Pubblicazioni

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers

2018 - AMERICAN JOURNAL OF MEDICAL GENETICS. PART A

Unolt, Marta; Versacci, Paolo; Anaclerio, Silvia; Lambiase, Caterina; Calcagni, Giulio; Trezzi, Matteo; Carotti, Adriano; Crowley, Terrence Blaine; Zackai, Elaine H.; Goldmuntz, Elizabeth; Gaynor, James William; Digilio, Maria Cristina; Mcdonald-Mcginn, Donna M.; Marino, Bruno

An allelic variant in the intergenic region between ERAP1 and ERAP2 correlates with an inverse expression of the two genes

2018 - SCIENTIFIC REPORTS

Paladini, F; Fiorillo, Mt; Vitulano, C; Tedeschi, V; Piga, M; Cauli, A; Mathieu, A; Sorrentino, R

Combining Genetic Variants to Improve Risk Prediction for NAFLD and Its Progression to Cirrhosis: A Proof of Concept Study

2018 - CANADIAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY

Vespasiani-Gentilucci, Umberto; Dell'Unto, Chiara; De Vincentis, Antonio; Baiocchini, Andrea; Delle Monache, Marco; Cecere, Roberto; Pellicelli, Adriano Maria; Giannelli, Valerio; Carotti, Simone; Galati, Giovanni; Gallo, Paolo; Valentini, Francesco; Del Nonno, Franca; Rosati, Davide; Morini, Sergio; Antonelli-Incalzi, Raffaele; Picardi, Antonio