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G. Ricci · SciRah

Researcher profile · Semantic Scholar

G. Ricci

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G. Ricci — researcher profile on SciRah

h-index: 32
Works: 116
Citations: 3,126

Most-cited papers

Nusinersen safety and effects on motor function in adult spinal muscular atrophy type 2 and 3
L. Maggi, L. Bello, S. Bonanno, A. Govoni +37 more
2020Journal of Neurology Neurosurgery & Psychiatry149 citations Open access
Semantic Scholar
Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral muscular dystrophy.
I. Scionti, F. Greco, G. Ricci, M. Govi +20 more
2012American Journal of Human Genetics122 citations Open access
Semantic Scholar
Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy
G. Ricci, I. Scionti, F. Sera, M. Govi +30 more
2013Brain : a journal of neurology109 citations Open access
Semantic Scholar
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis
F. Magri, V. Nigro, C. Angelini, T. Mongini +29 more
2017Muscle and Nerve96 citations Open access
Semantic Scholar
Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
S. Baldanzi, F. Bevilacqua, R. Lorio, L. Volpi +8 more
2016Orphanet Journal of Rare Diseases86 citations Open access
Semantic Scholar
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes
G. Ricci, L. Ruggiero, L. Vercelli, F. Sera +24 more
2016Journal of Neurology84 citations Open access
Semantic Scholar
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients
M. Savarese, G. Di Fruscio, A. Torella, C. Fiorillo +54 more
2016Neurology82 citations Open access
Semantic Scholar
Next-Generation Sequencing Identifies Transportin 3 as the Causative Gene for LGMD1F
A. Torella, M. Fanin, M. Mutarelli, E. Peterle +10 more
2013PLoS ONE74 citations Open access
Semantic Scholar
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1–3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry
A. Nikolić, G. Ricci, F. Sera, E. Bucci +27 more
2016BMJ Open73 citations Open access
Semantic Scholar
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy
V. Barone, V. Del Re, A. Gamberucci, V. Polverino +17 more
2017Human Mutation71 citations Open access
Semantic Scholar
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates
D. Rossi, B. Vezzani, L. Galli, Cecilia Paolini +14 more
2014Human Mutation71 citations Open access
Semantic Scholar
Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients
I. Faravelli, M. Meneri, D. Saccomanno, D. Velardo +17 more
2020Journal of Cellular and Molecular Medicine70 citations Open access
Semantic Scholar
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype
S. Brioschi, F. Gualandi, C. Scotton, A. Armaroli +17 more
2012BMC Medical Genetics70 citations Open access
Semantic Scholar
Folate, Homocysteine, Vitamin B12, and Polymorphisms of Genes Participating in One-Carbon Metabolism in Late-Onset Alzheimer's Disease Patients and Healthy Controls
F. Coppedè, P. Tannorella, I. Pezzini, F. Migheli +9 more
2012Antioxidants and Redox Signaling69 citations
Semantic Scholar
Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling
I. Scionti, G. Fabbri, C. Fiorillo, G. Ricci +9 more
2012Journal of Medical Genetics60 citations Open access
Semantic Scholar
Oxidative Stress Treatment for Clinical Trials in Neurodegenerative Diseases
E. C. Ienco, Annalisa LoGerfo, C. Carlesi, D. Orsucci +3 more
2011Journal of Alzheimer's Disease56 citations
Semantic Scholar
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy
L. Ruggiero, F. Mele, F. Manganelli, D. Bruzzese +23 more
2020JAMA Network Open52 citations Open access
Semantic Scholar
CMR-verified interstitial myocardial fibrosis as a marker of subclinical cardiac involvement in LMNA mutation carriers.
M. Fontana, A. Barison, N. Botto, L. Panchetti +9 more
2013JACC Cardiovascular Imaging49 citations Open access
Semantic Scholar
LMNA-associated myopathies
L. Maggi, A. D'Amico, A. Pini, S. Sivo +26 more
2014Neurology48 citations
Semantic Scholar
“I have got something positive out of this situation”: psychological benefits of caregiving in relatives of young people with muscular dystrophy
L. Magliano, Melania Patalano, A. Sagliocchi, M. Scutifero +25 more
2013Journal of Neurology45 citations Open access
Semantic Scholar
Muscle exercise in limb girdle muscular dystrophies: pitfall and advantages
G. Siciliano, C. Simoncini, S. Giannotti, V. Zampa +2 more
2015Acta myologica44 citations
Semantic Scholar
Cardiac and Neuromuscular Features of Patients With LMNA-Related Cardiomyopathy
G. Peretto, C. Di Resta, J. Perversi, C. Forleo +36 more
2019Annals of Internal Medicine43 citations
Semantic Scholar
Effects of aerobic training on exercise-related oxidative stress in mitochondrial myopathies
G. Siciliano, C. Simoncini, A. L. Gerfo, D. Orsucci +2 more
2012Neuromuscular Disorders41 citations Open access
Semantic Scholar
Study of the porcine dermal collagen repair patch in morpho-functional recovery of the rotator cuff after minimum follow-up of 2.5 years.
S. Giannotti, M. Ghilardi, G. Dell'osso, L. Magistrelli +6 more
2014Surgical technology international40 citations
Semantic Scholar
Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears
G. Ricci, M. Zatz, R. Tupler
2014Current molecular medicine39 citations Open access
Semantic Scholar
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for “double trouble” overlapping syndromes
G. Ricci, I. Scionti, G. Alí, L. Volpi +6 more
2012Neuromuscular Disorders36 citations Open access
Semantic Scholar
A multicentre retrospective study of Charcot-Marie-Tooth disease type 4B (CMT4B) due to mutations in Myotubularin-related proteins (MTMRs)
D. Pareyson, T. Stojkovic, M. Reilly, S. Léonard-Louis +38 more
2019Annals of Neurology34 citations Open access
Semantic Scholar
Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes
