Viktor Umansky

7.3k total citations · 2 hit papers
94 papers, 5.6k citations indexed

About

Viktor Umansky is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Viktor Umansky has authored 94 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Immunology, 51 papers in Oncology and 31 papers in Molecular Biology. Recurrent topics in Viktor Umansky's work include Immune cells in cancer (50 papers), Immunotherapy and Immune Responses (26 papers) and Cancer Immunotherapy and Biomarkers (23 papers). Viktor Umansky is often cited by papers focused on Immune cells in cancer (50 papers), Immunotherapy and Immune Responses (26 papers) and Cancer Immunotherapy and Biomarkers (23 papers). Viktor Umansky collaborates with scholars based in Germany, United States and Israel. Viktor Umansky's co-authors include Jochen Utikal, Alexandra Sevko, Christoffer Gebhardt, Peter Altevogt, C Blattner, Rebekka Weber, Christopher Groth, Samantha Lasser, Ihor Arkhypov and Xiaoying Hu and has published in prestigious journals such as Journal of Biological Chemistry, Blood and The Journal of Immunology.

In The Last Decade

Viktor Umansky

91 papers receiving 5.5k citations

Hit Papers

Myeloid-Derived Suppressor Cells Hinder the Anti-Cancer A... 2018 2026 2020 2023 2018 2024 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Viktor Umansky Germany 42 3.6k 2.8k 1.7k 625 460 94 5.6k
Viktor Umansky Germany 31 4.4k 1.2× 2.9k 1.0× 1.7k 1.0× 605 1.0× 374 0.8× 60 6.3k
Marco Donia Denmark 45 3.8k 1.1× 4.3k 1.5× 2.0k 1.2× 490 0.8× 520 1.1× 195 6.7k
Andrea Schietinger United States 25 3.5k 1.0× 3.1k 1.1× 1.2k 0.7× 336 0.5× 305 0.7× 41 5.1k
Wojciech Szeliga United States 19 4.0k 1.1× 3.0k 1.1× 1.5k 0.8× 564 0.9× 367 0.8× 26 5.7k
Damya Laoui Belgium 31 3.6k 1.0× 2.3k 0.8× 1.9k 1.1× 858 1.4× 406 0.9× 60 5.5k
Susanna Mandruzzato Italy 36 6.1k 1.7× 3.2k 1.1× 2.0k 1.1× 693 1.1× 403 0.9× 77 7.8k
Marc Schmitz Germany 46 3.2k 0.9× 2.8k 1.0× 2.0k 1.2× 440 0.7× 530 1.2× 173 6.4k
Linda A. Snyder United States 25 2.7k 0.8× 2.4k 0.9× 1.5k 0.8× 614 1.0× 564 1.2× 46 4.6k
Sabina Sangaletti Italy 33 2.4k 0.7× 1.6k 0.6× 1.3k 0.8× 531 0.8× 473 1.0× 81 4.4k
Stefanie K. Wculek Spain 18 2.8k 0.8× 1.8k 0.6× 1.6k 0.9× 475 0.8× 406 0.9× 21 4.7k

Countries citing papers authored by Viktor Umansky

Since Specialization
Citations

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

Fields of papers citing papers by Viktor Umansky

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Viktor Umansky. 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 Viktor Umansky. The network helps show where Viktor Umansky may publish in the future.

