M. Falco

The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes

Cynthia J. Curry, Jill A. Rosenfeld, Erica T. Grant et al. · American Journal of Medical Genetics Part A · 2013 · 104 citations · Full text

Brain Development, Genetics, Duplication 17P13.3 +19

Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients

Lucia Grillo, S Reitano, Giovanni Belfiore et al. · European Journal of Medical Genetics · 2010 · 95 citations

Chromosome Xq22.1, Psychiatric Disorders, Psychiatry +13

1.5 Mb<i> de novo </i>22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features

A Alberti, Corrado Romano, M. Falco et al. · Clinical Genetics · 2007 · 53 citations

Developmental Cognitive Neuroscience, Genetics, Pathology +20

Analysis of the gastrin‐releasing peptide receptor gene in Italian patients with autism spectrum disorders

Gregorio Seidita, Mario G. Mirisola, Rosalba D’Anna et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2008 · 12 citations · Full text

Brain Development, Autism Spectrum Disorders, Genetics +22