STRAFELLA, CLAUDIA
STRAFELLA, CLAUDIA
Dipartimento di Biomedicina e Prevenzione
A Hybrid Machine Learning and Network Analysis Approach Reveals Two Parkinson?s Disease Subtypes from 115 RNA-Seq Post-Mortem Brain Samples
2022-01-01 Termine, A; Fabrizio, C; Strafella, C; Caputo, V; Petrosini, L; Caltagirone, C; Cascella, R; Giardina, E
Age and sex modulate sars-cov-2 viral load kinetics: a longitudinal analysis of 1735 subjects
2021-01-01 Caputo, V; Termine, A; Fabrizio, C; Calvino, G; Luzzi, L; Fusco, C; Ingrasc(\`i), A; Peconi, C; D?alessio, R; Mihali, S; Trastulli, G; Megalizzi, D; Cascella, R; Rossini, A; Salvia, A; Strafella, C; Giardina, E
Analysis of genetic variants associated with COVID-19 outcome highlights different distributions among populations
2022-01-01 Fabrizio, C; Termine, A; Caputo, V; Megalizzi, D; Calvino, G; Trastulli, G; Ingrasc(\`i), A; Ferrante, S; Peconi, C; Rossini, A; Salvia, A; Caltagirone, C; Strafella, C; Giardina, E; Cascella, R
Biallelic PAX7 variants cause a novel Satellite Cell-opathy with progressive muscle involvement resembling facioscapulohumeral muscular dystrophy
2026-01-01 Ganassi, M; Strafella, C; Savarese, M; Heher, P; Engquist, En; Mcguire, L; Johari, M; De Nicola, Gf; Bigot, A; Mouly, V; Bortolani, S; Torchia, E; Monforte, M; Megalizzi, D; Sabino, A; Ricci, E; Giardina, E; Zammit, Ps; Tasca, G
Bridging past and future: the evolution of genetic diagnosis in FSHD and the role of emerging technologies in a globalized framework
2026-01-01 Strafella, C; Erdmann, H; Bevilacqua, Ja; Ricci, E; Ravenscroft, G; Matsumura, T; Vishnu, Vy; Sherif, Re; Oflazer, P; Muratori, D; Figueiredo, F; Sansone, V; Sacconi, S; Ricci, G; Filosto, M; Evangelista, T; Rosa, Al; Belayew, A; Abicht, A; Magdinier, F; Giardina, E
Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian families
2024-01-01 Strafella, C; Colantoni, L; Megalizzi, D; Trastulli, G; Piorgo, Ep; Primiano, G; Sancricca, C; Ricci, G; Siciliano, G; Caltagirone, C; Filosto, M; Tasca, G; Ricci, E; Cascella, R; Giardina, E
D4Z4 methylation levels combined with a machine learning pipeline highlight single CpG sites as discriminating biomarkers for FSHD patients
2022-01-01 Caputo, V; Megalizzi, D; Fabrizio, C; Termine, A; Colantoni, L; Bax, C; Gimenez, J; Monforte, M; Tasca, G; Ricci, E; Caltagirone, C; Giardina, E; Cascella, R; Strafella, C
Deciphering the complexity of FSHD: a multimodal approach as a model for rare disorders
2024-10-11 Megalizzi, D; Trastulli, G; Colantoni, L; Proietti Piorgo, E; Primiano, G; Sancricca, C; Caltagirone, C; Cascella, R; Strafella, C; Giardina, E
Deregulation of ncRNA in Neurodegenerative Disease: Focus on circRNA, lncRNA and miRNA in Amyotrophic Lateral Sclerosis
2021-01-01 Ruffo, P; Strafella, C; Cascella, R; Caputo, V; Conforti, Fl; And(\`o), S; Giardina, E
Describing phenotypes in FSHD: an update of the comprehensive clinical evaluation form
2025-01-01 Ricci, G; Torri, F; Ruggiero, L; Vercelli, L; Gadaleta, G; Rolle, E; Risi, B; Carraro, E; Evangelista, T; Bugiardini, E; Dubuisson, N; Voermans, N; Siciliano, G; Mongini, T; Filosto, M; Verriello, L; Tonin, P; Vattemi, G; Tupler, R; Turri, M; Trabacca, A; Santoro, L; Sansone, Va; Sancricca, C; Rodolico, C; Monforte, M; Ricci, E; Renieri, A; Previtali, S; Politano, L; Petrucci, A; Angelini, C; Pegoraro, E; Nigro, V; Mata', S; Massa, R; Moroni, I; Maggi, L; Valentino, Ml; Liguori, R; Inghilleri, M; Grandis, M; Colantoni, L; Strafella, C; Giardina, E; Antonini, G; Garibaldi, M; Gabellini, D; Fiorillo, C; Di Muzio, G; Diella, E; D'Angelo, Mg; Sciacco, M; Moggio, M; Comi, G; Coccia, M; Berardinelli, A; Battini, R; Barp, A; Allegri, I
