Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients
2013-01-01 Lepre, T; Cascella, R; Ragazzo, M; Galli, E; Novelli, G; Giardina, E
Towards the application of precision medicine in Age-Related Macular Degeneration.
2018-01-01 Cascella, R; Strafella, C; Caputo, V; Errichiello, V; Zampatti, S; Milano, F; Potenza, S; Mauriello, S; Novelli, G; Ricci, F; Cusumano, A; Giardina, E.
Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD
2023-01-01 Strafella, Claudia; Caputo, Valerio; Bortolani, Sara; Torchia, Eleonora; Megalizzi, Domenica; Trastulli, Giulia; Monforte, Mauro; Colantoni, Luca; Caltagirone, Carlo; Ricci, Enzo; Tasca, Giorgio; Cascella, Raffaella; Giardina, Emiliano
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report
2019-01-01 Strafella, C; Campoli, G; Galota, Rm; Caputo, V; Pagliaroli, G; Carboni, S; Zampatti, S; Peconi, C; Mela, J; Sancricca, C; Primiano, G; Minozzi, G; Servidei, S; Cascella, R; 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, Rm; Caputo, V; Campoli, G; Pagliaroli, G; Carboni, S; Mela, J; Peconi, C; Gambardella, S; Cascella, R; Giardina, E
NGS Analysis for Molecular Diagnosis of Retinitis Pigmentosa (RP): Detection of a Novel Variant in PRPH2 Gene
2019-01-01 Strafella, C; Caputo, V; Pagliaroli, G; Iozzo, N; Campoli, G; Carboni, S; Peconi, C; Galota, Rm; Zampatti, S; Minozzi, G; Novelli, G; Giardina, E; Cascella, R
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing.
2018-01-01 Cascella, R; Strafella, C; Longo, G; Manzo, L; Ragazzo, M; De Felici, C; Gambardella, S; Marsella, Lt; Novelli, G; Borgiani, P; Sangiuolo, F; Cusumano, A; Ricci, F; Giardina, E.
FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation.
2015-01-01 Cascella, R; Strafella, C; Germani, C; Manzo, L; Marsella, Lt; Borgiani, P; Sobhy, N; Abdelmaksood, R; Gerou, S; Ioannides, D; Sangiuolo, F; Novelli, G; Hashad, D; Vakirlis, E; Giardina, E.
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7
2009-01-01 Giardina, E; Peconi, C; Cascella, R; Sinibaldi, C; Foti Cuzzola, V; Nardone, Am; Bramanti, P; Novelli, G
Genetic Variants Allegedly Linked to Antisocial Behaviour Are Equally Distributed Across Different Populations
2021-01-01 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
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: significant association of twelve variants
2017-01-01 Cascella, R; Claudia, Strafella; Giuliana, Longo; Michele, Ragazzo; Laura, Manzo; Cecilia De, Felici; Valeria, Errichiello; Valerio, Caputo; Francesco, Viola; Chiara Maria, Eandi; Giovanni, Staurenghi; Andrea, Cusumano; Silvestro, Mauriello; Luigi Tonino, Marsella; Cinzia, Ciccacci; Paola, Borgiani; Federica, Sangiuolo; Giuseppe, Novelli; Federico, Ricci; And Emiliano, Giardina
Genetic Counseling and NGS Screening for Recessive LGMD2A Families
2020-01-01 Strafella, C; Caputo, V; Campoli, G; Galota, Rm; Mela, J; Zampatti, S; Minozzi, G; Sancricca, C; Servidei, S; Giardina, E; Cascella, R
Comparative analysis between saliva and buccal swabs as source of DNA: lesson from HLA-B*57:01 testing
2015-01-01 Cascella, R; Stocchi, L; Strafella, C; Mezzaroma, I; Mannazzu, M; Vullo, V; Montella, F; Parruti, G; Borgiani, P; Sangiuolo, F; Novelli, G; Pirazzoli, A; Zampatti, S; Giardina, E.
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
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
KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility.
2017-01-01 Cascella, R; Strafella, C; Ragazzo, M; Manzo, L; Costanza, G; Bowes, J; Hüffmeier, U; Potenza, S; Sangiuolo, F; Reis, A; Barton, A; Novelli, G; Orlandi, A; Giardina, E.
Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations
2019-01-01 Strafella, C; Caputo, V; Minozzi, G; Milano, F; Arcangeli, M; Sobhy, N; Abdelmaksood, R; Hashad, D; Vakirlis, E; Novelli, G; Cascella, R; Giardina, E.
