Simona Capponi

Most-cited papers

1. Charcot‐Marie‐Tooth disease: frequency of genetic subtypes in a Southern Italy population

   F. Manganelli, S. Tozza, C. Pisciotta, E. Bellone +6 more

   2014Journal of the peripheral nervous system71 citations

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2. Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations

   A. Echaniz-Laguna, T. Geuens, P. Petiot, Y. Péréon +17 more

   2017Human Mutation68 citations Open access

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3. HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients

   Simona Capponi, Alessandro Geroldi, P. Fossa, M. Grandis +5 more

   2011Journal of the peripheral nervous system66 citations

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4. Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1

   Simona Capponi, T. Geuens, Alessandro Geroldi, P. Origone +11 more

   2016Human Mutation52 citations Open access

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5. TNFα induces the expression of genes associated with endothelial dysfunction through p38MAPK-mediated down-regulation of miR-149.

   D. Palmieri, Simona Capponi, Alessandro Geroldi, Marzia Mura +2 more

   2014Biochemical and Biophysical Research Communications - BBRC43 citations

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6. Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies

   P. Mandich, P. Fossa, Simona Capponi, Alessandro Geroldi +6 more

   2009European Journal of Human Genetics38 citations Open access

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7. Gain of glycosylation: a new pathomechanism of Myelin Protein Zero mutations

   V. Prada, M. Passalacqua, M. Bono, P. Luzzi +9 more

   2012Annals of Neurology23 citations Open access

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8. GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course.

   I. Pezzini, Alessandro Geroldi, Simona Capponi, Rossella Gulli +11 more

   2016Neuromuscular Disorders21 citations

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9. A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease.

   P. Ciotti, M. Luigetti, Alessandro Geroldi, Simona Capponi +7 more

   2014Journal of Neurological Sciences19 citations

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10. Early onset Charcot‐Marie‐Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2‐related neuropathy

    M. Tufano, G. Cappuccio, G. Terrone, F. Manganelli +4 more

    2015Journal of the peripheral nervous system15 citations

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11. A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family

    F. Manganelli, C. Pisciotta, M. Nolano, Simona Capponi +6 more

    2012Journal of the peripheral nervous system14 citations

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12. Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation

    V. Prada, Simona Capponi, G. Ursino, A. Albertí +7 more

    2015Neuropathology (Kyoto. 1993)3 citations

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13. Contribution of copy number variations in CMT1X: a retrospective study

    Simona Capponi, Alessandro Geroldi, I. Pezzini, Rossella Gulli +8 more

    2015European Journal of Neurology3 citations

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14. LITAF/SIMPLE MUTATION ANALYSIS IN DOMINANT DEMYELINATING CHARCOT- MARIE-TOOTH DISEASE: A NOVEL MUTATION

    P. Ciotti, Alessandro Geroldi, Simona Capponi, R. Massa +5 more

    20120 citations

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