Valery N. Bochkov

13.1k total citations · 1 hit paper
113 papers, 6.6k citations indexed

About

Valery N. Bochkov is a scholar working on Molecular Biology, Immunology and Biochemistry. According to data from OpenAlex, Valery N. Bochkov has authored 113 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 30 papers in Immunology and 21 papers in Biochemistry. Recurrent topics in Valery N. Bochkov's work include Antioxidant Activity and Oxidative Stress (20 papers), Atherosclerosis and Cardiovascular Diseases (13 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (12 papers). Valery N. Bochkov is often cited by papers focused on Antioxidant Activity and Oxidative Stress (20 papers), Atherosclerosis and Cardiovascular Diseases (13 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (12 papers). Valery N. Bochkov collaborates with scholars based in Austria, Switzerland and United States. Valery N. Bochkov's co-authors include Olga Oskolkova, Norbert Leitinger, Bernd R. Binder, Konstantin G. Birukov, Флориан Грубер, Joakim Huber, Alexandra Kadl, Johannes M. Breuss, Rudolf Bauer and Verena M. Dirsch and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Valery N. Bochkov

111 papers receiving 6.5k citations

Hit Papers

Discovery and resupply of... 2015 2026 2018 2022 2015 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valery N. Bochkov Austria 37 3.4k 1.4k 817 698 593 113 6.6k
Han Geuk Seo South Korea 48 3.3k 1.0× 948 0.7× 449 0.5× 534 0.8× 472 0.8× 214 7.1k
Takahiro Shibata Japan 38 4.2k 1.2× 604 0.4× 486 0.6× 299 0.4× 746 1.3× 216 6.7k
Hirofumi Tachibana Japan 46 2.4k 0.7× 1.0k 0.7× 1.4k 1.7× 421 0.6× 273 0.5× 256 6.8k
Mario Dicato Luxembourg 57 5.1k 1.5× 814 0.6× 546 0.7× 740 1.1× 204 0.3× 219 10.8k
Po‐Lin Kuo Taiwan 55 4.8k 1.4× 1.2k 0.9× 416 0.5× 889 1.3× 236 0.4× 199 9.0k
Valérie B. Schini‐Kerth France 48 2.5k 0.7× 686 0.5× 1.3k 1.5× 546 0.8× 561 0.9× 202 7.3k
Elke H. Heiß Austria 41 4.1k 1.2× 633 0.5× 880 1.1× 1.6k 2.3× 316 0.5× 125 7.9k
Jong‐Sup Bae South Korea 50 3.6k 1.0× 2.0k 1.4× 700 0.9× 856 1.2× 163 0.3× 341 9.1k
Jung Han Yoon Park South Korea 49 3.4k 1.0× 689 0.5× 655 0.8× 892 1.3× 186 0.3× 185 6.5k
Hye‐Kyung Na South Korea 43 3.4k 1.0× 458 0.3× 685 0.8× 485 0.7× 355 0.6× 106 5.9k

Countries citing papers authored by Valery N. Bochkov

Since Specialization
Citations

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

Fields of papers citing papers by Valery N. Bochkov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Valery N. Bochkov. 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 Valery N. Bochkov. The network helps show where Valery N. Bochkov may publish in the future.

