M. Spadaro

2.5k total citations
36 papers, 1.3k citations indexed

About

M. Spadaro is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, M. Spadaro has authored 36 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Cellular and Molecular Neuroscience, 14 papers in Molecular Biology and 11 papers in Neurology. Recurrent topics in M. Spadaro's work include Genetic Neurodegenerative Diseases (15 papers), Mitochondrial Function and Pathology (8 papers) and Neurological diseases and metabolism (5 papers). M. Spadaro is often cited by papers focused on Genetic Neurodegenerative Diseases (15 papers), Mitochondrial Function and Pathology (8 papers) and Neurological diseases and metabolism (5 papers). M. Spadaro collaborates with scholars based in Italy, France and United States. M. Spadaro's co-authors include Marina Frontali, Carla Jodice, Liana Veneziano, C Morocutti, Elide Mantuano, Giovanni Ristori, Silvia Romano, Rune R. Frants, Nicola Vanacore and Flavia Trettel and has published in prestigious journals such as Brain, Neurology and The Lancet Neurology.

In The Last Decade

M. Spadaro

35 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Spadaro Italy 18 829 818 434 174 166 36 1.3k
Sven Asger Sørensen Denmark 18 542 0.7× 411 0.5× 1.0k 2.3× 141 0.8× 123 0.7× 37 1.7k
John MacMillan Australia 17 1.0k 1.2× 849 1.0× 452 1.0× 77 0.4× 287 1.7× 27 1.7k
Jenny Fjell United States 15 652 0.8× 658 0.8× 215 0.5× 244 1.4× 34 0.2× 16 1.7k
H. F. M. Busch Netherlands 22 964 1.2× 646 0.8× 495 1.1× 69 0.4× 41 0.2× 58 1.8k
Francesco Nicita Italy 23 412 0.5× 244 0.3× 239 0.6× 99 0.6× 288 1.7× 94 1.3k
Riadh Gouider Tunisia 20 321 0.4× 803 1.0× 554 1.3× 153 0.9× 80 0.5× 127 1.5k
Arifumi Kosakai Japan 17 422 0.5× 329 0.4× 139 0.3× 48 0.3× 93 0.6× 25 1.0k
Hideji Hashida Japan 19 672 0.8× 520 0.6× 434 1.0× 172 1.0× 45 0.3× 49 1.2k
N. Rizzuto Italy 20 289 0.3× 502 0.6× 418 1.0× 54 0.3× 39 0.2× 62 1.1k
V. Volpini Spain 17 571 0.7× 369 0.5× 167 0.4× 70 0.4× 36 0.2× 33 996

Countries citing papers authored by M. Spadaro

Since Specialization
Citations

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

Fields of papers citing papers by M. Spadaro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Spadaro

This figure shows the co-authorship network connecting the top 25 collaborators of M. Spadaro. A scholar is included among the top collaborators of M. Spadaro 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 M. Spadaro. M. Spadaro 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.
Coarelli, Giulia, Silvia Romano, Lorena Travaglini, et al.. (2018). Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegia. Clinical Neurology and Neurosurgery. 168. 60–63. 7 indexed citations
2.
Romano, Silvia, Giulia Coarelli, Christian Marcotulli, et al.. (2015). Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trial. The Lancet Neurology. 14(10). 985–991. 146 indexed citations
3.
Veneziano, Liana, Elide Mantuano, Claudio Catalli, et al.. (2014). A shared haplotype for dentatorubropallidoluysian atrophy (DRPLA) in Italian families testifies of the recent introduction of the mutation. Journal of Human Genetics. 59(3). 153–157. 4 indexed citations
4.
Spadaro, M., Paola Giunti, Patrizia Lulli, et al.. (2009). HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds. Acta Neurologica Scandinavica. 85(4). 257–265. 8 indexed citations
5.
Spadaro, M., Simona Ursu, Frank Lehmann‐Horn, et al.. (2004). A G301R Na+/K+-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs. Neurogenetics. 5(3). 177–185. 108 indexed citations
6.
Bastianello, Stefano, Anna Pichiecchio, M. Spadaro, et al.. (2004). Atypical multiple sclerosis: MRI findings and differential diagnosis. Neurological Sciences. 25(S4). s356–s360. 8 indexed citations
7.
Blandamura, Stella, P Boccato, M. Spadaro, Pietro Litta, & Silvia Chiarelli. (2002). Endometrial Hyperplasia with Berrylike Squamous Metaplasia and Pilomatrixomalike Shadow Cells. Acta Cytologica. 46(5). 887–892. 3 indexed citations
8.
Pozzilli, Carlo, Giovanni Antonini, Francesca Bagnato, et al.. (2002). Monthly corticosteroids decrease neutralizing antibodies to IFNβ1b: a randomized trial in multiple sclerosis. Journal of Neurology. 249(1). 50–56. 63 indexed citations
9.
Guida, Serena, Flavia Trettel, Elide Mantuano, et al.. (2001). Complete Loss of P/Q Calcium Channel Activity Caused by a CACNA1A Missense Mutation Carried by Patients with Episodic Ataxia Type 2. The American Journal of Human Genetics. 68(3). 759–764. 112 indexed citations
10.
Parisi, Vincenzo, Francesco Pierelli, Rita Restuccia, et al.. (1998). Impaired VEP after photostress response in multiple sclerosis patients previously affected by optic neuritis. Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section. 108(1). 73–79. 26 indexed citations
11.
Jodice, Carla, Elide Mantuano, Liana Veneziano, et al.. (1997). Episodic Ataxia Type 2 (EA2) and Spinocerebellar Ataxia Type 6 (SCA6) Due to CAG Repeat Expansion in the CACNA1A Gene on Chromosome 19p. Human Molecular Genetics. 6(11). 1973–1978. 215 indexed citations
12.
Parisi, Luca, et al.. (1996). Pre-symptomatic neurological involvement in Behçet's disease: the diagnostic role of magnetic transcranial stimulation. Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control. 101(1). 42–47. 18 indexed citations
13.
Frontali, Marina, G. Sabbadini, Andrea Novelletto, et al.. (1996). Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions. Annals of Human Genetics. 60(5). 423–435. 17 indexed citations
14.
Giunti, Paola, M G Sweeney, M. Spadaro, et al.. (1994). The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias. Brain. 117(4). 645–649. 48 indexed citations
15.
Spadaro, M., et al.. (1993). Clinical study of large kindreds with autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) of late onset. Neurological Sciences. 14(1). 17–21. 3 indexed citations
16.
Frontali, Marina, Francesca Persichetti, Andrea Novelletto, et al.. (1993). The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci. Human Molecular Genetics. 2(9). 1383–1387. 19 indexed citations
17.
Malandrini, Alessandro, Paola Piomboni, Giulia Collodel, et al.. (1993). Ultrastructural sperm abnormalities and cerebellar atrophy: does a correlation exist? Report of two cases without endocrine hypogonadism.. PubMed. 25(3). 371–5. 2 indexed citations
18.
Tomelleri, G., Paola Tonin, M. Spadaro, et al.. (1992). AZT-induced mitochondrial myopathy. Neurological Sciences. 13(9). 723–728. 22 indexed citations
19.
Frontali, Marina, M. Spadaro, Paola Giunti, et al.. (1992). AUTOSOMAL DOMINANT PURE CEREBELLAR ATAXIA. Brain. 115(6). 1647–1654. 13 indexed citations
20.
Spadaro, M., et al.. (1991). Association of “top of the basilar” syndrome with megadolichobasilar artery. Clinical and neuroimaging evaluation. Neurological Sciences. 12(2). 169–173. 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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