Unraveling Tumor Heterogeneity in an Apparently Monolithic Disease: BCL2 and Other Players in the Genetic Landscape of Nodal Follicular Lymphoma

por Magnoli, Francesca, Tibiletti, Maria Grazia, Uccella, Silvia
Publicado 2019

EBV(+) and MSI Gastric Cancers Harbor High PD-L1/PD-1 Expression and High CD8(+) Intratumoral Lymphocytes

por De Rosa, Simona, Sahnane, Nora, Tibiletti, Maria Grazia, Magnoli, Francesca, Vanoli, Alessandro, Sessa, Fausto, Chiaravalli, Anna Maria
Publicado 2018

Case Report: Male Lobular Breast Cancer in Hereditary Cancer Syndromes

por Carnevali, Ileana, Tedaldi, Gianluca, Pensotti, Valeria, Sahnane, Nora, Micello, Donata, Rovera, Francesca, Sessa, Fausto, Tibiletti, Maria Grazia
Publicado 2022

MLH1 Promoter Methylation Could Be the Second Hit in Lynch Syndrome Carcinogenesis

por Carnevali, Ileana Wanda, Cini, Giulia, Libera, Laura, Sahnane, Nora, Facchi, Sofia, Viel, Alessandra, Sessa, Fausto, Tibiletti, Maria Grazia
Publicado 2023

Similarities and differences in gene expression profiles of BRCA1 methylated and mutated epithelial ovarian cancers

por Sahnane, Nora, Libera, Laura, Facchi, Sofia, Carnevali, Ileana, Ronchi, Susanna, Albeni, Chiara, Cromi, Antonella, Casarin, Jvan, Sessa, Fausto, Tibiletti, Maria Grazia
Publicado 2023

Phenotypic features and genetic characterization of male breast cancer families: identification of two recurrent BRCA2 mutations in north-east of Italy

por Miolo, GianMaria, Puppa, Lara Della, Santarosa, Manuela, De Giacomi, Clelia, Veronesi, Andrea, Bidoli, Ettore, Tibiletti, Maria Grazia, Viel, Alessandra, Dolcetti, Riccardo
Publicado 2006

Gut Microbiota Analysis in Postoperative Lynch Syndrome Patients

por Mori, Giorgia, Orena, Beatrice Silvia, Cultrera, Ilenia, Barbieri, Giulia, Albertini, Alessandra M., Ranzani, Guglielmina Nadia, Carnevali, Ileana, Tibiletti, Maria Grazia, Pasca, Maria Rosalia
Publicado 2019

Oxidative DNA damage induces hypomethylation in a compromised base excision repair colorectal tumourigenesis

por Furlan, Daniela, Trapani, Davide, Berrino, Enrico, Debernardi, Carla, Panero, Mara, Libera, Laura, Sahnane, Nora, Riva, Cristina, Tibiletti, Maria Grazia, Sessa, Fausto, Sapino, Anna, Venesio, Tiziana
Publicado 2017

OncoPan(®): An NGS-Based Screening Methodology to Identify Molecular Markers for Therapy and Risk Assessment in Pancreatic Ductal Adenocarcinoma

por Tibiletti, Maria Grazia, Carnevali, Ileana, Pensotti, Valeria, Chiaravalli, Anna Maria, Facchi, Sofia, Volorio, Sara, Mariette, Frederique, Mariani, Paolo, Fortuzzi, Stefano, Pierotti, Marco Alessandro, Sessa, Fausto
Publicado 2022

BRCA Methylation Testing Identifies a Subset of Ovarian Carcinomas without Germline Variants That Can Benefit from PARP Inhibitor

por Sahnane, Nora, Carnevali, Ileana, Formenti, Giorgio, Casarin, Jvan, Facchi, Sofia, Bombelli, Raffaella, Di Lauro, Eleonora, Memoli, Domenico, Salvati, Annamaria, Rizzo, Francesca, Sessa, Fausto, Tibiletti, Maria Grazia
Publicado 2020

Aberrant DNA methylation profiles of inherited and sporadic colorectal cancer

por Sahnane, Nora, Magnoli, Francesca, Bernasconi, Barbara, Tibiletti, Maria Grazia, Romualdi, Chiara, Pedroni, Monica, Ponz de Leon, Maurizio, Magnani, Giulia, Reggiani-Bonetti, Luca, Bertario, Lucio, Signoroni, Stefano, Capella, Carlo, Sessa, Fausto, Furlan, Daniela
Publicado 2015

Transcriptome of Male Breast Cancer Matched with Germline Profiling Reveals Novel Molecular Subtypes with Possible Clinical Relevance

por Zelli, Veronica, Silvestri, Valentina, Valentini, Virginia, Bucalo, Agostino, Rizzolo, Piera, Zanna, Ines, Bianchi, Simonetta, Coppa, Anna, Giannini, Giuseppe, Cortesi, Laura, Calistri, Daniele, Tibiletti, Maria Grazia, Fox, Stephen B., Palli, Domenico, Ottini, Laura
Publicado 2021

