R. Giorda

Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population

N. Bresolin, G. Comi, R. Cagliani, 2003, Neuromuscular Disorders.

Alterations of the Birt-Hogg-Dubé gene (BHD) in sporadic colorectal tumours

R. Borgatti, C. Windpassinger, C. Gagliardi, 2003 .

An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia

C. Marino, S. Mascheretti, R. Giorda, 2015, Human Genetics.

Influence of the OPRM1 gene polymorphism upon children's degree of withdrawal and brain activation in response to facial expressions

R. Giorda, M. Battaglia, A. Zanoni, 2012, Developmental Cognitive Neuroscience.

CNGA3 mutations in hereditary cone photoreceptor disorders.

S. Jacobson, R. Salati, L. Sharpe, 2001, American journal of human genetics.