Antonio Petrucci

2.6k total citations
44 papers, 1.1k citations indexed

About

Antonio Petrucci is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Antonio Petrucci has authored 44 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Neurology, 23 papers in Cellular and Molecular Neuroscience and 17 papers in Molecular Biology. Recurrent topics in Antonio Petrucci's work include Genetic Neurodegenerative Diseases (21 papers), Parkinson's Disease Mechanisms and Treatments (14 papers) and Muscle Physiology and Disorders (7 papers). Antonio Petrucci is often cited by papers focused on Genetic Neurodegenerative Diseases (21 papers), Parkinson's Disease Mechanisms and Treatments (14 papers) and Muscle Physiology and Disorders (7 papers). Antonio Petrucci collaborates with scholars based in Italy, United Kingdom and Lebanon. Antonio Petrucci's co-authors include Gabriella Silvestri, Luca Leonardi, Gabriele Siciliano, Carlo Casali, Manlio Giacanelli, E. Valle, G. Pozzessere, Nicola Vanacore, Marco Bozzali and Carlo Caltagirone and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neurology.

In The Last Decade

Antonio Petrucci

40 papers receiving 1.0k citations

Peers

Antonio Petrucci
Antonio Petrucci
Citations per year, relative to Antonio Petrucci Antonio Petrucci (= 1×) peers Jonas Alex Morales Saute

Countries citing papers authored by Antonio Petrucci

Since Specialization
Citations

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

Fields of papers citing papers by Antonio Petrucci

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonio Petrucci

This figure shows the co-authorship network connecting the top 25 collaborators of Antonio Petrucci. A scholar is included among the top collaborators of Antonio Petrucci 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 Antonio Petrucci. Antonio Petrucci 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.
Brunetti, Valerio, Salvatore Rossi, Enrico Di Stasio, et al.. (2025). Prevalence and Clinical Correlates of Sleep Disorders in RFC1‐Spectrum Disorders: A Cross‐Sectional Study. Movement Disorders. 40(9). 1990–1995.
2.
Cioffi, Ettore, Alessandra Tessa, Antonio Petrucci, et al.. (2024). Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 variants in a series of Italian patients, shedding light upon genetic and phenotypic variability. Neurological Sciences. 45(8). 3845–3852.
3.
Colaizzo, Elisa, Luca Prosperini, Antonio Petrucci, & Alessia Perna. (2024). Creutzfeldt–Jakob Disease Associated with E200K Mutation and SARS-CoV-2 Infection: Pure Coincidence or Neurodegenerative Acceleration?. SHILAP Revista de lepidopterología. 8(2). 16–16.
4.
Spada, Enea, Marco Ceccanti, Umbertina Villano, et al.. (2024). Chronic inflammatory demyelinating polyneuropathy and HEV antibody status: A case-control study from Lazio, Italy. Journal of the Neurological Sciences. 459. 122959–122959. 1 indexed citations
5.
Luigetti, Marco, Valeria Guglielmino, Giovanni Antonini, et al.. (2021). ATTRv in Lazio-Italy: A High-Prevalence Region in a Non-Endemic Country. Genes. 12(6). 829–829. 14 indexed citations
6.
Serra, Laura, Davide Esposito, Giovanni Giulietti, et al.. (2021). Lesion distribution and substrate of white matter damage in myotonic dystrophy type 1: Comparison with multiple sclerosis. NeuroImage Clinical. 29. 102562–102562. 8 indexed citations
7.
Petrucci, Antonio, Guido Primiano, Marco Savarese, et al.. (2021). Novel TNNT1 mutation and mild nemaline myopathy phenotype in an Italian patient. Neuromuscular Disorders. 31(6). 532–538. 11 indexed citations
8.
Botta, Annalisa, Paola Bisceglia, Mario Bengala, et al.. (2021). A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles. Frontiers in Genetics. 12. 668094–668094. 3 indexed citations
9.
Ceccanti, Marco, Valeria Pozzilli, Chiara Cambieri, et al.. (2020). Creatine Kinase and Progression Rate in Amyotrophic Lateral Sclerosis. Cells. 9(5). 1174–1174. 25 indexed citations
10.
Ceccanti, Marco, Chiara Cambieri, Emanuela Onesti, et al.. (2019). Heteronymous H reflex in temporal muscle as sign of hyperexcitability in ALS patients. Clinical Neurophysiology. 130(8). 1455–1459. 6 indexed citations
11.
Chico, Lucia, Elena Caldarazzo Ienco, Annalisa Lo Gerfo, et al.. (2018). Amyotrophic Lateral Sclerosis and Oxidative Stress: A Double-Blind Therapeutic Trial After Curcumin Supplementation. CNS & Neurological Disorders - Drug Targets. 17(10). 767–779. 67 indexed citations
12.
Leonardi, Luca, et al.. (2017). Longitudinal neurophysiological assessment of intramuscular type-A botulin toxin in healthy humans. Neurological Sciences. 39(2). 329–332. 8 indexed citations
13.
Vanacore, Nicola, Emanuele Rastelli, Giovanni Antonini, et al.. (2016). An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy. Neuroepidemiology. 46(3). 191–197. 32 indexed citations
14.
Baldanzi, Sigrid, Francesca Bevilacqua, L. Volpi, et al.. (2016). Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study. Orphanet Journal of Rare Diseases. 11(1). 34–34. 64 indexed citations
15.
Bianchi, Maria Laura Ester, Emanuele Leoncini, Marcella Masciullo, et al.. (2016). Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors. Journal of Neurology. 263(3). 492–498. 23 indexed citations
16.
Campione, Elena, Annalisa Botta, Monia Di Prete, et al.. (2016). Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis. Neuromuscular Disorders. 27(2). 163–169. 15 indexed citations
17.
Astrea, Guja, Antonio Petrucci, Denise Cassandrini, et al.. (2016). Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features – a case report. BMC Medical Genetics. 17(1). 25–25. 5 indexed citations
18.
Sensi, M., Susanna Morano, E. Valle, et al.. (1999). EFFECT OF ISLET TRANSPLANTATION ON NEUROELECTROPHYSIOLOGICAL ABNORMALITIES IN DIABETIC INBRED LEWIS RATS: COMPARISON OF PRIMARY VERSUS SECONDARY PREVENTION1. Transplantation. 68(10). 1453–1459. 1 indexed citations
19.
Sensi, M., Susanna Morano, Maria Grazia Rossi, et al.. (1997). Neuroelectrophysiological abnormalities are related to metabolic and advanced non-enzymatic glycation changes in prospectively evaluated diabetic Sprague-Dawley rats. Cineca Institutional Research Information System (Tor Vergata University). 10(3). 101–109. 1 indexed citations
20.
Morano, Susanna, M. Sensi, Silvana Di Gregorio, et al.. (1996). Peripheral, but not Central, Nervous System Abnormalities are Reversed by Pancreatic Islet Transplantation in Diabetic Lewis Rats. European Journal of Neuroscience. 8(6). 1117–1123. 19 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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