Cancer risk associated with STK11/LKB1 germline mutations in Peutz–Jeghers syndrome patients: Results of an Italian multicenter studyNicoletta Resta, Maurizio Ponz de Leòn, Carlo Sabbà et al.|Digestive and Liver Disease|2013Cited by 158
Stability of BAT26 in tumours of hereditary nonpolyposis colorectal cancer patients with MSH2 intragenic deletionChiara Pastrello, Alessandra Viel, Silvana Baglioni et al.|European Journal of Human Genetics|2005Cited by 41
Integrated analysis of unclassified variants in mismatch repair genesChiara Pastrello, Alessandra Viel, Elisa Pin et al.|Genetics in Medicine|2011Cited by 36
Reply to Jaskowski et alChiara Pastrello, Alessandra Viel, Rossella Tricarico et al.|European Journal of Human Genetics|2006Cited by 0
Characterization of the Most Frequent MUTYH Mutation C.933+3a>C (Ivs10+3a>C) in the Northeastern Italian PopulationElisa Pin, Mara Fornasarig, Rossella Tricarico et al.|Gastroenterology|2011Cited by 0