Browsing by Author Brunet, Joan

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Issue DateTitleAuthor(s)
23-Jan-2021BARD1 Pathogenic Variants are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer CohortRofes, Paula; Valle, Jesús del; Torres Esquius, Sara; Feliubadaló i Elorza, Maria Lídia; Stradella, Agostina; Moreno Cabrera, José Marcos; López Dóriga Guerra, Adriana; Munté, Elisabet; Cid, Rafael de; Campos, Olga; Cuesta, Raquel; Teulé-Vega, Àlex; Grau Garcés, Èlia; Sanz, Judit; Capellá, G. (Gabriel); Díez Gibert, Orland; Brunet, Joan; Balmaña, Judith; Lázaro García, Conxi
4-Jan-2017Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary CancerFeliubadaló i Elorza, Maria Lídia; Tonda, Raul; Gausachs Romero, Mireia; Trotta, Jean Rémi; Castellanos, Elisabeth; López Dóriga Guerra, Adriana; Teulé-Vega, Àlex; Tornero, Eva; Valle Domínguez, Jesús del; Gel, Bernat; Gut, Marta; Pineda Riu, Marta; González, Sara; Menéndez Vilà, Mireia; Navarro, Matilde; Capellá, G. (Gabriel); Gut, Ivo G.; Serra Arenas, Eduard; Brunet, Joan; Beltran i Agulló, Sergi; Lázaro García, Conxi
2-Feb-2024Biological basis of extensive pleiotropy between blood traits and cancer riskGómez, Antonio; Pardo Cea, Miguel A.; Farré, Xavier; Esteve, Anna; Palade, Joanna; Espín, Roderic; Mateo González, Francesca; Alsop, Eric; Alorda, Marc; Blay, Natalia; Baiges, Alexandra; Shabbir, Arzoo; Comellas, Francesc; Arnan, Montserrat; Teulé Vega, Àlex; Salinas Masdeu, Mònica; Berrocal, Laura; Brunet, Joan; Rofes, Paula; Lázaro, Conxi; Conesa, Miquel; Rojas, Juan Jose; Velten, Lars; Fendler, Wojciech; Smyczynska, Urszula; Chowdhury, Dipanjan; Zeng, Yong; Hansen He, Housheng; Li, Rong; Van Keuren‑Jensen, Kendall; Cid, Rafael de; Pujana Genestar, M. Ángel
28-Jul-2021Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk ScoresBarnes, Daniel R.; Angel Pujana, Miquel; Teulé Vega, Àlex; Balmaña, Judith; GEMO Study Collaborators; EMBRACE Collaborators; KConFab Investigators; HEBON Investigators; Consortium Of Investigators Of Modifiers Of Brca1 And Brca2, The; Brunet, Joan; Darder, Esther; Valle Domínguez, Jesús del; Diez, Orland; Feliubadaló i Elorza, Maria Lídia; Izquierdo, Angel; Lazaro, Conxi; López Fernández, Adrià
28-Sep-2022Cancer risks by sex and variant type in PTEN hamartoma tumor syndromeHendricks, Linda A. J.; Hoogerbrugge, Nicoline; Mensenkamp, Arjen R.; Brunet, Joan; Lleuger Pujol, Roser; Høberg-Vetti, Hildegunn; Tveit Haavind, Marianne; Innella, Giovanni; Turchetti, Daniela; Aretz, Stefan; Spier, Isabel; Tischkowitz, Marc; Jahn, Arne; Links, Thera P.; Olderode-Berends, Maran J. W.; Blatnik, Ana; Leter, Edward M.; Evans, D. Gareth; Woodward, Emma R.; Steinke-Lange, Verena; Anastasiadou, Violetta C.; Colas, Chrystelle; Villy, Marie Charlotte; Benusiglio, Patrick R.; Gerasimenko, Anna; Barili, Valeria; Branchaud, Maud; Houdayer, Claude; Tesi, Bianca; Yazicioglu, M. Omer; Post, Rachel S. van der; Schuurs-Hoeijmakers, Janneke H. M.; Hest, Liselotte P. van; Adank, Muriel A.; Duijkers, Floor; Nielsen, Maartje; Verbeek, Katja C. J.; Ierland, Yvette van; Giltay, Jacques C.; Vos, Janet R.; PTEN Study Group
24-Dec-2021Clinical Management of COVID-19 in Cancer Patients with the STAT3 Inhibitor SilibininBosch Barrera, Joaquim; Roqué, Ariadna; Teixidor, Eduard; Carmona García, M. Carmen; Arbusà, Aina; Brunet, Joan; Martin Castillo, Begoña; Cuyàs, Elisabet; Verdura, Sara; Menendez, Javier A.
