Emilia D'angelo

Naples, Italy

Last Updated: 09/26/2026

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Found 9 publications

Loss of maternal PADI6 disrupts DNA methylation and genomic imprinting maintenance in late preimplantation mouse embryos.

Loss of maternal PADI6 disrupts DNA methylation and genomic imprinting maintenance in late preimplantation mouse embryos.

Journal: Epigenetics & chromatin

Published: January 09, 2026

DNA Methylation and Transcriptomic Profiles of Wilms Tumour Reveal New Deregulated Genes and Epigenetic Processes Relevant for Tumour Stratification and Management.

DNA Methylation and Transcriptomic Profiles of Wilms Tumour Reveal New Deregulated Genes and Epigenetic Processes Relevant for Tumour Stratification and Management.

Journal: International journal of cancer

Published: December 12, 2025

Adult-Onset β-Thalassemia Major as Acquired Imprinting Disorder.

Adult-Onset β-Thalassemia Major as Acquired Imprinting Disorder.

Journal: American journal of hematology

Published: November 24, 2025

Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome.

Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome.

Journal: Clinical epigenetics

Published: September 23, 2025

Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances.

Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances.

Journal: Clinical epigenetics

Published: May 27, 2025

Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans.

Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans.

Journal: Epigenetics & chromatin

Published: April 09, 2025

ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming.

ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming.

Journal: Biomolecules

Published: August 02, 2023

Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?

Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?

Journal: Frontiers in cell and developmental biology

Published: June 09, 2023

Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer.

Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer.

Journal: Cancers

Published: January 30, 2023

Showing 1-9 of 9

Last Updated: 09/26/2026