Monica Sciacco

5.8k total citations
90 papers, 2.9k citations indexed

About

Monica Sciacco is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Monica Sciacco has authored 90 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 32 papers in Clinical Biochemistry and 20 papers in Cellular and Molecular Neuroscience. Recurrent topics in Monica Sciacco's work include Mitochondrial Function and Pathology (44 papers), Metabolism and Genetic Disorders (32 papers) and Muscle Physiology and Disorders (23 papers). Monica Sciacco is often cited by papers focused on Mitochondrial Function and Pathology (44 papers), Metabolism and Genetic Disorders (32 papers) and Muscle Physiology and Disorders (23 papers). Monica Sciacco collaborates with scholars based in Italy, United States and United Kingdom. Monica Sciacco's co-authors include Maurizio Moggio, Giacomo P. Comi, Eduardo Bonilla, Nereo Bresolin, G. Scarlato, A. Prelle, Andreina Bordoni, E. Bonilla, Eric A. Schon and S. DiMauro and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Monica Sciacco

88 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Monica Sciacco Italy 29 2.2k 1.1k 497 462 247 90 2.9k
Massimiliano Filosto Italy 30 1.6k 0.7× 786 0.7× 544 1.1× 527 1.1× 501 2.0× 140 2.7k
Marcus Deschauer Germany 31 1.8k 0.8× 756 0.7× 477 1.0× 491 1.1× 665 2.7× 139 3.0k
Angela Pyle United Kingdom 36 2.6k 1.1× 881 0.8× 699 1.4× 470 1.0× 322 1.3× 90 3.4k
Yolanda Campos Spain 31 1.9k 0.8× 1.1k 1.0× 330 0.7× 263 0.6× 292 1.2× 118 2.7k
Chuanzhu Yan China 24 1.4k 0.6× 407 0.4× 311 0.6× 328 0.7× 366 1.5× 172 2.4k
Stefano DiDonato Italy 35 3.4k 1.5× 2.1k 2.0× 738 1.5× 311 0.7× 294 1.2× 63 4.0k
Gerald Pfeffer Canada 22 1.2k 0.5× 449 0.4× 307 0.6× 271 0.6× 105 0.4× 75 1.9k
Olimpia Musumeci Italy 32 1.4k 0.6× 389 0.4× 438 0.9× 331 0.7× 805 3.3× 110 2.8k
Hiroki Kato Japan 21 1.9k 0.8× 365 0.3× 410 0.8× 146 0.3× 379 1.5× 54 2.5k
Dario Ronchi Italy 24 1.3k 0.6× 392 0.4× 286 0.6× 468 1.0× 259 1.0× 86 2.1k

Countries citing papers authored by Monica Sciacco

Since Specialization
Citations

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

Fields of papers citing papers by Monica Sciacco

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monica Sciacco

This figure shows the co-authorship network connecting the top 25 collaborators of Monica Sciacco. A scholar is included among the top collaborators of Monica Sciacco 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 Monica Sciacco. Monica Sciacco 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.
Piga, Daniela, Simona Zanotti, Michela Ripolone, et al.. (2024). Association between ZASP/LDB3 Pro26Ser and Inclusion Body Myopathy. International Journal of Molecular Sciences. 25(12). 6547–6547. 1 indexed citations
2.
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.
3.
Ripolone, Michela, Simona Zanotti, Laura Napoli, et al.. (2023). MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization. Journal of Personalized Medicine. 13(1). 147–147. 4 indexed citations
4.
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
5.
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
6.
Gagliardi, Delia, Gianluca Costamagna, Elena Abati, et al.. (2021). Impact of COVID‐19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy. Muscle & Nerve. 64(4). 474–482. 7 indexed citations
7.
Pagliarani, Serena, Patrizia Ciscato, Gigliola Fagiolari, et al.. (2020). MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form. Molecular Genetics & Genomic Medicine. 8(9). e1320–e1320. 11 indexed citations
8.
Ronchi, Dario, Leonardo Caporali, Megi Meneri, et al.. (2020). TYMP Variants Result in Late-Onset Mitochondrial Myopathy With Altered Muscle Mitochondrial DNA Homeostasis. Frontiers in Genetics. 11. 860–860. 6 indexed citations
9.
Ronchi, Dario, Caterina Garone, Andrea Bordoni, et al.. (2012). Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions. Brain. 135(11). 3404–3415. 73 indexed citations
10.
Ronchi, Dario, Andreina Bordoni, Mafalda Rizzuti, et al.. (2011). Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation. Biochemical and Biophysical Research Communications. 412(2). 245–248. 12 indexed citations
11.
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
12.
Lamperti, Costanza, Valeria Lucchini, Dario Ronchi, et al.. (2010). Mitochondrial Respiratory Chain Dysfunction in Muscle From Patients With Amyotrophic Lateral Sclerosis. Archives of Neurology. 67(7). 849–54. 114 indexed citations
13.
Crimi, Marco, Roberto Del Bo, Sara Galbiati, et al.. (2003). Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion. European Journal of Human Genetics. 11(11). 896–898. 17 indexed citations
14.
Bo, Roberto Del, Andreina Bordoni, Filippo Martinelli Boneschi, et al.. (2002). Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients. Journal of the Neurological Sciences. 202(1-2). 85–91. 35 indexed citations
15.
Prelle, A., Lucia Tancredi, Monica Sciacco, et al.. (2002). Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levels. Journal of Neurology. 249(3). 305–311. 82 indexed citations
16.
Tancredi, Lucia, Elio Scarpini, Monica Sciacco, et al.. (2000). Severe polyneuropathy in a patient with Churg‐Strauss syndrome. Journal of the Peripheral Nervous System. 5(2). 106–110. 2 indexed citations
17.
Sciacco, Monica & Eduardo Bonilla. (1996). [43]Cytochemistry and immunocytochemistry of mitochondria in tissue sections. Methods in enzymology on CD-ROM/Methods in enzymology. 264. 509–521. 167 indexed citations
18.
Santorelli, Filippo M., Monica Sciacco, Kurenai Tanji, et al.. (1996). Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients. Annals of Neurology. 39(6). 789–795. 97 indexed citations
19.
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
20.

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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