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CERRATO, Flavia

CERRATO, Flavia  

Dipartimento di Scienze e Tecnologie Ambientali Biologiche e Farmaceutiche (DISTABiF)  

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Adult‐Onset β‐Thalassemia Major as Acquired Imprinting Disorder 1-gen-2026 D'Angelo, Emilia; Mandrile, Giorgia; Tesio, Nicolò; Cecere, Francesco; Ceglie, Teresa; De Maria, Rosa Maria; Mellone, Simona; Giordano, Mara; Kargutar, Neha Sanjay; Cerrato, Flavia; Riccio, Andrea; Ferrero, Giovanni Battista
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
Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome 1-gen-2025 D'Angelo, Emilia; Pignata, Laura; Cecere, Francesco; Vimercati, Alessandro; Cubellis, Maria Vittoria; Saadat, Abu; Giaccari, Carlo; Thibaud, Nathalie; Eggermann, Thomas; Fernández-Fructuoso, Jose Ramon; Russo, Silvia; Netchine, Irène; Cerrato, Flavia; Riccio, Andrea; Brioude, Frédéric
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
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 1-gen-2024 Giaccari, Carlo; Cecere, Francesco; Argenziano, Lucia; Pagano, Angela; Galvao, Antonio; Acampora, Dario; Rossi, Gianna; Hay Mele, Bruno; Acurzio, Basilia; Coonrod, Scott; Cubellis, Maria Vittoria; Cerrato, Flavia; Andrews, Simon; Cecconi, Sandra; Kelsey, Gavin; Riccio, Andrea
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis 1-gen-2024 G Mackay, Deborah J; Gazdagh, Gabriella; Monk, David; Brioude, Frederic; Giabicani, Eloise; M Krzyzewska, Izabela; M Kalish, Jennifer; M Maas, Saskia; Kagami, Masayo; Beygo, Jasmin; Kahre, Tiina; Tenorio-Castano, Jair; Ambrozaitytė, Laima; Burnytė, Birutė; Cerrato, Flavia; H Davies, Justin; Battista Ferrero, Giovanni; Fjodorova, Olga; Manero-Azua, Africa; Pereda, Arrate; Russo, Silvia; Tannorella, Pierpaola; I Temple, Karen; Õunap, Katrin; Riccio, Andrea; Perez de Nanclares, Guiomar; R Maher, Eamonn; Lapunzina, Pablo; Netchine, Irène; Eggermann, Thomas; Bliek, Jet; Tümer, Zeynep
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 1-gen-2023 Elefante, Pierandrea; Spedicati, Beatrice; Faletra, Flavio; Pignata, Laura; Cerrato, Flavia; Riccio, Andrea; Barbi, Egidio; Memo, Luigi; Travan, Laura
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.
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques 1-gen-2022 Carli, Diana; Operti, Matteo; Russo, Silvia; Cocchi, Guido; Milani, Donatella; Leoni, Chiara; Prada, Elisabetta; Melis, Daniela; Falco, Mariateresa; Spina, Jennifer; Uliana, Vera; Sara, Osimani; Sirchia, Fabio; Tarani, Luigi; Macchiaiolo, Marina; Cerrato, Flavia; Sparago, Angela; Pignata, Laura; Tannorella, Pierpaola; Cardaropoli, Simona; Bartuli, Andrea; Riccio, Andrea; Ferrero, Giovanni Battista; Mussa, Alessandro
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum 1-gen-2022 Passaretti, Francesco; Pignata, Laura; Vitiello, Giuseppina; Alesi, Viola; D'Elia, Gemma; Cecere, Francesco; Acquaviva, Fabio; De Brasi, Daniele; Novelli, Antonio; Riccio, Andrea; Iolascon, Achille; Cerrato, Flavia
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances 1-gen-2022 Pignata, Laura; Cecere, Francesco; Verma, Ankit; Hay Mele, Bruno; Monticelli, Maria; Acurzio, Basilia; Giaccari, Carlo; Sparago, Angela; Hernandez Mora, Jose Ramon; Monteagudo-Sánchez, Ana; Esteller, Manel; Pereda, Arrate; Tenorio-Castano, Jair; Palumbo, Orazio; Carella, Massimo; Prontera, Paolo; Piscopo, Carmelo; Accadia, Maria; Lapunzina, Pablo; Cubellis, Maria Vittoria; de Nanclares, Guiomar Perez; Monk, David; Riccio, Andrea; Cerrato, Flavia
Mosaic segmental and whole-chromosome upd(11)mat in silver-russell syndrome 1-gen-2021 Pignata, L.; Sparago, A.; Palumbo, O.; Andreucci, E.; Lapi, E.; Tenconi, R.; Carella, M.; Riccio, A.; Cerrato, F.
The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model 1-gen-2021 Freschi, A.; Del Prete, R.; Pignata, L.; Cecere, F.; Manfrevola, F.; Mattia, M.; Cobellis, G.; Sparago, A.; Bartolomei, M. S.; Riccio, A.; Cerrato, F.
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 1-gen-2021 Sparago, A.; Cerrato, F.; Pignata, L.; Cammarata-Scalisi, F.; Garavelli, L.; Piscopo, C.; Vancini, A.; Riccio, A.
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 1-gen-2021 Acurzio, B.; Verma, A.; Polito, A.; Giaccari, C.; Cecere, F.; Fioriniello, S.; Della Ragione, F.; Fico, A.; Cerrato, F.; Angelini, C.; Feil, R.; Riccio, A.
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 1-gen-2020 Pignata, L.; Palumbo, O.; Cerrato, F.; Acurzio, B.; de Alava, E.; Roma, J.; Gallego, S.; Mora, J.; Carella, M.; Riccio, A.; Verde, G.
DNA Methylation in the Diagnosis of Monogenic Diseases 1-gen-2020 Cerrato, F.; Sparago, A.; Ariani, F.; Brugnoletti, F.; Calzari, L.; Coppede, F.; De Luca, A.; Gervasini, C.; Giardina, E.; Gurrieri, F.; Lo Nigro, C.; Merla, G.; Miozzo, M.; Russo, S.; Sangiorgi, E.; Sirchia, S. M.; Squeo, G. M.; Tabano, S.; Tabolacci, E.; Torrente, I.; Genuardi, M.; Neri, G.; Riccio, A.
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 1-gen-2020 Cubellis, M. V.; Pignata, L.; Verma, A.; Sparago, A.; Del Prete, R.; Monticelli, M.; Calzari, L.; Antona, V.; Melis, D.; Tenconi, R.; Russo, S.; Cerrato, F.; Riccio, A.
Beckwith-Wiedemann Syndrome 1-gen-2019 Mussa, A; Kalish, J; Cerrato, F; Riccio, A; Ferrero, Gb