Sandra Soligo

3.3k total citations · 1 hit paper
11 papers, 2.4k citations indexed

About

Sandra Soligo is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Sandra Soligo has authored 11 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Oncology and 2 papers in Cell Biology. Recurrent topics in Sandra Soligo's work include TGF-β signaling in diseases (6 papers), Cancer-related Molecular Pathways (3 papers) and Cancer-related gene regulation (3 papers). Sandra Soligo is often cited by papers focused on TGF-β signaling in diseases (6 papers), Cancer-related Molecular Pathways (3 papers) and Cancer-related gene regulation (3 papers). Sandra Soligo collaborates with scholars based in Italy, United States and Israel. Sandra Soligo's co-authors include Stefano Piccolo, Michelangelo Cordenonsi, Sirio Dupont, Luca Zacchigna, Maddalena Adorno, Elena Enzo, Luca Azzolin, Chiara Frasson, Giuseppe Basso and Silvio Bicciato and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Sandra Soligo

11 papers receiving 2.4k citations

Hit Papers

YAP/TAZ Incorporation in ... 2014 2026 2018 2022 2014 250 500 750

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Sandra Soligo 1.8k 855 487 309 161 11 2.4k
Chungyee Leung-Hagesteijn 1.8k 1.0× 928 1.1× 418 0.9× 385 1.2× 113 0.7× 19 2.9k
Chenbei Chang 2.9k 1.6× 375 0.4× 504 1.0× 230 0.7× 372 2.3× 59 3.3k
Tomoo Tsukazaki 1.8k 1.0× 301 0.4× 452 0.9× 231 0.7× 148 0.9× 31 2.4k
Giusy Battilana 1.4k 0.8× 1.6k 1.9× 382 0.8× 205 0.7× 51 0.3× 16 2.5k
Nobuyuki Onishi 1.7k 0.9× 346 0.4× 694 1.4× 501 1.6× 152 0.9× 36 2.3k
Deborah Lang 1.3k 0.7× 409 0.5× 381 0.8× 268 0.9× 242 1.5× 37 2.0k
Tracy Tang 1.9k 1.0× 328 0.4× 759 1.6× 225 0.7× 291 1.8× 25 2.4k
Catherine D. Van Raamsdonk 1.7k 0.9× 652 0.8× 1.1k 2.3× 298 1.0× 236 1.5× 26 3.0k
Naoki Oshimori 968 0.5× 360 0.4× 461 0.9× 257 0.8× 80 0.5× 17 1.5k
Angela Denzel 2.5k 1.4× 377 0.4× 905 1.9× 436 1.4× 378 2.3× 13 3.2k

Countries citing papers authored by Sandra Soligo

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Soligo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Soligo

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Soligo. A scholar is included among the top collaborators of Sandra Soligo 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 Sandra Soligo. Sandra Soligo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
Panciera, Tito, Luca Azzolin, Atsushi Fujimura, et al.. (2016). Induction of Expandable Tissue-Specific Stem/Progenitor Cells through Transient Expression of YAP/TAZ. Cell stem cell. 19(6). 725–737. 197 indexed citations
2.
Azzolin, Luca, Tito Panciera, Sandra Soligo, et al.. (2014). YAP/TAZ Incorporation in the β-Catenin Destruction Complex Orchestrates the Wnt Response. Cell. 158(1). 157–170. 850 indexed citations breakdown →
3.
Mamidi, Anant, Masafumi Inui, Andrea Manfrin, et al.. (2012). Signaling crosstalk between TGFβ and Dishevelled/Par1b. Cell Death and Differentiation. 19(10). 1689–1697. 9 indexed citations
4.
Inui, Masafumi, Marco Montagner, Danny Ben‐Zvi, et al.. (2012). Self-regulation of the head-inducing properties of the Spemann organizer. Proceedings of the National Academy of Sciences. 109(38). 15354–15359. 19 indexed citations
5.
Inui, Masafumi, Andrea Manfrin, Anant Mamidi, et al.. (2011). USP15 is a deubiquitylating enzyme for receptor-activated SMADs. Nature Cell Biology. 13(11). 1368–1375. 159 indexed citations
6.
Morsut, Leonardo, Kai-Ping Yan, Elena Enzo, et al.. (2010). Negative control of Smad activity by ectodermin/Tif1γ patterns the mammalian embryo. Development. 137(15). 2571–2578. 76 indexed citations
7.
Dupont, Sirio, Anant Mamidi, Michelangelo Cordenonsi, et al.. (2009). FAM/USP9x, a Deubiquitinating Enzyme Essential for TGFβ Signaling, Controls Smad4 Monoubiquitination. Cell. 136(1). 123–135. 415 indexed citations
8.
Cordenonsi, Michelangelo, Marco Montagner, Maddalena Adorno, et al.. (2007). Integration of TGF-ß and Ras/MAPK Signaling Through p53 Phosphorylation. Science. 315(5813). 840–843. 163 indexed citations
9.
Martello, Graziano, Luca Zacchigna, Masafumi Inui, et al.. (2007). MicroRNA control of Nodal signalling. Nature. 449(7159). 183–188. 159 indexed citations
10.
Dupont, Sirio, Luca Zacchigna, Michelangelo Cordenonsi, et al.. (2005). Germ-Layer Specification and Control of Cell Growth by Ectodermin, a Smad4 Ubiquitin Ligase. Cell. 121(1). 87–99. 277 indexed citations
11.
Dupont, Sirio, Luca Zacchigna, Maddalena Adorno, et al.. (2004). Convergence of p53 and TGF-beta signaling networks. Cancer Letters. 213(2). 129–138. 59 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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