Enrico Bugiardini

2.2k total citations
44 papers, 932 citations indexed

About

Enrico Bugiardini is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Enrico Bugiardini has authored 44 papers receiving a total of 932 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 20 papers in Cellular and Molecular Neuroscience and 9 papers in Neurology. Recurrent topics in Enrico Bugiardini's work include Genetic Neurodegenerative Diseases (18 papers), Mitochondrial Function and Pathology (16 papers) and Muscle Physiology and Disorders (11 papers). Enrico Bugiardini is often cited by papers focused on Genetic Neurodegenerative Diseases (18 papers), Mitochondrial Function and Pathology (16 papers) and Muscle Physiology and Disorders (11 papers). Enrico Bugiardini collaborates with scholars based in Italy, United Kingdom and Sweden. Enrico Bugiardini's co-authors include G. Meola, Rosanna Cardani, Michael G. Hanna, Rocco Liguori, Vincenzo Donadio, Agostino Baruzzi, Pasquale Montagna, Emma Matthews, Mikael Elam and Annalisa Botta and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and Brain.

In The Last Decade

Enrico Bugiardini

42 papers receiving 918 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Enrico Bugiardini Italy 20 567 439 252 151 139 44 932
Antonio Petrucci Italy 20 509 0.9× 537 1.2× 492 2.0× 121 0.8× 45 0.3× 44 1.1k
Bruno Moulard Switzerland 11 663 1.2× 523 1.2× 263 1.0× 66 0.4× 84 0.6× 20 1.3k
Fumi Urano Japan 12 653 1.2× 417 0.9× 121 0.5× 134 0.9× 43 0.3× 21 1.1k
Velina Guergueltcheva Bulgaria 23 899 1.6× 561 1.3× 408 1.6× 86 0.6× 114 0.8× 52 1.6k
Robyn Labrum United Kingdom 14 488 0.9× 400 0.9× 175 0.7× 32 0.2× 145 1.0× 21 772
Hiroyuki Morino Japan 20 685 1.2× 564 1.3× 494 2.0× 163 1.1× 33 0.2× 78 1.2k
Satoshi Kashii Japan 17 413 0.7× 266 0.6× 137 0.5× 203 1.3× 23 0.2× 40 979
Lucie Guyant‐Maréchal France 15 398 0.7× 282 0.6× 421 1.7× 289 1.9× 16 0.1× 31 1.0k
Mikko Kärppä Finland 14 651 1.1× 133 0.3× 92 0.4× 70 0.5× 75 0.5× 38 951
Sally Spendiff Canada 16 389 0.7× 109 0.2× 117 0.5× 217 1.4× 54 0.4× 35 711

Countries citing papers authored by Enrico Bugiardini

Since Specialization
Citations

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

Fields of papers citing papers by Enrico Bugiardini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Enrico Bugiardini

