Roman V. Uzhachenko

1.2k total citations
36 papers, 860 citations indexed

About

Roman V. Uzhachenko is a scholar working on Molecular Biology, Immunology and Oncology. According to data from OpenAlex, Roman V. Uzhachenko has authored 36 papers receiving a total of 860 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Immunology and 10 papers in Oncology. Recurrent topics in Roman V. Uzhachenko's work include Immunotherapy and Immune Responses (8 papers), Mitochondrial Function and Pathology (7 papers) and Immune Cell Function and Interaction (7 papers). Roman V. Uzhachenko is often cited by papers focused on Immunotherapy and Immune Responses (8 papers), Mitochondrial Function and Pathology (7 papers) and Immune Cell Function and Interaction (7 papers). Roman V. Uzhachenko collaborates with scholars based in United States, Russia and France. Roman V. Uzhachenko's co-authors include Anil Shanker, Anna Dikalova, Sergey Dikalov, Alla V. Ivanova, Charles R. Flynn, William G. McMaster, Jorge Gamboa, Hana A. Itani, David G. Harrison and Rafal R. Nazarewicz and has published in prestigious journals such as The Journal of Immunology, Circulation Research and Cancer Research.

In The Last Decade

Roman V. Uzhachenko

36 papers receiving 851 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roman V. Uzhachenko United States 17 370 222 200 108 94 36 860
Vemika Chandra India 15 411 1.1× 235 1.1× 99 0.5× 130 1.2× 262 2.8× 19 949
Mourad Zerfaoui United States 22 633 1.7× 388 1.7× 469 2.3× 139 1.3× 107 1.1× 49 1.5k
Takuya Yashiro Japan 18 337 0.9× 335 1.5× 95 0.5× 126 1.2× 57 0.6× 53 845
Ho Joong Sung South Korea 17 579 1.6× 96 0.4× 184 0.9× 162 1.5× 69 0.7× 40 961
Xiaoxia Jin China 17 397 1.1× 78 0.4× 97 0.5× 77 0.7× 48 0.5× 36 747
Victoria A. McGuire United Kingdom 14 667 1.8× 315 1.4× 240 1.2× 74 0.7× 129 1.4× 21 1.2k
Noélie Davezac France 19 845 2.3× 156 0.7× 73 0.4× 162 1.5× 106 1.1× 28 1.3k
Carlos J. Orihuela United States 12 526 1.4× 369 1.7× 95 0.5× 417 3.9× 304 3.2× 13 1.5k
Kyaw Zaw Hein United States 11 262 0.7× 61 0.3× 93 0.5× 95 0.9× 77 0.8× 16 732

Countries citing papers authored by Roman V. Uzhachenko

Since Specialization
Citations

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

Fields of papers citing papers by Roman V. Uzhachenko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roman V. Uzhachenko. 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 Roman V. Uzhachenko. The network helps show where Roman V. Uzhachenko may publish in the future.

