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Birth Defects Research|July 10, 2024
Intrauterine growth in chromatinopathies: A long road for better understanding and for improving clinical managementLaura Avagliano, Silvia Castiglioni, Antonella Lettieri, et al.
Frontiers in Cell and Developmental Biology|May 7, 2021
Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and ChromatinopathiesChiara Parodi, Elisabetta Di Fede, Angela Peron, et al.
American Journal of Medical Genetics. Part A|April 5, 2025
Cohesins: Crossroad Between Cornelia de Lange Spectrum and Cancer PredispositionLaura Rigotti, Stefano Rebellato, Antonella Lettieri, et al.
Molecular Pharmaceutics|October 17, 2022
Caffeic Acid-Grafted PLGA as a Novel Material for the Design of Fluvastatin-Eluting Nanoparticles for the Prevention of Neointimal HyperplasiaStefano Bellosta, Francesca Selmin, Giulia Magri, et al.
Frontiers in Cell and Developmental Biology|October 13, 2022
Epigenetic disorders: Lessons from the animals-animal models in chromatinopathiesElisabetta Di Fede, Paolo Grazioli, Antonella Lettieri, et al.
Cells|May 1, 2020
Impact of <i>BDNF</i> Val66Met Polymorphism on Myocardial Infarction: Exploring the Macrophage PhenotypeLeonardo Sandrini, Laura Castiglioni, Patrizia Amadio, et al.
Human Genetics|May 16, 2024
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathiesElisabetta Di Fede, Antonella Lettieri, Esi Taci, et al.
American Journal of Medical Genetics. Part A|March 10, 2022
Identical EP300 variant leading to Rubinstein-Taybi syndrome with different clinical and immunologic phenotypeFrancesco Saettini, Grazia Fazio, Maria Teresa Bonati, et al.
Orphanet Journal of Rare Diseases|December 20, 2024
Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matterSilvia Castiglioni, Laura Pezzoli, Lidia Pezzani, et al.
Genes|March 25, 2022
<i>KMT2A</i>: Umbrella Gene for Multiple DiseasesSilvia Castiglioni, Elisabetta Di Fede, Clara Bernardelli, et al.
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