F. R. Di Raimo

Intrafamilial communication of hereditary breast and ovarian cancer genetic information in Italian women: towards a personalised approach

M. Genuardi, E. Lucci-Cordisco, A. Poscia, 2020, European Journal of Human Genetics.

Insertion of 16 amino acids in the BAR domain of the oligophrenin 1 protein causes mental retardation and cerebellar hypoplasia in an Italian family

E. Bertini, P. Billuart, G. Neri, 2011, Human mutation.

POPDC1(S201F) causes muscular dystrophy and arrhythmia by affecting protein trafficking.

E. Bertini, Hui Jiang, E. Arbustini, 2016, The Journal of clinical investigation.

Implementing carrier screening for cystic fibrosis outside the clinic: ethical analysis in the light of the personalist view.

V. Lucidi, A. A. Teleman, P. Refolo, 2018, La Clinica terapeutica.

Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy

C. Scapoli, E. Bertini, M. Pane, 2020, Frontiers in Genetics.

Treatment with valproic acid ameliorates ADHD symptoms in fragile X syndrome boys

G. Neri, M. Torrioli, D. Martinelli, 2010, American journal of medical genetics. Part A.

[Genetic test for cancer and intra-family communication: freedom vs. responsibility].

P. Refolo, A. Teleman, F. R. Di Raimo, 2015, La Clinica terapeutica.