Co-authorship network of co-authors of Roman V. Uzhachenko

This figure shows the co-authorship network connecting the top 25 collaborators of Roman V. Uzhachenko. A scholar is included among the top collaborators of Roman V. Uzhachenko 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 Roman V. Uzhachenko. Roman V. Uzhachenko 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.
Uzhachenko, Roman V., Thanigaivelan Kanagasabai, Menaka C. Thounaojam, et al.. (2025). CD8+ T–NK cell crosstalk establishes preemptive immunosurveillance to eliminate antigen–escape tumors. Frontiers in Immunology. 16. 1593913–1593913. 1 indexed citations
2.
Kumar, Amrendra, Vijay Ramani, Vijaya Bharti, et al.. (2023). Dendritic cell therapy augments antitumor immunity triggered by CDK4/6 inhibition and immune checkpoint blockade by unleashing systemic CD4 T-cell responses. Journal for ImmunoTherapy of Cancer. 11(5). e006019–e006019. 10 indexed citations
3.
Uzhachenko, Roman V., Akiko Shimamoto, Sanika Chirwa, et al.. (2022). Mitochondrial Fus1/Tusc2 and cellular Ca2+ homeostasis: tumor suppressor, anti-inflammatory and anti-aging implications. Cancer Gene Therapy. 29(10). 1307–1320. 10 indexed citations
4.
Uzhachenko, Roman V., Vijaya Bharti, Zhufeng Ouyang, et al.. (2021). Metabolic modulation by CDK4/6 inhibitor promotes chemokine-mediated recruitment of T cells into mammary tumors. Cell Reports. 35(1). 108944–108944. 61 indexed citations
5.
Tchekneva, Elena E., Roman V. Uzhachenko, Michael J. Koenig, et al.. (2019). Determinant roles of dendritic cell-expressed Notch Delta-like and Jagged ligands on anti-tumor T cell immunity. Journal for ImmunoTherapy of Cancer. 7(1). 95–95. 35 indexed citations
6.
Uzhachenko, Roman V. & Anil Shanker. (2019). CD8+ T Lymphocyte and NK Cell Network: Circuitry in the Cytotoxic Domain of Immunity. Frontiers in Immunology. 10. 1906–1906. 85 indexed citations
7.
Mayorov, Vladimir, Peter Uchakin, Venkataraman Amarnath, et al.. (2019). Targeting of reactive isolevuglandins in mitochondrial dysfunction and inflammation. Redox Biology. 26. 101300–101300. 16 indexed citations
8.
Shanker, Anil, et al.. (2018). Glutamate receptors provide costimulatory signals to improve T cell immune response.. The Journal of Immunology. 200(Supplement_1). 47.24–47.24. 4 indexed citations
9.
Dikalova, Anna, Hana A. Itani, Rafal R. Nazarewicz, et al.. (2017). Sirt3 Impairment and SOD2 Hyperacetylation in Vascular Oxidative Stress and Hypertension. Circulation Research. 121(5). 564–574. 235 indexed citations
10.
Uzhachenko, Roman V. & Anil Shanker. (2016). Notching tumor: Signaling through Notch receptors improves antitumor T cell immunity. OncoImmunology. 5(5). e1122864–e1122864. 6 indexed citations
11.
Uzhachenko, Roman V., Kyungho Park, Anwari Akhter, et al.. (2015). Multivalent Forms of the Notch Ligand DLL-1 Enhance Antitumor T-cell Immunity in Lung Cancer and Improve Efficacy of EGFR-Targeted Therapy. Cancer Research. 75(22). 4728–4741. 46 indexed citations
12.
Uzhachenko, Roman V., J. Shawn Goodwin, Lino Costa, et al.. (2015). Abstract 4059: Crosstalk between CD8+ T and NK cells: fine-tuning of antitumor immune response. Cancer Research. 75(15_Supplement). 4059–4059. 1 indexed citations
13.
Uzhachenko, Roman V., et al.. (2015). Common gamma chain cytokines in combinatorial immune strategies against cancer. Immunology Letters. 169. 61–72. 38 indexed citations
14.
Uzhachenko, Roman V., Sergey V. Ivanov, Wendell G. Yarbrough, et al.. (2013). Fus1/Tusc2 Is a Novel Regulator of Mitochondrial Calcium Handling, Ca 2+ -Coupled Mitochondrial Processes, and Ca 2+ -Dependent NFAT and NF-κB Pathways in CD4 + T Cells. Antioxidants and Redox Signaling. 20(10). 1533–1547. 33 indexed citations
15.
Yazlovitskaya, Eugenia M., Roman V. Uzhachenko, Paul Voziyan, Wendell G. Yarbrough, & Alla V. Ivanova. (2013). A novel radioprotective function for the mitochondrial tumor suppressor protein Fus1. Cell Death and Disease. 4(6). e687–e687. 14 indexed citations
16.
Uzhachenko, Roman V., Natalia Issaeva, Kelli L. Boyd, et al.. (2012). Tumour suppressor Fus1 provides a molecular link between inflammatory response and mitochondrial homeostasis. The Journal of Pathology. 227(4). 456–469. 16 indexed citations
17.
Sharshov, Kirill, Roman V. Uzhachenko, Anna V. Zaykovskaya, et al.. (2010). Genetic and biological characterization of avian influenza H5N1 viruses isolated from wild birds and poultry in Western Siberia. Archives of Virology. 155(7). 1145–1150. 23 indexed citations
19.
Маслов, Л. Н., et al.. (2004). Selective cannabinoid receptor agonist HU-210 decreases pump function of isolated perfused heart: Role of cAMP and cGMP. Bulletin of Experimental Biology and Medicine. 138(6). 550–553. 12 indexed citations
20.
Крылатов, А. В., Roman V. Uzhachenko, Л. Н. Маслов, et al.. (2002). Endogenous Cannabinoids Improve Myocardial Resistance to Arrhythmogenic Effects of Coronary Occlusion and Reperfusion: a Possible Mechanism. Bulletin of Experimental Biology and Medicine. 133(2). 122–124. 26 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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