Evaluation of CYP17A1 and CYP1B1 polymorphisms in male breast cancer risk

por Rizzolo, Piera, Silvestri, Valentina, Valentini, Virginia, Zelli, Veronica, Bucalo, Agostino, Zanna, Ines, Bianchi, Simonetta, Tibiletti, Maria Grazia, Russo, Antonio, Varesco, Liliana, Tedaldi, Gianluca, Bonanni, Bernardo, Azzollini, Jacopo, Manoukian, Siranoush, Coppa, Anna, Giannini, Giuseppe, Cortesi, Laura, Viel, Alessandra, Montagna, Marco, Peterlongo, Paolo, Radice, Paolo, Palli, Domenico, Ottini, Laura
Publicado 2019

Contribution of MUTYH Variants to Male Breast Cancer Risk: Results From a Multicenter Study in Italy

por Rizzolo, Piera, Silvestri, Valentina, Bucalo, Agostino, Zelli, Veronica, Valentini, Virginia, Catucci, Irene, Zanna, Ines, Masala, Giovanna, Bianchi, Simonetta, Spinelli, Alessandro Mauro, Tommasi, Stefania, Tibiletti, Maria Grazia, Russo, Antonio, Varesco, Liliana, Coppa, Anna, Calistri, Daniele, Cortesi, Laura, Viel, Alessandra, Bonanni, Bernardo, Azzollini, Jacopo, Manoukian, Siranoush, Montagna, Marco, Radice, Paolo, Palli, Domenico, Peterlongo, Paolo, Ottini, Laura
Publicado 2018

Detection of Germline Variants in 450 Breast/Ovarian Cancer Families with a Multi-Gene Panel Including Coding and Regulatory Regions

por Guglielmi, Chiara, Scarpitta, Rosa, Gambino, Gaetana, Conti, Eleonora, Bellè, Francesca, Tancredi, Mariella, Cervelli, Tiziana, Falaschi, Elisabetta, Cosini, Cinzia, Aretini, Paolo, Congregati, Caterina, Marino, Marco, Patruno, Margherita, Pilato, Brunella, Spina, Francesca, Balestrino, Luisa, Tenedini, Elena, Carnevali, Ileana, Cortesi, Laura, Tagliafico, Enrico, Tibiletti, Maria Grazia, Tommasi, Stefania, Ghilli, Matteo, Vivanet, Caterina, Galli, Alvaro, Caligo, Maria Adelaide
Publicado 2021

Insights into Genetic Susceptibility to Melanoma by Gene Panel Testing: Potential Pathogenic Variants in ACD, ATM, BAP1, and POT1

por Pastorino, Lorenza, Andreotti, Virginia, Dalmasso, Bruna, Vanni, Irene, Ciccarese, Giulia, Mandalà, Mario, Spadola, Giuseppe, Pizzichetta, Maria Antonietta, Ponti, Giovanni, Tibiletti, Maria Grazia, Sala, Elena, Genuardi, Maurizio, Chiurazzi, Pietro, Maccanti, Gabriele, Manoukian, Siranoush, Sestini, Serena, Danesi, Rita, Zampiga, Valentina, La Starza, Roberta, Stanganelli, Ignazio, Ballestrero, Alberto, Mastracci, Luca, Grillo, Federica, Sciallero, Stefania, Cecchi, Federica, Tanda, Enrica Teresa, Spagnolo, Francesco, Queirolo, Paola, Goldstein, Alisa M., Bruno, William, Ghiorzo, Paola
Publicado 2020

Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome Database

por Dominguez-Valentin, Mev, Seppälä, Toni T., Engel, Christoph, Aretz, Stefan, Macrae, Finlay, Winship, Ingrid, Capella, Gabriel, Thomas, Huw, Hovig, Eivind, Nielsen, Maartje, Sijmons, Rolf H, Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Mints, Miriam, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A., Green, Kate, Lalloo, Fiona, Hill, James, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Strauß, Hans-Georg, Tecklenburg, Johanna, Holinski-Feder, Elke, Steinke-Lange, Verena, Mecklin, Jukka-Pekka, Plazzer, John-Paul, Pineda, Marta, Navarro, Matilde, Vidal, Joan Brunet, Kariv, Revital, Rosner, Guy, Piñero, Tamara Alejandra, Gonzalez, María Laura, Kalfayan, Pablo, Sampson, Julian R., Ryan, Neil A. J., Evans, D. Gareth, Møller, Pål, Crosbie, Emma J.
Publicado 2020

Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement

por Møller, Pal, Seppälä, Toni T., Ahadova, Aysel, Crosbie, Emma J., Holinski-Feder, Elke, Scott, Rodney, Haupt, Saskia, Möslein, Gabriela, Winship, Ingrid, Broeke, Sanne W. Bajwa-ten, Kohut, Kelly E., Ryan, Neil, Bauerfeind, Peter, Thomas, Laura E., Evans, D. Gareth, Aretz, Stefan, Sijmons, Rolf H., Half, Elizabeth, Heinimann, Karl, Horisberger, Karoline, Monahan, Kevin, Engel, Christoph, Cavestro, Giulia Martina, Fruscio, Robert, Abu-Freha, Naim, Zohar, Levi, Laghi, Luigi, Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria Grazia, Lino-Silva, Leonardo S., Vaccaro, Carlos, Valle, Adriana Della, Rossi, Benedito Mauro, da Silva, Leandro Apolinário, de Oliveira Nascimento, Ivana Lucia, Rossi, Norma Teresa, Dębniak, Tadeusz, Mecklin, Jukka-Pekka, Bernstein, Inge, Lindblom, Annika, Sunde, Lone, Nakken, Sigve, Heuveline, Vincent, Burn, John, Hovig, Eivind, Kloor, Matthias, Sampson, Julian R., Dominguez-Valentin, Mev
Publicado 2023

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

por Dominguez-Valentin, Mev, Crosbie, Emma J., Engel, Christoph, Aretz, Stefan, Macrae, Finlay, Winship, Ingrid, Capella, Gabriel, Thomas, Huw, Nakken, Sigve, Hovig, Eivind, Nielsen, Maartje, Sijmons, Rolf H., Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Mints, Miriam, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A., Green, Kate, Lalloo, Fiona, Hill, James, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Strauß, Hans-Georg, Tecklenburg, Johanna, Holinski-Feder, Elke, Steinke-Lange, Verena, Mecklin, Jukka-Pekka, Plazzer, John-Paul, Pineda, Marta, Navarro, Matilde, Vidal, Joan Brunet, Kariv, Revital, Rosner, Guy, Piñero, Tamara Alejandra, Gonzalez, María Laura, Kalfayan, Pablo, Ryan, Neil, ten Broeke, Sanne W., Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Burn, John, Greenblatt, Marc, de Vos tot Nederveen Cappel, Wouter H., Della Valle, Adriana, Lopez-Koestner, Francisco, Alvarez, Karin, Büttner, Reinhard, Görgens, Heike, Morak, Monika, Holzapfel, Stefanie, Hüneburg, Robert, von Knebel Doeberitz, Magnus, Loeffler, Markus, Rahner, Nils, Weitz, Jürgen, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Auranen, Annika, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Therkildsen, Christina, Okkels, Henrik, Ketabi, Zohreh, Denton, Oliver G., Rødland, Einar Andreas, Vasen, Hans, Neffa, Florencia, Esperon, Patricia, Tjandra, Douglas, Möslein, Gabriela, Sampson, Julian R., Evans, D. Gareth, Seppälä, Toni T., Møller, Pål
Publicado 2020

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

por Dominguez-Valentin, Mev, Sampson, Julian R., Seppälä, Toni T., ten Broeke, Sanne W., Plazzer, John-Paul, Nakken, Sigve, Engel, Christoph, Aretz, Stefan, Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Capella, Gabriel, Balaguer, Francesc, Thomas, Huw, Evans, D. Gareth, Burn, John, Greenblatt, Marc, Hovig, Eivind, de Vos tot Nederveen Cappel, Wouter H., Sijmons, Rolf H., Bertario, Lucio, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Lindblom, Annika, Della Valle, Adriana, Lopez-Köstner, Francisco, Gluck, Nathan, Katz, Lior H., Heinimann, Karl, Vaccaro, Carlos A., Büttner, Reinhard, Görgens, Heike, Holinski-Feder, Elke, Morak, Monika, Holzapfel, Stefanie, Hüneburg, Robert, Knebel Doeberitz, Magnus von, Loeffler, Markus, Rahner, Nils, Schackert, Hans K., Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Wadt, Karin, Therkildsen, Christina, Okkels, Henrik, Ketabi, Zohreh, Moreira, Leticia, Sánchez, Ariadna, Serra-Burriel, Miquel, Pineda, Marta, Navarro, Matilde, Blanco, Ignacio, Green, Kate, Lalloo, Fiona, Crosbie, Emma J., Hill, James, Denton, Oliver G., Frayling, Ian M., Rødland, Einar Andreas, Vasen, Hans, Mints, Miriam, Neffa, Florencia, Esperon, Patricia, Alvarez, Karin, Kariv, Revital, Rosner, Guy, Pinero, Tamara Alejandra, Gonzalez, María Laura, Kalfayan, Pablo, Tjandra, Douglas, Winship, Ingrid M., Macrae, Finlay, Möslein, Gabriela, Mecklin, Jukka-Pekka, Nielsen, Maartje, Møller, Pål
Publicado 2019