A. Rosseto

Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin‐binding dynamics

F. Cardarelli, A. Renieri, F. Mari, 2012, Clinical genetics.

Molecular work-up of patients with the congenital variant of Rett syndrome: analysis of the 14q12 region

A. Rosseto, Ariele Rosseto, 2010 .

Pervasive mutations of JAK-STAT pathway genes in classical Hodgkin lymphoma.

Alexander V Penson, L. Pasqualucci, R. Rabadán, 2018, Blood.