Co-authorship network of co-authors of Valery N. Bochkov

This figure shows the co-authorship network connecting the top 25 collaborators of Valery N. Bochkov. A scholar is included among the top collaborators of Valery N. Bochkov 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 Valery N. Bochkov. Valery N. Bochkov 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.
O’Donnell, Valerie B. & Valery N. Bochkov. (2025). Oxidized phospholipids in ferroptosis, immunity and inflammation. ORCA Online Research @Cardiff (Cardiff University). 14. 100061–100061.
2.
Übelhart, Rudolf, et al.. (2024). Identification of plasma proteins binding oxidized phospholipids using pull-down proteomics and OxLDL masking assay. Journal of Lipid Research. 66(1). 100704–100704. 1 indexed citations
3.
Afonyushkin, Taras, Olga Oskolkova, Bernd Gesslbauer, et al.. (2022). Low Concentrations of Oxidized Phospholipids Increase Stress Tolerance of Endothelial Cells. Antioxidants. 11(9). 1741–1741. 2 indexed citations
4.
Lainšček, Duško, Bernd Gesslbauer, Eva Jarc Jovičić, et al.. (2020). Synergy between 15-lipoxygenase and secreted PLA 2 promotes inflammation by formation of TLR4 agonists from extracellular vesicles. Proceedings of the National Academy of Sciences. 117(41). 25679–25689. 17 indexed citations
5.
Afonyushkin, Taras, Olga Oskolkova, & Valery N. Bochkov. (2018). Oxidized phospholipids stimulate production of stem cell factor via NRF2-dependent mechanisms. Angiogenesis. 21(2). 229–236. 5 indexed citations
6.
Narzt, Marie‐Sophie, Ionela‐Mariana Nagelreiter, Olga Oskolkova, et al.. (2018). 1137 A novel role for NUPR1 in the keratinocyte stress response to UV oxidized phospholipids. Journal of Investigative Dermatology. 138(5). S193–S193. 4 indexed citations
7.
Philippova, Maria, et al.. (2016). Hormetic and anti-inflammatory properties of oxidized phospholipids. Molecular Aspects of Medicine. 49. 78–90. 35 indexed citations
8.
Birukova, Anna A., Patrick A. Singleton, Grzegorz Gawlak, et al.. (2014). GRP78 is a novel receptor initiating a vascular barrier protective response to oxidized phospholipids. Molecular Biology of the Cell. 25(13). 2006–2016. 45 indexed citations
9.
Pollreisz, Andreas, Taras Afonyushkin, Olga Oskolkova, et al.. (2013). Retinal pigment epithelium cells produce VEGF in response to oxidized phospholipids through mechanisms involving ATF4 and protein kinase CK2. Experimental Eye Research. 116. 177–184. 26 indexed citations
10.
Starosta, Vitaliy, Tinghuai Wu, Alejandro Zimman, et al.. (2011). Differential Regulation of Endothelial Cell Permeability by High and Low Doses of Oxidized 1-Palmitoyl-2-Arachidonyl- sn -Glycero-3-Phosphocholine. American Journal of Respiratory Cell and Molecular Biology. 46(3). 331–341. 46 indexed citations
11.
Uderhardt, Stefan, Martin Herrmann, Olga Oskolkova, et al.. (2011). 12/15-lipoxygenase orchestrates the clearance of apoptotic cells and maintains immunologic tolerance. Journal of Translational Medicine. 9(S2). 12 indexed citations
12.
Bochkov, Valery N., Olga Oskolkova, Konstantin G. Birukov, et al.. (2009). Generation and Biological Activities of Oxidized Phospholipids. Antioxidants and Redox Signaling. 12(8). 1009–1059. 465 indexed citations
13.
Blüml, Stephan, Stefanie Kirchberger, Valery N. Bochkov, et al.. (2008). Oxidized phospholipids induce anergy in human peripheral blood T cells. European Journal of Immunology. 38(3). 778–787. 31 indexed citations
14.
Blüml, Stephan, Ákos M. Lőrincz, Stefanie Kirchberger, et al.. (2008). The Oxidation State of Phospholipids Controls the Oxidative Burst in Neutrophil Granulocytes. The Journal of Immunology. 181(6). 4347–4353. 32 indexed citations
15.
Грубер, Флориан, Olga Oskolkova, Alexander Leitner, et al.. (2007). Photooxidation Generates Biologically Active Phospholipids That Induce Heme Oxygenase-1 in Skin Cells. Journal of Biological Chemistry. 282(23). 16934–16941. 49 indexed citations
16.
Demyanets, Svitlana, Stefan Pfaffenberger, Christoph Kaun, et al.. (2006). The estrogen metabolite 17beta-dihydroequilenin counteracts interleukin-1alpha induced expression of inflammatory mediators in human endothelial cells in vitro via NF-kappaB pathway.. PubMed. 95(1). 107–16. 16 indexed citations
17.
Kaun, Christoph, Gersina Rega‐Kaun, Walter S. Speidl, et al.. (2005). The estrogen metabolite 17β-dihydroequilenin counteracts interleukin-1α induced expression of inflammatory mediators in human endothelial cells in vitro via NF-κB pathway. Thrombosis and Haemostasis. 95(1). 107–116. 18 indexed citations
18.
Bochkov, Valery N., Yelena Parfyonova, Tkachuk Va, et al.. (2002). Expression of adhesion molecule T-cadherin is increased during neointima formation in experimental restenosis. Histochemistry and Cell Biology. 118(4). 281–290. 64 indexed citations
19.
Stambolsky, Dmitry, et al.. (1999). Identification of 130 kDa cell surface LDL-binding protein from smooth muscle cells as a partially processed T-cadherin precursor. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1416(1-2). 155–160. 19 indexed citations
20.
Resink, Thérèse J., Fritz R. Bühler, Alfred Hahn, Valery N. Bochkov, & Tkachuk Va. (1994). INTERACTION BETWEEN PLASMA-LIPOPROTEINS AND VASCULAR SMOOTH-MUSCLE CELLS - HOW RELEVANT IS IT TO ARTERIAL-HYPERTENSION. Nutrition Metabolism and Cardiovascular Diseases. 4(3). 163–170. 4 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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