Eugenia Morselli

19.8k total citations
78 papers, 6.5k citations indexed

About

Eugenia Morselli is a scholar working on Epidemiology, Molecular Biology and Genetics. According to data from OpenAlex, Eugenia Morselli has authored 78 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Epidemiology, 35 papers in Molecular Biology and 15 papers in Genetics. Recurrent topics in Eugenia Morselli's work include Autophagy in Disease and Therapy (44 papers), Epigenetics and DNA Methylation (11 papers) and Cancer-related Molecular Pathways (10 papers). Eugenia Morselli is often cited by papers focused on Autophagy in Disease and Therapy (44 papers), Epigenetics and DNA Methylation (11 papers) and Cancer-related Molecular Pathways (10 papers). Eugenia Morselli collaborates with scholars based in Chile, France and United States. Eugenia Morselli's co-authors include Guido Kroemer, Lorenzo Galluzzi, Alfredo Criollo, Maria Chiara Maiuri, Oliver Kepp, Shoaib Ahmad Malik, Ezgi Tasdemir, Ilio Vitale, Deborah J. Clegg and Nektarios Tavernarakis and has published in prestigious journals such as Circulation, The EMBO Journal and Cell Metabolism.

In The Last Decade

Eugenia Morselli

78 papers receiving 6.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eugenia Morselli Chile 39 3.4k 2.9k 884 819 749 78 6.5k
Ciro Isidoro Italy 43 2.9k 0.9× 1.9k 0.7× 934 1.1× 803 1.0× 536 0.7× 183 6.2k
Alfredo Criollo Chile 45 4.5k 1.3× 3.9k 1.4× 1.1k 1.2× 915 1.1× 1.0k 1.4× 75 8.9k
Federico Pietrocola France 31 2.9k 0.9× 1.6k 0.6× 764 0.9× 899 1.1× 663 0.9× 55 5.5k
Guillermo Mariño France 34 5.2k 1.6× 5.9k 2.1× 1.1k 1.3× 1.3k 1.6× 546 0.7× 55 10.3k
Yu‐shin Sou Japan 23 5.2k 1.6× 5.1k 1.8× 549 0.6× 774 0.9× 419 0.6× 28 8.5k
Yong‐Keun Jung South Korea 48 5.5k 1.6× 2.2k 0.8× 776 0.9× 1.6k 1.9× 826 1.1× 147 8.7k
Young Chul Kim South Korea 31 3.7k 1.1× 1.7k 0.6× 625 0.7× 518 0.6× 675 0.9× 140 6.9k
Malene Hansen United States 39 4.7k 1.4× 3.7k 1.3× 567 0.6× 1.9k 2.3× 240 0.3× 61 9.8k
Chunxin Wang United States 35 7.0k 2.1× 4.6k 1.6× 604 0.7× 1.3k 1.6× 361 0.5× 59 10.5k
Hilde Nilsen Norway 31 4.0k 1.2× 1.2k 0.4× 550 0.6× 1.0k 1.3× 605 0.8× 99 6.0k

Countries citing papers authored by Eugenia Morselli

Since Specialization
Citations

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

Fields of papers citing papers by Eugenia Morselli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eugenia Morselli

