A. Prelle

9.0k total citations
112 papers, 4.7k citations indexed

About

A. Prelle is a scholar working on Molecular Biology, Neurology and Clinical Biochemistry. According to data from OpenAlex, A. Prelle has authored 112 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 30 papers in Neurology and 26 papers in Clinical Biochemistry. Recurrent topics in A. Prelle's work include Mitochondrial Function and Pathology (33 papers), Muscle Physiology and Disorders (32 papers) and Metabolism and Genetic Disorders (26 papers). A. Prelle is often cited by papers focused on Mitochondrial Function and Pathology (33 papers), Muscle Physiology and Disorders (32 papers) and Metabolism and Genetic Disorders (26 papers). A. Prelle collaborates with scholars based in Italy, United States and United Kingdom. A. Prelle's co-authors include Maurizio Moggio, Nereo Bresolin, Giacomo P. Comi, Massimo Zeviani, Massimo Filippi, Federica Agosta, G. Scarlato, Monica Sciacco, Gigliola Fagiolari and Domenico Caputo and has published in prestigious journals such as Nature, Nature Medicine and PLoS ONE.

In The Last Decade

A. Prelle

110 papers receiving 4.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Prelle Italy 38 2.6k 1.5k 836 792 709 112 4.7k
Maurizio Moggio Italy 44 4.4k 1.7× 1.0k 0.7× 785 0.9× 1.1k 1.4× 1.0k 1.4× 195 6.2k
Cinzia Gellera Italy 41 3.7k 1.4× 1.7k 1.1× 813 1.0× 1.2k 1.5× 2.3k 3.2× 155 5.5k
Matthias Vorgerd Germany 41 3.1k 1.2× 686 0.4× 408 0.5× 299 0.4× 1.4k 2.0× 183 5.1k
Eisaku Ohama Japan 37 2.1k 0.8× 3.3k 2.1× 699 0.8× 352 0.4× 1.4k 2.0× 160 5.9k
Gabriella Silvestri Italy 35 3.5k 1.3× 666 0.4× 261 0.3× 1.4k 1.8× 1.3k 1.8× 126 4.4k
Carlo Minetti Italy 50 5.4k 2.1× 475 0.3× 617 0.7× 571 0.7× 805 1.1× 190 7.5k
Federico Zara Italy 46 3.0k 1.2× 878 0.6× 204 0.2× 399 0.5× 1.3k 1.9× 242 6.6k
I.F.M. de Coo Netherlands 45 4.4k 1.7× 428 0.3× 195 0.2× 1.8k 2.2× 600 0.8× 159 6.1k
Kiyomitsu Oyanagi Japan 38 1.2k 0.5× 1.9k 1.3× 423 0.5× 226 0.3× 1.1k 1.6× 173 4.2k
Makito Hirano Japan 29 994 0.4× 1.4k 0.9× 435 0.5× 178 0.2× 884 1.2× 149 3.0k

Countries citing papers authored by A. Prelle

Since Specialization
Citations

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

Fields of papers citing papers by A. Prelle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Prelle

This figure shows the co-authorship network connecting the top 25 collaborators of A. Prelle. A scholar is included among the top collaborators of A. Prelle 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 A. Prelle. A. Prelle 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.
Canu, Elisa, Federica Agosta, Nilo Riva, et al.. (2011). The Topography of Brain Microstructural Damage in Amyotrophic Lateral Sclerosis Assessed Using Diffusion Tensor MR Imaging. American Journal of Neuroradiology. 32(7). 1307–1314. 55 indexed citations
2.
Agosta, Federica, Paola Valsasina, Martina Absinta, et al.. (2011). Sensorimotor Functional Connectivity Changes in Amyotrophic Lateral Sclerosis. Cerebral Cortex. 21(10). 2291–2298. 96 indexed citations
3.
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
4.
Bo, Roberto Del, Serena Ghezzi, Stefania Corti, et al.. (2009). TARDBP (TDP‐43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations. European Journal of Neurology. 16(6). 727–732. 81 indexed citations
5.
Bo, Roberto Del, Marina Scarlato, Serena Ghezzi, et al.. (2006). Absence of angiogenic genes modification in Italian ALS patients. Neurobiology of Aging. 29(2). 314–316. 35 indexed citations
6.
7.
Gabellini, Davide, Giuseppe D’Antona, Maurizio Moggio, et al.. (2005). Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1. Nature. 439(7079). 973–977. 170 indexed citations
8.
Zanotti, Simona, Tiziana Negri, Cristina Cappelletti, et al.. (2005). Decorin and biglycan expression is differentially altered in several muscular dystrophies. Brain. 128(11). 2546–2555. 71 indexed citations
9.
Lamperti, Costanza, Ali Naini, Valeria Lucchini, et al.. (2005). Muscle Coenzyme Q10 Level in Statin-Related Myopathy. Archives of Neurology. 62(11). 1709–1709. 123 indexed citations
10.
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
11.
Bo, Roberto Del, Pierluigi Baron, A. Prelle, et al.. (2003). Novel missense mutation and large deletion of GNE gene in autosomal‐recessive inclusion‐body myopathy. Muscle & Nerve. 28(1). 113–117. 29 indexed citations
12.
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
13.
Baron, Pierluigi, Daniela Galimberti, Lucia Meda, et al.. (2000). Synergistic effect of  -amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cells. Brain. 123(2). 374–379. 23 indexed citations
14.
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
15.
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
16.
Toscano, António, Libero Vitiello, Giacomo P. Comi, et al.. (1995). Duplication of dystrophin gene and dissimilar clinical phenotype in the same family. Neuromuscular Disorders. 5(6). 475–481. 7 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.
Checcarelli, Nicoletta, A. Prelle, Maurizio Moggio, et al.. (1994). Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy. Journal of the Neurological Sciences. 123(1-2). 74–79. 24 indexed citations
19.
Prelle, A., Maurizio Moggio, Nicoletta Checcarelli, et al.. (1993). Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis. Journal of the Neurological Sciences. 117(1-2). 24–27. 12 indexed citations
20.
Prelle, A., R. Medori, Maurizio Moggio, et al.. (1992). Dystrophin deficiency in a case of congenital myopathy. Journal of Neurology. 239(2). 76–78. 13 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

Breakdown of academic impact, for papers by Maurizio Moggio Breakdown of academic impact, for papers by Cinzia Gellera Breakdown of academic impact, for papers by Matthias Vorgerd Breakdown of academic impact, for papers by Eisaku Ohama Breakdown of academic impact, for papers by Gabriella Silvestri Breakdown of academic impact, for papers by Carlo Minetti Breakdown of academic impact, for papers by Federico Zara Breakdown of academic impact, for papers by I.F.M. de Coo Breakdown of academic impact, for papers by Kiyomitsu Oyanagi Breakdown of academic impact, for papers by Makito Hirano
Rankless by CCL
2026