The origins and genetic interactions of KRAS mutations are allele- and tissue-specific

por Cook, Joshua H., Melloni, Giorgio E. M., Gulhan, Doga C., Park, Peter J., Haigis, Kevin M.
Publicado 2021

LowMACA: exploiting protein family analysis for the identification of rare driver mutations in cancer

por Melloni, Giorgio E. M., de Pretis, Stefano, Riva, Laura, Pelizzola, Mattia, Céol, Arnaud, Costanza, Jole, Müller, Heiko, Zammataro, Luca
Publicado 2016

A knowledge-based framework for the discovery of cancer-predisposing variants using large-scale sequencing breast cancer data

por Melloni, Giorgio E. M., Mazzarella, Luca, Bernard, Loris, Bodini, Margherita, Russo, Anna, Luzi, Lucilla, Pelicci, Pier Giuseppe, Riva, Laura
Publicado 2017

Very low-depth whole-genome sequencing in complex trait association studies

por Gilly, Arthur, Southam, Lorraine, Suveges, Daniel, Kuchenbaecker, Karoline, Moore, Rachel, Melloni, Giorgio E M, Hatzikotoulas, Konstantinos, Farmaki, Aliki-Eleni, Ritchie, Graham, Schwartzentruber, Jeremy, Danecek, Petr, Kilian, Britt, Pollard, Martin O, Ge, Xiangyu, Tsafantakis, Emmanouil, Dedoussis, George, Zeggini, Eleftheria
Publicado 2019

Mutations targeting the coagulation pathway are enriched in brain metastases

por Richichi, Cristina, Fornasari, Lorenzo, Melloni, Giorgio E. M., Brescia, Paola, Patanè, Monica, Del Bene, Massimiliano, Mustafa, Dana A. M., Kros, Johan M., Pollo, Bianca, Pruneri, Giancarlo, Sciandivasci, Angela, Munzone, Elisabetta, DiMeco, Francesco, Pelicci, Pier Giuseppe, Riva, Laura, Pelicci, Giuliana
Publicado 2017