Ada Sacchi

10.1k total citations
162 papers, 8.4k citations indexed

About

Ada Sacchi is a scholar working on Molecular Biology, Oncology and Biotechnology. According to data from OpenAlex, Ada Sacchi has authored 162 papers receiving a total of 8.4k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Molecular Biology, 95 papers in Oncology and 32 papers in Biotechnology. Recurrent topics in Ada Sacchi's work include Cancer-related Molecular Pathways (68 papers), Cancer Research and Treatments (32 papers) and Cell Adhesion Molecules Research (22 papers). Ada Sacchi is often cited by papers focused on Cancer-related Molecular Pathways (68 papers), Cancer Research and Treatments (32 papers) and Cell Adhesion Molecules Research (22 papers). Ada Sacchi collaborates with scholars based in Italy, United States and India. Ada Sacchi's co-authors include Giovanni Blandino, Sabrina Strano, Silvia Soddu, Giulia Piaggio, Giulia Fontemaggi, Gabriella D’Orazi, Rita Falcioni, Gianluca Bossi, Marco Crescenzi and Alfredo Pontecorvi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Ada Sacchi

161 papers receiving 8.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ada Sacchi Italy	55	5.8k	3.7k	1.5k	1.2k	868	162	8.4k
Jean Y. J. Wang United States	56	8.3k 1.4×	4.5k 1.2×	1.2k 0.8×	1.4k 1.2×	452 0.5×	127	11.6k
James M. Roberts United States	40	7.2k 1.3×	4.8k 1.3×	1.0k 0.7×	2.2k 1.8×	415 0.5×	52	9.6k
Sam W. Lee United States	48	5.0k 0.9×	2.3k 0.6×	1.1k 0.7×	906 0.7×	335 0.4×	93	7.1k
W. J. Pledger United States	42	5.0k 0.9×	2.5k 0.7×	1.0k 0.7×	1.2k 1.0×	193 0.2×	114	7.9k
David T. Weaver United States	49	6.5k 1.1×	2.6k 0.7×	1.3k 0.9×	747 0.6×	284 0.3×	150	9.0k
Joana Liu Donaher United States	11	5.1k 0.9×	4.4k 1.2×	1.9k 1.3×	1.0k 0.8×	334 0.4×	11	7.7k
Joanna Roberts United States	18	8.3k 1.4×	7.2k 2.0×	1.6k 1.0×	1.9k 1.6×	630 0.7×	33	12.1k
Julio A. Aguirre‐Ghiso United States	51	4.7k 0.8×	4.9k 1.3×	3.2k 2.2×	2.0k 1.6×	607 0.7×	98	9.9k
Giulia Taraboletti Italy	47	4.0k 0.7×	2.1k 0.6×	2.2k 1.5×	827 0.7×	279 0.3×	112	7.1k
Richard A. Ashmun United States	30	5.9k 1.0×	4.5k 1.2×	917 0.6×	1.0k 0.8×	530 0.6×	53	8.4k

Countries citing papers authored by Ada Sacchi

Since Specialization

Citations

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

Fields of papers citing papers by Ada Sacchi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ada Sacchi

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

All Works

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20 of 20 papers shown

Goeman, Frauke, Isabella Manni, Simona Artuso, et al.. (2012). Molecular imaging of nuclear factor-Y transcriptional activity maps proliferation sites in live animals. Molecular Biology of the Cell. 23(8). 1467–1474. 29 indexed citations

Gurtner, Aymone, Paola Fuschi, Fabio Martelli, et al.. (2010). Transcription Factor NF-Y Induces Apoptosis in Cells Expressing Wild-Type p53 through E2F1 Upregulation and p53 Activation. Cancer Research. 70(23). 9711–9720. 34 indexed citations

Bon, Giulia, Selene E. Di Carlo, Valentina Folgiero, et al.. (2009). Negative Regulation of β4 Integrin Transcription by Homeodomain-Interacting Protein Kinase 2 and p53 Impairs Tumor Progression. Cancer Research. 69(14). 5978–5986. 44 indexed citations

Rinaldo, Cinzia, Andrea Prodosmo, Francesca Siepi, et al.. (2009). HIPK2 Regulation by MDM2 Determines Tumor Cell Response to the p53-Reactivating Drugs Nutlin-3 and RITA. Cancer Research. 69(15). 6241–6248. 41 indexed citations

Marampon, Francesco, Gianluca Bossi, Carmela Ciccarelli, et al.. (2009). MEK/ERK inhibitor U0126 affects in vitro and in vivo growth of embryonal rhabdomyosarcoma. Molecular Cancer Therapeutics. 8(3). 543–551. 85 indexed citations

