E. Grillo

Investigation of modifier genes within copy number variations in Rett syndrome

J. LaSalle, A. Renieri, M. Mucciolo, 2012, Journal of Human Genetics.

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

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

Analysis of the Phenotypes in the Rett Networked Database

A. Vignoli, A. Clarke, J. Armstrong, 2019, International journal of genomics.

Revealing the Complexity of a Monogenic Disease: Rett Syndrome Exome Sequencing

S. Furini, A. Renieri, F. Mari, 2013, PloS one.

Rett networked database: An integrated clinical and genetic network of rett syndrome databases

A. Vignoli, A. Clarke, J. Armstrong, 2012, Human mutation.

NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype

M. Sanson, J. Soulier, I. Bièche, 2010, Human mutation.

Investigation of modifier genes within copy number variations in Rett syndrome

J. LaSalle, A. Renieri, M. Mucciolo, 2011, Journal of Human Genetics.

Two genes are responsible for Griscelli syndrome at the same 15q21 locus.

A. Fischer, I. Tezcan, F. Ersoy, 2000, Genomics.