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

द्वारा Pellegrini, Stefania, Elefanti, Lisa, Dall’Olmo, Luigi, Menin, Chiara
में प्रकाशित Genes (Basel) (2021)

TLR7 Gln11Leu single nucleotide polymorphism and susceptibility to cutaneous melanoma

द्वारा ELEFANTI, LISA, SACCO, GIORGIA, STAGNI, CAMILLA, RASTRELLI, MARCO, MENIN, CHIARA, RUSSO, IRENE, ALAIBAC, MAURO
में प्रकाशित Oncol Lett (2016)

MDM2 SNP309 accelerates colorectal tumour formation in women

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

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

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

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

द्वारा 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
में प्रकाशित Cancers (Basel) (2020)

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

द्वारा 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
में प्रकाशित Cancers (Basel) (2020)

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

द्वारा 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
में प्रकाशित PLoS Genet (2019)

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

द्वारा 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.
प्रकाशित 2009

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

द्वारा 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
में प्रकाशित 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

द्वारा 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
में प्रकाशित 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

द्वारा 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
प्रकाशित 2012

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

द्वारा 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
में प्रकाशित Melanoma Res (2020)

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

द्वारा 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.
में प्रकाशित Hum Mutat (2017)

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

द्वारा 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
में प्रकाशित Hum Mol Genet (2018)

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

द्वारा 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
में प्रकाशित Lancet Child Adolesc Health (2019)

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

द्वारा 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.
में प्रकाशित Nat Genet (2020)