Silvana Beri

Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome

María Clara Bonaglia, Roberto Giorda, Silvana Beri et al. · PLoS Genetics · 2011 · 223 citations · Full text

Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation

Renata Bocciardi, Roberto Giorda, Jens Buttgereit et al. · Human Mutation · 2007 · 130 citations

Genotype–phenotype relationship in three cases with overlapping 19p13.12 microdeletions

María Clara Bonaglia, Susan Marelli, Francesca Novara et al. · European Journal of Human Genetics · 2010 · 123 citations · Full text

Population Genetics, Genetics, Genotype-phenotype Association +1

Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3

Annalisa Vetro, Mohammadreza Dehghani, Lilia Kraoua et al. · European Journal of Human Genetics · 2014 · 108 citations · Full text

Spermatogenesis, Biology, Developmental Biology +13

A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia

Cecilia Marino, Roberto Giorda, Maria Luisa Lorusso et al. · European Journal of Human Genetics · 2005 · 92 citations · Full text

Neurodevelopmental Disorders, Genetic Disorder, Genetics +9