Silvia Fré

3.5k total citations · 1 hit paper
30 papers, 2.2k citations indexed

About

Silvia Fré is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Silvia Fré has authored 30 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 20 papers in Oncology and 6 papers in Cancer Research. Recurrent topics in Silvia Fré's work include Cancer Cells and Metastasis (20 papers), Developmental Biology and Gene Regulation (9 papers) and Wnt/β-catenin signaling in development and cancer (7 papers). Silvia Fré is often cited by papers focused on Cancer Cells and Metastasis (20 papers), Developmental Biology and Gene Regulation (9 papers) and Wnt/β-catenin signaling in development and cancer (7 papers). Silvia Fré collaborates with scholars based in France, United States and United Kingdom. Silvia Fré's co-authors include Mathilde Huyghe, Daniel Louvard, Sylvie Robine, Spyros Artavanis‐Tsakonas, Philippos Mourikis, Pier Paolo Di Fiore, Pietro De Camilli, Vladimir I. Slepnev, Margaret H. Butler and Kohji Takei and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Silvia Fré

25 papers receiving 2.2k citations

Hit Papers

Notch signals control the fate of immature progenitor cel... 2005 2026 2012 2019 2005 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Silvia Fré France 14 1.6k 696 571 348 234 30 2.2k
Pierre Roux France 27 1.6k 1.0× 656 0.9× 454 0.8× 258 0.7× 332 1.4× 49 2.4k
Fatima El Marjou France 17 1.5k 1.0× 769 1.1× 400 0.7× 499 1.4× 312 1.3× 23 2.5k
Theo van Laar Netherlands 29 2.0k 1.2× 1.2k 1.7× 390 0.7× 417 1.2× 446 1.9× 47 2.9k
Stefan Gaubatz Germany 28 2.7k 1.7× 1.4k 1.9× 462 0.8× 343 1.0× 305 1.3× 45 3.4k
Andrea C. Carrano United States 15 2.5k 1.6× 1.5k 2.1× 576 1.0× 269 0.8× 297 1.3× 17 3.1k
Zoi Lygerou Greece 32 3.5k 2.2× 708 1.0× 757 1.3× 527 1.5× 352 1.5× 85 4.0k
Wang L. Cheung United States 18 2.5k 1.6× 356 0.5× 315 0.6× 275 0.8× 161 0.7× 36 3.1k
Julia K. Pagan United States 17 1.7k 1.1× 510 0.7× 404 0.7× 152 0.4× 183 0.8× 23 2.1k
David Micklem Norway 21 1.8k 1.1× 623 0.9× 271 0.5× 181 0.5× 227 1.0× 59 2.7k
Sally P. Wheatley United Kingdom 28 2.2k 1.4× 689 1.0× 1.3k 2.4× 197 0.6× 188 0.8× 48 2.8k