This figure shows the co-authorship network connecting the top 25 collaborators of Enrico Bugiardini. A scholar is included among the top collaborators of Enrico Bugiardini 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 Enrico Bugiardini. Enrico Bugiardini 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.
Ricci, Giulia, Lucia Ruggiero, Liliana Vercelli, et al.. (2025). Describing phenotypes in FSHD: an update of the comprehensive clinical evaluation form. Neurological Sciences. 46(9). 4633–4643. 1 indexed citations
2.
Vishnu, Venugopalan Y., Richard J.L.F. Lemmers, T. Ahmad, et al.. (2024). The first genetically confirmed cohort of Facioscapulohumeral Muscular Dystrophy from Northern India. European Journal of Human Genetics. 32(9). 1053–1064. 4 indexed citations
3.
Facchini, Stefano, Natalia Dominik, Arianna Manini, et al.. (2023). Optical Genome Mapping Enables Detection and Accurate Sizing of RFC1 Repeat Expansions. Biomolecules. 13(10). 1546–1546. 11 indexed citations
4.
Bugiardini, Enrico, Emanuela Bottani, Silvia Marchet, et al.. (2020). Expanding the molecular and phenotypic spectrum of truncating MT-ATP6 mutations. Neurology Genetics. 6(1). e381–e381. 25 indexed citations
5.
Vivekanandam, Vinojini, Enrico Bugiardini, Ashirwad Merve, et al.. (2020). Differential Diagnoses of Inclusion Body Myositis. Neurologic Clinics. 38(3). 697–710. 2 indexed citations
6.
Gandhi, Sonia, Silvia Marino, Enrico Bugiardini, et al.. (2019). Adult-onset Leigh syndrome linked to the novel stop codon mutation m.6579G>A in MT-CO1. Mitochondrion. 47. 294–297. 8 indexed citations
7.
Bugiardini, Enrico, Jasper M. Morrow, Sachit Shah, et al.. (2018). The Diagnostic Value of MRI Pattern Recognition in Distal Myopathies. Frontiers in Neurology. 9. 456–456. 33 indexed citations
8.
Bugiardini, Enrico, Ilaria Rivolta, Anna Binda, et al.. (2015). SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype. Neuromuscular Disorders. 25(4). 301–307. 38 indexed citations
9.
Perfetti, Alessandra, Simona Greco, Enrico Bugiardini, et al.. (2014). Plasma microRNAs as biomarkers for myotonic dystrophy type 1. Neuromuscular Disorders. 24(6). 509–515. 57 indexed citations
10.
Bugiardini, Enrico & G. Meola. (2014). Consensus on cerebral involvement in myotonic dystrophy. Neuromuscular Disorders. 24(5). 445–452. 33 indexed citations
11.
Perfetti, Alessandra, Simona Greco, Pasquale Fasanaro, et al.. (2014). Genome Wide Identification of Aberrant Alternative Splicing Events in Myotonic Dystrophy Type 2. PLoS ONE. 9(4). e93983–e93983. 20 indexed citations
12.
Cardani, Rosanna, Marzia Giagnacovo, Giulia De Rossi, et al.. (2014). Progression of muscle histopathology but not of spliceopathy in myotonic dystrophy type 2. Neuromuscular Disorders. 24(12). 1042–1053. 14 indexed citations
13.
Cardani, Rosanna, Enrico Bugiardini, Laura Valentina Renna, et al.. (2013). Overexpression of CUGBP1 in Skeletal Muscle from Adult Classic Myotonic Dystrophy Type 1 but Not from Myotonic Dystrophy Type 2. PLoS ONE. 8(12). e83777–e83777. 34 indexed citations
14.
Passeri, Elena, Enrico Bugiardini, Valeria Sansone, et al.. (2013). Vitamin D, parathyroid hormone and muscle impairment in myotonic dystrophies. Journal of the Neurological Sciences. 331(1-2). 132–135. 26 indexed citations
15.
Cardani, Rosanna, Marzia Giagnacovo, Annalisa Botta, et al.. (2012). Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2. Journal of Neurology. 259(10). 2090–2099. 36 indexed citations
16.
Jones, Karlie, Christina Wei, Polina Iakova, et al.. (2012). GSK3β mediates muscle pathology in myotonic dystrophy. Journal of Clinical Investigation. 122(12). 4461–4472. 106 indexed citations
17.
Liguori, Rocco, Vitantonio Di Stasi, Enrico Bugiardini, et al.. (2010). Small fiber neuropathy in female patients with fabry disease. Muscle & Nerve. 41(3). 409–412. 47 indexed citations
18.
Donadio, Vincenzo, Pietro Cortelli, Mikael Elam, et al.. (2010). Autonomic innervation in multiple system atrophy and pure autonomic failure. Journal of Neurology Neurosurgery & Psychiatry. 81(12). 1327–1335. 62 indexed citations
19.
Donadio, Vincenzo, Giuseppe Plazzi, Stefano Vandi, et al.. (2008). Sympathetic and cardiovascular activity during cataplexy in narcolepsy. Journal of Sleep Research. 17(4). 458–463. 29 indexed citations
20.
Donadio, Vincenzo, Pietro Cortelli, Francesca Maria Antonella Falzone, et al.. (2008). Isolated generalised anhidrosis induced by postganglionic sympathetic skin nerve fibre degeneration: an incomplete Ross syndrome?. Journal of Neurology Neurosurgery & Psychiatry. 79(8). 959–961. 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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