Epigenetic profiling of the D4Z4 locus: optimization of the protocol for studying DNA methylation at single CpG site level
2023-01-01 Megalizzi, D; Trastulli, G; Caputo, V; Colantoni, L; Caltagirone, C; Strafella, C; Cascella, R; Giardina, E
Expanding Genetic and Clinical Spectra of Inherited Retinal Dystrophies: Identification of Three Novel PRPH2 Variants
2025-01-01 Cascella, R; Sebastiani, J; Strafella, C; Calvino, G; Andreucci, S; D'Ambrosio, M; Zampatti, S; Levialdi Ghiron, Jh; Falsini, B; Cusumano, A; Giardina, E
From Genomics to AI: Revolutionizing Precision Medicine in Oncology
2025-01-01 Calvino, G; Farro, J; Zampatti, S; Peconi, C; Megalizzi, D; Trastulli, G; Andreucci, S; Cascella, R; Strafella, C; Caltagirone, C; Grifalchi, F; Giardina, E
Identification of genetic networks reveals complex associations and risk trajectory linking mild cognitive impairment to Alzheimer's disease
2022-01-01 Strafella, C; Caputo, V; Termine, A; Fabrizio, C; Calvino, G; Megalizzi, D; Ruffo, P; Toppi, E; Banaj, N; Bassi, A; Boss(\`u), P; Caltagirone, C; Spalletta, G; Giardina, E; Cascella, R
Innovations in medicine: exploring ChatGPT's impact on rare disorder management
2024-03-28 Zampatti, S; Peconi, C; Megalizzi, D; Calvino, G; Trastulli, G; Cascella, R; Strafella, C; Caltagirone, C; Giardina, E
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients
2024-10-22 Strafella, C; Megalizzi, D; Trastulli, G; Proietti Piorgo, E; Colantoni, L; Tasca, G; Monforte, M; Zampatti, S; Primiano, G; Sancricca, C; Bortolani, S; Torchia, E; Ravera, B; Torri, F; Gadaleta, G; Risi, B; Caria, F; Gerardi, F; Carraro, E; Gioiosa, V; Garibaldi, M; Tufano, L; Frezza, E; Massa, R; Caltagirone, C; Pennisi, Em; Petrucci, A; Pane, M; Frongia, A; Gragnani, F; Scutifero, M; Mandich, P; Grandis, M; Maioli, Ma; Casali, C; Manfroi, E; Politano, L; Passamano, L; Petillo, R; Rodolico, C; Pugliese, A; Previtali, Sc; Sansone, V; Vercelli, L; Mongini, Te; Ricci, G; Siciliano, G; Filosto, M; Ricci, E; Cascella, R; Giardina, E; Null, N
Investigation of genetic variations of il6 and il6r as potential prognostic and pharmacogenetics biomarkers: Implications for covid19 and neuroin ammatory disorders
2020-01-01 Strafella, C; Caputo, V; Termine, A; Barati, S; Caltagirone, C; Giardina, E; Cascella, R
Long-read sequencing and the evolving landscape of facioscapulohumeral muscular dystrophy diagnosis
2026-01-01 Giardina, E; Strafella, C
Pharmacogenomics: an update on biologics and small-molecule drugs in the treatment of psoriasis
2021-01-01 Caputo, V; Strafella, C; Cosio, T; Lanna, C; Campione, E; Novelli, G; Giardina, E; Cascella, R
Precision medicine into clinical practice: a web-based tool enables real?time pharmacogenetic assessment of tailored treatments in psychiatric disorders
2021-01-01 Zampatti, S; Fabrizio, C; Ragazzo, M; Campoli, G; Caputo, V; Strafella, C; Pellicano, C; Cascella, R; Spalletta, G; Petrosini, L; Caltagirone, C; Termine, A; Giardina, E
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2022 | A Hybrid Machine Learning and Network Analysis Approach Reveals Two Parkinson?s Disease Subtypes from 115 RNA-Seq Post-Mortem Brain Samples | Termine, A; Fabrizio, C; Strafella, C; Caputo, V; Petrosini, L; Caltagirone, C; Cascella, R; Giardina, E | Articolo su rivista | |
