MEGALIZZI, DOMENICA
MEGALIZZI, DOMENICA
Dipartimento di Ingegneria Civile e Ingegneria informatica
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
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
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
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
Relationship between nutrition, lifestyle, and neurodegenerative disease: lessons from ADH1B, CYP1A2 and MTHFR
2022-01-01 Barati, S; Fabrizio, C; Strafella, C; Cascella, R; Caputo, V; Megalizzi, D; Peconi, C; Mela, J; Colantoni, L; Caltagirone, C; Termine, A; Giardina, E
RHO variants and autosomal dominant retinitis pigmentosa: insights from the italian genetic landscape
2024-09-02 Trastulli, G; Megalizzi, D; Calvino, G; Andreucci, S; Zampatti, S; Strafella, C; Caltagirone, C; Giardina, E; Cascella, R
Update on the molecular aspects and methods underlying the complex architecture of FSHD
2022-01-01 Caputo, V; Megalizzi, D; Fabrizio, C; Termine, A; Colantoni, L; Caltagirone, C; Giardina, E; Cascella, R; Strafella, C
Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD
2023-01-01 Strafella, C; Caputo, V; Bortolani, S; Torchia, E; Megalizzi, D; Trastulli, G; Monforte, M; Colantoni, L; Caltagirone, C; Ricci, E; Tasca, G; Cascella, R; Giardina, E
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 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-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-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-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-2022 | Relationship between nutrition, lifestyle, and neurodegenerative disease: lessons from ADH1B, CYP1A2 and MTHFR | Barati, S; Fabrizio, C; Strafella, C; Cascella, R; Caputo, V; Megalizzi, D; Peconi, C; Mela, J; Colantoni, L; Caltagirone, C; Termine, A; Giardina, E | Articolo su rivista | |
| 2-set-2024 | RHO variants and autosomal dominant retinitis pigmentosa: insights from the italian genetic landscape | Trastulli, G; Megalizzi, D; Calvino, G; Andreucci, S; Zampatti, S; Strafella, C; Caltagirone, C; Giardina, E; Cascella, R | Articolo su rivista | |
| 1-gen-2022 | Update on the molecular aspects and methods underlying the complex architecture of FSHD | Caputo, V; Megalizzi, D; Fabrizio, C; Termine, A; Colantoni, L; Caltagirone, C; Giardina, E; Cascella, R; Strafella, C | Articolo su rivista | |
| 1-gen-2023 | Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD | Strafella, C; Caputo, V; Bortolani, S; Torchia, E; Megalizzi, D; Trastulli, G; Monforte, M; Colantoni, L; Caltagirone, C; Ricci, E; Tasca, G; Cascella, R; Giardina, E | Articolo su rivista |