Michelangelo Cao

Most-cited papers

1. A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score

   C. Lamperti, G. Fabbri, L. Vercelli, R. D'Amico +23 more

   2010Muscle and Nerve158 citations Open access

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2. 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 Genetics123 citations Open access

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3. 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

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4. 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

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5. 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

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6. FSHD1 and FSHD2 form a disease continuum

   S. Sacconi, A. Briand-Suleau, M. Gros, C. Baudoin +22 more

   2019Neurology71 citations Open access

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7. 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

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8. Atypical onset in a series of 122 cases with FacioScapuloHumeral Muscular Dystrophy

   E. Pastorello, Michelangelo Cao, C. Trevisan

   2012Clinical neurology and neurosurgery (Dutch-Flemish ed. Print)54 citations Open access

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9. Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations

   Michelangelo Cao, M. Donà, Lucia Valentino, C. Semplicini +12 more

   2015Neurogenetics36 citations

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10. No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype

    C. Bertolin, G. Querin, E. DaRe, A. Sagnelli +12 more

    2016European Journal of Neurology8 citations Open access

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11. G.P.15.09 Unexpected high percentage of asymptomatic subjects carrying the FSHD molecular defect: Which factors contribute to the disease mechanism?

    E. Bonifazi, C. Lamperti, C. Fiorillo, L. Vercelli +29 more

    20092 citations

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12. Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations

    Michelangelo Cao, M. Donà, Maria Lucia Valentino, C. Semplicini +12 more

    2016Neurogenetics1 citations Open access

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13. Chromosome X inactivation pattern in FSHD female patients

    Michelangelo Cao, C. Bertolin, S. Tripodi, Luca Bello +2 more

    20170 citations

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14. Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations

    Michelangelo Cao, M. Donà, M. L. Valentino, C. Semplicini +12 more

    2016Neurogenetics0 citations

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15. D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations.

    J. Daolio, A. Nikolić, G. Ricci, M. Govi +20 more

    20130 citations

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16. D.P.1.02 A robust tool to quantify disability in patients affected by facioscapulohumeral muscular dystrophy

    C. Lamperti, G. Fabbri, Francesca Greco, M. Servida +25 more

    20080 citations

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