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E. Picillo · SciRah

Researcher profile · Semantic Scholar

E. Picillo

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E. Picillo — researcher profile on SciRah

h-index: 18
Works: 55
Citations: 1,374

Most-cited papers

Improvement of survival in Duchenne Muscular Dystrophy: retrospective analysis of 835 patients
L. Passamano, A. Taglia, A. Palladino, E. Viggiano +10 more
2012Acta myologica384 citations
Semantic Scholar
Real-time PCR assay in Leishmania-infected dogs treated with meglumine antimoniate and allopurinol.
L. Manna, S. Reale, F. Vitale, E. Picillo +2 more
2008The Veterinary Journal109 citations
Semantic Scholar
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy
L. Bello, L. Piva, A. Barp, A. Taglia +33 more
2012Neurology84 citations Open access
Semantic Scholar
Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy
E. Viggiano, M. Ergoli, E. Picillo, L. Politano
2016Human Genetics80 citations
Semantic Scholar
Study of efficacy of miltefosine and allopurinol in dogs with leishmaniosis.
L. Manna, F. Vitale, S. Reale, E. Picillo +3 more
2009The Veterinary Journal78 citations
Semantic Scholar
Comparison of X‐chromosome inactivation in Duchenne muscle/myocardium‐manifesting carriers, non‐manifesting carriers and related daughters
E. Viggiano, E. Picillo, A. Cirillo, L. Politano
2013Clinical Genetics54 citations
Semantic Scholar
Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene
A. Taglia, Roberta Petillo, P. D'Ambrosio, E. Picillo +8 more
2015Acta myologica53 citations
Semantic Scholar
Leishmania DNA Quantification by Real‐time PCR in Naturally Infected Dogs Treated with Miltefosine
L. Manna, Angelo Elio Gravino, E. Picillo, N. Decaro +1 more
2008Annals of the New York Academy of Sciences46 citations
Semantic Scholar
Cardiac involvement in patients with Spinal Muscular Atrophies
A. Palladino, L. Passamano, A. Taglia, P. D'Ambrosio +8 more
2011Acta myologica42 citations
Semantic Scholar
Interferon-gamma (INF-gamma), IL4 expression levels and Leishmania DNA load as prognostic markers for monitoring response to treatment of leishmaniotic dogs with miltefosine and allopurinol.
L. Manna, S. Reale, E. Picillo, F. Vitale +1 more
2008Cytokine42 citations
Semantic Scholar
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study
G. Astrea, Alessandro Romano, C. Angelini, C. Antozzi +32 more
2018Orphanet Journal of Rare Diseases41 citations Open access
Semantic Scholar
Urine Sampling for Real-Time Polymerase Chain Reaction-Based Diagnosis of Canine Leishmaniasis
L. Manna, S. Reale, E. Picillo, F. Vitale +1 more
2008Journal of Veterinary Diagnostic Investigation35 citations Open access
Semantic Scholar
Cross‐sectional serum metabolomic study of multiple forms of muscular dystrophy
P. Spitali, K. Hettne, R. Tsonaka, Ekrem Sabir +7 more
2018Journal of Cellular and Molecular Medicine34 citations Open access
Semantic Scholar
Skewed X‐chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy
E. Viggiano, E. Picillo, M. Ergoli, A. Cirillo +2 more
2017Journal of Gene Medicine31 citations
Semantic Scholar
Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy
E. Viggiano, E. Picillo, L. Passamano, Maria Elena Onore +5 more
2023Genes24 citations Open access
Semantic Scholar
Novel mutations in LMNA A/C gene and associated phenotypes
Roberta Petillo, P. D'Ambrosio, A. Torella, A. Taglia +7 more
2015Acta myologica22 citations
Semantic Scholar
Molecular evidence of apoptotic pathway activation in semen samples with high DNA fragmentation.
Lucrezia Manente, S. Pecoraro, E. Picillo, Umberto Gargiulo +3 more
2015In Vivo21 citations
Semantic Scholar
Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function
M. Ergoli, Massimo Venditti, E. Picillo, S. Minucci +1 more
