CAPUTO, VALERIO
CAPUTO, VALERIO
Dipartimento di Biomedicina e Prevenzione
Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications
2020-01-01 Strafella, C; Caputo, V; Termine, A; Barati, S; Gambardella, S; Borgiani, P; Caltagirone, C; Novelli, G; Giardina, E; Cascella, R
Application of precision medicine in neurodegenerative diseases
2018-01-01 Strafella, C; Caputo, V; Galota, Mr; Zampatti, S; Marella, G; Mauriello, S; Cascella, R; Giardina, E
Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations.
2019-06-04 Strafella, C; Caputo, V; Minozzi, G; Milano, F; Arcangeli, M; Sobhy, N; Abdelmaksood, R; Hashad, D; Vakirlis, E; Novelli, G; Cascella, R; Giardina, E
Case report: Sars-CoV-2 infection in a vaccinated individual: evaluation of the immunological profile and virus transmission risk
2021-06-01 Strafella, C; Caputo, V; Guerrera, G; Termine, A; Fabrizio, C; Cascella, R; Picozza, M; Caltagirone, C; Rossini, A; Balice, Mp; Salvia, A; Battistini, L; Borsellino, G; Giardina, E
Characterization of a natural variant of human NDP52 and its functional consequences on mitophagy
2021-08-01 Di Rita, A; Angelini, D; Maiorino, T; Caputo, V; Cascella, R; Kumar, M; Tiberti, M; Lambrughi, M; Wesch, N; Löhr, F; Dötsch, V; Carinci, M; D'Acunzo, P; Chiurchiù, V; Papaleo, E; Rogov, V; Giardina, E; Battistini, L; Strappazzon, F
Comparative analysis of antigen and molecular tests for the detection of Sars-CoV-2 and related variants: a study on 4266 samples
2021-07-01 Caputo, V; Bax, C; Colantoni, L; Peconi, C; Termine, A; Fabrizio, C; Calvino, G; Luzzi, L; Panunzi, G; Fusco, C; Strafella, C; Cascella, R; Battistini, L; Caltagirone, C; Salvia, A; Sancesario, G; Giardina, E
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations
2020-01-01 Sbardella, D; Tundo, Gr; Cunsolo, V; Grasso, G; Cascella, R; Caputo, V; Santoro, Am; Milardi, D; Pecorelli, A; Ciaccio, C; Di Pierro, D; Leoncini, S; Campagnolo, L; Pironi, V; Oddone, F; Manni, P; Foti, S; Giardina, E; De Felice, C; Hayek, J; Curatolo, P; Galasso, C; Valacchi, G; Coletta, M; Graziani, G; Marini, S
Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD
2018-01-01 Cascella, R; Strafella, C; Caputo, V; Galota, Rm; Errichiello, V; Scutifero, M; Petillo, R; Marella, Gl; Arcangeli, M; Colantoni, L; Zampatti, S; Ricci, E; Deidda, G; Politano, L; Giardina, E
Effects of micro-textured polystyrene substrates by compression molding on cell adhesion and proliferation
2018-01-01 Bellisario, D; Quadrini, F; Santolim, G; Tedde, Gm; Caputo, V; Spitalieri, P; Sangiuolo, F; Santo, L
Epigenomic signatures in age-related macular degeneration: Focus on their role as disease modifiers and therapeutic targets
2021-01-01 Caputo, V; Strafella, C; Termine, A; Fabrizio, C; Ruffo, P; Cusumano, A; Giardina, E; Ricci, F; Cascella, R
Evaluation of OpenArray™ as a genotyping method for forensic DNA phenotyping and human identification
2021-02-01 Ragazzo, M; Puleri, G; Errichiello, V; Manzo, L; Luzzi, L; Potenza, S; Strafella, C; Peconi, C; Nicastro, F; Caputo, V; Giardina, E
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era.
