C. Scotton

1.2k citations

20 papers · 541 indexed · h-index 14

Co-authors: Alessandra Ferlini Chiara Passarelli Francesca Gualandi Marcella Neri Maria Sofia Falzarano Matteo Bovolenta Rita Selvatici Annarita Armaroli
Topics: Muscle Physiology and Disorders (13 papers)RNA Research and Splicing (5 papers)Genetic Neurodegenerative Diseases (4 papers)
Cited by: Sensory Systems Molecular Biology Genetics
Journals: PLoS ONE Molecules Experimental Cell Research
Partner nations: Italy United Kingdom United States

In The Last Decade

C. Scotton

18 papers receiving 530 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Impact of intermittently scanned continuous glucose monitoring with alarms on sleep and metabolic outcomes in children and adolescents with type 1 diabetes 2022 ·Acta Diabetologica ·Roberto Franceschi,C. Scotton,(unknown),Vittoria Cauvin,Evelina Maines,Marco Angriman,(unknown),Francesca Valent,Massimo Soffiati,Ugo Faraguna	7
2	Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients 2021 ·Frontiers in Physiology ·Rachele Rossi,Maria Sofia Falzarano,(unknown),Annarita Armaroli,C. Scotton,Paola Mantuano,(unknown),Ornella Cappellari,Elena Schwartz,Anton Yuryev,Eugenio Mercuri,Enrico Bertini,Adele D’Amico,Marina Mora,Camilla Johansson,Cristina Al‐Khalili Szigyarto,Annamaria De Luca,Alessandra Ferlini	5
3	Report of a novel ATP7A mutation causing distal motor neuropathy 2019 ·Neuromuscular Disorders ·Francesca Gualandi,Elisabetta Sette,F. Fortunato,Stefania Bigoni,D. De Grandis,C. Scotton,Rita Selvatici,Marcella Neri,Alex Incensi,Rocco Liguori,Markus Storbeck,Mert Karakaya,V. Simioni,Stefano Squarzoni,Vincent Timmerman,Brunhilde Wirth,Vincenzo Donadio,V. Tugnoli,Alessandra Ferlini	13
4	Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression 2017 ·Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms ·Samuele Gherardi,Matteo Bovolenta,Chiara Passarelli,Maria Sofia Falzarano,(unknown),C. Scotton,Marcella Neri,Annarita Armaroli,(unknown),Rita Selvatici,Francesca Gualandi,Alessandra Recchia,Marina Mora,Pia Bernasconi,Lorenzo Maggi,Lucía Morandi,Alessandra Ferlini,Giovanni Perini	8
5	Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains 2017 ·Neuromuscular Disorders ·Elizabeth Harris,(unknown),(unknown),Marcella Neri,C. Scotton,Judith A. Hudson,Marta Bertoli,Teresinha Evangelista,Bas Vroling,Tuomo Polvikoski,Mark Roberts,Ana Töpf,Kate Bushby,(unknown),Hanns Lochmüller,Alessandra Ferlini,Volker Straub,Rita Barresi	36
6	Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 2016 ·Human Gene Therapy ·Maria Sofia Falzarano,Domenico D’Amario,A. Siracusano,Massimo Massetti,Antonio Amodeo,(unknown),(unknown),Eugenio Mercuri,(unknown),C. Scotton,Annarita Armaroli,Rachele Rossi,Rita Selvatici,Filippo Crea,Alessandra Ferlini	18
7	The Popeye Domain Containing Genes and Their Function in Striated Muscle 2016 ·Journal of Cardiovascular Development and Disease ·R. Schindler,C. Scotton,Vanessa French,Alessandra Ferlini,Thomas Brand	13
8	Paternal germline mosaicism in collagen VI related myopathies 2015 ·European Journal of Paediatric Neurology ·Annarita Armaroli,Cecilia Trabanelli,C. Scotton,(unknown),Rita Selvatici,Giacomo Brisca,Luciano Merlini,Claudio Bruno,Alessandra Ferlini,Francesca Gualandi	17
9	Duchenne Muscular Dystrophy: From Diagnosis to Therapy 2015 ·Molecules ·(unknown),C. Scotton,Chiara Passarelli,Alessandra Ferlini	194
10	Biomarkers in rare neuromuscular diseases 2014 ·Experimental Cell Research ·C. Scotton,Chiara Passarelli,Marcella Neri,Alessandra Ferlini	22
