The Interplay between Nevi and Melanoma Predisposition Unravels Nevi-Related and Nevi-Resistant Familial Melanoma

por Pellegrini, Stefania, Elefanti, Lisa, Dall’Olmo, Luigi, Menin, Chiara
Publicado en Genes (Basel) (2021)

TLR7 Gln11Leu single nucleotide polymorphism and susceptibility to cutaneous melanoma

por ELEFANTI, LISA, SACCO, GIORGIA, STAGNI, CAMILLA, RASTRELLI, MARCO, MENIN, CHIARA, RUSSO, IRENE, ALAIBAC, MAURO
Publicado en Oncol Lett (2016)

MDM2 SNP309 accelerates colorectal tumour formation in women

por Bond, Gareth L, Menin, Chiara, Bertorelle, Roberta, Alhopuro, Pia, Aaltonen, Lauri A, Levine, Arnold J
Publicado 2006

Gender-specific associations between polymorphisms of the circadian gene RORA and cutaneous melanoma susceptibility

por Benna, Clara, Rajendran, Senthilkumar, Spiro, Giovanna, Menin, Chiara, Dall’Olmo, Luigi, Rossi, Carlo Riccardo, Mocellin, Simone
Publicado en J Transl Med (2021)

TERT Promoter Mutations Differently Correlate with the Clinical Outcome of MAPK Inhibitor-Treated Melanoma Patients

por Del Bianco, Paola, Stagni, Camilla, Giunco, Silvia, Fabozzi, Alessio, Elefanti, Lisa, Pellegrini, Stefania, Vecchiato, Antonella, Pigozzo, Jacopo, Zamuner, Carolina, De Rossi, Anita, De Nicolo, Arcangela, Menin, Chiara
Publicado en Cancers (Basel) (2020)

Genetic Variants of the TERT Gene, Telomere Length, and Circulating TERT as Prognostic Markers in Rectal Cancer Patients

por Rampazzo, Enrica, Cecchin, Erika, Del Bianco, Paola, Menin, Chiara, Spolverato, Gaya, Giunco, Silvia, Lonardi, Sara, Malacrida, Sandro, De Paoli, Antonino, Toffoli, Giuseppe, Pucciarelli, Salvatore, De Rossi, Anita
Publicado en Cancers (Basel) (2020)

Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies

por Schlafly, Andrew, Pfeiffer, Ruth M., Nagore, Eduardo, Puig, Susana, Calista, Donato, Ghiorzo, Paola, Menin, Chiara, Fargnoli, Maria Concetta, Peris, Ketty, Song, Lei, Zhang, Tongwu, Shi, Jianxin, Landi, Maria Teresa, Sampson, Joshua Neil
Publicado en PLoS Genet (2019)

Altered tumor formation and evolutionary selection of genetic variants in the human MDM4 oncogene

por Atwal, Gurinder Singh, Kirchhoff, Tomas, Bond, Elisabeth E., Montagna, Marco, Menin, Chiara, Bertorelle, Roberta, Scaini, Maria Chiara, Bartel, Frank, Böhnke, Anja, Pempe, Christina, Gradhand, Elise, Hauptmann, Steffen, Offit, Kenneth, Levine, Arnold J., Bond, Gareth L.
Publicado 2009

The Molecular Landscape of Primary Acral Melanoma: A Multicenter Study of the Italian Melanoma Intergroup (IMI)

por Elefanti, Lisa, Zamuner, Carolina, Del Fiore, Paolo, Stagni, Camilla, Pellegrini, Stefania, Dall’Olmo, Luigi, Fabozzi, Alessio, Senetta, Rebecca, Ribero, Simone, Salmaso, Roberto, Mocellin, Simone, Bassetto, Franco, Cavallin, Francesco, Tosi, Anna Lisa, Galuppini, Francesca, Dei Tos, Angelo Paolo, Menin, Chiara, Cappellesso, Rocco
Publicado en Int J Mol Sci (2021)

MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: a pooled analysis from the M-SKIP project

por Tagliabue, Elena, Gandini, Sara, Bellocco, Rino, Maisonneuve, Patrick, Newton-Bishop, Julia, Polsky, David, Lazovich, DeAnn, Kanetsky, Peter A, Ghiorzo, Paola, Gruis, Nelleke A, Landi, Maria Teresa, Menin, Chiara, Fargnoli, Maria Concetta, García-Borrón, Jose Carlos, Han, Jiali, Little, Julian, Sera, Francesco, Raimondi, Sara
Publicado en Cancer Manag Res (2018)

