António Toscano

12.6k total citations
226 papers, 4.9k citations indexed

About

António Toscano is a scholar working on Molecular Biology, Rheumatology and Physiology. According to data from OpenAlex, António Toscano has authored 226 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Molecular Biology, 70 papers in Rheumatology and 58 papers in Physiology. Recurrent topics in António Toscano's work include Glycogen Storage Diseases and Myoclonus (62 papers), Lysosomal Storage Disorders Research (51 papers) and Mitochondrial Function and Pathology (31 papers). António Toscano is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (62 papers), Lysosomal Storage Disorders Research (51 papers) and Mitochondrial Function and Pathology (31 papers). António Toscano collaborates with scholars based in Italy, United States and United Kingdom. António Toscano's co-authors include Olimpia Musumeci, Carmelo Rodolico, Benedikt Schoser, Giuseppe Vita, Massimo Zeviani, Nereo Bresolin, C Messina, Giacomo P. Comi, Anna Mazzeo and Paolo Girlanda and has published in prestigious journals such as Brain, Neurology and PEDIATRICS.

In The Last Decade

António Toscano

216 papers receiving 4.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
António Toscano Italy 38 2.3k 1.4k 1.4k 856 820 226 4.9k
Pascal Laforêt France 47 3.8k 1.7× 2.0k 1.4× 1.8k 1.3× 989 1.2× 1.4k 1.7× 270 7.4k
D. Pongratz Germany 39 2.3k 1.0× 898 0.6× 740 0.5× 576 0.7× 743 0.9× 185 5.0k
Antoni L. Andreu Spain 44 3.7k 1.6× 776 0.6× 1.2k 0.9× 1.6k 1.9× 719 0.9× 175 5.5k
Oluf Andersen Sweden 39 2.0k 0.9× 642 0.5× 912 0.7× 400 0.5× 303 0.4× 135 5.9k
Benedikt Schoser Germany 52 4.1k 1.8× 2.3k 1.6× 1.7k 1.3× 379 0.4× 2.0k 2.5× 337 8.2k
Michèl A.A.P. Willemsen Netherlands 41 2.8k 1.2× 734 0.5× 396 0.3× 1.2k 1.4× 816 1.0× 199 5.7k
Zohar Argov Israel 41 3.5k 1.6× 890 0.6× 664 0.5× 369 0.4× 1.1k 1.4× 180 6.3k
Carlo Minetti Italy 50 5.4k 2.4× 1.0k 0.7× 516 0.4× 571 0.7× 805 1.0× 190 7.5k
Florian Eichler United States 34 2.2k 1.0× 1.0k 0.7× 240 0.2× 447 0.5× 375 0.5× 127 4.0k
Wolfgang Müller‐Felber Germany 31 1.2k 0.5× 912 0.7× 750 0.6× 135 0.2× 413 0.5× 135 3.2k

Countries citing papers authored by António Toscano

Since Specialization
Citations

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

Fields of papers citing papers by António Toscano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of António Toscano

