Prevalence of germline MUTYH mutations among Lynch-like syndrome patients von Castillejo, Adela, Vargas, Gardenia, Castillejo, María Isabel, Navarro, Matilde, Barberá, Víctor Manuel, González, Sara, Hernández-Illán, Eva, Brunet, Joan, Ramón y Cajal, Teresa, Balmaña, Judith, Oltra, Silvestre, Iglesias, Sílvia, Velasco, Àngela, Solanes, Ares, Campos, Olga, Sánchez Heras, Ana Beatriz, Gallego, Javier, Carrasco, Estela, González Juan, Dolors, Segura, Ángel, Chirivella, Isabel, Juan, María José, Tena, Isabel, Lázaro, Conxi, Blanco, Ignacio, Pineda, Marta, Capellá, Gabriel, Soto, José Luis

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MicroRNA signatures in hereditary breast cancer von Murria Estal, Rosa, Palanca Suela, Sarai, de Juan Jiménez, Inmaculada, Egoavil Rojas, Cecilia, García-Casado, Zaida, Juan Fita, María José, Sánchez Heras, Ana Beatriz, Segura Huerta, Ángel, Chirivella González, Isabel, Sánchez-Izquierdo, Dolors, Llop García, Marta, Barragán González, Eva, Bolufer Gilabert, Pascual

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Prevalence of Lynch syndrome among patients with newly diagnosed endometrial cancers von Egoavil, Cecilia, Alenda, Cristina, Castillejo, Adela, Paya, Artemio, Peiro, Gloria, Sánchez-Heras, Ana-Beatriz, Castillejo, Maria-Isabel, Rojas, Estefanía, Barberá, Víctor-Manuel, Cigüenza, Sonia, Lopez, Jose-Antonio, Piñero, Oscar, Román, Maria-Jose, Martínez-Escoriza, Juan-Carlos, Guarinos, Carla, Perez-Carbonell, Lucia, Aranda, Francisco-Ignacio, Soto, Jose-Luis

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Efficacy and safety of niraparib in patients aged 65 years and older with advanced ovarian cancer: Results from the PRIMA/ENGOT-OV26/GOG-3012 trial von Valabrega, Giorgio, Pothuri, Bhavana, Oaknin, Ana, Graybill, Whitney S., Sánchez, Ana Beatriz, McCormick, Colleen, Baurain, Jean-François, Tinker, Anna V., Denys, Hannelore, O’Cearbhaill, Roisin E., Hietanen, Sakari, Moore, Richard G., Knudsen, Anja Ør, de La Motte Rouge, Thibault, Heitz, Florian, Levy, Tally, York, Whitney, Gupta, Divya, Monk, Bradley J., González-Martín, Antonio

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Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair von Seguí, Nuria, Mina, Leonardo B, Lázaro, Conxi, Sanz-Pamplona, Rebeca, Pons, Tirso, Navarro, Matilde, Bellido, Fernando, López-Doriga, Adriana, Valdés-Mas, Rafael, Pineda, Marta, Guinó, Elisabet, Vidal, August, Soto, José Luís, Caldés, Trinidad, Durán, Mercedes, Urioste, Miguel, Rueda, Daniel, Brunet, Joan, Balbín, Milagros, Blay, Pilar, Iglesias, Silvia, Garré, Pilar, Lastra, Enrique, Sánchez-Heras, Ana Beatriz, Valencia, Alfonso, Moreno, Victor, Pujana, Miguel Ángel, Villanueva, Alberto, Blanco, Ignacio, Capellá, Gabriel, Surrallés, Jordi, Puente, Xose S, Valle, Laura

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Immune Response to Mucosal Brucella Infection von López-Santiago, Rubén, Sánchez-Argáez, Ana Beatriz, De Alba-Núñez, Liliana Gabriela, Baltierra-Uribe, Shantal Lizbeth, Moreno-Lafont, Martha Cecilia

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Use of multi-gene panels in patients at high risk of hereditary digestive cancer: position statement of AEG, SEOM, AEGH and IMPaCT-GENÓMICA consortium von Carballal, Sabela, Balaguer, Francesc, Bujanda, Luis, Capellá, Gabriel, González Santiago, Santiago, Jover, Rodrigo, Moreira, Leticia, Pineda, Marta, Ruiz-Ponte, Clara, Sánchez Heras, Ana Beatriz, Serrano Blanch, Raquel, Soto, José Luis, Vidal Tocino, Rosario, Cubiella, Joaquín

