| 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 A Freschi, R Del Prete, L Pignata, F Cecere, F Manfrevola, M Mattia, ... Human Molecular Genetics 30 (16), 1509-1520, 2021 | 15 | 2021 |
| Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi … L Pignata, F Cecere, A Verma, B Hay Mele, M Monticelli, B Acurzio, ... Clinical Epigenetics 14 (1), 1-15, 2022 | 12 | 2022 |
| Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs B Acurzio, A Verma, A Polito, C Giaccari, F Cecere, S Fioriniello, ... Scientific Reports 11 (1), 13802, 2021 | 10 | 2021 |
| ZBTB2 protein is a new partner of the Nucleosome Remodeling and Deacetylase (NuRD) complex R Russo, V Russo, F Cecere, M Valletta, MT Gentile, L Colucci-D'Amato, ... International Journal of Biological Macromolecules 168, 67-76, 2021 | 8 | 2021 |
| 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 C Giaccari, F Cecere, L Argenziano, A Pagano, A Galvao, D Acampora, ... Genes & Development 38 (3-4), 131-150, 2024 | 3 | 2024 |
| Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? L Pignata, F Cecere, F Acquaviva, E D’Angelo, D Cioffi, V Pellino, ... Frontiers in Cell and Developmental Biology 11, 1237629, 2023 | 3 | 2023 |
| Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer F Cecere, L Pignata, B Hay Mele, A Saadat, E D’Angelo, O Palumbo, ... Cancers 15 (7), 1944, 2023 | 3 | 2023 |
| Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome … F Passaretti, L Pignata, G Vitiello, V Alesi, G D’Elia, F Cecere, ... Genes 13 (10), 1875, 2022 | 3 | 2022 |
| Understanding the Variability of 22q11. 2 Deletion Syndrome: The Role of Epigenetic Factors F Cillo, E Coppola, F Habetswallner, F Cecere, L Pignata, E Toriello, ... Genes 15 (3), 321, 2024 | 2 | 2024 |
| The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex B Acurzio, F Cecere, C Giaccari, A Verma, R Russo, M Valletta, ... Epigenetics & Chromatin 15 (1), 1-13, 2022 | 1 | 2022 |
| A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency V Lullo, F Cecere, S Batti, S Allegretti, B Morone, S Fioriniello, L Pisapia, ... bioRxiv, 2024.04. 19.590250, 2024 | | 2024 |
| ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming A Verma, V Poondi Krishnan, F Cecere, E D’Angelo, V Lullo, M Strazzullo, ... Biomolecules 13 (12), 1717, 2023 | | 2023 |
| A maternal-effect Padi6 variant results in abnormal nuclear localization of DNMT1 and failure of epigenetic reprogramming and zygotic genome activation in mouse embryos C Giaccari, F Cecere, L Argenziano, A Galvao, D Acampora, G Rossi, ... bioRxiv, 2023.10. 09.561545, 2023 | | 2023 |
