Isabelle Corre

2.1k total citations · 1 hit paper
31 papers, 1.6k citations indexed

About

Isabelle Corre is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Isabelle Corre has authored 31 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 13 papers in Oncology and 6 papers in Genetics. Recurrent topics in Isabelle Corre's work include Cytokine Signaling Pathways and Interactions (6 papers), Sphingolipid Metabolism and Signaling (5 papers) and Angiogenesis and VEGF in Cancer (5 papers). Isabelle Corre is often cited by papers focused on Cytokine Signaling Pathways and Interactions (6 papers), Sphingolipid Metabolism and Signaling (5 papers) and Angiogenesis and VEGF in Cancer (5 papers). Isabelle Corre collaborates with scholars based in France, United States and United Kingdom. Isabelle Corre's co-authors include François Paris, Franck Verrecchia, Françoise Rédiní, Valérie Trichet, Nicolas Clere, Vincent Crenn, Sylvie Hermouet, Jacques Huot, Colin Niaudet and Marie‐Hélène Gaugler and has published in prestigious journals such as The Journal of Experimental Medicine, Blood and Cancer Research.

In The Last Decade

Isabelle Corre

30 papers receiving 1.6k citations

Hit Papers

The Osteosarcoma Microenvironment: A Complex but Targetab... 2020 2026 2022 2024 2020 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isabelle Corre France 20 869 349 328 275 251 31 1.6k
David R. Emlet United States 16 1.3k 1.5× 598 1.7× 231 0.7× 261 0.9× 216 0.9× 24 2.1k
Takaki Hiwasa Japan 25 1.3k 1.5× 474 1.4× 386 1.2× 397 1.4× 168 0.7× 132 2.1k
Yoshikazu Nakaoka Japan 26 1.1k 1.3× 462 1.3× 209 0.6× 366 1.3× 653 2.6× 76 2.5k
Maurizio Orlandini Italy 26 1.3k 1.5× 493 1.4× 217 0.7× 208 0.8× 94 0.4× 66 1.9k
Adriana Aguilar‐Mahecha Canada 19 835 1.0× 420 1.2× 637 1.9× 213 0.8× 169 0.7× 43 1.7k
Wei Ji China 28 1.2k 1.3× 516 1.5× 559 1.7× 255 0.9× 384 1.5× 94 2.1k
Susana Constantino Rosa Santos Portugal 17 664 0.8× 464 1.3× 250 0.8× 224 0.8× 105 0.4× 41 1.3k
Bing Liao China 22 670 0.8× 371 1.1× 444 1.4× 135 0.5× 301 1.2× 71 1.9k
Lisa Happerfield United Kingdom 27 995 1.1× 656 1.9× 658 2.0× 339 1.2× 204 0.8× 43 2.4k
Hanibal Bohnenberger Germany 22 690 0.8× 428 1.2× 238 0.7× 287 1.0× 163 0.6× 86 1.6k

Countries citing papers authored by Isabelle Corre

Since Specialization
Citations

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

Fields of papers citing papers by Isabelle Corre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Corre