2019-01-01 Zampatti, S; Colantoni, L; Strafella, C; Galota, R; Caputo, V; Campoli, G; Pagliaroli, G; Carboni, S; Mela, J; Peconi, C; Gambardella, S; Cascella, R; Giardina, E
Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis
2019-01-01 Musumeci, Ml; Fiorentini, F; Bianchi, L; Cascella, R; Giardina, E; Caputo, V; Micali, G
Gender and complex diseases: Insights into sex-specific epigenetic|Genere e malattie complesse: Meccanismi epigenetici sesso-specifici
2018-01-01 Caputo, V; Cascella, R; Strafella, C; Giardina, E; Novelli, G
Genetic counseling and NGS screening for recessive LGMD2A families
2020-01-01 Strafella, C; Caputo, V; Campoli, G; Galota, R; Mela, J; Zampatti, S; Minozzi, G; Sancricca, C; Servidei, S; Giardina, E; Cascella, R
Genetic counselling improves the molecular characterisation of dementing disorders
2021-01-01 Zampatti, S; Ragazzo, M; Peconi, C; Luciano, S; Gambardella, S; Caputo, V; Strafella, C; Cascella, R; Caltagirone, C; Giardina, E
Genetic determinants highlight the existence of shared etiopathogenetic mechanisms characterizing age-related macular degeneration and neurodegenerative disorders
2021-05-01 Strafella, C; Caputo, V; Termine, A; Fabrizio, C; Ruffo, P; Potenza, S; Cusumano, A; Ricci, F; Caltagirone, C; Giardina, E; Cascella, R
Genetic variants allegedly linked to antisocial behaviour are equally distributed across different populations
2021-03-01 Zampatti, S; Ragazzo, M; Fabrizio, C; Termine, A; Campoli, G; Caputo, V; Strafella, C; Cascella, R; Caltagirone, C; Giardina, E
Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs Interactions
2021-01-01 Strafella, C; Caputo, V; Termine, A; Assogna, F; Pellicano, C; Pontieri, Fe; Macchiusi, L; Minozzi, G; Gambardella, S; Centonze, D; Bossù, P; Spalletta, G; Caltagirone, C; Giardina, E; Cascella, R
Interpreting mixture profiles: comparison between precision ID GlobalFiler™ NGS STR panel v2 and traditional methods
2020-01-01 Ragazzo, M; Carboni, S; Caputo, V; Buttini, C; Manzo, L; Errichiello, V; Puleri, G; Giardina, E
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2020 | Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications | Strafella, C; Caputo, V; Termine, A; Barati, S; Gambardella, S; Borgiani, P; Caltagirone, C; Novelli, G; Giardina, E; Cascella, R | Articolo su rivista | |
| 1-gen-2018 | Application of precision medicine in neurodegenerative diseases | Strafella, C; Caputo, V; Galota, Mr; Zampatti, S; Marella, G; Mauriello, S; Cascella, R; Giardina, E | Articolo su rivista | |
| 4-giu-2019 | Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. | Strafella, C; Caputo, V; Minozzi, G; Milano, F; Arcangeli, M; Sobhy, N; Abdelmaksood, R; Hashad, D; Vakirlis, E; Novelli, G; Cascella, R; Giardina, E | Articolo su rivista | |
| 1-giu-2021 | Case report: Sars-CoV-2 infection in a vaccinated individual: evaluation of the immunological profile and virus transmission risk | Strafella, C; Caputo, V; Guerrera, G; Termine, A; Fabrizio, C; Cascella, R; Picozza, M; Caltagirone, C; Rossini, A; Balice, Mp; Salvia, A; Battistini, L; Borsellino, G; Giardina, E | Articolo su rivista | |
| 1-ago-2021 | Characterization of a natural variant of human NDP52 and its functional consequences on mitophagy | Di Rita, A; Angelini, D; Maiorino, T; Caputo, V; Cascella, R; Kumar, M; Tiberti, M; Lambrughi, M; Wesch, N; Löhr, F; Dötsch, V; Carinci, M; D'Acunzo, P; Chiurchiù, V; Papaleo, E; Rogov, V; Giardina, E; Battistini, L; Strappazzon, F | Articolo su rivista | |
| 1-lug-2021 | Comparative analysis of antigen and molecular tests for the detection of Sars-CoV-2 and related variants: a study on 4266 samples | Caputo, V; Bax, C; Colantoni, L; Peconi, C; Termine, A; Fabrizio, C; Calvino, G; Luzzi, L; Panunzi, G; Fusco, C; Strafella, C; Cascella, R; Battistini, L; Caltagirone, C; Salvia, A; Sancesario, G; Giardina, E | Articolo su rivista | |