This figure shows the co-authorship network connecting the top 25 collaborators of António Toscano. A scholar is included among the top collaborators of António Toscano 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 António Toscano. António Toscano 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.
Aleksovska, Katina, Theodoros Kyriakides, C. Angelini, et al.. (2025). What Are the Normal Serum Creatine Kinase Values for Skeletal Muscle? A Worldwide Systematic Review. European Journal of Neurology. 32(6). e70240–e70240. 2 indexed citations
2.
Musumeci, Olimpia, Anna Maria Pugliese, Ilaria Arena, et al.. (2025). Management of presymptomatic juvenile patients with late-onset Pompe disease (LOPD). Neuromuscular Disorders. 47. 105277–105277. 1 indexed citations
3.
Tessitore, Agostino, Carmela Casella, Antonio Ciacciarelli, et al.. (2024). Predictors of Good Functional Outcome in Patients with Tandem Occlusion After Revascularization Treatment: Single-Center Experience with 12-Month Follow-Up. World Neurosurgery. 188. e382–e389. 2 indexed citations
4.
Kishnani, Priya S., Barry J. Byrne, Kristl G. Claeys, et al.. (2024). Switching treatment to cipaglucosidase alfa plus miglustat positively affects patient-reported outcome measures in patients with late-onset Pompe disease. Journal of Patient-Reported Outcomes. 8(1). 132–132. 3 indexed citations
5.
Løkken, Nicoline, Andrea Martinuzzi, Miguel A. Martı́n, et al.. (2022). Muscle MRI in McArdle Disease. Neurology. 99(15). e1664–e1675. 5 indexed citations
6.
Gentile, Luca, Massimo Russo, Federica Taioli, et al.. (2021). Rare among Rare: Phenotypes of Uncommon CMT Genotypes. Brain Sciences. 11(12). 1616–1616. 1 indexed citations
7.
Gentile, Luca, Massimo Russo, Marco Luigetti, et al.. (2021). Patisiran in hATTR Amyloidosis: Six-Month Latency Period before Efficacy. Brain Sciences. 11(4). 515–515. 9 indexed citations
8.
Russo, Massimo, Luca Gentile, Vincenzo Di Stefano, et al.. (2021). Use of Drugs for ATTRv Amyloidosis in the Real World: How Therapy Is Changing Survival in a Non-Endemic Area. Brain Sciences. 11(5). 545–545. 21 indexed citations
9.
Gentile, Luca, Massimo Russo, Gian Maria Fabrizi, et al.. (2020). Charcot-Marie-Tooth disease: experience from a large Italian tertiary neuromuscular center. Neurological Sciences. 41(5). 1239–1243. 16 indexed citations
10.
Gentile, Luca, Gianluca Di Bella, Fabio Minutoli, et al.. (2020). Description of a large cohort of Caucasian patients with V122I ATTRv amyloidosis: Neurological and cardiological features. Journal of the Peripheral Nervous System. 25(3). 273–278. 16 indexed citations
11.
Russo, Massimo, Luca Gentile, António Toscano, et al.. (2020). Advances in Treatment of ATTRv Amyloidosis: State of the Art and Future Prospects. Brain Sciences. 10(12). 952–952. 11 indexed citations
12.
Ruggeri, Paolo, et al.. (2020). Ultrasound assessment of diaphragm function in patients with late-onset Pompe disease. Neurological Sciences. 41(8). 2175–2184. 22 indexed citations
13.
Iolascon, Giovanni, Michele Vitacca, Elena Carraro, et al.. (2019). Adapted physical activity and therapeutic exercise in late-onset Pompe disease (LOPD): a two-step rehabilitative approach. Neurological Sciences. 41(4). 859–868. 8 indexed citations
14.
Ambrosini, Anna, Daniela Calabrese, Guido Cavaletti, et al.. (2018). The Italian neuromuscular registry: a coordinated platform where patient organizations and clinicians collaborate for data collection and multiple usage. Orphanet Journal of Rare Diseases. 13(1). 176–176. 24 indexed citations
15.
Aguennouz, M., Marco Beccaria, Giorgia Purcaro, et al.. (2016). Analysis of lipid profile in lipid storage myopathy. Journal of Chromatography B. 1029-1030. 157–168. 7 indexed citations
16.
Schoser, Benedikt, et al.. (2015). Minutes of the European POmpe Consortium (EPOC) Meeting March 27 to 28, 2015, Munich, Germany.. PubMed. 34(2-3). 141–3. 4 indexed citations
17.
Russo, Massimo, Gian Luca Vita, António Toscano, et al.. (2008). Psychosocial impact of presymptomatic genetic testing for transthyretin amyloidotic polyneuropathy. Neuromuscular Disorders. 19(1). 44–48. 16 indexed citations
18.
Petersen, Poul Erik, et al.. (2003). Changing oral health status of 6- and 12-year-old schoolchildren in Portugal.. PubMed. 20(4). 211–6. 90 indexed citations
19.
Oreto, Giuseppe, Giuseppe Vita, Placido Gitto, et al.. (2002). Idiopathic restrictive cardiomyopathy in childhood. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 28(5). 412–415. 1 indexed citations
20.
Monici, Maria C., et al.. (1997). Dna fragmentation in metabolic myopathies. The Italian Journal of Neurological Sciences. 18(4). 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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