RNAseq-Based Prioritization Revealed COL6A5, COL8A1, COL10A1 and MIR146A as Common and Differential Susceptibility Biomarkers for Psoriasis and Psoriatic Arthritis: Confirmation from Genotyping Analysis of 1417 Italian Subjects
2020-01-01 Caputo, V; Strafella, C; Termine, A; Campione, E; Bianchi, L; Novelli, G; Giardina, E; Cascella, R
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis
2018-01-01 Zampatti, S; Mela, J; Peconi, C; Pagliaroli, G; Carboni, S; Barrano, G; Zito, I; Cascella, R; Marella, G; Milano, F; Arcangeli, M; Caltagirone, C; Novelli, A; Giardina, E.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients | 1-gen-2013 | Lepre, T; Cascella, R; Ragazzo, M; Galli, E; Novelli, G; Giardina, E | |
| Towards the application of precision medicine in Age-Related Macular Degeneration. | 1-gen-2018 | Cascella, R; Strafella, C; Caputo, V; Errichiello, V; Zampatti, S; Milano, F; Potenza, S; Mauriello, S; Novelli, G; Ricci, F; Cusumano, A; Giardina, E. | |
| Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD | 1-gen-2023 | Strafella, Claudia; Caputo, Valerio; Bortolani, Sara; Torchia, Eleonora; Megalizzi, Domenica; Trastulli, Giulia; Monforte, Mauro; Colantoni, Luca; Caltagirone, Carlo; Ricci, Enzo; Tasca, Giorgio; Cascella, Raffaella; Giardina, Emiliano | |
| Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report | 1-gen-2019 | Strafella, C; Campoli, G; Galota, Rm; Caputo, V; Pagliaroli, G; Carboni, S; Zampatti, S; Peconi, C; Mela, J; Sancricca, C; Primiano, G; Minozzi, G; Servidei, S; Cascella, R; Giardina, E. | |
| Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era | 1-gen-2019 | Zampatti, S; Colantoni, L; Strafella, C; Galota, Rm; Caputo, V; Campoli, G; Pagliaroli, G; Carboni, S; Mela, J; Peconi, C; Gambardella, S; Cascella, R; Giardina, E | |
| NGS Analysis for Molecular Diagnosis of Retinitis Pigmentosa (RP): Detection of a Novel Variant in PRPH2 Gene | 1-gen-2019 | Strafella, C; Caputo, V; Pagliaroli, G; Iozzo, N; Campoli, G; Carboni, S; Peconi, C; Galota, Rm; Zampatti, S; Minozzi, G; Novelli, G; Giardina, E; Cascella, R | |
| Assessing individual risk for AMD with genetic counseling, family history, and genetic testing. | 1-gen-2018 | Cascella, R; Strafella, C; Longo, G; Manzo, L; Ragazzo, M; De Felici, C; Gambardella, S; Marsella, Lt; Novelli, G; Borgiani, P; Sangiuolo, F; Cusumano, A; Ricci, F; Giardina, E. | |
| FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation. | 1-gen-2015 | Cascella, R; Strafella, C; Germani, C; Manzo, L; Marsella, Lt; Borgiani, P; Sobhy, N; Abdelmaksood, R; Gerou, S; Ioannides, D; Sangiuolo, F; Novelli, G; Hashad, D; Vakirlis, E; Giardina, E. | |
| A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7 | 1-gen-2009 | Giardina, E; Peconi, C; Cascella, R; Sinibaldi, C; Foti Cuzzola, V; Nardone, Am; Bramanti, P; Novelli, G | |
| Genetic Variants Allegedly Linked to Antisocial Behaviour Are Equally Distributed Across Different Populations | 1-gen-2021 | 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 | 1-gen-2021 | 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 | |
| Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: significant association of twelve variants | 1-gen-2017 | Cascella, R; Claudia, Strafella; Giuliana, Longo; Michele, Ragazzo; Laura, Manzo; Cecilia De, Felici; Valeria, Errichiello; Valerio, Caputo; Francesco, Viola; Chiara Maria, Eandi; Giovanni, Staurenghi; Andrea, Cusumano; Silvestro, Mauriello; Luigi Tonino, Marsella; Cinzia, Ciccacci; Paola, Borgiani; Federica, Sangiuolo; Giuseppe, Novelli; Federico, Ricci; And Emiliano, Giardina | |
| Genetic Counseling and NGS Screening for Recessive LGMD2A Families | 1-gen-2020 | Strafella, C; Caputo, V; Campoli, G; Galota, Rm; Mela, J; Zampatti, S; Minozzi, G; Sancricca, C; Servidei, S; Giardina, E; Cascella, R | |
| Comparative analysis between saliva and buccal swabs as source of DNA: lesson from HLA-B*57:01 testing | 1-gen-2015 | Cascella, R; Stocchi, L; Strafella, C; Mezzaroma, I; Mannazzu, M; Vullo, V; Montella, F; Parruti, G; Borgiani, P; Sangiuolo, F; Novelli, G; Pirazzoli, A; Zampatti, S; Giardina, E. | |
| Pharmacogenomics: An Update on Biologics and Small-Molecule Drugs in the Treatment of Psoriasis | 1-gen-2021 | Caputo, V; Strafella, C; Cosio, T; Lanna, C; Campione, E; Novelli, G; Giardina, E; Cascella, R | |
| A Hybrid Machine Learning and Network Analysis Approach Reveals Two Parkinson's Disease Subtypes from 115 RNA-Seq Post-Mortem Brain Samples | 1-gen-2022 | Termine, A; Fabrizio, C; Strafella, C; Caputo, V; Petrosini, L; Caltagirone, C; Cascella, R; Giardina, E | |
| KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility. | 1-gen-2017 | Cascella, R; Strafella, C; Ragazzo, M; Manzo, L; Costanza, G; Bowes, J; Hüffmeier, U; Potenza, S; Sangiuolo, F; Reis, A; Barton, A; Novelli, G; Orlandi, A; Giardina, E. | |
| Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations | 1-gen-2019 | Strafella, C; Caputo, V; Minozzi, G; Milano, F; Arcangeli, M; Sobhy, N; Abdelmaksood, R; Hashad, D; Vakirlis, E; Novelli, G; Cascella, R; Giardina, E. | |
| RNAseq-Based Prioritization Revealed COL6A5, COL8A1, COL10A1 and MIR146A as Common and Differential Susceptibility Biomarkers for Psoriasis and Psoriatic Arthritis: Confirmation from Genotyping Analysis of 1417 Italian Subjects | 1-gen-2020 | Caputo, V; Strafella, C; Termine, A; Campione, E; Bianchi, L; Novelli, G; Giardina, E; Cascella, R | |
| Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis | 1-gen-2018 | Zampatti, S; Mela, J; Peconi, C; Pagliaroli, G; Carboni, S; Barrano, G; Zito, I; Cascella, R; Marella, G; Milano, F; Arcangeli, M; Caltagirone, C; Novelli, A; Giardina, E. |
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