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Trends in Genetics : TIG|July 2, 2024
New insights into oocyte cytoplasmic lattice-associated proteinsCarlo Giaccari, Francesco Cecere, Lucia Argenziano, et al.
Life (Basel, Switzerland)|June 27, 2024
An Update on Physiopathological Roles of Akt in the ReprodAKTive Mammalian OvaryCarlo Giaccari, Sevastiani Antonouli, George Anifandis, et al.
Epigenetics & Chromatin|August 2, 2022
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complexBasilia Acurzio, Francesco Cecere, Carlo Giaccari, et al.
Scientific Reports|July 6, 2021
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCsBasilia Acurzio, Ankit Verma, Alessia Polito, 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 & 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.
Reproduction (Cambridge, England)|June 26, 2025
Single-cell multiomic analysis reveals methylome and transcriptome deviations following oocyte maturation in vitroCamilla Benedetti, Carlo Giaccari, Francesco Cecere, et al.
Clinical Epigenetics|October 4, 2025
Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbancesFrancesco Cecere, Laura Pignata, Emilia D'Angelo, et al.
Clinical Epigenetics|June 1, 2022
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 disturbancesLaura Pignata, Francesco Cecere, Ankit Verma, et al.
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