Sfoglia per Autore
YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction
2017 M. Gabriele, A.T. Vulto van Silfhout, P. Germain, A. Vitriolo, R. Kumar, E. Douglas, E. Haan, K. Kosaki, T. Takenouchi, A. Rauch, K. Steindl, E. Frengen, D. Misceo, C.R.J. Pedurupillay, P. Stromme, J.A. Rosenfeld, Y. Shao, W.J. Craigen, C.P. Schaaf, D. Rodriguez Buritica, L. Farach, J. Friedman, P. Thulin, S.D. Mclean, K.M. Nugent, J. Morton, J. Nicholl, J. Andrieux, A. Stray Pedersen, P. Chambon, S. Patrier, S.A. Lynch, S. Kjaergaard, P.M. Tørring, C. Brasch Andersen, A. Ronan, A. van Haeringen, P.J. Anderson, Z. Powis, H.G. Brunner, R. Pfundt, J.H.M. Schuurs Hoeijmakers, B.W.M. van Bon, S. Lelieveld, C. Gilissen, W.M. Nillesen, L.E.L.M. Vissers, J. Gecz, D.A. Koolen, G. Testa, B.B.A. de Vries
The chromatin basis of neurodevelopmental disorders: Rethinking dysfunction along the molecular and temporal axes
2018 M. Gabriele, A. Lopez Tobon, G. D'Agostino, G. Testa
THE DEVELOPMENTAL LOGIC OF ENHANCEROPATHIES CAUSED BY KMT2D AND YY1 HAPLOINSUFFICIENCY THROUGH PATIENT-DERIVED DISEASE MODELING PLATFORMS
2019 M. Gabriele
From enhanceropathies to the epigenetic manifold underlying human cognition
2019 A. Vitriolo, M. Gabriele, G. Testa
High-throughput screening identifies histone deacetylase inhibitors that modulate GTF2I expression in 7q11.23 microduplication autism spectrum disorder patient-derived cortical neurons
2020 F. Cavallo, F. Troglio, G. Faga, D. Fancelli, R. Shyti, S. Trattaro, M. Zanella, G. D'Agostino, J.M. Hughes, M.R. Cera, M. Pasi, M. Gabriele, M. Lazzarin, M. Mihailovich, F. Kooy, A. Rosa, C. Mercurio, M. Varasi, G. Testa
KMT2B and Neuronal Transdifferentiation: Bridging Basic Chromatin Mechanisms to Disease Actionability
2020 G. Barbagiovanni, M. Gabriele, G. Testa
Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders
2022 K. Linda, E.I. Lewerissa, A.H.A. Verboven, M. Gabriele, M. Frega, T.M. Klein Gunnewiek, L. Devilee, E. Ulferts, M. Hommersom, A. Oudakker, C. Schoenmaker, H. van Bokhoven, D. Schubert, G. Testa, D.A. Koolen, B.B.A. de Vries, N. Nadif Kasri
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