CECERE, FRANCESCO
CECERE, FRANCESCO
Istituto per le applicazioni del calcolo - IAC - Sede Secondaria Napoli
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
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
A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos
2024 Giaccari, Carlo; Cecere, Francesco; Argenziano, Lucia; Pagano, Angela; Galvao, Antonio; Acampora, Dario; Rossi, Gianna; Hay Mele, Bruno; Acurzio, Basilia; Coonrod, Scott; Vittoria Cubellis, Maria; Cerrato, Flavia; Andrews, Simon; Cecconi, Sandra; Kelsey, Gavin; Andrea Riccio, And
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency
2024 Lullo, Vincenzo; Cecere, Francesco; Batti, Saveria; Allegretti, Sara; Morone, Barbara; Fioriniello, Salvatore; Pisapia, Laura; Genesio, Rita; Della Ragione, Floriana; Giardino, Giuliana; Pignata, Claudio; Riccio, Andrea; Matarazzo, Maria R.; Strazzullo, Maria
New insights into oocyte cytoplasmic lattice-associated proteins
2024 Giaccari, C.; Cecere, F.; Argenziano, L.; Pagano, A.; Riccio, A.
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors
2024 Cillo, F.; Coppola, E.; Habetswallner, F.; Cecere, F.; Pignata, L.; Toriello, E.; De Rosa, A.; Grilli, L.; Ammendola, A.; Salerno, P.; Romano, R.; Cirillo, E.; Merla, G.; Riccio, A.; Pignata, C.; Giardino, G.
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer
2023 Cecere, Francesco; Pignata, Laura; Hay Mele, Bruno; Saadat, Abu; D'Angelo, Emilia; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Scarano, Gioacchino; Battista Rossi, Giovanni; Angelini, Claudia; Sparago, Angela; Cerrato, Flavia; Riccio, Andrea
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
ICF1 Syndrome Associated DNMT3B Mutations Prevent de novo Methylation at a subset of Imprinted Loci During iPSC Reprogramming
2023 Verma, Ankit; Poondi Krishnan, Varsha; Cecere, Francesco; D'Angelo, Emilia; Lullo, Vincenzo; Strazzullo, Maria; Selig, Sara; Angelini, Claudia; Matarazzo, MARIA ROSARIA; Riccio, Andrea
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum.
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.
2022 Pignata, Laura; Cecere, Francesco; Verma, Ankit; Hay Mele, Bruno; Monticelli, Maria; Acurzio, Basilia; Giaccari, Carlo; Sparago, Angela; Ramon Hernandez Mora, Jose; Monteagudosánchez, Ana; Esteller, Manel; Pereda, Arrate; Tenoriocastano, Jair; Palumbo, Orazio; Carella, Massimo; Prontera, Paolo; Piscopo, Carmelo; Accadia, Maria; Lapunzina, Pablo; Vittoria Cubellis, Maria; Perez de Nanclares, Guiomar; Monk, David; Riccio, Andrea; Cerrato, Flavia
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex.
2022 Acurzio, Basilia; Cecere, Francesco; Giaccari, Carlo; Verma, Ankit; Russo, Rosita; Valletta, Mariangela; Hay Mele, Bruno; Angelini, Claudia; Chambery, Angela; Riccio, Andrea
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
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.
ZBTB2 protein is a new partner of the Nucleosome Remodeling and Deacetylase (NuRD) complex
2021 Russo, Rosita; Russo, Veronica; Cecere, Francesco; Valletta, Mariangela; Teresa Gentile, Maria; Lucacoluccid'Amato, ; Angelini, Claudia; Riccio, Andrea; Vincenzo Pedone, Paolo; Chambery, Angela; Baglivo, Ilaria
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs
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
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| 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-effect Padi6 variant 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; Vittoria Cubellis, Maria; Cerrato, Flavia; Andrews, Simon; Cecconi, Sandra; Kelsey, Gavin; Andrea Riccio, And | |
| A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency | 1-gen-2024 | Lullo, Vincenzo; Cecere, Francesco; Batti, Saveria; Allegretti, Sara; Morone, Barbara; Fioriniello, Salvatore; Pisapia, Laura; Genesio, Rita; Della Ragione, Floriana; Giardino, Giuliana; Pignata, Claudio; Riccio, Andrea; Matarazzo, Maria R.; Strazzullo, Maria | |
| New insights into oocyte cytoplasmic lattice-associated proteins | 1-gen-2024 | Giaccari, C.; Cecere, F.; Argenziano, L.; Pagano, A.; Riccio, A. | |
| Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors | 1-gen-2024 | Cillo, F.; Coppola, E.; Habetswallner, F.; Cecere, F.; Pignata, L.; Toriello, E.; De Rosa, A.; Grilli, L.; Ammendola, A.; Salerno, P.; Romano, R.; Cirillo, E.; Merla, G.; Riccio, A.; Pignata, C.; Giardino, G. | |
| Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer | 1-gen-2023 | Cecere, Francesco; Pignata, Laura; Hay Mele, Bruno; Saadat, Abu; D'Angelo, Emilia; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Scarano, Gioacchino; Battista Rossi, Giovanni; Angelini, Claudia; Sparago, Angela; Cerrato, Flavia; Riccio, Andrea | |
| 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 | |
| ICF1 Syndrome Associated DNMT3B Mutations Prevent de novo Methylation at a subset of Imprinted Loci During iPSC Reprogramming | 1-gen-2023 | Verma, Ankit; Poondi Krishnan, Varsha; Cecere, Francesco; D'Angelo, Emilia; Lullo, Vincenzo; Strazzullo, Maria; Selig, Sara; Angelini, Claudia; Matarazzo, MARIA ROSARIA; Riccio, Andrea | |
| 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; Ramon Hernandez Mora, Jose; Monteagudosánchez, Ana; Esteller, Manel; Pereda, Arrate; Tenoriocastano, Jair; Palumbo, Orazio; Carella, Massimo; Prontera, Paolo; Piscopo, Carmelo; Accadia, Maria; Lapunzina, Pablo; Vittoria Cubellis, Maria; Perez de Nanclares, Guiomar; Monk, David; Riccio, Andrea; Cerrato, Flavia | |
| The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex. | 1-gen-2022 | Acurzio, Basilia; Cecere, Francesco; Giaccari, Carlo; Verma, Ankit; Russo, Rosita; Valletta, Mariangela; Hay Mele, Bruno; Angelini, Claudia; Chambery, Angela; Riccio, Andrea | |
| 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. | |
| ZBTB2 protein is a new partner of the Nucleosome Remodeling and Deacetylase (NuRD) complex | 1-gen-2021 | Russo, Rosita; Russo, Veronica; Cecere, Francesco; Valletta, Mariangela; Teresa Gentile, Maria; Lucacoluccid'Amato, ; Angelini, Claudia; Riccio, Andrea; Vincenzo Pedone, Paolo; Chambery, Angela; Baglivo, Ilaria | |
| 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 |