The p53 Codon 72 Pro/Pro Genotype Identifies Poor-Prognosis Neuroblastoma Patients: Correlation with Reduced Apoptosis and Enhanced Senescence by the p53-72P Isoform

por Cattelani, Sara, Ferrari-Amorotti, Giovanna, Galavotti, Sara, Defferrari, Raffaella, Tanno, Barbara, Cialfi, Samantha, Vergalli, Jenny, Fragliasso, Valentina, Guerzoni, Clara, Manzotti, Gloria, Soliera, Angela Rachele, Menin, Chiara, Bertorelle, Roberta, McDowell, Heather P, Inserra, Alessandro, Belli, Maria Luisa, Varesio, Luigi, Tweddle, Deborah, Tonini, Gian Paolo, Altavista, Pierluigi, Dominici, Carlo, Raschellà, Giuseppe, Calabretta, Bruno
Publicado 2012

MC1R variants and cutaneous melanoma risk according to histological type, body site, and Breslow thickness: a pooled analysis from the M-SKIP project

por Caini, Saverio, Gandini, Sara, Botta, Francesca, Tagliabue, Elena, Raimondi, Sara, Nagore, Eduardo, Zanna, Ines, Maisonneuve, Patrick, Newton-Bishop, Julia, Polsky, David, Lazovich, DeAnn, Kumar, Rajiv, Kanetsky, Peter A., Hoiom, Veronica, Ghiorzo, Paola, Landi, Maria Teresa, Ribas, Gloria, Menin, Chiara, Stratigos, Alexander J., Palmieri, Giuseppe, Guida, Gabriella, García-Borrón, Jose Carlos, Nan, Hongmei, Little, Julian, Sera, Francesco, Puig, Susana, Fargnoli, Maria Concetta
Publicado en Melanoma Res (2020)

Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI

por Carraro, Marco, Minervini, Giovanni, Giollo, Manuel, Bromberg, Yana, Capriotti, Emidio, Casadio, Rita, Dunbrack, Roland, Elefanti, Lisa, Fariselli, Pietro, Ferrari, Carlo, Gough, Julian, Katsonis, Panagiotis, Leonardi, Emanuela, Lichtarge, Olivier, Menin, Chiara, Martelli, Pier Luigi, Niroula, Abhishek, Pal, Lipika R., Repo, Susanna, Scaini, Maria Chiara, Vihinen, Mauno, Wei, Qiong, Xu, Qifang, Yang, Yuedong, Yin, Yizhou, Zaucha, Jan, Zhao, Huiying, Zhou, Yaoqi, Brenner, Steven E., Moult, John, Tosatto, Silvio C.E.
Publicado en Hum Mutat (2017)

Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma

por Gu, Fangyi, Chen, Ting-Huei, Pfeiffer, Ruth M, Fargnoli, Maria Concetta, Calista, Donato, Ghiorzo, Paola, Peris, Ketty, Puig, Susana, Menin, Chiara, De Nicolo, Arcangela, Rodolfo, Monica, Pellegrini, Cristina, Pastorino, Lorenza, Evangelou, Evangelos, Zhang, Tongwu, Hua, Xing, DellaValle, Curt T, Timothy Bishop, D, MacGregor, Stuart, Iles, Mark I, Law, Matthew H, Cust, Anne, Brown, Kevin M, Stratigos, Alexander J, Nagore, Eduardo, Chanock, Stephen, Shi, Jianxin, Consortium, Melanoma Meta-Analysis, Consortium, MelaNostrum, Landi, Maria Teresa
Publicado en Hum Mol Genet (2018)

MC1R variants in childhood and adolescent melanoma: A pooled-analysis from a large worldwide multicenter cohort of patients

por Pellegrini, Cristina, Botta, Francesca, Massi, Daniela, Martorelli, Claudia, Facchetti, Fabio, Gandini, Sara, Maisonneuve, Patrick, Avril, Marie-Françoise, Demenais, Florence, Paillerets, Brigitte Bressac-de, Hoiom, Veronica, Cust, Anne E., Anton-Culver, Hoda, Gruber, Stephen B., Gallagher, Richard P., Marrett, Loraine, Zanetti, Roberto, Dwyer, Terence, Thomas, Nancy E., Begg, Colin B., Berwick, Marianne, Puig, Susana, Potrony, Miriam, Nagore, Eduardo, Ghiorzo, Paola, Menin, Chiara, Manganoni, Ausilia Maria, Rodolfo, Monica, Brugnara, Sonia, Passoni, Emanuela, Sekulovic, Lidija Kandolf, Baldini, Federica, Guida, Gabriella, Stratigos, Alexandras, Ozdemir, Fezal, Ayala, Fabrizio, Fernandez-de-Misa, Ricardo, Quaglino, Pietro, Ribas, Gloria, Romanini, Antonella, Migliano, Emilia, Stanganelli, Ignazio, Kanetsky, Peter A., Pizzichetta, Maria Antonietta, García-Borrón, Jose Carlos, Nan, Hongmei, Landi, Maria Teresa, Little, Julian, Newton-Bishop, Julia, Sera, Francesco, Fargnoli, Maria Concetta, Raimondi, Sara
Publicado en Lancet Child Adolesc Health (2019)

Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility

por Landi, Maria Teresa, Bishop, D. Timothy, MacGregor, Stuart, Machiela, Mitchell J., Stratigos, Alexander J., Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Choi, Jiyeon, Fargnoli, Maria Concetta, Zhang, Tongwu, Rodolfo, Monica, Trower, Adam J., Menin, Chiara, Martinez, Jacobo, Hadjisavvas, Andreas, Song, Lei, Stefanaki, Irene, Scolyer, Richard, Yang, Rose, Goldstein, Alisa M., Potrony, Miriam, Kypreou, Katerina P., Pastorino, Lorenza, Queirolo, Paola, Pellegrini, Cristina, Cattaneo, Laura, Zawistowski, Matthew, Gimenez-Xavier, Pol, Rodriguez, Arantxa, Elefanti, Lisa, Manoukian, Siranoush, Rivoltini, Licia, Smith, Blair H., Loizidou, Maria A., Regno, Laura Del, Massi, Daniela, Mandala, Mario, Khosrotehrani, Kiarash, Akslen, Lars A., Amos, Christopher I., Andresen, Per A., Avril, Marie-Françoise, Azizi, Esther, Soyer, H. Peter, Bataille, Veronique, Dalmasso, Bruna, Bowdler, Lisa M., Burdon, Kathryn P., Chen, Wei V., Codd, Veryan, Craig, Jamie E., Dębniak, Tadeusz, Falchi, Mario, Fang, Shenying, Friedman, Eitan, Simi, Sarah, Galan, Pilar, Garcia-Casado, Zaida, Gillanders, Elizabeth M., Gordon, Scott, Green, Adele, Gruis, Nelleke A., Hansson, Johan, Harland, Mark, Harris, Jessica, Helsing, Per, Henders, Anjali, Hočevar, Marko, Höiom, Veronica, Hunter, David, Ingvar, Christian, Kumar, Rajiv, Lang, Julie, Lathrop, G. Mark, Lee, Jeffrey E., Li, Xin, Lubiński, Jan, Mackie, Rona M., Malt, Maryrose, Malvehy, Josep, McAloney, Kerrie, Mohamdi, Hamida, Molven, Anders, Moses, Eric K., Neale, Rachel E., Novaković, Srdjan, Nyholt, Dale R., Olsson, Håkan, Orr, Nicholas, Fritsche, Lars G., Puig-Butille, Joan Anton, Qureshi, Abrar A., Radford-Smith, Graham L., Randerson-Moor, Juliette, Requena, Celia, Rowe, Casey, Samani, Nilesh J., Sanna, Marianna, Schadendorf, Dirk, Schulze, Hans-Joachim, Simms, Lisa A., Smithers, Mark, Song, Fengju, Swerdlow, Anthony J., van der Stoep, Nienke, Kukutsch, Nicole A., Visconti, Alessia, Wallace, Leanne, Ward, Sarah V., Wheeler, Lawrie, Sturm, Richard A., Hutchinson, Amy, Jones, Kristine, Malasky, Michael, Vogt, Aurelie, Zhou, Weiyin, Pooley, Karen A., Elder, David E., Han, Jiali, Hicks, Belynda, Hayward, Nicholas K., Kanetsky, Peter A., Brummett, Chad, Montgomery, Grant W., Olsen, Catherine M, Hayward, Caroline, Dunning, Alison M., Martin, Nicholas G., Evangelou, Evangelos, Mann, Graham J., Long, Georgina, Pharoah, Paul D. P., Easton, Douglas F., Barrett, Jennifer H., Cust, Anne E., Abecasis, Goncalo, Duffy, David L., Whiteman, David C., Gogas, Helen, De Nicolo, Arcangela, Tucker, Margaret A., Bishop, Julia A. Newton, Peris, Ketty, Chanock, Stephen J., Demenais, Florence, Brown, Kevin M., Puig, Susana, Nagore, Eduardo, Shi, Jianxin, Iles, Mark M., Law, Matthew H.
Publicado en Nat Genet (2020)