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R. Campopiano · SciRah

Researcher profile · Semantic Scholar

R. Campopiano

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R. Campopiano — researcher profile on SciRah

h-index: 9
Works: 24
Citations: 404

Most-cited papers

ccf-mtDNA as a Potential Link Between the Brain and Immune System in Neuro-Immunological Disorders
S. Gambardella, F. Limanaqi, R. Ferese, F. Biagioni +3 more
2019Frontiers in Immunology135 citations Open access
Semantic Scholar
Four Copies of SNCA Responsible for Autosomal Dominant Parkinson's Disease in Two Italian Siblings
R. Ferese, N. Modugno, R. Campopiano, M. Santilli +9 more
2015Parkinson's Disease71 citations Open access
Semantic Scholar
Circulating miR-127-3p as a Potential Biomarker for Differential Diagnosis in Frontotemporal Dementia
P. Piscopo, M. Grasso, M. Puopolo, E. D’Acunto +9 more
2018Journal of Alzheimer's Disease60 citations Open access
Semantic Scholar
C9orf72-Related Neurodegenerative Diseases: From Clinical Diagnosis to Therapeutic Strategies
S. Zampatti, C. Peconi, R. Campopiano, S. Gambardella +2 more
2022Frontiers in Aging Neuroscience23 citations Open access
Semantic Scholar
Functional analysis of a conserved site mutation in the DNA end processing enzyme PNKP leading to ataxia with oculomotor apraxia type 4 in humans
A. Islam, Anirban Chakraborty, S. Gambardella, R. Campopiano +3 more
2023Journal of Biological Chemistry15 citations Open access
Semantic Scholar
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS)
R. Ferese, S. Zampatti, A. Griguoli, F. Fornai +7 more
2016Journal of Molecular Neuroscience14 citations
Semantic Scholar
The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson’s Disease Owing Genetic and Anatomical Specificity
S. Gambardella, R. Ferese, F. Biagioni, C. Busceti +6 more
2017Frontiers in Cellular Neuroscience13 citations Open access
Semantic Scholar
Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study
A. di Fonzo, Marco Percetti, E. Monfrini, Ilaria Palmieri +26 more
2023Movement Disorders11 citations Open access
Semantic Scholar
Migrainous Infarction in a Patient With Sporadic Hemiplegic Migraine and Cystic Fibrosis: A 99mTc‐HMPAO Brain SPECT Study
V. Mancini, G. Mastria, Viviana Frantellizzi, P. Troiani +11 more
2019Headache9 citations
Semantic Scholar
A novel POLR3A genotype leads to leukodystrophy type-7 in two siblings with unusually late age of onset
R. Campopiano, R. Ferese, S. Zampatti, E. Giardina +10 more
2020BMC Neurology8 citations Open access
Semantic Scholar
Distribution of the C9orf72 hexanucleotide repeat expansion in healthy subjects: a multicenter study promoted by the Italian IRCCS network of neuroscience and neurorehabilitation
E. Giardina, P. Mandich, R. Ghidoni, N. Ticozzi +40 more
2024Frontiers in Neurology7 citations Open access
Semantic Scholar
Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants
R. Ferese, R. Campopiano, Simona Scala, C. D’Alessio +14 more
2021Frontiers in Genetics7 citations Open access
Semantic Scholar
Compassionate drug uses and saving for the national health system: the case study of Fondazione Policlinico Gemelli.
D. Pilunni, V. Daloisio, R. Campopiano, M. Pani +1 more
2021European Review for Medical and Pharmacological Sciences6 citations
Semantic Scholar
A Large Family with p.Arg554His Mutation in ABCD1: Clinical Features and Genotype/Phenotype Correlation in Female Carriers
R. Campopiano, C. Femiano, Maria Antonietta Chiaravalloti, R. Ferese +11 more
2021Genes6 citations Open access
Semantic Scholar
Cohort analysis of novel SPAST variants in SPG4 patients and implementation of in vitro and in vivo studies to identify the pathogenic mechanism caused by splicing mutations
R. Ferese, Simona Scala, A. Suppa, R. Campopiano +15 more
2023Frontiers in Neurology5 citations Open access
Semantic Scholar
A Novel Homozygous Variant in the Fork-Head-Associated Domain of Polynucleotide Kinase Phosphatase in a Patient Affected by Late-Onset Ataxia With Oculomotor Apraxia Type 4
R. Campopiano, R. Ferese, F. Buttari, C. Femiano +8 more
2020Frontiers in Neurology5 citations Open access
Semantic Scholar
Decipher non‐canonical SPAST splicing mutations with the help of functional assays in patients affected by spastic paraplegia 4 (SPG4)
R. Ferese, Simona Scala, A. Suppa, R. Campopiano +16 more
2022Clinical Genetics4 citations Open access
Semantic Scholar
Unusual Segregation of APP Mutations in Monogenic Alzheimer Disease
G. Mastromoro, S. Gambardella, E. Marchionni, R. Campopiano +3 more
2019Neurodegenerative Diseases3 citations
Semantic Scholar
Next Generation Sequencing and ALS: known genes, different phenotyphes.
R. Campopiano, L. Ryskalin, E. Giardina, S. Zampatti +6 more
2017Archives Italiennes de Biologie2 citations
Semantic Scholar
Expanding the Clinical and Mutational Spectrum of FBXO7-Related Parkinsonism: A Novel Italian Family and Comprehensive Literature Review
S. Zampatti, C. Strafella, R. Campopiano, C. Peconi +7 more
2026Genes0 citations Open access
Semantic Scholar
New variants and genotype–phenotype correlation in KIF5A mutation: the contribution of a large Italian cohort
R. Ferese, A. Suppa, R. Campopiano, Simona Scala +20 more
2025Journal of Medical Genetics0 citations Open access
Semantic Scholar
Structural modeling of altered CLCN1 conformation following a novel mutation in a patient affected by autosomal dominant myotonia congenita (Thomsen disease).
R. Ferese, V. Albano, M. Falconi, F. Iacovelli +11 more
2017Archives Italiennes de Biologie0 citations
Semantic Scholar
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS)
R. Ferese, S. Zampatti, A. Griguoli, F. Fornai +7 more
2016Journal of Molecular Neuroscience0 citations
Semantic Scholar
Short history of the “Genomic Revolution” and implication for neurological institutes
S. Gambardella, V. Albano, R. Campopiano, R. Ferese +4 more
2015La Rivista Italiana della Medicina di Laboratorio - Italian Journal of Laboratory Medicine0 citations
Semantic Scholar

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