Silvia Russo

X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations

Antonio Musio, Angelo Selicorni, Maria Luisa Focarelli et al. · Nature Genetics · 2006 · 476 citations

Mendelian Disorder, Genetic Disorder, Pathology +5

Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly

Maila Giannandrea, Veronica Bianchi, Maria Lidia Mignogna et al. · The American Journal of Human Genetics · 2010 · 234 citations · Full text

Syndromic Autism, Genetic Disorder, Genetics +8

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome

Jet Bliek, Gaetano Verde, Jonathan L A Callaway et al. · European Journal of Human Genetics · 2008 · 232 citations · Full text

Developmental Biology, Genetic Disorder, Epigenetic Change +7

(Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome

Alessandro Mussa, Silvia Russo, Agostina De Crescenzo et al. · European Journal of Human Genetics · 2015 · 185 citations · Full text

Clinical Disorders, Genetic Disorder, Genetics +7

Genistein in the Metabolic Syndrome: Results of a Randomized Clinical Trial

Francesco Squadrito, Herbert Marini, Alessandra Bitto et al. · The Journal of Clinical Endocrinology & Metabolism · 2013 · 174 citations · Full text