Countries citing papers authored by Silvia Fré

Since Specialization
Citations

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

Fields of papers citing papers by Silvia Fré

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvia Fré

This figure shows the co-authorship network connecting the top 25 collaborators of Silvia Fré. A scholar is included among the top collaborators of Silvia Fré 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 Silvia Fré. Silvia Fré 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
2.
Faraldo, Marisa M., et al.. (2025). Contractile fibroblasts form a transient niche for the branching mammary epithelium. Nature Communications. 16(1). 8576–8576.
3.
Fré, Silvia, et al.. (2024). Fibroblast-induced mammary epithelial branching depends on fibroblast contractility. PLoS Biology. 22(1). e3002093–e3002093. 8 indexed citations
4.
Faraldo, Marisa M., et al.. (2024). Alpha-6 integrin deletion delays the formation of Brca1/p53-deficient basal-like breast tumors by restricting luminal progenitor cell expansion. Breast Cancer Research. 26(1). 91–91. 4 indexed citations
5.
6.
Fré, Silvia, et al.. (2023). Fourteenth Annual ENBDC Workshop: Methods in Mammary Gland Biology and Breast Cancer. Journal of Mammary Gland Biology and Neoplasia. 28(1). 22–22.
7.
Amerongen, Renée van, Mohamed Bentires‐Alj, Antonius L. van Boxtel, et al.. (2023). Imagine beyond: recent breakthroughs and next challenges in mammary gland biology and breast cancer research. Journal of Mammary Gland Biology and Neoplasia. 28(1). 17–17. 3 indexed citations
8.
Urbanus, Jos, Jason Cosgrove, Joost B. Beltman, et al.. (2023). DRAG in situ barcoding reveals an increased number of HSPCs contributing to myelopoiesis with age. Nature Communications. 14(1). 2184–2184. 11 indexed citations
9.
Lloyd‐Lewis, Bethan, et al.. (2022). In vivo imaging of mammary epithelial cell dynamics in response to lineage-biased Wnt/β-catenin activation. Cell Reports. 38(10). 110461–110461. 9 indexed citations
10.
Lloyd‐Lewis, Bethan, Philippos Mourikis, & Silvia Fré. (2019). Notch signalling: sensor and instructor of the microenvironment to coordinate cell fate and organ morphogenesis. Current Opinion in Cell Biology. 61. 16–23. 39 indexed citations
11.
Jacquemin, Guillaume, et al.. (2019). Lineage tracing of Notch1-expressing cells in intestinal tumours reveals a distinct population of cancer stem cells. Scientific Reports. 9(1). 888–888. 12 indexed citations
12.
Lilja, Anna M., Verónica Rodilla, Mathilde Huyghe, et al.. (2018). Clonal analysis of Notch1-expressing cells reveals the existence of unipotent stem cells that retain long-term plasticity in the embryonic mammary gland. Nature Cell Biology. 20(6). 677–687. 99 indexed citations
13.
Rodilla, Verónica & Silvia Fré. (2018). Cellular Plasticity of Mammary Epithelial Cells Underlies Heterogeneity of Breast Cancer. Biomedicines. 6(4). 103–103. 14 indexed citations
14.
Fré, Silvia, Allison J. Bardin, Sylvie Robine, & Daniel Louvard. (2011). Notch signaling in intestinal homeostasis across species: the cases of Drosophila, Zebrafish and the mouse. Experimental Cell Research. 317(19). 2740–2747. 41 indexed citations
15.
Fré, Silvia, Édouard Hannezo, Sanja Šale, et al.. (2011). Notch Lineages and Activity in Intestinal Stem Cells Determined by a New Set of Knock-In Mice. PLoS ONE. 6(10). e25785–e25785. 107 indexed citations
16.
Fré, Silvia, Danijela Matic Vignjevic, Marie Schoumacher, et al.. (2008). Epithelial Morphogenesis and Intestinal Cancer: New Insights in Signaling Mechanisms. Advances in cancer research. 100. 85–111. 15 indexed citations
17.
Vignjevic, Danijela Matic, Silvia Fré, Daniel Louvard, & Sylvie Robine. (2007). Conditional Mouse Models of Cancer. Handbook of experimental pharmacology. 263–287. 5 indexed citations
18.
Fré, Silvia, Mathilde Huyghe, Philippos Mourikis, et al.. (2005). Notch signals control the fate of immature progenitor cells in the intestine. Nature. 435(7044). 964–968. 708 indexed citations breakdown →
19.
Robine, Sylvie, Silvia Fré, Mathilde Huyghe, Spyros Artavanis‐Tsakonas, & Daniel Louvard. (2005). Notch, un gène clé de l’équilibre entre prolifération et différenciation des cellules épithéliales de l’intestin. médecine/sciences. 21(8-9). 780–782. 7 indexed citations
20.
Chen, Hong, Silvia Fré, Vladimir I. Slepnev, et al.. (1998). Epsin is an EH-domain-binding protein implicated in clathrin-mediated endocytosis. Nature. 394(6695). 793–797. 479 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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