This figure shows the co-authorship network connecting the top 25 collaborators of Eugenia Morselli. A scholar is included among the top collaborators of Eugenia Morselli 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 Eugenia Morselli. Eugenia Morselli 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.
Rivagorda, Manon, François Mailliet, Valérie Boitez, et al.. (2025). A primary cilia–autophagy axis in hippocampal neurons is essential to maintain cognitive resilience. Nature Aging. 5(3). 450–467. 8 indexed citations
2.
3.
Toledo, Jorge, Mauricio Budini, Valentina Parra, et al.. (2024). PKD2 regulates autophagy and forms a protein complex with BECN1 at the primary cilium of hypothalamic neuronal cells. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870(6). 167256–167256. 1 indexed citations
4.
Díaz‐Castro, Francisco, Patricia Rivera, Javier Botella, et al.. (2024). A single bout of resistance exercise triggers mitophagy, potentially involving the ejection of mitochondria in human skeletal muscle. Acta Physiologica. 240(9). e14203–e14203. 5 indexed citations
5.
Corchado, Juan M., Matías Monsalves‐Álvarez, Isabel Matias, et al.. (2023). The CB1 cannabinoid receptor regulates autophagy in the tibialis anterior skeletal muscle in mice. Biological Research. 56(1). 14–14. 5 indexed citations
6.
Espinosa, Rodrigo, Pablo Galaz‐Davison, César A. Ramírez‐Sarmiento, et al.. (2022). Palmitic and Stearic Acids Inhibit Chaperone-Mediated Autophagy (CMA) in POMC-like Neurons In Vitro. Cells. 11(6). 920–920. 3 indexed citations
7.
Ravasio, Andrea, Eugenia Morselli, & Cristina Bertocchi. (2022). Mechanoautophagy: Synergies Between Autophagy and Cell Mechanotransduction at Adhesive Complexes. Frontiers in Cell and Developmental Biology. 10. 917662–917662. 9 indexed citations
8.
Moreno‐Tapia, Daniela, Felipe Melo-González, Geraldyne A. Salazar, et al.. (2022). Limited Heme Oxygenase Contribution to Modulating the Severity of Salmonella enterica serovar Typhimurium Infection. Antioxidants. 11(6). 1040–1040. 3 indexed citations
9.
Peña‐Oyarzún, Daniel, Francesca Burgos‐Bravo, Cristian Sotomayor-Flores, et al.. (2020). PKD2/polycystin-2 induces autophagy by forming a complex with BECN1. Autophagy. 17(7). 1714–1728. 30 indexed citations
10.
Peña‐Oyarzún, Daniel, Montserrat Reyes, Eugenia Morselli, et al.. (2020). Role of Autophagy in the Microenvironment of Oral Squamous Cell Carcinoma. Frontiers in Oncology. 10. 602661–602661. 31 indexed citations
11.
Criollo, Alfredo, Francisco Altamirano, Zully Pedrozo, et al.. (2018). Polycystin-2-dependent control of cardiomyocyte autophagy. Journal of Molecular and Cellular Cardiology. 118. 110–121. 29 indexed citations
12.
Morselli, Eugenia, Aaron P. Frank, Biff F. Palmer, et al.. (2015). A sexually dimorphic hypothalamic response to chronic high-fat diet consumption. International Journal of Obesity. 40(2). 206–209. 63 indexed citations
13.
Morselli, Eugenia, Esther Fuente-Martín, Brian Finan, et al.. (2014). Hypothalamic PGC-1α Protects Against High-Fat Diet Exposure by Regulating ERα. Cell Reports. 9(2). 633–645. 162 indexed citations
14.
Galluzzi, Lorenzo, Eugenia Morselli, Ilio Vitale, et al.. (2010). miR-181a and miR-630 Regulate Cisplatin-Induced Cancer Cell Death. Cancer Research. 70(5). 1793–1803. 239 indexed citations
15.
Morselli, Eugenia, Lorenzo Galluzzi, Oliver Kepp, et al.. (2009). Anti- and pro-tumor functions of autophagy. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793(9). 1524–1532. 319 indexed citations
16.
Galluzzi, Lorenzo, Catherine Brenner, Eugenia Morselli, Zahia Touat, & Guido Kroemer. (2008). Viral Control of Mitochondrial Apoptosis. PLoS Pathogens. 4(5). e1000018–e1000018. 364 indexed citations
17.
Vicencio, José M., Lorenzo Galluzzi, Nicolas Tajeddine, et al.. (2008). Senescence, Apoptosis or Autophagy?. Gerontology. 54(2). 92–99. 205 indexed citations
18.
Tajeddine, Nicolas, Lorenzo Galluzzi, Oliver Kepp, et al.. (2008). Hierarchical involvement of Bak, VDAC1 and Bax in cisplatin-induced cell death. Oncogene. 27(30). 4221–4232. 172 indexed citations
19.
Tasdemir, Ezgi, Maria Chiara Maiuri, Idil Orhon, et al.. (2008). p53 represses autophagy in a cell cycle-dependent fashion. Cell Cycle. 7(19). 3006–3011. 82 indexed citations
20.
Tasdemir, Ezgi, Maria Chiara Maiuri, Eugenia Morselli, et al.. (2008). A dual role of p53 in the control of autophagy. Autophagy. 4(6). 810–814. 273 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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