Edoardo Nusco

2.4k total citations · 1 hit paper
37 papers, 1.5k citations indexed

About

Edoardo Nusco is a scholar working on Molecular Biology, Physiology and Epidemiology. According to data from OpenAlex, Edoardo Nusco has authored 37 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 17 papers in Physiology and 13 papers in Epidemiology. Recurrent topics in Edoardo Nusco's work include Lysosomal Storage Disorders Research (15 papers), Virus-based gene therapy research (9 papers) and Retinal Development and Disorders (6 papers). Edoardo Nusco is often cited by papers focused on Lysosomal Storage Disorders Research (15 papers), Virus-based gene therapy research (9 papers) and Retinal Development and Disorders (6 papers). Edoardo Nusco collaborates with scholars based in Italy, United States and Germany. Edoardo Nusco's co-authors include Andrea Ballabio, Carmine Settembre, Elena Polishchuk, Alessandro Fraldi, Nicola Brunetti‐Pierri, Alberto Auricchio, Roman Polishchuk, Rosa Ferriero, Giuseppe Manco and Maria Pia Cosma and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Edoardo Nusco

36 papers receiving 1.5k citations

Hit Papers

A substrate-specific mTORC1 pathway underlies Birt–Hogg–D... 2020 2026 2022 2024 2020 50 100 150 200

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edoardo Nusco Italy 22 720 532 519 319 220 37 1.5k
Jeong‐A Lim United States 13 647 0.9× 650 1.2× 711 1.4× 305 1.0× 142 0.6× 23 1.6k
Calogera M. Simonaro United States 23 503 0.7× 1.4k 2.7× 450 0.9× 308 1.0× 137 0.6× 56 1.9k
Gouri Yogalingam Australia 20 448 0.6× 617 1.2× 393 0.8× 266 0.8× 135 0.6× 33 1.2k
Lishu Li United States 6 446 0.6× 482 0.9× 552 1.1× 242 0.8× 61 0.3× 8 1.1k
Karen Jardine Canada 23 1.3k 1.8× 736 1.4× 497 1.0× 108 0.3× 363 1.6× 42 3.0k
Rie Asada Japan 22 917 1.3× 281 0.5× 428 0.8× 764 2.4× 192 0.9× 37 1.8k
Mitsutoki Hatta Japan 19 1.8k 2.5× 483 0.9× 266 0.5× 154 0.5× 164 0.7× 41 2.4k
Conrad C. Weihl United States 15 885 1.2× 278 0.5× 970 1.9× 495 1.6× 38 0.2× 17 1.7k
Junru Wang China 9 798 1.1× 167 0.3× 1.0k 2.0× 319 1.0× 45 0.2× 21 1.7k