2019Molecular Reproduction and Development19 citations
Semantic Scholar
Improvement of survival in DuchenneMuscular Dystrophy: retrospective analysisof 835 patients
L. Passamano, A. Taglia, A. Palladino, E. Viggiano +10 more
201218 citations
Semantic Scholar
Nucleoside hydrolase DNA vaccine against canine visceral leishmaniasis
G. P. Borja-Cabrera, F. B. Santos, E. Picillo, Angelo Elio Gravino +2 more
2009Procedia in Vaccinology17 citations Open access
Semantic Scholar
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity.
Domenico Gorgoglione, Daniele Sabbatini, Pietro Riguzzi, Giuliana Capece +59 more
2024Brain : a journal of neurology15 citations Open access
Semantic Scholar
X-Linked Emery–Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female Carriers
E. Viggiano, A. Madej-Pilarczyk, Nicola Carboni, E. Picillo +6 more
2019Genes15 citations Open access
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
Copy Number Variants Account for a Tiny Fraction of Undiagnosed Myopathic Patients
Teresa Giugliano, M. Savarese, A. Garofalo, E. Picillo +29 more
2018Genes13 citations Open access
Semantic Scholar
CLCN1 Molecular Characterization in 19 South-Italian Patients With Dominant and Recessive Type of Myotonia Congenita
C. Orsini, Roberta Petillo, P. D'Ambrosio, M. Ergoli +5 more
2020Frontiers in Neurology12 citations Open access
Semantic Scholar
Genetic counseling in Pompe disease
A. Taglia, E. Picillo, P. D'Ambrosio, Maria Rosaria Cecio +2 more
2011Acta myologica12 citations
Semantic Scholar
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature
Antonella Pizza, E. Picillo, Maria Elena Onore, M. Scutifero +3 more
2023Acta myologica10 citations
Semantic Scholar
DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemia
M. Traverso, S. Baratto, M. Iacomino, M. Di Duca +15 more
2024European Journal of Human Genetics9 citations Open access
Semantic Scholar
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function
Maria Elena Onore, M. Savarese, E. Picillo, L. Passamano +2 more
2022International Journal of Molecular Sciences9 citations Open access
Semantic Scholar
Patients on treatment with risdiplam in Italy: challenges in the interpretation of the real-world data
E. Albamonte, Adrea Lizio, G. Coratti, L. Maggi +46 more
2025Neurological Sciences6 citations
Semantic Scholar
Alu-Mediated Insertions in the DMD Gene: A Difficult Puzzle to Interpret Clinically
A. Torella, Alberto Budillon, Mariateresa Zanobio, F. Del Vecchio Blanco +4 more
2023International Journal of Molecular Sciences6 citations Open access
Semantic Scholar
Phenotypic Variability of Andersen–Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene—A New Family Case Report
Maria Elena Onore, E. Picillo, P. D'Ambrosio, Salvatore Morra +2 more
2024Biomolecules3 citations Open access
Semantic Scholar
A rare co-occurrence of phosphorylase kinase deficiency (GSD type IXd) and alpha-glycosidase deficiency (GSD Type II) in a 53-year-old man presenting with an atypical glycogen storage disease phenotype
E. Picillo, Maria Elena Onore, L. Passamano, V. Nigro +1 more
2024Acta myologica3 citations
Semantic Scholar
Study of anti-Müllerian hormone levels in patients with Myotonic Dystrophy Type 1. Preliminary results.
M. Ergoli, Massimo Venditti, R. Dotolo, E. Picillo +2 more
2017Acta myologica3 citations
Semantic Scholar
DMD Phenotype in Girls with a de novo Balanced X;3 Autosome Translocation: A Case Report
L. Politano, E. Picillo, E. Viggiano
20133 citations
Semantic Scholar
Landscape Analysis of COL6A1, COL6A2, and COL6A3 Pathogenic Variants in a Large Italian Cohort Presenting with Collagen VI-Related Myopathies: A Nationwide Report
F. Fortunato, Laura Fiocco, A. Margutti, Marcella Neri +34 more
2025Biomolecules2 citations Open access
