Ina Kurth

1.8k total citations
38 papers, 1.2k citations indexed

About

Ina Kurth is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Ina Kurth has authored 38 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Oncology and 12 papers in Cancer Research. Recurrent topics in Ina Kurth's work include Cancer Cells and Metastasis (12 papers), Cancer, Hypoxia, and Metabolism (6 papers) and Cancer Genomics and Diagnostics (4 papers). Ina Kurth is often cited by papers focused on Cancer Cells and Metastasis (12 papers), Cancer, Hypoxia, and Metabolism (6 papers) and Cancer Genomics and Diagnostics (4 papers). Ina Kurth collaborates with scholars based in Germany, United States and Israel. Ina Kurth's co-authors include Anna Dubrovska, Claudia Peitzsch, Michaël Baumann, Leoni A. Kunz‐Schughart, Monica Cojoc, Katrin Mäbert, Mechthild Krause, Martin Bornhäuser, Franziska Trautmann and Carsten Werner and has published in prestigious journals such as Cancer Research, Oncogene and International Journal of Cancer.

In The Last Decade

Ina Kurth

36 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ina Kurth Germany 18 600 544 400 240 140 38 1.2k
Zhaomei Mu United States 22 577 1.0× 752 1.4× 605 1.5× 304 1.3× 176 1.3× 43 1.3k
Woondong Jeong United States 9 974 1.6× 732 1.3× 402 1.0× 164 0.7× 61 0.4× 23 1.5k
Elizabeth A. Kuczynski Canada 12 681 1.1× 373 0.7× 454 1.1× 203 0.8× 124 0.9× 16 1.1k
Tiffany M. Phillips United States 8 817 1.4× 903 1.7× 436 1.1× 214 0.9× 83 0.6× 11 1.5k
Kazuharu Kai Japan 18 487 0.8× 577 1.1× 443 1.1× 141 0.6× 187 1.3× 38 1.2k
Andrey Ugolkov United States 24 899 1.5× 453 0.8× 325 0.8× 188 0.8× 141 1.0× 44 1.5k
Robert Lemos United States 15 878 1.5× 438 0.8× 531 1.3× 207 0.9× 107 0.8× 20 1.4k
Nicolas Floc’h United Kingdom 14 587 1.0× 464 0.9× 223 0.6× 493 2.1× 82 0.6× 30 1.2k

Countries citing papers authored by Ina Kurth

Since Specialization
Citations

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

Fields of papers citing papers by Ina Kurth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ina Kurth