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Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome von Sánchez-Heras, Ana Beatriz, Dámaso, Estela, Castillejo, Adela, Robledo, Mercedes, Teulé, Alexandre, Lázaro, Conxi, Sánchez-Martínez, Rosario, Zúñiga, Ángel, López-Fernández, Adrià, Balmaña, Judith, Robles, Luis, Ramon Y Cajal, Teresa, Castillejo, M Isabel, Ibañez, Raquel Perea, Sevila, Carmen Martínez, Sánchez-Mira, Andrea, Escandell, Inés, Gómez, Luís, Berbel, Pere, Soto, José Luis

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Co‐occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome von Ferrer‐Avargues, Rosario, Castillejo, María Isabel, Dámaso, Estela, Díez‐Obrero, Virginia, Garrigos, Noemí, Molina, Tatiana, Codoñer‐Alejos, Alan, Segura, Ángel, Sánchez‐Heras, Ana Beatriz, Castillejo, Adela, Soto, José Luis

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Characterization of a novel POLD1 missense founder mutation in a Spanish population von Ferrer‐Avargues, Rosario, Díez‐Obrero, Virginia, Martín‐Tomás, Ester, Hernández‐Illán, Eva, Castillejo, María‐Isabel, Codoñer‐Alejos, Alan, Barberá, Víctor‐Manuel, Sánchez‐Heras, Ana‐Beatriz, Segura, Ángel, Juan, María‐José, Tena, Isabel, Castillejo, Adela, Soto, José‐Luis

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Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (F... von Ramírez-Calvo, Marta, García-Casado, Zaida, Fernández-Serra, Antonio, de Juan, Inmaculada, Palanca, Sarai, Oltra, Silvestre, Soto, José Luis, Castillejo, Adela, Barbera, Víctor M, Juan-Fita, Ma José, Segura, Ángel, Chirivella, Isabel, Sánchez, Ana Beatriz, Tena, Isabel, Chaparro, Carolina, Salas, Dolores, López-Guerrero, José Antonio

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Laboratory Cross-Comparison and Ring Test Trial for Tumor BRCA Testing in a Multicenter Epithelial Ovarian Cancer Series: The BORNEO GEICO 60-0 Study von Garcia-Casado, Zaida, Oaknin, Ana, Mendiola, Marta, Alkorta-Aranburu, Gorka, Antunez-Lopez, Jose Ramon, Moreno-Bueno, Gema, Palacios, Jose, Yubero, Alfonso, Marquez, Raul, Gallego, Alejandro, Sanchez-Heras, Ana Beatriz, Lopez-Guerrero, Jose Antonio, Perez-Segura, Cristina, Barretina-Ginesta, Pilar, Alarcon, Jesus, Gaba, Lydia, Marquez, Antonia, Matito, Judit, Cueva, Juan, Palacio, Isabel, Iglesias, Maria, Arcusa, Angels, Sanchez-Lorenzo, Luisa, Guerra-Alia, Eva, Romero, Ignacio, Vivancos, Ana

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Mammographic density and breast cancer in women from high risk families von Ramón Y Cajal, Teresa, Chirivella, Isabel, Miranda, Josefa, Teule, Alexandre, Izquierdo, Ángel, Balmaña, Judith, Sánchez-Heras, Ana Beatriz, Llort, Gemma, Fisas, David, Lope, Virginia, Hernández-Agudo, Elena, Juan-Fita, María José, Tena, Isabel, Robles, Luis, Guillén-Ponce, Carmen, Pérez-Segura, Pedro, Luque-Molina, Mari Sol, Hernando-Polo, Susana, Salinas, Mónica, Brunet, Joan, Salas-Trejo, María Dolores, Barnadas, Agustí, Pollán, Marina

