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S. Zanotti · SciRah

Researcher profile · Semantic Scholar

S. Zanotti

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S. Zanotti — researcher profile on SciRah

h-index: 22
Works: 63
Citations: 1,394

Most-cited papers

Altered extracellular matrix transcript expression and protein modulation in primary Duchenne muscular dystrophy myotubes.
S. Zanotti, S. Saredi, A. Ruggieri, M. Fabbri +4 more
2007Matrix Biology94 citations
Semantic Scholar
Decorin and biglycan expression is differentially altered in several muscular dystrophies.
S. Zanotti, T. Negri, C. Cappelletti, P. Bernasconi +9 more
2005Brain : a journal of neurology91 citations Open access
Semantic Scholar
Exosomes and exosomal miRNAs from muscle-derived fibroblasts promote skeletal muscle fibrosis
S. Zanotti, S. Gibertini, F. Blàsevich, C. Bragato +7 more
2018bioRxiv85 citations Open access
Semantic Scholar
Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy.
S. Zanotti, S. Gibertini, Maurizio Curcio, P. Savadori +5 more
2015Biochimica et Biophysica Acta85 citations Open access
Semantic Scholar
Role of the TFG N-terminus and coiled-coil domain in the transforming activity of the thyroid TRK-T3 oncogene
A. Greco, L. Fusetti, C. Miranda, Riccardo Villa +3 more
1998Oncogene80 citations Open access
Semantic Scholar
Changes of Synaptotagmin Interaction with t‐SNARE Proteins In Vitro After Calcium/Calmodulin‐Dependent Phosphorylation
M. Verona, S. Zanotti, T. Schäfer, G. Racagni +1 more
2000Journal of Neurochemistry65 citations
Semantic Scholar
Osteopontin is highly expressed in severely dystrophic muscle and seems to play a role in muscle regeneration and fibrosis
S. Zanotti, S. Gibertini, C. Di Blasi, C. Cappelletti +4 more
2011Histopathology63 citations
Semantic Scholar
Altered production of extra-cellular matrix components by muscle-derived Duchenne muscular dystrophy fibroblasts before and after TGF-β1 treatment
S. Zanotti, S. Gibertini, M. Mora
2010Cell and Tissue Research58 citations
Semantic Scholar
Engineering an Environment for the Study of Fibrosis: A 3D Human Muscle Model with Endothelium Specificity and Endomysium.
S. Bersini, M. Gilardi, Giovanni Stefano Ugolini, V. Sansoni +9 more
2018Cell Reports57 citations Open access
Semantic Scholar
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy
A. Ruggieri, F. Brancati, S. Zanotti, L. Maggi +14 more
2015Acta Neuropathologica Communications55 citations Open access
Semantic Scholar
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
Q. Gang, C. Bettencourt, P. Machado, Stefen Brady +50 more
2016Neurobiology of Aging52 citations Open access
Semantic Scholar
Genetic and Epigenetic Characteristics of FSHD-Associated 4q and 10q D4Z4 that are Distinct from Non-4q/10q D4Z4 Homologs
Weihua Zeng, Yen-yun Chen, Daniel A. Newkirk, Bei-Bei Wu +9 more
2014Human Mutation51 citations Open access
Semantic Scholar
Tackling muscle fibrosis: From molecular mechanisms to next generation engineered models to predict drug delivery.
S. Bersini, M. Gilardi, Marina Mora, S. Krol +4 more
2018Advanced Drug Delivery Reviews45 citations Open access
Semantic Scholar
CASQ1 mutations impair calsequestrin polymerization and cause tubular aggregate myopathy
J. Böhm, X. Lornage, F. Chevessier, C. Birck +11 more
2017Acta Neuropathologica45 citations
Semantic Scholar
DNAJB6 Myopathies: Focused Review on an Emerging and Expanding Group of Myopathies
A. Ruggieri, S. Saredi, S. Zanotti, M. Pasanisi +2 more
2016Frontiers in Molecular Biosciences41 citations Open access
Semantic Scholar
Anti-fibrotic effect of pirfenidone in muscle derived-fibroblasts from Duchenne muscular dystrophy patients.
