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Cells|December 23, 2022
<i>D4Z4</i> Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD PatientsValerio Caputo, Domenica Megalizzi, Carlo Fabrizio, et al.
Pharmacogenomics|August 1, 2015
Comparative analysis between saliva and buccal swabs as source of DNA: lesson from HLA-B*57:01 testingRaffaella Cascella, Laura Stocchi, Claudia Strafella, et al.
Frontiers in Immunology|July 12, 2021
Case Report: Sars-CoV-2 Infection in a Vaccinated Individual: Evaluation of the Immunological Profile and Virus Transmission RiskClaudia Strafella, Valerio Caputo, Gisella Guerrera, et al.
Human Molecular Genetics|October 11, 2019
The variability of SMCHD1 gene in FSHD patients: evidence of new mutationsClaudia Strafella, Valerio Caputo, Rosaria Maria Galota, et al.
Frontiers in Aging Neuroscience|March 7, 2022
Identification of Genetic Networks Reveals Complex Associations and Risk Trajectory Linking Mild Cognitive Impairment to Alzheimer's DiseaseClaudia Strafella, Valerio Caputo, Andrea Termine, et al.
Journal of Personalized Medicine|December 29, 2022
Analysis of Genetic Variants Associated with COVID-19 Outcome Highlights Different Distributions among PopulationsCarlo Fabrizio, Andrea Termine, Valerio Caputo, et al.
Frontiers in Neurology|July 3, 2019
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case ReportClaudia Strafella, Giulia Campoli, Rosaria Maria Galota, et al.
Clinical Genetics|December 2, 2023
Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian familiesClaudia Strafella, Luca Colantoni, Domenica Megalizzi, et al.
Frontiers in Genetics|June 21, 2021
Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs InteractionsClaudia Strafella, Valerio Caputo, Andrea Termine, et al.
Frontiers in Neurology|December 15, 2018
Digenic Inheritance of Shortened Repeat Units of the D4Z4 Region and a Loss-of-Function Variant in <i>SMCHD1</i> in a Family With FSHDRaffaella Cascella, Claudia Strafella, Valerio Caputo, et al.
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