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Alessandro Geroldi

Observed names: A. GEROLDI, A. Geroldi, Geroldi, A, Geroldi, Alessandro
Institution: University of Genoa
ORCID: 0000-0002-2208-9195
Observed ORCID: 0000-0002-2208-9195
OpenAlex ID: A5035853364
Charcot‐Marie‐Tooth disease: frequency of genetic subtypes in a Southern Italy population
2014 · Fiore Manganelli, Stefano Tozza, et al. · Journal of the Peripheral Nervous System · 78
HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients
2011 · Simona Capponi, Alessandro Geroldi, et al. · Journal of the Peripheral Nervous System · 72
Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1
2016 · Simona Capponi, Thomas Geuens, et al. · Human Mutation · 60
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Expanding the spectrum of genes responsible for hereditary motor neuropathies
2019 · Stefano C. Previtali, Edward Zhao, et al. · Journal of Neurology Neurosurgery & Psychiatry · 57
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TNFα induces the expression of genes associated with endothelial dysfunction through p38MAPK-mediated down-regulation of miR-149
2013 · Daniela Palmieri, Simona Capponi, et al. · Biochemical and Biophysical Research Communications · 43
Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies
2009 · Paola Mandich, Paola Fossa, et al. · European Journal of Human Genetics · 42
A multicenter retrospective study of charcot‐marie‐tooth disease type 4B (CMT4B) associated with mutations in myotubularin‐related proteins (MTMRs)
2019 · Davide Pareyson, Tanya Stojkovic, et al. · Annals of Neurology · 41
Severe Neuropathy After Diphtheria-Tetanus-Pertussis Vaccination in a Child Carrying a Novel Frame-Shift Mutation in the Small Heat-Shock Protein 27 Gene
2009 · Paola Mandich, Marina Grandis, et al. · Journal of Child Neurology · 33
Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype
2019 · Ilaria Callegari, C. Gemelli, et al. · Journal of Neurology · 32
Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients
2018 · Paola Origone, Alessandro Geroldi, et al. · Neurodegenerative Diseases · 29
Diagnostic Value of Sural Nerve Biopsy: Retrospective Analysis of Clinical Cases From 1981 to 2017
2019 · Valeria Prada, Sara Massucco, et al. · Frontiers in Neurology · 25
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GDAP1 mutations in Italian axonal Charcot–Marie–Tooth patients: Phenotypic features and clinical course
2015 · I. Pezzini, A. Geroldi, et al. · Neuromuscular Disorders · 23
Twenty years of molecular analyses in amyotrophic lateral sclerosis: genetic landscape of Italian patients
2018 · Merit Lamp, Paola Origone, et al. · Neurobiology of Aging · 22
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot–Marie–Tooth disease
2014 · Paola Ciotti, Marco Luigetti, et al. · Journal of the Neurological Sciences · 19
A novel mutation of Twinkle in Perrault syndrome: A not rare diagnosis?
2020 · Fabio Gotta, Merit Lamp, et al. · Annals of Human Genetics · 18
Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA repeats carrier
2018 · Paola Origone, Fabio Gotta, et al. · Cerebellum & Ataxias · 18
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Alternative Splicing in the HumanPMP22Gene: Implications in CMT1A Neuropathy
2015 · Davide Visigalli, Patrizio Castagnola, et al. · Human Mutation · 17
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Fast course ALS presenting with vocal cord paralysis: Clinical features, bioinformatic and modelling analysis of the novel SOD1 Gly147Ser mutation
2011 · Paola Origone, Claudia Caponnetto, et al. · Amyotrophic Lateral Sclerosis · 17
Early onset Charcot‐Marie‐Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2 ‐related neuropathy
2015 · Maria Tufano, Gerarda Cappuccio, et al. · Journal of the Peripheral Nervous System · 16
Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease
2008 · Paola Mandich, Marina Grandis, et al. · Journal of Human Genetics · 16
A novel mutation in COL3A1 associates to vascular Ehlers–Danlos syndrome with predominant musculoskeletal involvement
2021 · Federica Ruscitti, Lucia Trevisan, et al. · Molecular Genetics & Genomic Medicine · 15
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The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment
2022 · Chiara Fiorillo, Giovanna Capodivento, et al. · Neuropathology and Applied Neurobiology · 14
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A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family
2012 · Fiore Manganelli, Chiara Pisciotta, et al. · Journal of the Peripheral Nervous System · 13
A novel mutation in the N-terminal acting-binding domain of Filamin C protein causing a distal myofibrillar myopathy
2019 · Chiara Gemelli, Valeria Prada, et al. · Journal of the Neurological Sciences · 11
Accelerated repair and reduced mutagenicity of oxidative DNA damage in human bladder cells expressing the E. coli FPG protein
2005 · Monica Ropolo, Alessandro Geroldi, et al. · International Journal of Cancer · 11
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Works count: 52
Citation count: 836
H-index: 17
I10-index: 29
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