| 1-gen-2021 | Age and sex modulate sars-cov-2 viral load kinetics: a longitudinal analysis of 1735 subjects | Caputo, V; Termine, A; Fabrizio, C; Calvino, G; Luzzi, L; Fusco, C; Ingrasc(\`i), A; Peconi, C; D?alessio, R; Mihali, S; Trastulli, G; Megalizzi, D; Cascella, R; Rossini, A; Salvia, A; Strafella, C; Giardina, E | Articolo su rivista | |
| 1-gen-2022 | Analysis of genetic variants associated with COVID-19 outcome highlights different distributions among populations | Fabrizio, C; Termine, A; Caputo, V; Megalizzi, D; Calvino, G; Trastulli, G; Ingrasc(\`i), A; Ferrante, S; Peconi, C; Rossini, A; Salvia, A; Caltagirone, C; Strafella, C; Giardina, E; Cascella, R | Articolo su rivista | |
| 1-gen-2026 | Biallelic PAX7 variants cause a novel Satellite Cell-opathy with progressive muscle involvement resembling facioscapulohumeral muscular dystrophy | Ganassi, M; Strafella, C; Savarese, M; Heher, P; Engquist, En; Mcguire, L; Johari, M; De Nicola, Gf; Bigot, A; Mouly, V; Bortolani, S; Torchia, E; Monforte, M; Megalizzi, D; Sabino, A; Ricci, E; Giardina, E; Zammit, Ps; Tasca, G | Articolo su rivista | |
| 1-gen-2026 | Bridging past and future: the evolution of genetic diagnosis in FSHD and the role of emerging technologies in a globalized framework | Strafella, C; Erdmann, H; Bevilacqua, Ja; Ricci, E; Ravenscroft, G; Matsumura, T; Vishnu, Vy; Sherif, Re; Oflazer, P; Muratori, D; Figueiredo, F; Sansone, V; Sacconi, S; Ricci, G; Filosto, M; Evangelista, T; Rosa, Al; Belayew, A; Abicht, A; Magdinier, F; Giardina, E | Articolo su rivista | |
| 1-gen-2024 | Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian families | Strafella, C; Colantoni, L; Megalizzi, D; Trastulli, G; Piorgo, Ep; Primiano, G; Sancricca, C; Ricci, G; Siciliano, G; Caltagirone, C; Filosto, M; Tasca, G; Ricci, E; Cascella, R; Giardina, E | Articolo su rivista | |
| 1-gen-2022 | D4Z4 methylation levels combined with a machine learning pipeline highlight single CpG sites as discriminating biomarkers for FSHD patients | Caputo, V; Megalizzi, D; Fabrizio, C; Termine, A; Colantoni, L; Bax, C; Gimenez, J; Monforte, M; Tasca, G; Ricci, E; Caltagirone, C; Giardina, E; Cascella, R; Strafella, C | Articolo su rivista | |
| 11-ott-2024 | Deciphering the complexity of FSHD: a multimodal approach as a model for rare disorders | Megalizzi, D; Trastulli, G; Colantoni, L; Proietti Piorgo, E; Primiano, G; Sancricca, C; Caltagirone, C; Cascella, R; Strafella, C; Giardina, E | Articolo su rivista | |
| 1-gen-2021 | Deregulation of ncRNA in Neurodegenerative Disease: Focus on circRNA, lncRNA and miRNA in Amyotrophic Lateral Sclerosis | Ruffo, P; Strafella, C; Cascella, R; Caputo, V; Conforti, Fl; And(\`o), S; Giardina, E | Articolo su rivista | |
| 1-gen-2025 | Describing phenotypes in FSHD: an update of the comprehensive clinical evaluation form | Ricci, G; Torri, F; Ruggiero, L; Vercelli, L; Gadaleta, G; Rolle, E; Risi, B; Carraro, E; Evangelista, T; Bugiardini, E; Dubuisson, N; Voermans, N; Siciliano, G; Mongini, T; Filosto, M; Verriello, L; Tonin, P; Vattemi, G; Tupler, R; Turri, M; Trabacca, A; Santoro, L; Sansone, Va; Sancricca, C; Rodolico, C; Monforte, M; Ricci, E; Renieri, A; Previtali, S; Politano, L; Petrucci, A; Angelini, C; Pegoraro, E; Nigro, V; Mata', S; Massa, R; Moroni, I; Maggi, L; Valentino, Ml; Liguori, R; Inghilleri, M; Grandis, M; Colantoni, L; Strafella, C; Giardina, E; Antonini, G; Garibaldi, M; Gabellini, D; Fiorillo, C; Di Muzio, G; Diella, E; D'Angelo, Mg; Sciacco, M; Moggio, M; Comi, G; Coccia, M; Berardinelli, A; Battini, R; Barp, A; Allegri, I | Articolo su rivista | |