11	Muscle Proteomics Reveals Novel Insights into the Pathophysiological Mechanisms of Collagen VI Myopathies 2014 ·Journal of Proteome Research ·Sara De Palma,Daniele Capitanio,Michele Vasso,Paola Braghetta,C. Scotton,Paolo Bonaldo,Hanns Lochmüller,Francesco Muntoni,Alessandra Ferlini,Cecilia Gelfi	32
12	A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 2013 ·Neuromuscular Disorders ·Marcella Neri,Rita Selvatici,C. Scotton,Cecilia Trabanelli,Annarita Armaroli,D. De Grandis,Nicolas Lévy,Francesca Gualandi,Alessandra Ferlini	19
13	SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers 2013 ·Molecular Genetics and Metabolism ·Valeria Guglielmi,Gaetano Vattemi,Francesca Gualandi,Nicol C. Voermans,Matteo Marini,C. Scotton,Elena Pegoraro,Arie Oosterhof,(unknown),Ernő Zádor,Enza Maria Valente,D. De Grandis,Marcella Neri,(unknown),Antonio Novelli,Toin H. Van Kuppevelt,Bruno Dallapiccola,Baziel G.M. van Engelen,Alessandra Ferlini,Giuliano Tomelleri	26
14	Biomarkers in Rare Diseases 2013 ·Public Health Genomics ·Alessandra Ferlini,C. Scotton,Giuseppe Novelli	15
15	Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3 2013 ·Neurogenetics ·Ginevra Zanni,C. Scotton,Chiara Passarelli,Mingyan Fang,Sabina Barresi,Bruno Dallapiccola,Bin Wu,Francesca Gualandi,Alessandra Ferlini,Enrico Bertini,Wei Wang	24
16	Brody syndrome: A clinically heterogeneous entity distinct from Brody disease 2012 ·Neuromuscular Disorders ·Nicol C. Voermans,(unknown),Arie Oosterhof,Toin H. Van Kuppevelt,Gea Drost,Martin Lammens,Erik‐Jan Kamsteeg,C. Scotton,Francesca Gualandi,Valeria Guglielmi,Lambertus P. van den Heuvel,Gaetano Vattemi,Baziel G.M. van Engelen	31
17	The DMD Locus Harbours Multiple Long Non-Coding RNAs Which Orchestrate and Control Transcription of Muscle Dystrophin mRNA Isoforms 2012 ·PLoS ONE ·Matteo Bovolenta,(unknown),Emanuele Valli,Simona Brioschi,C. Scotton,Marcella Neri,Maria Sofia Falzarano,Samuele Gherardi,M. Fabris,Paola Rimessi,Francesca Gualandi,Giovanni Perini,Alessandra Ferlini	43
18	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 2012 ·Neuromuscular Disorders ·Nicol C. Voermans,(unknown),Arie Oosterhof,(unknown),Gea Drost,Martin Lammens,Erik-Jan Kamsteeg,C. Scotton,Francesca Gualandi,Valeria Guglielmi,Lambert van den Heuvel,Gaetano Vattemi,Baziel G.M. van Engelen	0
19	D.P.9 Whole exome sequencing filtered by novel candidate genes as tool for gene discovery in a recessive family with Parkinson and ataxia 2012 ·Neuromuscular Disorders ·Marcella Neri,Matteo Bovolenta,C. Scotton,D. De Grandis,Tiziana Castrignanò,Bruno Dallapiccola,Francesca Gualandi,Alessandra Ferlini	0
20	Rapid, comprehensive analysis of the dystrophin transcript by a custom micro-fluidic exome array 2011 ·Human Mutation ·Matteo Bovolenta,C. Scotton,Maria Sofia Falzarano,Francesca Gualandi,Alessandra Ferlini	18

About C. Scotton

C. Scotton is a scholar working on Developmental Biology, Molecular Biology and Cellular and Molecular Neuroscience, having authored 20 papers that have together received 541 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (13 papers), RNA Research and Splicing (5 papers) and Genetic Neurodegenerative Diseases (4 papers). The work is most often cited by research in Sensory Systems (34 citations), Molecular Biology (443 citations) and Genetics (65 citations). C. Scotton has collaborated with scholars based in Italy, United Kingdom and United States. Frequent 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. Their work appears in journals such as PLoS ONE, Molecules and Experimental Cell Research.

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