Countries citing papers authored by Edoardo Nusco

Since Specialization
Citations

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

Fields of papers citing papers by Edoardo Nusco

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edoardo Nusco

This figure shows the co-authorship network connecting the top 25 collaborators of Edoardo Nusco. A scholar is included among the top collaborators of Edoardo Nusco 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 Edoardo Nusco. Edoardo Nusco 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.
Piccolo, Pasquale, Rosa Ferriero, Edoardo Nusco, et al.. (2025). Hepatocyte delivery of miR-34b/c reduces hepatic stellate cell activation and improves liver fibrosis. Molecular Therapy — Nucleic Acids. 36(3). 102593–102593.
2.
Montefusco, Sandro, Edoardo Nusco, Antonella Capuozzo, et al.. (2024). TRPML-1 Dysfunction and Renal Tubulopathy in Mucolipidosis Type IV. Journal of the American Society of Nephrology. 36(4). 587–601. 1 indexed citations
3.
Spinelli, Michele, Edoardo Nusco, Severo Campione, et al.. (2023). Genome editing without nucleases confers proliferative advantage to edited hepatocytes and corrects Wilson disease. JCI Insight. 8(21). 11 indexed citations
4.
Pastore, Nunzia, R. Colonna, Elena Polishchuk, et al.. (2023). Increased expression or activation of TRPML1 reduces hepatic storage of toxic Z alpha-1 antitrypsin. Molecular Therapy. 31(9). 2651–2661. 5 indexed citations
5.
Tornabene, Patrizia, Antonella Iuliano, Edoardo Nusco, et al.. (2022). Liver gene therapy with intein‐mediated F8 trans ‐splicing corrects mouse haemophilia A. EMBO Molecular Medicine. 14(6). e15199–e15199. 10 indexed citations
6.
Intartaglia, Daniela, et al.. (2022). Induction of Autophagy Promotes Clearance of RHOP23H Aggregates and Protects From Retinal Degeneration. Frontiers in Aging Neuroscience. 14. 878958–878958. 12 indexed citations
7.
Petruzzelli, Raffaella, Stephanie J. Church, Severo Campione, et al.. (2022). Full-length ATP7B reconstituted through protein trans-splicing corrects Wilson disease in mice. Molecular Therapy — Methods & Clinical Development. 26. 495–504. 24 indexed citations
8.
Ferla, Rita, Edoardo Nusco, John M. Cullen, et al.. (2020). Low incidence of hepatocellular carcinoma in mice and cats treated with systemic adeno-associated viral vectors. Molecular Therapy — Methods & Clinical Development. 20. 247–257. 35 indexed citations
9.
Napolitano, Gennaro, Chiara Di Malta, Alessandra Esposito, et al.. (2020). A substrate-specific mTORC1 pathway underlies Birt–Hogg–Dubé syndrome. Nature. 585(7826). 597–602. 208 indexed citations breakdown →
10.
Ferriero, Rosa, Gwladys Gernoux, Rossella De Cegli, et al.. (2020). CHOP and c-JUN up-regulate the mutant Z α1-antitrypsin, exacerbating its aggregation and liver proteotoxicity. Journal of Biological Chemistry. 295(38). 13213–13223. 16 indexed citations
11.
Sorrentino, Nicolina Cristina, Maria De Risi, Sandra Strollo, et al.. (2019). Enhancing the Therapeutic Potential of Sulfamidase for the Treatment of Mucopolysaccharidosis IIIA. Molecular Therapy — Methods & Clinical Development. 15. 333–342. 14 indexed citations
12.
Soria, Leandro R., Gabriella Allegri, Dominique Melck, et al.. (2017). Enhancement of hepatic autophagy increases ureagenesis and protects against hyperammonemia. Proceedings of the National Academy of Sciences. 115(2). 391–396. 46 indexed citations
13.
Bartolomeo, Rosa, Laura Cinque, Chiara De Leonibus, et al.. (2017). mTORC1 hyperactivation arrests bone growth in lysosomal storage disorders by suppressing autophagy. Journal of Clinical Investigation. 127(10). 3717–3729. 74 indexed citations
14.
Gatto, Francesca, Barbara Rossi, Antonietta Tarallo, et al.. (2017). AAV-mediated transcription factor EB (TFEB) gene delivery ameliorates muscle pathology and function in the murine model of Pompe Disease. Scientific Reports. 7(1). 15089–15089. 42 indexed citations
15.
Cinque, Laura, Alison Forrester, Rosa Bartolomeo, et al.. (2015). FGF signalling regulates bone growth through autophagy. Nature. 528(7581). 272–275. 163 indexed citations
16.
Pastore, Nunzia, Edoardo Nusco, Pasquale Piccolo, et al.. (2013). Improved Efficacy and Reduced Toxicity by Ultrasound-Guided Intrahepatic Injections of Helper-Dependent Adenoviral Vector in Gunn Rats. Human Gene Therapy Methods. 24(5). 321–327. 7 indexed citations
17.
Pastore, Nunzia, Edoardo Nusco, Jana Vaníková, et al.. (2012). Sustained Reduction of Hyperbilirubinemia in Gunn Rats After Adeno-Associated Virus-Mediated Gene Transfer of Bilirubin UDP-Glucuronosyltransferase Isozyme 1A1 to Skeletal Muscle. Human Gene Therapy. 23(10). 1082–1089. 6 indexed citations
18.
Saide, Assunta, et al.. (2012). Impaired parkin-mediated mitochondrial targeting to autophagosomes differentially contributes to tissue pathology in lysosomal storage diseases. Human Molecular Genetics. 21(8). 1770–1781. 42 indexed citations
19.
Polito, Vinicia Assunta, et al.. (2010). Correction of CNS defects in the MPSII mouse model via systemic enzyme replacement therapy. Human Molecular Genetics. 19(24). 4871–4885. 39 indexed citations
20.
Domenico, Carmela Di, G. Villani, Daniele Di Napoli, et al.. (2009). Intracranial gene delivery of LV‐NAGLU vector corrects neuropathology in murine MPS IIIB. American Journal of Medical Genetics Part A. 149A(6). 1209–1218. 31 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026