Simona Capponi

678 total citations
16 papers, 405 citations indexed

About

Simona Capponi is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Simona Capponi has authored 16 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 8 papers in Molecular Biology and 6 papers in Neurology. Recurrent topics in Simona Capponi's work include Hereditary Neurological Disorders (10 papers), Botulinum Toxin and Related Neurological Disorders (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Simona Capponi is often cited by papers focused on Hereditary Neurological Disorders (10 papers), Botulinum Toxin and Related Neurological Disorders (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Simona Capponi collaborates with scholars based in Italy, United States and Germany. Simona Capponi's co-authors include Paola Mandich, Alessandro Geroldi, Emilia Bellone, Fiore Manganelli, Marina Grandis, Paola Fossa, Rossella Gulli, Chiara Pisciotta, Paola Ciotti and Angelo Schenone and has published in prestigious journals such as Nature Communications, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Simona Capponi

16 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simona Capponi Italy 12 222 211 92 76 74 16 405
Alessandro Geroldi Italy 13 285 1.3× 214 1.0× 134 1.5× 90 1.2× 94 1.3× 30 461
Estelle Arnaud Switzerland 7 194 0.9× 227 1.1× 58 0.6× 73 1.0× 63 0.9× 7 381
Dorothée Bleckmann Switzerland 8 172 0.8× 228 1.1× 81 0.9× 38 0.5× 31 0.4× 9 334
Alexander P. Drew Australia 10 148 0.7× 152 0.7× 35 0.4× 45 0.6× 84 1.1× 15 303
M. Zimoń Belgium 8 142 0.6× 134 0.6× 41 0.4× 73 1.0× 62 0.8× 10 301
Helle Høyer Norway 8 243 1.1× 97 0.5× 96 1.0× 50 0.7× 105 1.4× 17 329
Charles A. Wuertzer United States 7 194 0.9× 232 1.1× 271 2.9× 26 0.3× 60 0.8× 8 524
Isabelle Cournu‐Rebeix France 8 135 0.6× 219 1.0× 41 0.4× 68 0.9× 112 1.5× 12 443
Jeff Goldy United States 5 144 0.6× 168 0.8× 52 0.6× 43 0.6× 57 0.8× 5 316
Martina Marinello France 9 174 0.8× 349 1.7× 48 0.5× 81 1.1× 20 0.3× 11 438

Countries citing papers authored by Simona Capponi

Since Specialization
Citations

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

Fields of papers citing papers by Simona Capponi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simona Capponi

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

All Works

16 of 16 papers shown
1.
Capponi, Simona, Ellen B. Penney, Karen Grütz, et al.. (2021). Dissection of TAF1 neuronal splicing and implications for neurodegeneration in X-linked dystonia-parkinsonism. Brain Communications. 3(4). fcab253–fcab253. 10 indexed citations
2.
Conic, Sascha, Florian Mueller, Farrah El-Saafin, et al.. (2019). Co-translational assembly of mammalian nuclear multisubunit complexes. Nature Communications. 10(1). 1740–1740. 70 indexed citations
3.
Capponi, Simona, Manuel Irimia, F.M.A. van Schaik, et al.. (2019). Neuronal-specific microexon splicing of TAF1 mRNA is directly regulated by SRRM4/nSR100. RNA Biology. 17(1). 62–74. 17 indexed citations
4.
Parmeggiani, Antonia, Simona Capponi, Luca Spinardi, et al.. (2018). Neuropsychological profile in Italian children with neurofibromatosis type 1 (NF1) and their relationships with neuroradiological data: Preliminary results. European Journal of Paediatric Neurology. 22(5). 822–830. 13 indexed citations
5.
Capponi, Simona, Thomas Geuens, Alessandro Geroldi, et al.. (2016). Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1. Human Mutation. 37(11). 1202–1208. 39 indexed citations
6.
Pezzini, Ilaria, Alessandro Geroldi, Simona Capponi, et al.. (2015). GDAP1 mutations in Italian axonal Charcot–Marie–Tooth patients: Phenotypic features and clinical course. Neuromuscular Disorders. 26(1). 26–32. 17 indexed citations
7.
Tufano, Maria Antonietta, Gerarda Cappuccio, Gaetano Terrone, et al.. (2015). Early onset Charcot‐Marie‐Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2‐related neuropathy. Journal of the Peripheral Nervous System. 20(4). 415–418. 10 indexed citations
8.
Ciotti, Paola, Marco Luigetti, Alessandro Geroldi, et al.. (2014). A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot–Marie–Tooth disease. Journal of the Neurological Sciences. 343(1-2). 183–186. 15 indexed citations
9.
Manganelli, Fiore, Stefano Tozza, Chiara Pisciotta, et al.. (2014). Charcot‐Marie‐Tooth disease: frequency of genetic subtypes in a Southern Italy population. Journal of the Peripheral Nervous System. 19(4). 292–298. 61 indexed citations
10.
Capponi, Simona, Alessandro Geroldi, Ilaria Pezzini, et al.. (2014). Contribution of copy number variations in CMT1X: a retrospective study. European Journal of Neurology. 22(2). 406–409. 2 indexed citations
11.
Prada, Valeria, Simona Capponi, Antonia Albertí, et al.. (2014). Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation. Neuropathology. 35(3). 254–259. 3 indexed citations
12.
Palmieri, Daniela, et al.. (2013). TNFα induces the expression of genes associated with endothelial dysfunction through p38MAPK-mediated down-regulation of miR-149. Biochemical and Biophysical Research Communications. 443(1). 246–251. 34 indexed citations
13.
Manganelli, Fiore, Chiara Pisciotta, Maria Nolano, et al.. (2012). A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family. Journal of the Peripheral Nervous System. 17(3). 351–355. 11 indexed citations
14.
Capponi, Simona, Alessandro Geroldi, Paola Fossa, et al.. (2011). HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients. Journal of the Peripheral Nervous System. 16(4). 287–294. 51 indexed citations
15.
Prada, Valeria, Mario Passalacqua, Marı́a Rosa Bono, et al.. (2011). Gain of glycosylation: A new pathomechanism of myelin protein zero mutations. Annals of Neurology. 71(3). 427–431. 21 indexed citations
16.
Mandich, Paola, Paola Fossa, Simona Capponi, et al.. (2009). Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies. European Journal of Human Genetics. 17(9). 1129–1134. 31 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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