This figure shows the co-authorship network connecting the top 25 collaborators of Ina Kurth. A scholar is included among the top collaborators of Ina Kurth 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 Ina Kurth. Ina Kurth 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.
Visioli, Fernanda, Mahnaz Bonrouhi, Kinga Pajdzik, et al.. (2024). The Role of SOX2 and SOX9 in Radioresistance and Tumor Recurrence. Cancers. 16(2). 439–439. 9 indexed citations
2.
Elkabets, Moshe, et al.. (2024). Unravelling the Complexity of HNSCC Using Single-Cell Transcriptomics. Cancers. 16(19). 3265–3265. 2 indexed citations
3.
Richter, Susan, Steffen Löck, Annett Linge, et al.. (2024). Epigenetic Targeting to Overcome Radioresistance in Head and Neck Cancer. Cancers. 16(4). 730–730. 6 indexed citations
4.
5.
Chan, Kenneth Chun‐Ho, Nina Hofmann, Mareike Roscher, et al.. (2024). HGG-38. COMBINING TARGETED THERAPY AND RADIATION OUTPERFORMS SINGLE TREATMENTS IN PEDIATRIC HIGH-GRADE GLIOMA. Neuro-Oncology. 26(Supplement_4). 0–0. 1 indexed citations
6.
Stögbauer, Fabian, Kristian Unger, Julia Heß, et al.. (2023). A Novel Subgroup of UCHL1-Related Cancers Is Associated with Genomic Instability and Sensitivity to DNA-Damaging Treatment. Cancers. 15(6). 1655–1655. 1 indexed citations
7.
Kurth, Ina, et al.. (2023). Private and Collaborative Kaplan-Meier Estimators. 212–241.
8.
Poleszczuk, Jan, Susan Richter, Mirko Peitzsch, et al.. (2022). Cellular plasticity upon proton irradiation determines tumor cell radiosensitivity. Cell Reports. 38(8). 110422–110422. 12 indexed citations
9.
Linge, Annett, Steffen Löck, Antje Dietrich, et al.. (2022). Plasticity within Aldehyde Dehydrogenase–Positive Cells Determines Prostate Cancer Radiosensitivity. Molecular Cancer Research. 20(5). 794–809. 11 indexed citations
10.
Kurth, Ina, Dana Holzinger, Christa Flechtenmacher, et al.. (2021). Establishment of a Plasticity-Associated Risk Model Based on a SOX2- and SOX9-Related Gene Set in Head and Neck Squamous Cell Carcinoma. Molecular Cancer Research. 19(10). 1676–1687. 6 indexed citations
11.
Koi, Lydia, Michaël Baumann, Mechthild Krause, et al.. (2021). Tyrosine Kinase c-MET as Therapeutic Target for Radiosensitization of Head and Neck Squamous Cell Carcinomas. Cancers. 13(8). 1865–1865. 13 indexed citations
12.
Lohaus, Fabian, Martina Rauner, Martina Benešová, et al.. (2021). Metastatic Spread in Prostate Cancer Patients Influencing Radiotherapy Response. Frontiers in Oncology. 10. 627379–627379. 37 indexed citations
13.
Baumann, Michaël, et al.. (2020). What will radiation oncology look like in 2050? A look at a changing professional landscape in Europe and beyond. Molecular Oncology. 14(7). 1577–1585. 22 indexed citations
14.
Peitzsch, Claudia, et al.. (2019). Cancer stem cells in radiation response: current views and future perspectives in radiation oncology. International Journal of Radiation Biology. 95(7). 900–911. 26 indexed citations
15.
Peitzsch, Claudia, Monica Cojoc, Ina Kurth, et al.. (2016). An Epigenetic Reprogramming Strategy to Resensitize Radioresistant Prostate Cancer Cells. Cancer Research. 76(9). 2637–2651. 57 indexed citations
16.
Zscheppang, Katja, et al.. (2016). Efficacy of Beta1 Integrin and EGFR Targeting in Sphere-Forming Human Head and Neck Cancer Cells. Journal of Cancer. 7(6). 736–745. 12 indexed citations
17.
Cojoc, Monica, Claudia Peitzsch, Ina Kurth, et al.. (2015). Aldehyde Dehydrogenase Is Regulated by β-Catenin/TCF and Promotes Radioresistance in Prostate Cancer Progenitor Cells. Cancer Research. 75(7). 1482–1494. 187 indexed citations
18.
Trautmann, Franziska, Monica Cojoc, Ina Kurth, et al.. (2014). CXCR4 as biomarker for radioresistant cancer stem cells. International Journal of Radiation Biology. 90(8). 687–699. 68 indexed citations
19.
Peitzsch, Claudia, Ina Kurth, Leoni A. Kunz‐Schughart, Michaël Baumann, & Anna Dubrovska. (2013). Discovery of the cancer stem cell related determinants of radioresistance. Radiotherapy and Oncology. 108(3). 378–387. 147 indexed citations
20.
Kurth, Ina, Katja Franke, W. Pompe, Martin Bornhäuser, & Carsten Werner. (2011). Extracellular Matrix Functionalized Microcavities to Control Hematopoietic Stem and Progenitor Cell Fate. Macromolecular Bioscience. 11(6). 739–747. 38 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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