| 1-gen-2023 | Epigenetic profiling of the D4Z4 locus: optimization of the protocol for studying DNA methylation at single CpG site level | Megalizzi, D; Trastulli, G; Caputo, V; Colantoni, L; Caltagirone, C; Strafella, C; Cascella, R; Giardina, E | Articolo su rivista | |
| 1-gen-2025 | Expanding Genetic and Clinical Spectra of Inherited Retinal Dystrophies: Identification of Three Novel PRPH2 Variants | Cascella, R; Sebastiani, J; Strafella, C; Calvino, G; Andreucci, S; D'Ambrosio, M; Zampatti, S; Levialdi Ghiron, Jh; Falsini, B; Cusumano, A; Giardina, E | Articolo su rivista | |
| 1-gen-2025 | From Genomics to AI: Revolutionizing Precision Medicine in Oncology | Calvino, G; Farro, J; Zampatti, S; Peconi, C; Megalizzi, D; Trastulli, G; Andreucci, S; Cascella, R; Strafella, C; Caltagirone, C; Grifalchi, F; Giardina, E | Articolo su rivista | |
| 1-gen-2022 | Identification of genetic networks reveals complex associations and risk trajectory linking mild cognitive impairment to Alzheimer's disease | Strafella, C; Caputo, V; Termine, A; Fabrizio, C; Calvino, G; Megalizzi, D; Ruffo, P; Toppi, E; Banaj, N; Bassi, A; Boss(\`u), P; Caltagirone, C; Spalletta, G; Giardina, E; Cascella, R | Articolo su rivista | |
| 28-mar-2024 | Innovations in medicine: exploring ChatGPT's impact on rare disorder management | Zampatti, S; Peconi, C; Megalizzi, D; Calvino, G; Trastulli, G; Cascella, R; Strafella, C; Caltagirone, C; Giardina, E | Articolo su rivista | |
| 22-ott-2024 | Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients | Strafella, C; Megalizzi, D; Trastulli, G; Proietti Piorgo, E; Colantoni, L; Tasca, G; Monforte, M; Zampatti, S; Primiano, G; Sancricca, C; Bortolani, S; Torchia, E; Ravera, B; Torri, F; Gadaleta, G; Risi, B; Caria, F; Gerardi, F; Carraro, E; Gioiosa, V; Garibaldi, M; Tufano, L; Frezza, E; Massa, R; Caltagirone, C; Pennisi, Em; Petrucci, A; Pane, M; Frongia, A; Gragnani, F; Scutifero, M; Mandich, P; Grandis, M; Maioli, Ma; Casali, C; Manfroi, E; Politano, L; Passamano, L; Petillo, R; Rodolico, C; Pugliese, A; Previtali, Sc; Sansone, V; Vercelli, L; Mongini, Te; Ricci, G; Siciliano, G; Filosto, M; Ricci, E; Cascella, R; Giardina, E; Null, N | Articolo su rivista | |
| 1-gen-2020 | Investigation of genetic variations of il6 and il6r as potential prognostic and pharmacogenetics biomarkers: Implications for covid19 and neuroin ammatory disorders | Strafella, C; Caputo, V; Termine, A; Barati, S; Caltagirone, C; Giardina, E; Cascella, R | Articolo su rivista | |
| 1-gen-2026 | Long-read sequencing and the evolving landscape of facioscapulohumeral muscular dystrophy diagnosis | Giardina, E; Strafella, C | Articolo su rivista | |
| 1-gen-2021 | Pharmacogenomics: an update on biologics and small-molecule drugs in the treatment of psoriasis | Caputo, V; Strafella, C; Cosio, T; Lanna, C; Campione, E; Novelli, G; Giardina, E; Cascella, R | Articolo su rivista | |
| 1-gen-2021 | Precision medicine into clinical practice: a web-based tool enables real?time pharmacogenetic assessment of tailored treatments in psychiatric disorders | Zampatti, S; Fabrizio, C; Ragazzo, M; Campoli, G; Caputo, V; Strafella, C; Pellicano, C; Cascella, R; Spalletta, G; Petrosini, L; Caltagirone, C; Termine, A; Giardina, E | Articolo su rivista |