Micaela Quarto

2.5k total citations
18 papers, 1.9k citations indexed

About

Micaela Quarto is a scholar working on Molecular Biology, Oncology and Neurology. According to data from OpenAlex, Micaela Quarto has authored 18 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Oncology and 4 papers in Neurology. Recurrent topics in Micaela Quarto's work include Cancer-related Molecular Pathways (6 papers), Protein Degradation and Inhibitors (4 papers) and Ubiquitin and proteasome pathways (4 papers). Micaela Quarto is often cited by papers focused on Cancer-related Molecular Pathways (6 papers), Protein Degradation and Inhibitors (4 papers) and Ubiquitin and proteasome pathways (4 papers). Micaela Quarto collaborates with scholars based in Italy, United States and Denmark. Micaela Quarto's co-authors include Maria Capra, Kristian Helin, Stefano Confalonieri, Esther Hulleman, Paolo Nucíforo, Pier Paolo Di Fiore, Giuseppe Viale, Suzanne Lam, Aart G. Jochemsen and Dianna A. Johnson and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Micaela Quarto

18 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Micaela Quarto Italy 16 1.5k 773 318 204 159 18 1.9k
Sarah Francoz Belgium 11 1.4k 0.9× 1.2k 1.6× 310 1.0× 106 0.5× 160 1.0× 12 1.8k
Yongping Crawford United States 14 1.1k 0.7× 581 0.8× 450 1.4× 157 0.8× 56 0.4× 16 1.5k
Verline Justilien United States 21 1.3k 0.9× 475 0.6× 328 1.0× 97 0.5× 176 1.1× 31 1.7k
Faison Nuckolls United States 7 1.7k 1.1× 933 1.2× 369 1.2× 160 0.8× 55 0.3× 9 2.1k
Deborah L. Burkhart United States 10 927 0.6× 816 1.1× 308 1.0× 235 1.2× 97 0.6× 15 1.5k
Paul Meltzer United States 7 1.8k 1.2× 768 1.0× 824 2.6× 233 1.1× 98 0.6× 10 2.4k
Ingrid J. Apel United States 19 1.3k 0.9× 561 0.7× 733 2.3× 211 1.0× 54 0.3× 26 2.1k
Greg H. Enders United States 19 1.8k 1.2× 979 1.3× 938 2.9× 140 0.7× 50 0.3× 31 2.4k
Donné Majoor Netherlands 7 1.3k 0.8× 800 1.0× 238 0.7× 321 1.6× 29 0.2× 8 2.0k
Graeme J. Walker Australia 23 1.4k 0.9× 1.3k 1.7× 585 1.8× 332 1.6× 58 0.4× 66 2.3k

Countries citing papers authored by Micaela Quarto

Since Specialization
Citations

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

Fields of papers citing papers by Micaela Quarto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Micaela Quarto

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

All Works

18 of 18 papers shown
1.
Beznoussenko, Galina V., Flora Ascione, Qingsen Li, et al.. (2023). Cell stretching activates an ATM mechano-transduction pathway that remodels cytoskeleton and chromatin. Cell Reports. 42(12). 113555–113555. 23 indexed citations
2.
Aceto, Nicola, Nina Sausgruber, Heike Brinkhaus, et al.. (2012). Tyrosine phosphatase SHP2 promotes breast cancer progression and maintains tumor-initiating cells via activation of key transcription factors and a positive feedback signaling loop. Nature Medicine. 18(4). 529–537. 210 indexed citations
3.
Hudlebusch, Heidi Rye, Julie Skotte, Eric Santoni‐Rugiu, et al.. (2011). MMSET Is Highly Expressed and Associated with Aggressiveness in Neuroblastoma. Cancer Research. 71(12). 4226–4235. 50 indexed citations
4.
Gaetani, Paolo, Esther Hulleman, Daniel S. Levi, et al.. (2010). Expression of the Transcription Factor HEY1 in Glioblastoma: A Preliminary Clinical Study. Tumori Journal. 96(1). 97–102. 21 indexed citations
5.
Fanelli, Mirco, Stefano Amatori, Iros Barozzi, et al.. (2010). Pathology tissue–chromatin immunoprecipitation, coupled with high-throughput sequencing, allows the epigenetic profiling of patient samples. Proceedings of the National Academy of Sciences. 107(50). 21535–21540. 48 indexed citations
6.
Cirò, Marco, Elena Prosperini, Micaela Quarto, et al.. (2009). ATAD2 Is a Novel Cofactor for MYC, Overexpressed and Amplified in Aggressive Tumors. Cancer Research. 69(21). 8491–8498. 185 indexed citations
7.
Confalonieri, Stefano, Micaela Quarto, Paolo Nucíforo, et al.. (2009). Alterations of ubiquitin ligases in human cancer and their association with the natural history of the tumor. Oncogene. 28(33). 2959–2968. 80 indexed citations
8.
Hulleman, Esther, Micaela Quarto, Giacomo Masserdotti, et al.. (2008). A role for the transcription factor HEY1 in glioblastoma. Journal of Cellular and Molecular Medicine. 13(1). 136–146. 63 indexed citations
9.
Fagiani, Ernesta, Giuseppina Giardina, Lucilla Luzi, et al.. (2007). RaLP, a New Member of the Src Homology and Collagen Family, Regulates Cell Migration and Tumor Growth of Metastatic Melanomas. Cancer Research. 67(7). 3064–3073. 58 indexed citations
10.
Vecchi, Manuela, Paolo Nucíforo, Solange Romagnoli, et al.. (2007). Gene expression analysis of early and advanced gastric cancers. Oncogene. 26(29). 4284–4294. 67 indexed citations
11.
Peviani, Marco, Cristina Cheroni, Flavia Troglio, et al.. (2007). Lack of changes in the PI3K/AKT survival pathway in the spinal cord motor neurons of a mouse model of familial amyotrophic lateral sclerosis. Molecular and Cellular Neuroscience. 34(4). 592–602. 24 indexed citations
12.
Capra, Maria, Paolo Nucíforo, Stefano Confalonieri, et al.. (2006). Frequent Alterations in the Expression of Serine/Threonine Kinases in Human Cancers. Cancer Research. 66(16). 8147–8154. 150 indexed citations
13.
Finocchiaro, Giacomo, et al.. (2006). Lap2α Expression is Controlled by E2F and Deregulated in Various Human Tumors. Cell Cycle. 5(12). 1331–1341. 27 indexed citations
14.
Carro, Maria Stella, Fabio M. Spiga, Micaela Quarto, et al.. (2006). DEK Expression is Controlled by E2F and Deregulated in Diverse Tumor Type. Cell Cycle. 5(11). 1202–1207. 95 indexed citations
15.
Laurie, Nikia A., Stacy L. Donovan, Chie-Schin Shih, et al.. (2006). Inactivation of the p53 pathway in retinoblastoma. Nature. 444(7115). 61–66. 453 indexed citations
16.
Hock, Andreas, Esther Hulleman, Nikita Popov, et al.. (2005). The Ubiquitin Ligase HectH9 Regulates Transcriptional Activation by Myc and Is Essential for Tumor Cell Proliferation. Cell. 123(3). 409–421. 315 indexed citations
17.
Quarto, Micaela, et al.. (2003). Long-lasting induction of Notch2 in the hippocampus of kainate-treated adult mice. Neuroreport. 14(7). 917–921. 10 indexed citations
18.
Quarto, Micaela, et al.. (2003). Long-lasting induction of Notch2 in the hippocampus of kainate-treated adult mice. Neuroreport. 14(7). 917–921. 9 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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