Federica Palumbo

Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene

A. Mai, L. Pacini, G. Maulucci, 2020, Human Genetics.

Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome†

G. Neri, E. Tabolacci, Veronica Nobile, 2016, Genes.

Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells

M. Helmer-Citterich, F. Ferrè, Stella Lanni, 2016, Epigenetics & Chromatin.

Defining the role of the CGGBP1 protein in FMR1 gene expression

Stella Lanni, G. Neri, P. Chiurazzi, 2015, European Journal of Human Genetics.