Semantic Scholar
Upper limb progression in Duchenne muscular dystrophy: Insights from a 36-month longitudinal study using the PUL 20
G. Coratti, M. Pane, Sophia Paolucci, Luca Bello +28 more
2025Journal of Neuromuscular Diseases2 citations Open access
Semantic Scholar
Brucella DNA is not detected in in-vitro produced embryos derived from ovaries of naturally infected buffaloes
G. Neglia, L. Zicarelli, Pa-Lo Di, E. Picillo +9 more
20072 citations Open access
Semantic Scholar
Autosomal dominant Ullrich congenital muscular dystrophy due to a de novo mutation in COL6A3 gene. A case report
E. Picillo, A. Torella, L. Passamano, V. Nigro +1 more
2022Acta myologica1 citations
Semantic Scholar
A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy
S. Sampaolo, Luca Lombardi, A. Pascarella, E. Picillo +4 more
2015Journal of Neuromuscular Diseases1 citations Open access
Semantic Scholar
Preliminary results on ghrelin mRNA quantification in buffalo calves during fasting and refeeding by real-time reverse transcription PCR assay
L. Manna, E. Picillo, G. Esposito, M. Réndina +5 more
20071 citations Open access
Semantic Scholar
Intraocular pressure and corneal biomechanics in patients affected by myotonic dystrophy type 1
Michele Lanza, Rosa Boccia, M. Scutifero, Luigi Serra +5 more
2026Graefe's Archive for Clinical and Experimental Ophthalmology0 citations Open access
Semantic Scholar
Risdiplam therapy in adult patients with Spinal muscular Atrophy (SMA). A 24-month-real-world experience at a single muscular centre
Elia Cesarone, E. Picillo, M. Scutifero, L. Passamano +1 more
2026Acta myologica0 citations
Semantic Scholar
3.32eP Expanding the molecular basis of glycogen storage disease due to muscle phosphorylase kinase deficiency: a novel candidate gene through exome sequencing
Giovanni Vicidomini, Pasquale Di Letto, Margherita Scarpato, F. Palmieri +11 more
2026Neuromuscular Disorders0 citations
Semantic Scholar
Development of Italian centile curves for the North Star Ambulatory Assessment and timed items.
Sophia Paolucci, Nicolò Lentini, G. Coratti, Federica Ricci +45 more
2026Neuromuscular Disorders0 citations Open access
Semantic Scholar
Risk of Cardiac Arrhythmias in Patients with Late-Onset Pompe Disease—Results from a Long Follow-Up in a Group of 12 Patients and Review of Literature
A. Palladino, L. Passamano, M. Scutifero, Salvatore Morra +4 more
2024Cardiogenetics0 citations Open access
Semantic Scholar
PROCEEDINGS OF THE 4th ENMD CONGRESS E-HEALTH & INNOVATION TO OVERCOME BARRIERS IN NEUROMUSCULAR DISEASES
C. Angelini, A. Annunziata, Zohar Argov, E. Bertini +88 more
2023Acta myologica0 citations
Semantic Scholar
Metabolomics analysis in serum of muscular dystrophy patients
P. Spitali, Kristina M. Hettne, Roula Tsonaka, Ekrem Sabir +7 more
20180 citations
Semantic Scholar
Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy
E. Viggiano, M. Ergoli, E. Picillo, L. Politano
2016Human Genetics0 citations
Semantic Scholar
XV CONGRESS OF THE ITALIAN SOCIETY OF MYOLOGY Naples, Italy - May 20-23, 2015 - Program (Summary)
A. Zaccaro, U. Balottin, M. Camia, M. C. Motta +496 more
2015Acta myologica0 citations
Semantic Scholar

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L. Politano×30
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L. Politano — researcher profile on SciRah
V. Nigro×19
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V. Nigro — researcher profile on SciRah
L. Passamano×13
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M. Scutifero×13
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E. Viggiano — researcher profile on SciRah

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A. Taglia — researcher profile on SciRah

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