Maurizio Moggio

13.7k total citations
195 papers, 6.2k citations indexed

About

Maurizio Moggio is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Maurizio Moggio has authored 195 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 132 papers in Molecular Biology, 39 papers in Cellular and Molecular Neuroscience and 36 papers in Clinical Biochemistry. Recurrent topics in Maurizio Moggio's work include Mitochondrial Function and Pathology (58 papers), Muscle Physiology and Disorders (53 papers) and Metabolism and Genetic Disorders (36 papers). Maurizio Moggio is often cited by papers focused on Mitochondrial Function and Pathology (58 papers), Muscle Physiology and Disorders (53 papers) and Metabolism and Genetic Disorders (36 papers). Maurizio Moggio collaborates with scholars based in Italy, United States and United Kingdom. Maurizio Moggio's co-authors include Giacomo P. Comi, Nereo Bresolin, A. Prelle, G. Scarlato, Monica Sciacco, Andreina Bordoni, Gigliola Fagiolari, Massimo Zeviani, Costanza Lamperti and Francesco Fortunato and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and PLoS ONE.

In The Last Decade

Maurizio Moggio

191 papers receiving 6.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maurizio Moggio Italy 44 4.4k 1.1k 1.0k 1.0k 883 195 6.2k
A. Prelle Italy 38 2.6k 0.6× 792 0.7× 1.5k 1.5× 709 0.7× 683 0.8× 112 4.7k
Pascal Laforêt France 47 3.8k 0.9× 989 0.9× 1.1k 1.1× 1.4k 1.4× 2.0k 2.2× 270 7.4k
Akihiko Taguchi Japan 40 2.3k 0.5× 1.5k 1.3× 474 0.5× 750 0.7× 778 0.9× 115 6.8k
Kurenai Tanji United States 39 3.5k 0.8× 1.7k 1.5× 404 0.4× 618 0.6× 621 0.7× 119 5.2k
Hannu Somer Finland 37 3.2k 0.7× 604 0.5× 448 0.4× 917 0.9× 524 0.6× 108 4.7k
Carlo Minetti Italy 50 5.4k 1.2× 571 0.5× 475 0.5× 805 0.8× 1.0k 1.2× 190 7.5k
Laurence A. Bindoff Norway 48 6.3k 1.4× 3.4k 3.0× 878 0.8× 1.4k 1.4× 696 0.8× 187 8.0k
Eduardo Bonilla United States 49 6.9k 1.6× 3.5k 3.1× 361 0.3× 963 0.9× 943 1.1× 127 9.0k
Benedikt Schoser Germany 52 4.1k 0.9× 379 0.3× 1.7k 1.7× 2.0k 2.0× 2.3k 2.6× 337 8.2k
Marcus Deschauer Germany 31 1.8k 0.4× 756 0.7× 491 0.5× 477 0.5× 665 0.8× 139 3.0k

Countries citing papers authored by Maurizio Moggio

Since Specialization
Citations

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

Fields of papers citing papers by Maurizio Moggio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maurizio Moggio

This figure shows the co-authorship network connecting the top 25 collaborators of Maurizio Moggio. A scholar is included among the top collaborators of Maurizio Moggio 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 Maurizio Moggio. Maurizio Moggio 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.
Magri, Francesca, Laura Napoli, Michela Ripolone, et al.. (2023). The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls. International Journal of Molecular Sciences. 24(24). 17402–17402.
2.
Rimoldi, M., Daniele Velardo, Megi Meneri, et al.. (2023). Lafora Disease: A Case Report and Evolving Treatment Advancements. Brain Sciences. 13(12). 1679–1679. 2 indexed citations
3.
Rimoldi, M., Francesca Magri, Michela Ripolone, et al.. (2023). Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant. Frontiers in Genetics. 14. 1278572–1278572. 3 indexed citations
4.
Zanotti, Simona, Francesca Magri, Michela Ripolone, et al.. (2022). Immunofluorescence signal intensity measurements as a semi-quantitative tool to assess sarcoglycan complex expression in muscle biopsy. European Journal of Histochemistry. 66(3). 5 indexed citations
5.
Magri, Francesca, Simona Zanotti, Sabrina Salani, et al.. (2022). Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the SGCB Gene. International Journal of Molecular Sciences. 23(17). 9817–9817. 1 indexed citations
6.
Moriggi, Manuela, Daniele Capitanio, Enrica Torretta, et al.. (2021). Muscle Proteomic Profile before and after Enzyme Replacement Therapy in Late-Onset Pompe Disease. International Journal of Molecular Sciences. 22(6). 2850–2850. 27 indexed citations
7.
Monfrini, Edoardo, Filippo Cogiamanian, Sabrina Salani, et al.. (2021). A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia. Annals of Neurology. 89(4). 834–839. 18 indexed citations
8.
Filosto, Massimiliano, Stefano Cotti Piccinelli, Costanza Lamperti, et al.. (2019). Muscle pain in mitochondrial diseases: a picture from the Italian network. Journal of Neurology. 266(4). 953–959. 6 indexed citations
9.
Reyes, Aurelio, Laura Melchionda, Alessia Nasca, et al.. (2015). RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy. The American Journal of Human Genetics. 97(1). 186–193. 80 indexed citations
10.
Mancuso, Michelangelo, C. Angelini, Enrico Bertini, et al.. (2012). Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases. Neuromuscular Disorders. 22. S226–S229. 38 indexed citations
11.
Lunetta, Christian, A. Prelle, Paolo Magni, et al.. (2011). Impaired expression of insulin‐like growth factor‐1 system in skeletal muscle of amyotrophic lateral sclerosis patients. Muscle & Nerve. 45(2). 200–208. 37 indexed citations
12.
Ciammola, Andrea, Jenny Sassone, Monica Sciacco, et al.. (2010). Low anaerobic threshold and increased skeletal muscle lactate production in subjects with Huntington's disease. Movement Disorders. 26(1). 130–137. 47 indexed citations
13.
Lucchiari, Sabrina, Serena Pagliarani, Stefania Corti, et al.. (2008). Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion. Journal of the Neurological Sciences. 275(1-2). 159–163. 9 indexed citations
14.
Eisenberg, Iris, Alal Eran, Ichizo Nishino, et al.. (2007). Distinctive patterns of microRNA expression in primary muscular disorders. Proceedings of the National Academy of Sciences. 104(43). 17016–17021. 407 indexed citations
15.
Crimi, Marco, Sara Galbiati, Isabella Moroni, et al.. (2003). A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome. Neurology. 60(11). 1857–1861. 59 indexed citations
16.
Prelle, A., Patrizia Ciscato, Maurizio Moggio, et al.. (1995). Utrophin expression during human fetal development. International Journal of Developmental Neuroscience. 13(6). 585–593. 13 indexed citations
17.
Moggio, Maurizio, A. Prelle, Gigliola Fagiolari, et al.. (1994). Anionic phospholipids calcium binding sites in Duchenne and murine X‐linked muscular dystrophy. Muscle & Nerve. 17(5). 485–488. 1 indexed citations
18.
Scarpini, Elio, et al.. (1992). Phenotypic and proliferative properties of Schwann cells from nerves of diabetic patients.. PubMed. 12(5-6). 211–5. 7 indexed citations
19.
Biral, Donatella, Ernesto Damiani, Elio Scarpini, et al.. (1987). Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features. Neurology. 37(10). 1658–1658. 1 indexed citations
20.
Pellegrini, G., et al.. (1979). Ophthalmoplegia plus. A multisystem disorder of unknown etiopathogenesis. Neurological Sciences. 1(1). 85–94. 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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