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

Bằng Pellegrini, Stefania, Elefanti, Lisa, Dall’Olmo, Luigi, Menin, Chiara
Xuất bản năm Genes (Basel) (2021)

TLR7 Gln11Leu single nucleotide polymorphism and susceptibility to cutaneous melanoma

Bằng ELEFANTI, LISA, SACCO, GIORGIA, STAGNI, CAMILLA, RASTRELLI, MARCO, MENIN, CHIARA, RUSSO, IRENE, ALAIBAC, MAURO
Xuất bản năm Oncol Lett (2016)

MDM2 SNP309 accelerates colorectal tumour formation in women

Bằng Bond, Gareth L, Menin, Chiara, Bertorelle, Roberta, Alhopuro, Pia, Aaltonen, Lauri A, Levine, Arnold J
Được phát hành 2006

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

Bằng Benna, Clara, Rajendran, Senthilkumar, Spiro, Giovanna, Menin, Chiara, Dall’Olmo, Luigi, Rossi, Carlo Riccardo, Mocellin, Simone
Xuất bản năm J Transl Med (2021)

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

Bằng 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
Xuất bản năm Cancers (Basel) (2020)

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

Bằng 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
Xuất bản năm Cancers (Basel) (2020)

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

Bằng 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
Xuất bản năm PLoS Genet (2019)

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

Bằng 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.
Được phát hành 2009

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

Bằng 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
Xuất bản năm 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

Bằng 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
Xuất bản năm 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

Bằng 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
Được phát hành 2012

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

Bằng 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
Xuất bản năm Melanoma Res (2020)

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

Bằng 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.
Xuất bản năm Hum Mutat (2017)

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

Bằng 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
Xuất bản năm Hum Mol Genet (2018)

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

Bằng 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
Xuất bản năm Lancet Child Adolesc Health (2019)

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

Bằng 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.
Xuất bản năm Nat Genet (2020)