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IFN‐γ stimulates Paneth cell secretion through necroptosis mTORC1 dependent von Encarnacion‐Garcia, Maria R., De la Torre‐Baez, Raúl, Hernandez‐Cueto, María A., Velázquez‐Villegas, Laura A., Candelario‐Martinez, Aurora, Sánchez‐Argáez, Ana Beatriz, Horta‐López, Perla H., Montoya‐García, Armando, Jaimes‐Ortega, Gustavo Alberto, Lopez‐Bailon, Luis, Piedra‐Quintero, Zayda, Carrasco‐Torres, Gabriela, De Ita, Marlon, Figueroa‐Corona, María del Pilar, Muñoz‐Medina, José Esteban, Sánchez‐Uribe, Magdalena, Ortiz‐Fernández, Arturo, Meraz‐Ríos, Marco Antonio, Silva‐Olivares, Angélica, Betanzos, Abigail, Baay‐Guzman, Guillermina Juliana, Navarro‐Garcia, Fernando, Villa‐Treviño, Saúl, Garcia‐Sierra, Francisco, Cisneros, Bulmaro, Schnoor, Michael, Ortíz‐Navarrete, Vianney F., Villegas‐Sepúlveda, Nicolás, Valle‐Rios, Ricardo, Medina‐Contreras, Oscar, Noriega, Lilia G., Nava, Porfirio

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Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome von Castillejo, Adela, Guarinos, Carla, Martinez-Canto, Ana, Barbera, Victor-Manuel, Egoavil, Cecilia, Castillejo, Maria-Isabel, Perez-Carbonell, Lucia, Sanchez-Heras, Ana-Beatriz, Segura, Angel, Ochoa, Enrique, Lazaro, Rafael, Ruiz-Ponte, Clara, Bujanda, Luis, Andreu, Montserrat, Castells, Antoni, Carracedo, Angel, Llor, Xavier, Clofent, Juan, Alenda, Cristina, Paya, Artemio, Jover, Rodrigo, Soto, Jose-Luis

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INOVATYON/ ENGOT-ov5 study: Randomized phase III international study comparing trabectedin/pegylated liposomal doxorubicin (PLD) followed by platinum at progression vs carboplatin/... von Colombo, N., Gadducci, A., Sehouli, J., Rulli, E., Mäenpää, J., Sessa, C., Montes, A., Ottevanger, N. B., Berger, R., Vergote, I., D’Incalci, M., Churruca Galaz, C., Chekerov, R., Nyvang, G. B., Riniker, S., Herbertson, R., Fossati, R., Barretina-Ginesta, M. P., Deryal, M., Mirza, M. R., Biagioli, E., Iglesias, M., Funari, G., Romeo, M., Tasca, G., Pardo, B., Tognon, G., Rubio-Pérez, M. J., DeCensi, A., De Giorgi, U., Zola, P., Benedetti Panici, P., Aglietta, M., Arcangeli, V., Zamagni, C., Bologna, A., Westermann, A., Heinzelmann-Schwarz, V., Tsibulak, I., Wimberger, P., Poveda, A.

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Relationship of immunohistochemistry, copy number aberrations and epigenetic disorders with BRCAness pattern in hereditary and sporadic breast cancer von Murria Estal, Rosa, Palanca Suela, Sarai, de Juan Jiménez, Inmaculada, Alenda Gonzalez, Cristina, Egoavil Rojas, Cecilia, García-Casado, Zaida, López Guerrero, Jose Antonio, Juan Fita, María José, Sánchez Heras, Ana Beatriz, Segura Huerta, Ángel, Santaballa Bertrán, Ana, Chirivella González, Isabel, Llop García, Marta, Pérez Simó, Gema, Barragán González, Eva, Bolufer Gilabert, Pascual

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SEOM clinical guideline on heritable TP53-related cancer syndrome (2022) von Sánchez-Heras, Ana Beatriz, Ramon y Cajal, Teresa, Pineda, Marta, Aguirre, Elena, Graña, Begoña, Chirivella, Isabel, Balmaña, Judit, Brunet, Joan

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Recurrent testicular germ cell tumors in a family with MYH-associated polyposis von Castillejo, Adela, Sanchez-Heras, Ana Beatriz, Jover, Rodrigo, Castillejo, Maria Isabel, Guarinos, Carla, Oltra, Silvestre, Martínez-Canto, Ana, Barbera, Victor Manuel, Laforga, Juan, Paya, Artemio, Alenda, Cristina, Soto, Jose Luis

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Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells von Andrianova, Maria A, Seplyarskiy, Vladimir B, Terradas, Mariona, Sánchez-Heras, Ana Beatriz, Mur, Pilar, Soto, José Luis, Aiza, Gemma, Borràs, Emma, Kondrashov, Fyodor A, Kondrashov, Alexey S, Bazykin, Georgii A, Valle, Laura

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