S. Zanotti, C. Bragato, Andrea Zucchella, L. Maggi +3 more
2016Life Science35 citations
Semantic Scholar
Genetic dissection of dome formation in a mammary cell line: identification of two genes with opposing action.
I. Zucchi, C. Montagna, L. Susani, R. Montesano +5 more
1999Proceedings of the National Academy of Sciences of the United States of America33 citations Open access
Semantic Scholar
Fibroblasts from the muscles of Duchenne muscular dystrophy patients are resistant to cell detachment apoptosis.
S. Zanotti, S. Gibertini, C. Bragato, R. Mantegazza +2 more
2011Experimental Cell Research32 citations
Semantic Scholar
Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein
M. Hanel, C. Sun, Takako I. Jones, Steven W. Long +3 more
2011Differentiation; research in biological diversity30 citations Open access
Semantic Scholar
LAMA2 gene analysis in congenital muscular dystrophy: new mutations, prenatal diagnosis, and founder effect.
C. Di Blasi, D. Piga, P. Brioschi, I. Moroni +11 more
2005Archives of Neurology29 citations
Semantic Scholar
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy
M. Ripolone, D. Velardo, S. Mondello, S. Zanotti +10 more
2022Acta Neuropathologica Communications28 citations Open access
Semantic Scholar
Fibrosis and inflammation are greater in muscles of beta-sarcoglycan-null mouse than mdx mouse
S. Gibertini, S. Zanotti, P. Savadori, Maurizio Curcio +6 more
2014Cell and Tissue Research27 citations
Semantic Scholar
The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis
Q. Gang, C. Bettencourt, P. Machado, Z. Fox +20 more
2015Neurobiology of Aging20 citations Open access
Semantic Scholar
A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia
C. Di Blasi, Serena Sansanelli, A. Ruggieri, M. Moriggi +11 more
2015Journal of Medical Genetics19 citations
Semantic Scholar
A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylation.
S. Saredi, S. Gibertini, A. Ardissone, I. Fusco +5 more
2014European journal of paediatric neurology17 citations
Semantic Scholar
Duchenne muscular dystrophy fibroblast nodules: a cell-based assay for screening anti-fibrotic agents
S. Zanotti, S. Gibertini, P. Savadori, R. Mantegazza +1 more
2013Cell and Tissue Research17 citations
Semantic Scholar
A rare mutation in MYH7 gene occurs with overlapping phenotype.
L. Ruggiero, C. Fiorillo, S. Gibertini, F. de Stefano +7 more
2015Biochemical and Biophysical Research Communications - BBRC16 citations
Semantic Scholar
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes
S. Zanotti, F. Magri, S. Salani, L. Napoli +12 more
2023International Journal of Molecular Sciences14 citations Open access
Semantic Scholar
Megaconial congenital muscular dystrophy due to novel CHKB variants: a case report and literature review
F. Magri, Sara Antognozzi, M. Ripolone, S. Zanotti +13 more
2022Skeletal Muscle13 citations Open access
Semantic Scholar
Genetic defects are common in myopathies with tubular aggregates
Q. Gang, C. Bettencourt, S. Brady, J. Holton +16 more
2021Annals of Clinical and Translational Neurology13 citations Open access
Semantic Scholar
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy
D. Ronchi, M. Garbellini, F. Magri, F. Menni +22 more
2023European Journal of Human Genetics11 citations Open access
Semantic Scholar
A novel RRM2B mutation associated with mitochondrial DNA depletion syndrome
M. Fumagalli, D. Ronchi, M. Bedeschi, Arianna Manini +11 more
2022Molecular Genetics and Metabolism Reports9 citations Open access
Semantic Scholar
Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvement
S. Saredi, A. Ruggieri, E. Mottarelli, A. Ardissone +5 more
2009Muscle and Nerve8 citations
Semantic Scholar
