Ralph Pries

2.3k total citations
98 papers, 1.7k citations indexed

About

Ralph Pries is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Ralph Pries has authored 98 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Immunology, 31 papers in Oncology and 30 papers in Molecular Biology. Recurrent topics in Ralph Pries's work include Immune Cell Function and Interaction (15 papers), Immunotherapy and Immune Responses (14 papers) and Immune Response and Inflammation (14 papers). Ralph Pries is often cited by papers focused on Immune Cell Function and Interaction (15 papers), Immunotherapy and Immune Responses (14 papers) and Immune Response and Inflammation (14 papers). Ralph Pries collaborates with scholars based in Germany, United States and United Kingdom. Ralph Pries's co-authors include Barbara Wollenberg, Karl‐Ludwig Bruchhage, Thomas Trenkle, Stefan Nitsch, Rebecca Kesselring, Annette Thiel, Samer G. Hakim, Gerhard H. Braus, David Juhl and Andreas Thiel and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and PLoS ONE.

In The Last Decade

Ralph Pries

93 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ralph Pries Germany 23 611 561 524 223 200 98 1.7k
Ahmad Waseem United Kingdom 30 159 0.3× 349 0.6× 1.2k 2.3× 307 1.4× 85 0.4× 62 2.5k
Tetsuro Ikebe Japan 28 251 0.4× 1.0k 1.8× 1.2k 2.4× 680 3.0× 89 0.4× 81 2.5k
Xin Pang China 21 252 0.4× 284 0.5× 554 1.1× 390 1.7× 58 0.3× 40 1.2k
Howard Edington United States 24 1.8k 2.9× 1.7k 3.0× 1.0k 1.9× 179 0.8× 69 0.3× 53 3.5k
Yuichiro Kuratomi Japan 24 150 0.2× 669 1.2× 731 1.4× 401 1.8× 206 1.0× 96 2.1k
Urszula Mazurek Poland 22 321 0.5× 229 0.4× 634 1.2× 226 1.0× 29 0.1× 201 1.8k
Zewen Kelvin Tuong Australia 24 903 1.5× 349 0.6× 643 1.2× 186 0.8× 28 0.1× 63 2.0k
Qingxuan Wang China 21 152 0.2× 143 0.3× 589 1.1× 195 0.9× 62 0.3× 56 1.4k
Tengfei Liu China 18 478 0.8× 336 0.6× 610 1.2× 147 0.7× 17 0.1× 53 1.6k
Chen Qu China 23 251 0.4× 367 0.7× 847 1.6× 379 1.7× 52 0.3× 74 1.6k