Nucera, Carmelo, Cecilia Tiveron, Antonella Farsetti, et al.. (2009). Maternal thyroid hormones are transcriptionally active during embryo–foetal development: results from a novel transgenic mouse model. Journal of Cellular and Molecular Medicine. 14(10). 2417–2435. 21 indexed citations

Puca, Rosa, Lavinia Nardinocchi, Hilah Gal, et al.. (2008). Reversible Dysfunction of Wild-Type p53 following Homeodomain-Interacting Protein Kinase-2 Knockdown. Cancer Research. 68(10). 3707–3714. 62 indexed citations

Manni, Isabella, Giuseppina Caretti, Simona Artuso, et al.. (2008). Posttranslational Regulation of NF-YA Modulates NF-Y Transcriptional Activity. Molecular Biology of the Cell. 19(12). 5203–5213. 42 indexed citations

Folgiero, Valentina, Robin E. Bachelder, Giulia Bon, et al.. (2007). The α6β4 Integrin Can Regulate ErbB-3 Expression: Implications for α6β4 Signaling and Function. Cancer Research. 67(4). 1645–1652. 50 indexed citations

10.

Agostino, Silvia Di, Sabrina Strano, Valentina Zerbini, et al.. (2006). Gain of function of mutant p53: The mutant p53/NF-Y protein complex reveals an aberrant transcriptional mechanism of cell cycle regulation. Cancer Cell. 10(3). 191–202. 344 indexed citations

11.

Giglio, Simona, Francesca Mancini, Lara Felicioni, et al.. (2005). Identification of an Aberrantly Spliced Form of HDMX in Human Tumors: A New Mechanism for HDM2 Stabilization. Cancer Research. 65(21). 9687–9694. 47 indexed citations

12.

Strano, Sabrina, Olimpia Monti, Natalia Pediconi, et al.. (2005). The Transcriptional Coactivator Yes-Associated Protein Drives p73 Gene-Target Specificity in Response to DNA Damage. Molecular Cell. 18(4). 447–459. 299 indexed citations

13.

Bossi, Gianluca, et al.. (2004). Wild-type p53 gene transfer is not detrimental to normal cells in vivo: implications for tumor gene therapy. Oncogene. 23(2). 418–425. 24 indexed citations

14.

Gurtner, Aymone, Isabella Manni, Paola Fuschi, et al.. (2003). Requirement for Down-Regulation of the CCAAT-binding Activity of the NF-Y Transcription Factor during Skeletal Muscle Differentiation. Molecular Biology of the Cell. 14(7). 2706–2715. 76 indexed citations

15.

Nanni, Simona, Fabiola Moretti, Annalisa Grasselli, et al.. (2002). Signaling through estrogen receptors modulates telomerase activity in human prostate cancer. Journal of Clinical Investigation. 110(2). 219–227. 76 indexed citations

16.

Manni, Isabella, Patrizia Tunici, N. Cirenei, et al.. (2002). Mxi1 inhibits the proliferation of U87 glioma cells through down-regulation of cyclin B1 gene expression. British Journal of Cancer. 86(3). 477–484. 30 indexed citations

17.

Bossi, Gianluca, Raffaella Scardigli, Piero Musiani, et al.. (2000). Development of a murine orthotopic model of leukemia: Evaluation of TP53 gene therapy efficacy. Cancer Gene Therapy. 7(1). 135–143. 3 indexed citations

18.

Prisco, Marco di, Atsushi Hongo, Maria Giulia Rizzo, Ada Sacchi, & Renato Baserga. (1997). The Insulin-Like Growth Factor I Receptor as a Physiologically Relevant Target of p53 in Apoptosis Caused by Interleukin-3 Withdrawal. Molecular and Cellular Biology. 17(3). 1084–1092. 127 indexed citations

19.

Giacomini, Patrizio, Raffaele Tecce, Roberto Gambari, et al.. (1988). Recombinant human IFN-gamma, but not IFN- alpha or IFN- beta , enhances MHC- and non-MHC-encoded glycoproteins by a protein synthesis-dependent mechanism.. The Journal of Immunology. 140(9). 3073–3081. 40 indexed citations

20.

Sacchi, Ada, Gianni Chinali, & Umberto Ferrini. (1983). Association of elongation factor 2 with ribosomes during growth of a murine ascitic tumor.. PubMed. 6(3). 179–87. 1 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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