5-Mar-2023Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidenceHassanin, Emadeldin; Spier, Isabel; Bobbili, Dheeraj R.; Aldisi, Rana; Klinkhammer, Hannah; David, Friederike; Dueñas, Nuria; Hüneburg, Robert; Perne, Claudia; Brunet, Joan; Capella, Gabriel; Nöthen, Markus M.; Forstner, Andreas J.; Mayr, Andreas; Krawitz, Peter; May, Patrick; Aretz, Stefan; Maj, Carlo
1-Oct-2022Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortiumMøller, Pål; Seppälä, Toni T.; Dowty, James G.; Haupt, Saskia; Dominguez Valentin, Mev; Sunde, Lone; Bernstein, Inge; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capellá, G. (Gabriel); Lindblom, Annika; Gluck, Nathan; Kalfayan, Pablo; Torrezan, Giovana Tardin; Winship, Ingrid; Plazzer, John Paul; Sijmons, Rolf; Backman, Ann Sofie; De Vargas, Aída Falcón; Vangala, Deepak; Lautrup, Charlotte K.; Laghi, Luigi; Valle, Adriana Della; Abu Freha, Naim; Winter, Des; Bohorquez, Mabel; Horisberger, Karoline; Heinimann, Karl; Half, Elizabeth; Lopez Koestner, Francisco; Alvarez Valenzuela, Karin; Van Hest, Liselotte P.; Scott, Rodney J.; Ligtenberg, Marjolijn J. L.; Katz, Lior; Da Silva, Leandro Apolinário; Zahary, Mohd N.; Laish, Ido; Rossi, Norma Teresa; Morrison, Patrick J.; Vainer, Elez; Nascimento, Ivana; Steinke Lange, Verena; Vaccaro, Carlos Alberto; Carraro, Dirce Maria; Thomas, Huw; Zaránd, Attila; Poplawski, Nicola; Aronson, Melyssa; Kohonen Corish, Maija R. J.; Lee, Grant; Mecklin, Jukka Pekka; Pylvänäinen, Kirsi; Schmiegel, Wolff; Hüneburg, Robert; Gerdes, Anne Marie; Snyder, Carrie; Renkonen Sinisalo, Laura; Lepisto, Anna; Peltomäki, Päivi; Therkildsen, Christina; Lindberg, Lars Joachim; Lindor, Noralane; Thorlacius Ussing, Ole; Stoffel, Elena; Newcomb, Polly A.; Von Knebel Doeberitz, Magnus; Palmero, Edenir; Thibodeau, Stephen N.; Loeffler, Markus; Amor, David; Hoogerbrugge, Nicoline; Rahner, Nils; Duijkers, Floor; Hall, Michael J.; Buchanan, Daniel D.; Le Marchand, Loïc; Win, Aung Ko; Hovig, Eivind; Hampel, Heather; Williams, Heinric; Ricciardiello, Luigi; Southey, Melissa; Samadder, N. Jewel; James, Paul; Okkels, Henrik; Lubiński, Jan; Reece, Jeanette; Ngeow, Joanne; Bassaneze, Thiago; Guillem, Jose G.; Ahadova, Aysel; Arnold, Julie; Pai, Rish; Jenkins, Mark A.; Wadt, Karin; Ankathil, Ravindran; Holinski Feder, Elke; Monahan, Kevin; Chen Shtoyerman, Rakefet; Heuveline, Vincent; Senter, Leigha; Rasmussen, Lene J.; Ward, Robyn; Parry, Susan; Evans, D. Gareth; Sampson, Julian R.; Moslein, Gabriela; Bonanni, Bernardo; Dębniak, Tadeusz; John, Thomas; Hopper, John L.; Gallinger, Steven; Figueiredo, Jane; Ten Broeke, Sanne W.; Van Overeem Hansen, Thomas; Caldés, Trinidad; Yamaguchi, Tatsuro; Barca Tierno, Verónica; Garre, Pilar; Kennelly, Rory; Cavestro, Giulia Martina; Dueñas, Nuria; Greenblatt, Marc; Weitz, Jürgen; Pineda, Marta; Lino Silva, Leonardo S.; Redler, Silke; Nakken, Sigve; Burn, John; Büttner, Reinhard; Brunet, Joan; Green, Kate; Sheth, Harsh; Rossi, Benedito Mauro; Stakelum, Aine; Portenkirchner, Carmen; Lalloo, Fiona; Newton, Katie; Martin, Claudia; Kloor, Matthias; The European Hereditary Tumour Group (ehtg) And The International Mismatch Repair Consortium (imrc); Bertario, Lucio; Crosbie, Emma J.; Mints, Miriam; Tjandra, Douglas; Neffa, Florencia; Perne, Claudia; Esperon, Patricia; Latchford, Andrew; Kariv, Revital; Macrae, Finlay; Guillén Ponce, Carmen; Rosner, Guy; Levi, Zohar; Tibiletti, Maria Grazia; Pavicic, Walter Hernán