Countries citing papers authored by Ralph Pries

Since Specialization
Citations

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

Fields of papers citing papers by Ralph Pries

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ralph Pries

This figure shows the co-authorship network connecting the top 25 collaborators of Ralph Pries. A scholar is included among the top collaborators of Ralph Pries 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 Ralph Pries. Ralph Pries 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.
Meyhöfer, Svenja, Armin Steffen, Jens U. Marquardt, et al.. (2024). Obesity-related Plasma CXCL10 Drives CX3CR1-dependent Monocytic Secretion of Macrophage Migration Inhibitory Factor. ImmunoHorizons. 8(1). 19–28. 1 indexed citations
2.
3.
Theodoraki, Marie‐Nicole, Christian Idel, Cornelia Brunner, et al.. (2024). Type 2-like polarization and elevated CXCL4 secretion of monocyte derived macrophages upon internalization of plasma-derived exosomes from head and neck cancer patients. BMC Cancer. 24(1). 1173–1173. 4 indexed citations
4.
Pries, Ralph, et al.. (2023). Modes of Action of 1,8-Cineol in Infections and Inflammation. Metabolites. 13(6). 751–751. 22 indexed citations
5.
Meyhöfer, Svenja, Armin Steffen, Christian M. Lange, et al.. (2023). Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets. ImmunoHorizons. 7(3). 191–199. 3 indexed citations
6.
Rades, Dirk, Tamer Soror, Christian Idel, et al.. (2023). Chemoradiation with Cisplatin vs. Carboplatin for Squamous Cell Carcinoma of the Head and Neck (SCCHN). Cancers. 15(13). 3278–3278. 9 indexed citations
7.
Theodoraki, Marie‐Nicole, Cornelia Brunner, Thomas K. Hoffmann, et al.. (2023). Plasma‑derived CD16 exosomes and peripheral blood monocytes as correlating biomarkers in head and neck cancer. Oncology Letters. 25(5). 200–200. 2 indexed citations
8.
Soror, Tamer, Christian Idel, Ralph Pries, et al.. (2023). First Results of Concurrent Chemoradiation with Two Courses of 5 × 25 mg/m2 Cisplatin for Locally Advanced Head and Neck Cancer. Journal of Personalized Medicine. 13(6). 1006–1006.
9.
Pries, Ralph, et al.. (2020). Platelet Induced Functional Alteration of CD4+ and CD8+ T Cells in HNSCC. International Journal of Molecular Sciences. 21(20). 7507–7507. 13 indexed citations
10.
Steffen, Armin, et al.. (2020). Redistribution of Monocyte Subsets in Obstructive Sleep Apnea Syndrome Patients Leads to an Imbalanced PD-1/PD-L1 Cross-Talk with CD4/CD8 T Cells. The Journal of Immunology. 206(1). 51–58. 32 indexed citations
11.
Valentiner, Ursula, Ralph Pries, Till S. Clauditz, et al.. (2019). Selectin Binding Sites Are Involved in Cell Adhesive Properties of Head and Neck Squamous Cell Carcinoma. Cancers. 11(11). 1672–1672. 5 indexed citations
12.
Wicklein, Daniel, et al.. (2019). Immunohistochemical Analysis of Transcription Factors and Markers of Epithelial–Mesenchymal Transition (EMT) in Human Tumors. Anticancer Research. 39(10). 5437–5448. 10 indexed citations
13.
Bruchhage, Karl‐Ludwig, et al.. (2018). Increased phosphorylation of eNOS in nasal polyps of chronic rhinosinusitis patients can be diminished by 1,8-cineol. Nitric Oxide. 78. 89–94. 10 indexed citations
14.
Böscke, Robert, Eszter K. Vladar, Ralph Pries, et al.. (2017). Wnt Signaling in Chronic Rhinosinusitis with Nasal Polyps. American Journal of Respiratory Cell and Molecular Biology. 56(5). 575–584. 30 indexed citations
15.
Lindemann, Antje, et al.. (2014). Biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells. International Journal of Nanomedicine. 9. 5025–5025. 45 indexed citations
16.
Kesselring, Rebecca, Annette Thiel, Ralph Pries, et al.. (2014). The complement receptors CD46, CD55 and CD59 are regulated by the tumour microenvironment of head and neck cancer to facilitate escape of complement attack. European Journal of Cancer. 50(12). 2152–2161. 51 indexed citations
17.
Kesselring, Rebecca, Annette Thiel, Ralph Pries, & Barbara Wollenberg. (2011). The number of CD161 positive Th17 cells are decreased in head and neck cancer patients. Cellular Immunology. 269(2). 74–77. 14 indexed citations
18.
Pries, Ralph, et al.. (2006). Secretion of tumor-promoting and immune suppressive cytokines by cell lines of head and neck squamous cell carcinoma.. PubMed. 20(1). 45–8. 37 indexed citations
19.
Pries, Ralph, et al.. (2006). Yeast Gcn4p Stabilization Is Initiated by the Dissociation of the Nuclear Pho85p/Pcl5p Complex. Molecular Biology of the Cell. 17(7). 2952–2962. 20 indexed citations
20.
Pries, Ralph, et al.. (2003). Polyadenylation of rRNA- and tRNA-based yeast transcripts cleaved by internal ribozyme activity. Current Genetics. 43(4). 255–262. 10 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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