This figure shows the co-authorship network connecting the top 25 collaborators of Isabelle Corre. A scholar is included among the top collaborators of Isabelle Corre 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 Isabelle Corre. Isabelle Corre 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.
Navarro, E., François Guillonneau, Catherine Guette, et al.. (2025). Secretomes From Non‐Small Cell Lung Cancer Cells Induce Endothelial Plasticity Through a Partial Endothelial‐to‐Mesenchymal Transition. Cancer Medicine. 14(5). e70707–e70707. 1 indexed citations
2.
Mancini, Stéphane J.C., Karl Balabanian, Isabelle Corre, et al.. (2021). Deciphering Tumor Niches: Lessons From Solid and Hematological Malignancies. Frontiers in Immunology. 12. 766275–766275. 19 indexed citations
3.
Morice, Sarah, Régis Brion, Benjamin Ory, et al.. (2021). Involvement of the TGF-β Signaling Pathway in the Development of YAP-Driven Osteosarcoma Lung Metastasis. Frontiers in Oncology. 11. 765711–765711. 10 indexed citations
4.
Aguesse, Audrey, Sébastien Gouard, Sophie Chiavassa, et al.. (2020). Secretion of Acid Sphingomyelinase and Ceramide by Endothelial Cells Contributes to Radiation-Induced Intestinal Toxicity. Cancer Research. 80(12). 2651–2662. 19 indexed citations
5.
Clere, Nicolas, et al.. (2020). Endothelial-to-Mesenchymal Transition in Cancer. Frontiers in Cell and Developmental Biology. 8. 747–747. 129 indexed citations
6.
Lézot, Frédéric, Isabelle Corre, Sarah Morice, Françoise Rédiní, & Franck Verrecchia. (2020). SHH Signaling Pathway Drives Pediatric Bone Sarcoma Progression. Cells. 9(3). 536–536. 20 indexed citations
7.
Faure, Sébastien, et al.. (2019). Endothelial-to-Mesenchymal Transition (EndoMT): Roles in Tumorigenesis, Metastatic Extravasation and Therapy Resistance. Journal of Oncology. 2019. 1–13. 75 indexed citations
8.
Niaudet, Colin, Stéphanie Bonnaud, Sébastien Gouard, et al.. (2017). Plasma membrane reorganization links acid sphingomyelinase/ceramide to p38 MAPK pathways in endothelial cells apoptosis. Cellular Signalling. 33. 10–21. 44 indexed citations
9.
Paris, François, et al.. (2016). Oxidative stress disassembles the p38/NPM/PP2A complex, which leads to modulation of nucleophosmin‐mediated signaling to DNA damage response. The FASEB Journal. 30(8). 2899–2914. 20 indexed citations
10.
Supiot, S., et al.. (2015). Radiothérapie hypofractionnée : quelles sont les règles à suivre ?. Cancer/Radiothérapie. 19(6-7). 421–425. 1 indexed citations
11.
Rousseau, Matthieu, Marie‐Hélène Gaugler, Audrey Rodallec, et al.. (2011). RhoA GTPase regulates radiation-induced alterations in endothelial cell adhesion and migration. Biochemical and Biophysical Research Communications. 414(4). 750–755. 39 indexed citations
12.
Bonnaud, Stéphanie, Colin Niaudet, François Legoux, et al.. (2010). Sphingosine-1-Phosphate Activates the AKT Pathway to Protect Small Intestines from Radiation-Induced Endothelial Apoptosis. Cancer Research. 70(23). 9905–9915. 72 indexed citations
13.
Clere, Nicolas, Isabelle Corre, Sébastien Faure, et al.. (2010). Deficiency or blockade of angiotensin II type 2 receptor delays tumorigenesis by inhibiting malignant cell proliferation and angiogenesis. International Journal of Cancer. 127(10). 2279–2291. 67 indexed citations
14.
Corre, Isabelle, Colin Niaudet, & François Paris. (2010). Plasma membrane signaling induced by ionizing radiation. Mutation Research/Reviews in Mutation Research. 704(1-3). 61–67. 101 indexed citations
16.
Hermouet, Sylvie, C. A. Sutton, Timothy M. Rose, et al.. (2003). Qualitative and quantitative analysis of human herpesviruses in chronic and acute B cell lymphocytic leukemia and in multiple myeloma. Leukemia. 17(1). 185–195. 45 indexed citations
17.
Hermouet, Sylvie, Anne Godard, Danielle Pineau, et al.. (2002). ABNORMAL PRODUCTION OF INTERLEUKIN (IL)-11 AND IL-8 IN POLYCYTHAEMIA VERA. Cytokine. 20(4). 178–183. 39 indexed citations
18.
Corre, Isabelle, et al.. (2001). Analysis of Thymocyte Development Reveals That the Gtpase Rhoa Is a Positive Regulator of T Cell Receptor Responses in Vivo. The Journal of Experimental Medicine. 194(7). 903–914. 64 indexed citations
19.
Corre, Isabelle, Danielle Pineau, & Sylvie Hermouet. (1999). Interleukin-8. Experimental Hematology. 27(1). 28–36. 35 indexed citations
20.
Corre, Isabelle, Heinz Baumann, & Sylvie Hermouet. (1999). Regulation by Gi2 proteins of v-fms-induced proliferation and transformation via Src-kinase and STAT3. Oncogene. 18(46). 6335–6342. 35 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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