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Orphanet Journal of Rare Diseases|June 2, 2019
Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum DisorderJulie Masson, Caroline Demily, Nicolas Chatron, et al.
The Hastings Center Report|February 25, 2021
Rethinking Human Embryo Research PoliciesKirstin R W Matthews, Ana S Iltis, Nuria Gallego Marquez, et al.
Cell Reports|April 6, 2022
CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectoriesCarlo Emanuele Villa, Cristina Cheroni, Christoph P Dotter, et al.
Cell Death & Disease|May 28, 2024
Tumor microenvironment-induced FOXM1 regulates ovarian cancer stemnessChiara Battistini, Hilary A Kenny, Melissa Zambuto, et al.
HLA|August 2, 2024
HLA alleles associated to susceptibility to gliptin-associated bullous pemphigoid in Italian patientsMarco Andreani, Feliciana Mariotti, Anna Pira, et al.
Molecular Autism|June 4, 2020
Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASDDanijela Drakulic, Srdjan Djurovic, Yasir Ahmed Syed, et al.
Stem Cell Reports|December 19, 2025
High resolution multi-scale profiling of embryonic germ cell-like cell derivation reveals pluripotent state transitions in humansSarah Stucchi, Lessly P Sepulveda-Rincon, Camille Dion, et al.
The Journal of Clinical Investigation|November 9, 2013
Germinal center dysregulation by histone methyltransferase EZH2 promotes lymphomagenesisMarieta Caganova, Chiara Carrisi, Gabriele Varano, et al.
Science Advances|November 29, 2023
GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disordersAlejandro López-Tobón, Reinald Shyti, Carlo Emanuele Villa, et al.
International Journal of Molecular Sciences|June 5, 2020
The ENDpoiNTs Project: Novel Testing Strategies for Endocrine Disruptors Linked to Developmental NeurotoxicityDiana Lupu, Patrik Andersson, Carl-Gustaf Bornehag, et al.
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