D'ANGELO, EMILIA
D'ANGELO, EMILIA
Dipartimento di Scienze e Tecnologie Ambientali Biologiche e Farmaceutiche (DISTABiF)
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?
2023 Pignata, Laura; Cecere, Francesco; Acquaviva, Fabio; D'Angelo, Emilia; Cioffi, Daniela; Pellino, Valeria; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Sparago, Angela; De Brasi, Daniele; Cerrato, Flavia; Riccio, Andrea
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer
2023 Cecere, F.; Pignata, L.; Hay Mele, B.; Saadat, A.; D'Angelo, E.; Palumbo, O.; Palumbo, P.; Carella, M.; Scarano, G.; Rossi, G. B.; Angelini, C.; Sparago, A.; Cerrato, F.; Riccio, A.
Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances
2025 Cecere, Francesco; Pignata, Laura; D'Angelo, Emilia; Giaccari, Carlo; Saadat, Abu; Sparago, Angela; Angelini, Claudia; Hay Mele, Bruno; Mussa, Alessandro; Ferrero, Giovanni Battista; Scarano, Gioacchino; Gori, Giulia; Di Maria, Emilio; Romano, Corrado; Tarani, Luigi; Piscopo, Carmelo; Scala, Iris; Tenorio, Jair Antonio; Lapunzina, Pablo; Cerrato, Flavia; Riccio, Andrea
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming
2023 Verma, A.; Poondi Krishnan, V.; Cecere, F.; D'Angelo, E.; Lullo, V.; Strazzullo, M.; Selig, S.; Angelini, C.; Matarazzo, M. R.; Riccio, A.
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans
2025 Cecere, Francesco; Relator, Raissa; Levy, Michael; Verma, Ankit; Mcconkey, Haley; Mele, Bruno Hay; Pignata, Laura; Giaccari, Carlo; D'Angelo, Emilia; Saha, Subham; Saadat, Abu; Sparago, Angela; Angelini, Claudia; Cerrato, Flavia; Sadikovic, Bekim; Riccio, Andrea
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? | 1-gen-2023 | Pignata, Laura; Cecere, Francesco; Acquaviva, Fabio; D'Angelo, Emilia; Cioffi, Daniela; Pellino, Valeria; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Sparago, Angela; De Brasi, Daniele; Cerrato, Flavia; Riccio, Andrea | |
| Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer | 1-gen-2023 | Cecere, F.; Pignata, L.; Hay Mele, B.; Saadat, A.; D'Angelo, E.; Palumbo, O.; Palumbo, P.; Carella, M.; Scarano, G.; Rossi, G. B.; Angelini, C.; Sparago, A.; Cerrato, F.; Riccio, A. | |
| Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances | 1-gen-2025 | Cecere, Francesco; Pignata, Laura; D'Angelo, Emilia; Giaccari, Carlo; Saadat, Abu; Sparago, Angela; Angelini, Claudia; Hay Mele, Bruno; Mussa, Alessandro; Ferrero, Giovanni Battista; Scarano, Gioacchino; Gori, Giulia; Di Maria, Emilio; Romano, Corrado; Tarani, Luigi; Piscopo, Carmelo; Scala, Iris; Tenorio, Jair Antonio; Lapunzina, Pablo; Cerrato, Flavia; Riccio, Andrea | |
| ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming | 1-gen-2023 | Verma, A.; Poondi Krishnan, V.; Cecere, F.; D'Angelo, E.; Lullo, V.; Strazzullo, M.; Selig, S.; Angelini, C.; Matarazzo, M. R.; Riccio, A. | |
| Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans | 1-gen-2025 | Cecere, Francesco; Relator, Raissa; Levy, Michael; Verma, Ankit; Mcconkey, Haley; Mele, Bruno Hay; Pignata, Laura; Giaccari, Carlo; D'Angelo, Emilia; Saha, Subham; Saadat, Abu; Sparago, Angela; Angelini, Claudia; Cerrato, Flavia; Sadikovic, Bekim; Riccio, Andrea |