Co-authorship network of co-authors of Viktor Umansky

This figure shows the co-authorship network connecting the top 25 collaborators of Viktor Umansky. A scholar is included among the top collaborators of Viktor Umansky 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 Viktor Umansky. Viktor Umansky 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.
Liu, Ke, Yuxin Zhang, Daniel Novak, et al.. (2025). Direct transdifferentiation of tumorigenic melanoma cells induces tumor cell reversion. Cell Death and Disease. 16(1). 563–563.
2.
Umansky, Viktor. (2025). MDSCs as major inducers of immunosuppression in melanoma. 8(CITIM). 24–24.
3.
Kurt, Feyza Gül Özbay, Carolina De La Torre, Volker Ast, et al.. (2024). S100A9 and HMGB1 orchestrate MDSC-mediated immunosuppression in melanoma through TLR4 signaling. Journal for ImmunoTherapy of Cancer. 12(9). e009552–e009552. 16 indexed citations
4.
Petrova, Vera, Christopher Groth, Ihor Arkhypov, et al.. (2023). Immunosuppressive capacity of circulating MDSC predicts response to immune checkpoint inhibitors in melanoma patients. Frontiers in Immunology. 14. 12 indexed citations
5.
Kurt, Feyza Gül Özbay, Carolina De La Torre, Samantha Lasser, et al.. (2022). STAT3 inhibitor Napabucasin abrogates MDSC immunosuppressive capacity and prolongs survival of melanoma-bearing mice. Journal for ImmunoTherapy of Cancer. 10(3). e004384–e004384. 56 indexed citations
6.
Arkhypov, Ihor, Feyza Gül Özbay Kurt, Daniel Novak, et al.. (2022). HSP90α induces immunosuppressive myeloid cells in melanoma via TLR4 signaling. Journal for ImmunoTherapy of Cancer. 10(9). e005551–e005551. 32 indexed citations
7.
Sun, Qian, et al.. (2022). ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6. Cancers. 14(4). 1071–1071. 15 indexed citations
8.
Groth, Christopher, Ludovica Arpinati, Merav E. Shaul, et al.. (2021). Blocking Migration of Polymorphonuclear Myeloid-Derived Suppressor Cells Inhibits Mouse Melanoma Progression. Cancers. 13(4). 726–726. 24 indexed citations
9.
Weber, Rebekka, Christopher Groth, Samantha Lasser, et al.. (2020). IL-6 as a major regulator of MDSC activity and possible target for cancer immunotherapy. Cellular Immunology. 359. 104254–104254. 219 indexed citations
10.
Gebhardt, Christoffer, Rebekka Weber, Raphael Reinhard, et al.. (2020). Potential therapeutic effect of low-dose paclitaxel in melanoma patients resistant to immune checkpoint blockade: A pilot study. Cellular Immunology. 360. 104274–104274. 19 indexed citations
11.
Federico, Aniello, Lionel Larribère, Daniel Novak, et al.. (2020). Mithramycin A and Mithralog EC-8042 Inhibit SETDB1 Expression and Its Oncogenic Activity in Malignant Melanoma. Molecular Therapy — Oncolytics. 18. 83–99. 26 indexed citations
12.
Fleming, Viktor, Xiaoying Hu, Rebekka Weber, et al.. (2019). Melanoma Extracellular Vesicles Generate Immunosuppressive Myeloid Cells by Upregulating PD-L1 via TLR4 Signaling. Cancer Research. 79(18). 4715–4728. 110 indexed citations
13.
Kappelmann‐Fenzl, Melanie, Silke Kuphal, Rosemarie Krupar, et al.. (2019). Complex Formation with Monomeric α-Tubulin and Importin 13 Fosters c-Jun Protein Stability and Is Required for c-Jun’s Nuclear Translocation and Activity. Cancers. 11(11). 1806–1806. 6 indexed citations
14.
Blattner, C, Viktor Fleming, Rebekka Weber, et al.. (2018). CCR5+ Myeloid-Derived Suppressor Cells Are Enriched and Activated in Melanoma Lesions. Cancer Research. 78(1). 157–167. 151 indexed citations
15.
Yamauchi, Yoshikane, Seyer Safi, C Blattner, et al.. (2018). Circulating and Tumor Myeloid-derived Suppressor Cells in Resectable Non–Small Cell Lung Cancer. American Journal of Respiratory and Critical Care Medicine. 198(6). 777–787. 131 indexed citations
16.
Utikal, Jochen, et al.. (2018). Opposing roles of eosinophils in cancer. Cancer Immunology Immunotherapy. 68(5). 823–833. 92 indexed citations
17.
Blacher, Eran, Lilach Abramovitz, Anat Klein, et al.. (2016). Incipient Melanoma Brain Metastases Instigate Astrogliosis and Neuroinflammation. Cancer Research. 76(15). 4359–4371. 68 indexed citations
18.
Berraondo, Pedro, Viktor Umansky, & Ignacio Melero. (2012). Changing the Tumor Microenvironment: New Strategies for Immunotherapy. Cancer Research. 72(20). 5159–5164. 21 indexed citations
19.
Michels, Tillmann, Galina V. Shurin, Hiam Naiditch, et al.. (2012). Paclitaxel promotes differentiation of myeloid-derived suppressor cells into dendritic cellsin vitroin a TLR4-independent manner. Journal of Immunotoxicology. 9(3). 292–300. 130 indexed citations
20.
Schneider, Thomas, Arne Warth, Philipp A. Schnabel, et al.. (2011). Foxp3+ Regulatory T Cells and Natural Killer Cells Distinctly Infiltrate Primary Tumors and Draining Lymph Nodes in Pulmonary Adenocarcinoma. Journal of Thoracic Oncology. 6(3). 432–438. 65 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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