Agostina De Crescenzo

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

Prevalence of beckwith–wiedemann syndrome in North West of Italy

Alessandro Mussa, Silvia Russo, Agostina De Crescenzo et al. · American Journal of Medical Genetics Part A · 2013 · 137 citations

The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases

Nicoletta Chiesa, Agostina De Crescenzo, Kankadeb Mishra et al. · Human Molecular Genetics · 2011 · 123 citations · Full text

Distinct Methylation Changes at the IGF2-H19 Locus in Congenital Growth Disorders and Cancer

Adele Murrell, Yoko Itō, Gaetano Verde et al. · PLoS ONE · 2008 · 103 citations · Full text