C. Scotton

1.2k total citations
20 papers, 541 citations indexed

About

C. Scotton is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, C. Scotton has authored 20 papers receiving a total of 541 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Neurology. Recurrent topics in C. Scotton's work include Muscle Physiology and Disorders (13 papers), RNA Research and Splicing (5 papers) and Genetic Neurodegenerative Diseases (4 papers). C. Scotton is often cited by papers focused on Muscle Physiology and Disorders (13 papers), RNA Research and Splicing (5 papers) and Genetic Neurodegenerative Diseases (4 papers). C. Scotton collaborates with scholars based in Italy, United Kingdom and United States. C. Scotton's co-authors include Alessandra Ferlini, Chiara Passarelli, Francesca Gualandi, Marcella Neri, Maria Sofia Falzarano, Matteo Bovolenta, Rita Selvatici, Annarita Armaroli, Giuseppe Novelli and Hanns Lochmüller and has published in prestigious journals such as PLoS ONE, Molecules and Experimental Cell Research.

In The Last Decade

C. Scotton

18 papers receiving 530 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. Scotton Italy 14 443 89 84 73 65 20 541
Zhijian Yang China 15 319 0.7× 57 0.6× 61 0.7× 129 1.8× 21 0.3× 52 585
Cíntia Yuri Matsumura Brazil 12 398 0.9× 61 0.7× 57 0.7× 28 0.4× 40 0.6× 22 510
Meriel McEntagart United Kingdom 14 273 0.6× 101 1.1× 157 1.9× 149 2.0× 66 1.0× 24 576
Wenjun Xu China 15 321 0.7× 124 1.4× 103 1.2× 45 0.6× 29 0.4× 54 615
S. Saredi Italy 13 376 0.8× 50 0.6× 131 1.6× 48 0.7× 49 0.8× 24 540
Robyn Labrum United Kingdom 14 488 1.1× 145 1.6× 400 4.8× 84 1.2× 44 0.7× 21 772
Tiziana Mongini Italy 14 399 0.9× 117 1.3× 141 1.7× 56 0.8× 48 0.7× 46 595
Mirko Vukcevic Switzerland 13 296 0.7× 124 1.4× 93 1.1× 10 0.1× 74 1.1× 17 462
M.L. Mostacciuolo Italy 12 289 0.7× 119 1.3× 113 1.3× 22 0.3× 88 1.4× 18 466

Countries citing papers authored by C. Scotton

Since Specialization
Citations

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

Fields of papers citing papers by C. Scotton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Scotton

This figure shows the co-authorship network connecting the top 25 collaborators of C. Scotton. A scholar is included among the top collaborators of C. Scotton 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 C. Scotton. C. Scotton 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.
Franceschi, Roberto, C. Scotton, Vittoria Cauvin, et al.. (2022). Impact of intermittently scanned continuous glucose monitoring with alarms on sleep and metabolic outcomes in children and adolescents with type 1 diabetes. Acta Diabetologica. 59(7). 911–919. 7 indexed citations
2.
Rossi, Rachele, Maria Sofia Falzarano, Annarita Armaroli, et al.. (2021). Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients. Frontiers in Physiology. 12. 678974–678974. 5 indexed citations
3.
Gualandi, Francesca, Elisabetta Sette, F. Fortunato, et al.. (2019). Report of a novel ATP7A mutation causing distal motor neuropathy. Neuromuscular Disorders. 29(10). 776–785. 13 indexed citations
4.
Gherardi, Samuele, Matteo Bovolenta, Chiara Passarelli, et al.. (2017). Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1860(11). 1138–1147. 8 indexed citations
5.
Harris, Elizabeth, Marcella Neri, C. Scotton, et al.. (2017). Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains. Neuromuscular Disorders. 27(9). 861–872. 36 indexed citations
6.
Falzarano, Maria Sofia, Domenico D’Amario, A. Siracusano, et al.. (2016). Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype. Human Gene Therapy. 27(10). 772–783. 18 indexed citations
7.
Schindler, R., C. Scotton, Vanessa French, Alessandra Ferlini, & Thomas Brand. (2016). The Popeye Domain Containing Genes and Their Function in Striated Muscle. Journal of Cardiovascular Development and Disease. 3(2). 22–22. 13 indexed citations
8.
Armaroli, Annarita, Cecilia Trabanelli, C. Scotton, et al.. (2015). Paternal germline mosaicism in collagen VI related myopathies. European Journal of Paediatric Neurology. 19(5). 533–536. 17 indexed citations
9.
Scotton, C., et al.. (2015). Duchenne Muscular Dystrophy: From Diagnosis to Therapy. Molecules. 20(10). 18168–18184. 194 indexed citations
10.
Scotton, C., Chiara Passarelli, Marcella Neri, & Alessandra Ferlini. (2014). Biomarkers in rare neuromuscular diseases. Experimental Cell Research. 325(1). 44–49. 22 indexed citations
11.
Palma, Sara De, Daniele Capitanio, Michele Vasso, et al.. (2014). Muscle Proteomics Reveals Novel Insights into the Pathophysiological Mechanisms of Collagen VI Myopathies. Journal of Proteome Research. 13(11). 5022–5030. 32 indexed citations
12.
Neri, Marcella, Rita Selvatici, C. Scotton, et al.. (2013). A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation. Neuromuscular Disorders. 23(6). 478–482. 19 indexed citations
13.
Guglielmi, Valeria, Gaetano Vattemi, Francesca Gualandi, et al.. (2013). SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. Molecular Genetics and Metabolism. 110(1-2). 162–169. 26 indexed citations
14.
Ferlini, Alessandra, C. Scotton, & Giuseppe Novelli. (2013). Biomarkers in Rare Diseases. Public Health Genomics. 16(6). 313–321. 15 indexed citations
15.
Zanni, Ginevra, C. Scotton, Chiara Passarelli, et al.. (2013). Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3. Neurogenetics. 14(3-4). 247–250. 24 indexed citations
16.
Voermans, Nicol C., Arie Oosterhof, Toin H. Van Kuppevelt, et al.. (2012). Brody syndrome: A clinically heterogeneous entity distinct from Brody disease. Neuromuscular Disorders. 22(11). 944–954. 31 indexed citations
17.
Bovolenta, Matteo, Emanuele Valli, Simona Brioschi, et al.. (2012). The DMD Locus Harbours Multiple Long Non-Coding RNAs Which Orchestrate and Control Transcription of Muscle Dystrophin mRNA Isoforms. PLoS ONE. 7(9). e45328–e45328. 43 indexed citations
18.
Voermans, Nicol C., Arie Oosterhof, Gea Drost, et al.. (2012). G.P.103 Brody syndrome: a clinically heterogeneous entity distinct from Brody disease: A review of literature and a cross-sectional clinical study in 17 patients. Neuromuscular Disorders. 22(9-10). 899–899.
19.
Neri, Marcella, Matteo Bovolenta, C. Scotton, et al.. (2012). D.P.9 Whole exome sequencing filtered by novel candidate genes as tool for gene discovery in a recessive family with Parkinson and ataxia. Neuromuscular Disorders. 22(9-10). 810–810.
20.
Bovolenta, Matteo, C. Scotton, Maria Sofia Falzarano, Francesca Gualandi, & Alessandra Ferlini. (2011). Rapid, comprehensive analysis of the dystrophin transcript by a custom micro-fluidic exome array. Human Mutation. 33(3). 572–581. 18 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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