Alexander Pietras

2.9k total citations · 2 hit papers
32 papers, 2.2k citations indexed

About

Alexander Pietras is a scholar working on Cancer Research, Molecular Biology and Genetics. According to data from OpenAlex, Alexander Pietras has authored 32 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cancer Research, 16 papers in Molecular Biology and 12 papers in Genetics. Recurrent topics in Alexander Pietras's work include Cancer, Hypoxia, and Metabolism (16 papers), Glioma Diagnosis and Treatment (12 papers) and Neuroblastoma Research and Treatments (9 papers). Alexander Pietras is often cited by papers focused on Cancer, Hypoxia, and Metabolism (16 papers), Glioma Diagnosis and Treatment (12 papers) and Neuroblastoma Research and Treatments (9 papers). Alexander Pietras collaborates with scholars based in Sweden, United States and Spain. Alexander Pietras's co-authors include Sven Påhlman, Erik Fredlund, Rosa Noguera, Lorenz Poellinger, Tobias Löfstedt, Linda Holmquist Mengelbier, Samuel Navarro, Eric C. Holland, Johan Vallon‐Christersson and Åke Borg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The EMBO Journal.

In The Last Decade

Alexander Pietras

31 papers receiving 2.2k citations

Hit Papers

Recruitment of HIF-1α and HIF-2α to common target genes i... 2006 2026 2012 2019 2006 2014 100 200 300 400 500

Peers

Alexander Pietras
Ichiro Nakano United States
Ruprecht Wiedemeyer United States
Eli E. Bar United States
Joseph Celestino United States
Mingyao Ying United States
Alexander Pietras
Citations per year, relative to Alexander Pietras Alexander Pietras (= 1×) peers Daniel Bexell

Countries citing papers authored by Alexander Pietras

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Pietras

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Pietras

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Pietras. A scholar is included among the top collaborators of Alexander Pietras 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 Alexander Pietras. Alexander Pietras 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.
Leandersson, Karin, David O’Connell, Valeria Governa, et al.. (2024). Complement Factor H Is an ICOS Ligand Modulating Tregs in the Glioma Microenvironment. Cancer Immunology Research. 13(1). 122–138. 4 indexed citations
2.
Tüysüz, Emre Can, Chrysostomi Gialeli, Valeria Governa, et al.. (2024). Tumor suppressor role of the complement inhibitor CSMD1 and its role in TNF-induced neuroinflammation in gliomas. Journal of Experimental & Clinical Cancer Research. 43(1). 98–98. 5 indexed citations
3.
Ceberg, Crister, et al.. (2023). TMIC-54. RADIOTHERAPY-INDUCED REMODELING OF THE GLIOBLASTOMA MICROENVIRONMENT. Neuro-Oncology. 25(Supplement_5). v290–v290.
4.
Berg, Tracy J. & Alexander Pietras. (2022). Radiotherapy-induced remodeling of the tumor microenvironment by stromal cells. Seminars in Cancer Biology. 86(Pt 3). 846–856. 42 indexed citations
5.
Pietras, Alexander. (2022). What (H)IF isoform matters? A deubiquitinase can tune the hypoxic response. The EMBO Journal. 41(7). e110819–e110819. 2 indexed citations
6.
Pantazopoulou, Vasiliki, et al.. (2021). Hypoxia-Induced Reactivity of Tumor-Associated Astrocytes Affects Glioma Cell Properties. Cells. 10(3). 613–613. 24 indexed citations
7.
Berg, Tracy J., Carolina Marques, Vasiliki Pantazopoulou, et al.. (2021). The Irradiated Brain Microenvironment Supports Glioma Stemness and Survival via Astrocyte-Derived Transglutaminase 2. Cancer Research. 81(8). 2101–2115. 32 indexed citations
8.
Grassi, Elisa, Pauline Jeannot, Vasiliki Pantazopoulou, Tracy J. Berg, & Alexander Pietras. (2020). Niche-derived soluble DLK1 promotes glioma growth. Neoplasia. 22(12). 689–701. 12 indexed citations
9.
Grassi, Elisa, Vasiliki Pantazopoulou, & Alexander Pietras. (2020). Hypoxia-induced release, nuclear translocation, and signaling activity of a DLK1 intracellular fragment in glioma. Oncogene. 39(20). 4028–4044. 24 indexed citations
10.
Grassi, Elisa, Vasiliki Pantazopoulou, Bei Tong, et al.. (2017). CD44 Interacts with HIF-2α to Modulate the Hypoxic Phenotype of Perinecrotic and Perivascular Glioma Cells. Cell Reports. 20(7). 1641–1653. 88 indexed citations
11.
Pietras, Alexander, Tatsuya Ozawa, Elena Bazzoli, et al.. (2016). ABCG2 regulates self-renewal and stem cell marker expression but not tumorigenicity or radiation resistance of glioma cells. Scientific Reports. 6(1). 25956–25956. 44 indexed citations
12.
Pietras, Alexander, Amanda Katz, Elin Ekström, et al.. (2014). Osteopontin-CD44 Signaling in the Glioma Perivascular Niche Enhances Cancer Stem Cell Phenotypes and Promotes Aggressive Tumor Growth. Cell stem cell. 14(3). 357–369. 403 indexed citations breakdown →
13.
Fomchenko, Elena I., Joseph D. Dougherty, Karim Y. Helmy, et al.. (2011). Recruited Cells Can Become Transformed and Overtake PDGF-Induced Murine Gliomas In Vivo during Tumor Progression. PLoS ONE. 6(7). e20605–e20605. 59 indexed citations
14.
Cifani, Paolo, Karin Hansson, Fredrik Levander, et al.. (2011). Hunting for Protein Markers of Hypoxia by Combining Plasma Membrane Enrichment with a New Approach to Membrane Protein Analysis. Journal of Proteome Research. 10(4). 1645–1656. 3 indexed citations
15.
Pietras, Alexander, A. Johnsson, & Sven Påhlman. (2010). The HIF-2α-Driven Pseudo-Hypoxic Phenotype in Tumor Aggressiveness, Differentiation, and Vascularization. Current topics in microbiology and immunology. 345. 1–20. 50 indexed citations
16.
Noguera, Rosa, Erik Fredlund, Marta Piqueras, et al.. (2009). HIF-1α and HIF-2α Are Differentially Regulated In vivo in Neuroblastoma: High HIF-1α Correlates Negatively to Advanced Clinical Stage and Tumor Vascularization. Clinical Cancer Research. 15(23). 7130–7136. 64 indexed citations
17.
Pietras, Alexander, Loen M. Hansford, A. Johnsson, et al.. (2009). HIF-2α maintains an undifferentiated state in neural crest-like human neuroblastoma tumor-initiating cells. Proceedings of the National Academy of Sciences. 106(39). 16805–16810. 111 indexed citations
18.
Sjölund, Jonas, Martin Johansson, Sugata Manna, et al.. (2008). Suppression of renal cell carcinoma growth by inhibition of Notch signaling in vitro and in vivo. Journal of Clinical Investigation. 118(1). 217–228. 147 indexed citations
19.
Karlsson, Jenny, et al.. (2007). Arsenic trioxide-induced neuroblastoma cell death is accompanied by proteolytic activation of nuclear Bax. Oncogene. 26(42). 6150–6159. 15 indexed citations
20.
Mengelbier, Linda Holmquist, Erik Fredlund, Tobias Löfstedt, et al.. (2006). Recruitment of HIF-1α and HIF-2α to common target genes is differentially regulated in neuroblastoma: HIF-2α promotes an aggressive phenotype. Cancer Cell. 10(5). 413–423. 594 indexed citations breakdown →

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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