P. Bernasconi, Nicola Carboni, G. Ricci, G. Siciliano +22 more
2018The Nucleus33 citations Open access
Semantic Scholar
Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis
G. Ricci, F. Mele, M. Govi, L. Ruggiero +26 more
2020Scientific Reports32 citations Open access
Semantic Scholar
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase
E. Mauri, Elena Abati, O. Musumeci, C. Rodolico +71 more
2020Acta myologica32 citations
Semantic Scholar
ClC‐1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype–phenotype correlation
P. Imbrici, L. Maggi, G. Mangiatordi, M. M. Dinardo +15 more
2015Journal of Physiology30 citations Open access
Semantic Scholar
Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies
A. Nikolić, Takako I. Jones, M. Govi, F. Mele +31 more
2020International Journal of Molecular Sciences28 citations Open access
Semantic Scholar
The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME.
J. Senderek, P. Laššuthová, D. Kabzińska, Lisa Abreu +53 more
2020Neurology27 citations Open access
Semantic Scholar
A 5-year clinical follow-up study from the Italian National Registry for FSHD
L. Vercelli, F. Mele, L. Ruggiero, F. Sera +23 more
2020Journal of Neurology26 citations Open access
Semantic Scholar
Therapeutic opportunities and clinical outcome measures in Duchenne muscular dystrophy
G. Ricci, L. Bello, F. Torri, E. Schirinzi +2 more
2022Neurological Sciences24 citations Open access
Semantic Scholar
Central Nervous System Involvement as Outcome Measure for Clinical Trials Efficacy in Myotonic Dystrophy Type 1
C. Simoncini, G. Spadoni, E. Lai, L. Santoni +3 more
2020Frontiers in Neurology24 citations Open access
Semantic Scholar
Exercise-Related Oxidative Stress as Mechanism to Fight Physical Dysfunction in Neuromuscular Disorders
G. Siciliano, L. Chico, Annalisa LoGerfo, C. Simoncini +2 more
2020Frontiers in Physiology23 citations Open access
Semantic Scholar
Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort
V. Montano, P. Lopriore, F. Gruosso, V. Carelli +20 more
2022Journal of Neurology22 citations Open access
Semantic Scholar
Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies
P. Imbrici, C. Altamura, G. Camerino, G. Mangiatordi +15 more
2016The FASEB Journal22 citations Open access
Semantic Scholar
Phenotype may predict the clinical course of facioscapolohumeral muscular dystrophy
G. Ricci, P. Cammish, G. Siciliano, R. Tupler +2 more
2019Muscle and Nerve20 citations Open access
Semantic Scholar
Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective study
I. Faravelli, Delia Gagliardi, Elena Abati, M. Meneri +14 more
2023Cellular and Molecular Life Sciences19 citations Open access
Semantic Scholar
Exercise therapy in muscle diseases: open issues and future perspectives
G. Siciliano, E. Schirinzi, C. Simoncini, G. Ricci
2019Acta myologica19 citations
Semantic Scholar
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease
L. Maggi, L. Bello, S. Bonanno, A. Govoni +41 more
2022Journal of Neurology Neurosurgery & Psychiatry18 citations
Semantic Scholar
Pathophysiology and Management of Fatigue in Neuromuscular Diseases
F. Torri, P. Lopriore, V. Montano, G. Siciliano +2 more
2023International Journal of Molecular Sciences17 citations Open access
Semantic Scholar
Psychosocial impact of sport activity in neuromuscular disorders
Giuseppe Vita, C. Stancanelli, S. La Foresta, C. Faraone +17 more
2020Neurological Sciences17 citations
Semantic Scholar
Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patients.
R. Brugnoni, L. Maggi, Eleonora Canioni, F. Verde +24 more
2020Neuromuscular Disorders17 citations
Semantic Scholar
Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross‐sectional study
Delia Gagliardi, I. Faravelli, M. Meneri, D. Saccomanno +6 more
2021Journal of Cellular and Molecular Medicine16 citations Open access
Semantic Scholar
A mobile app for patients with Pompe disease and its possible clinical applications.
G. Ricci, S. Baldanzi, Fabrizio Seidita, C. Proietti +20 more
2018Neuromuscular Disorders16 citations Open access
Semantic Scholar
Cross-talk between pathogenic mechanisms in neurodegeneration: the role of oxidative stress in Amyotrophic Lateral Sclerosis.
L. Chico, M. Modena, Annalisa LoGerfo, G. Ricci +4 more
2017Archives Italiennes de Biologie16 citations
Semantic Scholar
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience
F. Fortunato, Francesca Bianchi, G. Ricci, F. Torri +47 more
2023Orphanet Journal of Rare Diseases14 citations Open access
Semantic Scholar

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G. Siciliano×43
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G. Siciliano — researcher profile on SciRah
E. Pegoraro×18
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E. Pegoraro — researcher profile on SciRah
L. Maggi×17
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L. Maggi — researcher profile on SciRah
T. Mongini×17
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T. Mongini — researcher profile on SciRah

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C. Angelini — researcher profile on SciRah

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M. Filosto — researcher profile on SciRah

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L. Santoro — researcher profile on SciRah

A. Berardinelli×13

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A. Berardinelli — researcher profile on SciRah

L. Vercelli×13

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L. Vercelli — researcher profile on SciRah

C. Rodolico×13

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C. Rodolico — researcher profile on SciRah

L. Ruggiero×13

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L. Ruggiero — researcher profile on SciRah

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R. Tupler — researcher profile on SciRah