Carmelo Rodolico

5.3k total citations
123 papers, 2.1k citations indexed

About

Carmelo Rodolico is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Carmelo Rodolico has authored 123 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 44 papers in Neurology and 25 papers in Cellular and Molecular Neuroscience. Recurrent topics in Carmelo Rodolico's work include Muscle Physiology and Disorders (30 papers), Myasthenia Gravis and Thymoma (25 papers) and Genetic Neurodegenerative Diseases (20 papers). Carmelo Rodolico is often cited by papers focused on Muscle Physiology and Disorders (30 papers), Myasthenia Gravis and Thymoma (25 papers) and Genetic Neurodegenerative Diseases (20 papers). Carmelo Rodolico collaborates with scholars based in Italy, United States and United Kingdom. Carmelo Rodolico's co-authors include António Toscano, Giuseppe Vita, Olimpia Musumeci, M. Aguennouz, Sonia Messina, Anna Mazzeo, Simona Portaro, Emanuele Barca, Michele Gaeta and Salvatore Benvenga and has published in prestigious journals such as PLoS ONE, Neurology and PEDIATRICS.

In The Last Decade

Carmelo Rodolico

116 papers receiving 2.1k citations

Peers

Carmelo Rodolico

NEURO

PHYSI

RHEUM

CMN

Anna Mazzeo Italy

Christopher Lindberg Sweden

Monica Sciacco Italy

Tatsuo Kohriyama Japan

Francesco Fortunato Italy

Karim Wahbi France

Julia Wanschitz Austria

Takeo Abumiya Japan

Gerald Pfeffer Canada

Kohkichi Hosoda Japan

Anna Mazzeo Italy

Carmelo Rodolico

1.1k ×1.2

391 ×0.6

NEURO

263 ×0.6

PHYSI

163 ×0.4

RHEUM

360 ×1.1

CMN

Citations per year, relative to Carmelo Rodolico Carmelo Rodolico (= 1×) peers Anna Mazzeo

Countries citing papers authored by Carmelo Rodolico

Since Specialization

Citations

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

Fields of papers citing papers by Carmelo Rodolico

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carmelo Rodolico

This figure shows the co-authorship network connecting the top 25 collaborators of Carmelo Rodolico. A scholar is included among the top collaborators of Carmelo Rodolico 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 Carmelo Rodolico. Carmelo Rodolico is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

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

Pugliese, Alessia, et al.. (2023). Presynaptic Congenital Myasthenic Syndromes: Understanding Clinical Phenotypes through In vivo Models. Journal of Neuromuscular Diseases. 10(5). 731–759. 7 indexed citations

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

Lucchini, Matteo, Lorenzo Maggi, Elena Pegoraro, et al.. (2021). Anti-cN1A Antibodies Are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis. Cells. 10(5). 1146–1146. 25 indexed citations

Musumeci, Olimpia, Edoardo Ferlazzo, Carmelo Rodolico, et al.. (2020). A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies. Frontiers in Neurology. 11. 514–514. 3 indexed citations

Toscano, António, Carmelo Rodolico, & Olimpia Musumeci. (2019). Multisystem late onset Pompe disease (LOPD): an update on clinical aspects. Annals of Translational Medicine. 7(13). 284–284. 58 indexed citations

Vita, Gian Luca, Francesca Polito, Rosaria Oteri, et al.. (2018). Hippo signaling pathway is altered in Duchenne muscular dystrophy. PLoS ONE. 13(10). e0205514–e0205514. 33 indexed citations

Camerino, Giulia Maria, Olimpia Musumeci, Elena Conte, et al.. (2017). Risk of Myopathy in Patients in Therapy with Statins: Identification of Biological Markers in a Pilot Study. Frontiers in Pharmacology. 8. 500–500. 30 indexed citations

Marino, Marco, Olimpia Musumeci, Maria Cucinotta, et al.. (2016). Ischemic stroke due to hypoperfusion in a patient with a previously unrecognized Danon disease. Neuromuscular Disorders. 26(12). 890–894. 8 indexed citations

10.

Evoli, Amelia, Rocco Liguori, A. Romani, et al.. (2014). Italian recommendations for Lambert–Eaton myasthenic syndrome (LEMS) management. Neurological Sciences. 35(4). 515–520. 12 indexed citations

11.

Barca, Emanuele, M. Aguennouz, Anna Mazzeo, et al.. (2012). ANT1 is reduced in sporadic inclusion body myositis. Neurological Sciences. 34(2). 217–224. 7 indexed citations

12.

Musumeci, Olimpia, Emanuele Barca, Sabrina Ravaglia, et al.. (2012). Auditory system involvement in late onset Pompe disease: A study of 20 Italian patients. Molecular Genetics and Metabolism. 107(3). 480–484. 23 indexed citations

13.

Gaeta, Michele, Emanuele Scribano, Achille Mileto, et al.. (2011). Muscle Fat Fraction in Neuromuscular Disorders: Dual-Echo Dual-Flip-Angle Spoiled Gradient-Recalled MR Imaging Technique for Quantification—A Feasibility Study. Radiology. 259(2). 487–494. 78 indexed citations

14.

Musumeci, Olimpia, Claudio Bruno, Tiziana Mongini, et al.. (2011). Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII). Neuromuscular Disorders. 22(4). 325–330. 36 indexed citations

15.

Schara, Ulrike, Marja Hietala, Carmelo Rodolico, et al.. (2007). G.P.10.01 Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. Neuromuscular Disorders. 17(9-10). 818–818. 2 indexed citations

16.

Patitucci, A., M. Muglia, A. Magariello, et al.. (2005). Comparison of different techniques for detecting 17p12 duplication in CMT1A. Neuromuscular Disorders. 15(7). 488–492. 9 indexed citations

17.

Musumeci, Olimpia, Carmelo Rodolico, Ichizo Nishino, et al.. (2005). Asymptomatic hyperCKemia in a case of Danon disease due to a missense mutation in Lamp-2 gene. Neuromuscular Disorders. 15(6). 409–411. 27 indexed citations

18.

Fodale, Vincenzo, C Praticò, Paolo Girlanda, et al.. (2004). Acute motor axonal polyneuropathy after a cisatracurium infusion and concomitant corticosteroid therapy. British Journal of Anaesthesia. 92(2). 289–293. 6 indexed citations

19.

Cagliani, Rachele, Francesco Fortunato, Roberto Giorda, et al.. (2003). Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population. Neuromuscular Disorders. 13(10). 788–795. 38 indexed citations

20.

Monici, Maria C., Carmelo Rodolico, António Toscano, et al.. (2002). Apoptosis and apoptosis‐related proteins in thyroid myopathies. Muscle & Nerve. 26(3). 383–388. 4 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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