Immunofluorescence signal intensity measurements as a semi-quantitative tool to assess sarcoglycan complex expression in muscle biopsy
S. Zanotti, F. Magri, Francesca Poggetti, M. Ripolone +7 more
2022European Journal of Histochemistry6 citations Open access
Semantic Scholar
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene
S. Zanotti, M. Ripolone, L. Napoli, D. Velardo +11 more
2023Cells5 citations Open access
Semantic Scholar
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization
M. Ripolone, S. Zanotti, L. Napoli, D. Ronchi +4 more
2023Journal of Personalized Medicine5 citations Open access
Semantic Scholar
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant
M. Rimoldi, F. Magri, Sara Antognozzi, M. Ripolone +10 more
2023Frontiers in Genetics5 citations Open access
Semantic Scholar
Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
Arianna Manini, L. Caporali, M. Meneri, S. Zanotti +8 more
2022Frontiers in Genetics5 citations Open access
Semantic Scholar
MicroRNAs as serum biomarkers in Becker muscular dystrophy
Delia Gagliardi, M. Rizzuti, Roberta Brusa, M. Ripolone +11 more
2022Journal of Cellular and Molecular Medicine4 citations Open access
Semantic Scholar
Traumatic Brain Injury Triggers Neurodegeneration in a Mildly Symptomatic MELAS Patient: Implications on the Detrimental Role of Damaged Mitochondria in Determining Head Trauma Sequalae in the General Population
S. Zanotti, D. Velardo, M. Sciacco
2022Metabolites3 citations Open access
Semantic Scholar
Test of Antifibrotic Drugs in a Cellular Model of Fibrosis Based on Muscle-Derived Fibroblasts from Duchenne Muscular Dystrophy Patients.
S. Zanotti, M. Mora
2018Methods in molecular biology3 citations
Semantic Scholar
Botulinum toxin type A affects the transcriptome of cell cultures derived from muscle biopsies of controls and spastic patients.
S. Zanotti, D. Kapetis, S. Gibertini, F. Salerno +7 more
2018Toxicology in Vitro3 citations
Semantic Scholar
Biobank of Cells, Tissues and DNA from Patients with Neuromuscular Diseases: An Indispensable link between Clinical Centers and the Scientific Community
M. Mora, C. Bragato, S. Gibertini, S. Zanotti +11 more
20173 citations Open access
Semantic Scholar
Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy.
C. Di Blasi, F. Blàsevich, Emanuela Bellafiore, E. Mottarelli +6 more
2010Neuromuscular Disorders3 citations
Semantic Scholar
Proteoglycans are Differentially Altered in Muscular Dystrophies
S. Zanotti, M. Mora
2006TheScientificWorldJournal3 citations Open access
Semantic Scholar
Peculiar histological and ultrastructural skeletal muscle alterations in a patient with CMV infection and autoimmune myositis: case evaluation and brief literature review.
M. Ripolone, L. Napoli, V. Mantero, M. Sciacco +1 more
2022Acta myologica2 citations
Semantic Scholar
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the SGCB Gene
F. Magri, S. Zanotti, S. Salani, F. Fortunato +9 more
2022International Journal of Molecular Sciences2 citations Open access
Semantic Scholar
P20.4 Antithetic role of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy
S. Zanotti, S. Gibertini, Paolo Savadori, Maurizio Curcio +3 more
20132 citations
Semantic Scholar
P.131 Building a FORCETM platform-based DMD franchise for the treatment of individuals with mutations amenable to exon skipping
C. Desjardins, R. Venkatesan, E. O'Donnell, J. Hall +7 more
2022Neuromuscular Disorders1 citations
Semantic Scholar
SQSTM1 and VCP mutations in a series of 205 inclusion body myositis cases
Q. Gang, C. Bettencourt, Stefen Brady, J. Holton +25 more
20151 citations
Semantic Scholar

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