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International Journal of Biological Macromolecules|December 10, 2020
ZBTB2 protein is a new partner of the Nucleosome Remodeling and Deacetylase (NuRD) complexRosita Russo, Veronica Russo, Francesco Cecere, et al.
BMJ Open|July 25, 2025
New generation of paediatricians in the health care system: are paediatric residents ready to manage children without supervision? A survey using respiratory infections as a modelMargherita Del Bene, Alfredo Diana, Antonio Corsello, et al.
Frontiers in Cell and Developmental Biology|August 28, 2023
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?Laura Pignata, Francesco Cecere, Fabio Acquaviva, et al.
Frontiers in Immunology|July 23, 2024
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiencyVincenzo Lullo, Francesco Cecere, Saveria Batti, et al.
Cancers|April 13, 2023
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal CancerFrancesco Cecere, Laura Pignata, Bruno Hay Mele, et al.
Frontiers in Oncology|March 13, 2026
Impact of nutritional source modality on weight loss and BMI reduction after hematopoietic stem cell transplantationFrancesco Paolo Tambaro, Francesco Fabozzi, Riccardo Masetti, et al.
Epigenetics & Chromatin|July 24, 2025
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humansFrancesco Cecere, Raissa Relator, Michael Levy, et al.
Clinical Epigenetics|November 23, 2025
Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndromeEmilia D'Angelo, Laura Pignata, Francesco Cecere, et al.
Genes|March 28, 2024
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic FactorsFrancesca Cillo, Emma Coppola, Federico Habetswallner, et al.
Genes & Development|March 7, 2024
A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryosCarlo Giaccari, Francesco Cecere, Lucia Argenziano, et al.
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