.2× 112 0.6× 211 1.2× 45 0.4× 41 1.4k
Safiyyah Ziyad United States 15 551 1.0× 293 1.2× 111 0.6× 153 0.9× 55 0.4× 23 968
Ryuichi Ohgaki Japan 22 798 1.5× 209 0.8× 84 0.5× 106 0.6× 222 1.7× 45 1.4k
Ahmed F. Salem United States 21 799 1.5× 249 1.0× 134 0.8× 248 1.5× 80 0.6× 42 1.2k
Birgit Mosch Germany 16 484 0.9× 154 0.6× 158 0.9× 120 0.7× 79 0.6× 25 904
Urs Lüthi Switzerland 16 870 1.6× 213 0.9× 298 1.7× 135 0.8× 59 0.5× 34 1.6k
Ines Lohse United States 18 509 1.0× 425 1.7× 87 0.5× 394 2.3× 112 0.9× 43 1.2k
Astrid Zimmermann Germany 20 891 1.7× 397 1.6× 100 0.6× 210 1.2× 65 0.5× 76 1.7k

Countries citing papers authored by Elizabeth A. Kosmacek

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth A. Kosmacek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elizabeth A. Kosmacek

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth A. Kosmacek. A scholar is included among the top collaborators of Elizabeth A. Kosmacek 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 Elizabeth A. Kosmacek. Elizabeth A. Kosmacek 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
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2.
Chatterjee, Arpita, Elizabeth A. Kosmacek, Mei Liu, et al.. (2025). Identification of Potential Prophylactic Medical Countermeasures Against Acute Radiation Syndrome (ARS). International Journal of Molecular Sciences. 26(9). 4055–4055. 1 indexed citations
3.
Kosmacek, Elizabeth A., Divya Murthy, Pankaj K. Singh, et al.. (2025). Radiation Promotes Acute and Chronic Damage to Adipose Tissue. International Journal of Molecular Sciences. 26(12). 5626–5626. 4 indexed citations
4.
Jonnalagadda, Sravan K., Ling Duan, Elizabeth A. Kosmacek, et al.. (2024). Coumarin‐Based Aldo‐Keto Reductase Family 1C (AKR1C) 2 and 3 Inhibitors. ChemMedChem. 19(21). e202400081–e202400081. 1 indexed citations
5.
Kosmacek, Elizabeth A., et al.. (2024). Adipose Tissues Have Been Overlooked as Players in Prostate Cancer Progression. International Journal of Molecular Sciences. 25(22). 12137–12137. 3 indexed citations
6.
Kosmacek, Elizabeth A., Michael J. Baine, Arpita Chatterjee, et al.. (2024). Exogenous APN protects normal tissues from radiation-induced oxidative damage and fibrosis in mice and prostate cancer patients with higher levels of APN have less radiation-induced toxicities. Redox Biology. 73. 103219–103219. 9 indexed citations
7.
Kosmacek, Elizabeth A., et al.. (2022). CT vs. bioluminescence: A comparison of imaging techniques for orthotopic prostate tumors in mice. PLoS ONE. 17(11). e0277239–e0277239. 3 indexed citations
8.
Mir, Shakeel U.R., Brandon Griess, Raghupathy Vengoji, et al.. (2022). Upregulation of Nox4 induces a pro-survival Nrf2 response in cancer-associated fibroblasts that promotes tumorigenesis and metastasis, in part via Birc5 induction. Breast Cancer Research. 24(1). 48–48. 18 indexed citations
9.
Pekas, Elizabeth J., Elizabeth A. Kosmacek, Bryan T. Hackfort, et al.. (2021). Sympathoinhibition and vasodilation contribute to the acute hypotensive response of the superoxide dismutase mimic, MnTnBuOE-2-PyP5+, in hypertensive animals. SHILAP Revista de lepidopterología. 3. 100016–100016. 5 indexed citations
10.
Lin, Chi, Jean L. Grem, Kelsey Klute, et al.. (2021). The Phase I Results of a Phase 1/2 Trial for Patients With Newly Diagnosed Anal Cancer Treated With Concurrent Radiation Therapy, 5-Fluorouracil, Mitomycin and BMX-001. International Journal of Radiation Oncology*Biology*Physics. 111(3). S103–S103. 1 indexed citations
11.
Zhu, Yuxiang, Divya Murthy, Sai Sundeep Kollala, et al.. (2021). The central role of NADPH depletion in MnTE-2-PyP-induced prostate cancer cell growth inhibition. SHILAP Revista de lepidopterología. 3. 100025–100025. 2 indexed citations
12.
13.
Kosmacek, Elizabeth A., et al.. (2019). MnTnBuOE-2-PyP treatment protects from radioactive iodine (I-131) treatment-related side effects in thyroid cancer. Radiation and Environmental Biophysics. 59(1). 99–109. 8 indexed citations
14.
Kosmacek, Elizabeth A., et al.. (2019). Reactive Oxygen Species Drive Epigenetic Changes in Radiation-Induced Fibrosis. Oxidative Medicine and Cellular Longevity. 2019. 1–27. 70 indexed citations
15.
Miller, Dannah, Matthew A. Ingersoll, Arpita Chatterjee, et al.. (2019). p66Shc protein through a redox mechanism enhances the progression of prostate cancer cells towards castration-resistance. Free Radical Biology and Medicine. 139. 24–34. 17 indexed citations
16.
Perraud, Anne-Laure, et al.. (2018). The ion channel, TRPM2, contributes to the pathogenesis of radiodermatitis. Radiation and Environmental Biophysics. 58(1). 89–98. 5 indexed citations
17.
Chatterjee, Arpita, Elizabeth A. Kosmacek, & Rebecca E. Oberley‐Deegan. (2017). MnTE-2-PyP Treatment, or NOX4 Inhibition, Protects against Radiation-Induced Damage in Mouse Primary Prostate Fibroblasts by Inhibiting the TGF-Beta 1 Signaling Pathway. Radiation Research. 187(3). 367–367. 39 indexed citations
18.
Kosloski, Lisa M., Elizabeth A. Kosmacek, Katherine E. Olson, R. Lee Mosley, & Howard E. Gendelman. (2013). GM-CSF induces neuroprotective and anti-inflammatory responses in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine intoxicated mice. Journal of Neuroimmunology. 265(1-2). 1–10. 86 indexed citations
19.
Ērenpreisa, Jekaterina, Kristīne Salmiņa, Anda Huna, et al.. (2011). Polyploid tumour cells elicit paradiploid progeny through depolyploidizing divisions and regulated autophagic degradation. Cell Biology International. 35(7). 687–695. 75 indexed citations
20.
Ianzini, Fiorenza, Elizabeth A. Kosmacek, Eleonora Napoli, et al.. (2009). Activation of Meiosis-Specific Genes Is Associated with Depolyploidization of Human Tumor Cells following Radiation-Induced Mitotic Catastrophe. Cancer Research. 69(6). 2296–2304. 103 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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