| 1-gen-2020 | Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations | Sbardella, D; Tundo, Gr; Cunsolo, V; Grasso, G; Cascella, R; Caputo, V; Santoro, Am; Milardi, D; Pecorelli, A; Ciaccio, C; Di Pierro, D; Leoncini, S; Campagnolo, L; Pironi, V; Oddone, F; Manni, P; Foti, S; Giardina, E; De Felice, C; Hayek, J; Curatolo, P; Galasso, C; Valacchi, G; Coletta, M; Graziani, G; Marini, S | Articolo su rivista | |
| 1-gen-2018 | Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD | Cascella, R; Strafella, C; Caputo, V; Galota, Rm; Errichiello, V; Scutifero, M; Petillo, R; Marella, Gl; Arcangeli, M; Colantoni, L; Zampatti, S; Ricci, E; Deidda, G; Politano, L; Giardina, E | Articolo su rivista | |
| 1-gen-2018 | Effects of micro-textured polystyrene substrates by compression molding on cell adhesion and proliferation | Bellisario, D; Quadrini, F; Santolim, G; Tedde, Gm; Caputo, V; Spitalieri, P; Sangiuolo, F; Santo, L | Articolo su rivista | |
| 1-gen-2021 | Epigenomic signatures in age-related macular degeneration: Focus on their role as disease modifiers and therapeutic targets | Caputo, V; Strafella, C; Termine, A; Fabrizio, C; Ruffo, P; Cusumano, A; Giardina, E; Ricci, F; Cascella, R | Articolo su rivista | |
| 1-feb-2021 | Evaluation of OpenArray™ as a genotyping method for forensic DNA phenotyping and human identification | Ragazzo, M; Puleri, G; Errichiello, V; Manzo, L; Luzzi, L; Potenza, S; Strafella, C; Peconi, C; Nicastro, F; Caputo, V; Giardina, E | Articolo su rivista | |
| 1-gen-2019 | Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. | Zampatti, S; Colantoni, L; Strafella, C; Galota, R; Caputo, V; Campoli, G; Pagliaroli, G; Carboni, S; Mela, J; Peconi, C; Gambardella, S; Cascella, R; Giardina, E | Articolo su rivista | |
| 1-gen-2019 | Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis | Musumeci, Ml; Fiorentini, F; Bianchi, L; Cascella, R; Giardina, E; Caputo, V; Micali, G | Articolo su rivista | |
| 1-gen-2018 | Gender and complex diseases: Insights into sex-specific epigenetic|Genere e malattie complesse: Meccanismi epigenetici sesso-specifici | Caputo, V; Cascella, R; Strafella, C; Giardina, E; Novelli, G | Articolo su rivista | |
| 1-gen-2020 | Genetic counseling and NGS screening for recessive LGMD2A families | Strafella, C; Caputo, V; Campoli, G; Galota, R; Mela, J; Zampatti, S; Minozzi, G; Sancricca, C; Servidei, S; Giardina, E; Cascella, R | Articolo su rivista | |
| 1-gen-2021 | Genetic counselling improves the molecular characterisation of dementing disorders | Zampatti, S; Ragazzo, M; Peconi, C; Luciano, S; Gambardella, S; Caputo, V; Strafella, C; Cascella, R; Caltagirone, C; Giardina, E | Articolo su rivista | |
| 1-mag-2021 | Genetic determinants highlight the existence of shared etiopathogenetic mechanisms characterizing age-related macular degeneration and neurodegenerative disorders | Strafella, C; Caputo, V; Termine, A; Fabrizio, C; Ruffo, P; Potenza, S; Cusumano, A; Ricci, F; Caltagirone, C; Giardina, E; Cascella, R | Articolo su rivista | |
| 1-mar-2021 | Genetic variants allegedly linked to antisocial behaviour are equally distributed across different populations | Zampatti, S; Ragazzo, M; Fabrizio, C; Termine, A; Campoli, G; Caputo, V; Strafella, C; Cascella, R; Caltagirone, C; Giardina, E | Articolo su rivista | |
| 1-gen-2021 | Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs Interactions | Strafella, C; Caputo, V; Termine, A; Assogna, F; Pellicano, C; Pontieri, Fe; Macchiusi, L; Minozzi, G; Gambardella, S; Centonze, D; Bossù, P; Spalletta, G; Caltagirone, C; Giardina, E; Cascella, R | Articolo su rivista | |
| 1-gen-2020 | Interpreting mixture profiles: comparison between precision ID GlobalFiler™ NGS STR panel v2 and traditional methods | Ragazzo, M; Carboni, S; Caputo, V; Buttini, C; Manzo, L; Errichiello, V; Puleri, G; Giardina, E | Articolo su rivista |