29-Sep-2020Complete Loss of EPCAM Immunoexpression Identifies EPCAM Deletion Carriers in MSH2-Negative Colorectal NeoplasiaCuatrecasas Freixas, Miriam; Gorostiaga, Iñigo; Riera, Cristina; Saperas, Esteban; Llort, Gemma; Costa, Irmgard; Matias-Guiu, Xavier; Carrato, Cristina; Navarro, Matilde; Pineda Riu, Marta; Dueñas, Nuria; Brunet, Joan; Marco, Vicente; Trias, Isabel; Busteros, José Ignacio; Mateu, Gemma; Balaguer Prunés, Francesc; Fernández Figueras, María Teresa; Esteller, Manel; Musulén, Eva
1-Jul-2020Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like IndividualsDámaso, Estela; González Acosta, María Isabel; Vargas Parra, Gardenía María; Navarro, Matilde; Balmaña, Judith; Ramon y Cajal, Teresa; Tuset, Noemí; Thompson, Bryony A.; Marín, Fátima; Fernández, Anna; Gomez, Carolina; Velasco, Àngela; Solanes, Ares; Iglesias Casals, Sílvia; Urgel, Gisela; López, Consol; Valle, Jesús del; Campos, Olga; Santacana, Maria; Matias-Guiu, Xavier; Lázaro García, Conxi; Valle, Laura; Brunet, Joan; Pineda Riu, Marta; Capellá, G. (Gabriel)
22-Jun-2021Correction: Dueñas et al. Assessing effectiveness of colonic and gynecological risk reducing surgery in Lynch syndrome individuals. Cancers 2020, 12, 3419.Dueñas, Nuria; Navarro, Matilde; Teulé-Vega, Àlex; Solanes, Ares; Salinas Masdeu, Mònica; Iglesias Casals, Sílvia; Munté, Elisabet; Ponce i Sebastià, Jordi; Guardiola, Jordi; Kreisler, Esther; Carballas, Elvira; Cuadrado, Marta; Matias-Guiu, Xavier; Ossa, Napoleón de la; Lop, Joan; Lázaro García, Conxi; Capellá, G. (Gabriel); Pineda Riu, Marta; Brunet, Joan
6-Mar-2018Decapping Protein Edc4 Regulates Dna Repair And Phenocopies Brca1Hernández, Gonzalo; Ramírez, María José; Minguillón, Jordi; Quiles, Paco; Ruiz de Garibay, Gorka; Aza-Carmona, Miriam; Bogliolo, Massimo; Pujol, Roser; Prados-Carvajal, Rosario; Fernandez, Juana; Garcia, Nadia; López, Adriá; Gutiérrez Enríquez, Sara; Díez Gibert, Orland; Benitez, Javier; Salinas Masdeu, Mònica; Teulé-Vega, Àlex; Brunet, Joan; Radice, Paolo; Peterlongo, Paolo; Schindler, Detlev; Huertas, Pablo; Puente, Xose S.; Lázaro García, Conxi; Pujana Genestar, M. Ángel; Surrallés, Jordi
22-Dec-2018Does multilocus inherited neoplasia alleles syndrome have severe clinical expression?Stradella, Agostina; Valle, Jesús del; Rofes, Paula; Feliubadaló i Elorza, Maria Lídia; Grau Garcés, Èlia; Velasco, Àngela; González, Sara; Vargas Parra, Gardenía María; Izquierdo, Ángel; Campos, Olga; Tornero, Eva; Navarro, Matilde; Balmaña, Judith; Capellá, G. (Gabriel); Pineda Riu, Marta; Brunet, Joan; Lázaro García, Conxi
1-Dec-2020Evaluation of CNV detection tools for NGS panel data in genetic diagnosticsMoreno Cabrera, José Marcos; Valle Domínguez, Jesús del; Castellanos, Elisabeth; Feliubadaló i Elorza, Maria Lídia; Pineda Riu, Marta; Brunet, Joan; Serra, Eduard; Capellá, G. (Gabriel); Lázaro García, Conxi; Gel, Bernat
1-Aug-2023Evaluation of somatic mutations in cervicovaginal samples as a non-invasive method for the detection and molecular classification of endometrial cancerPelegrina, Beatriz; Paytubi Casabona, Sònia; Marín, Fátima; Martínez Delgado, José Manuel; Carmona, Álvaro; Frias Gomez, Jon; Peremiquel Trillas, Paula; Dorca Duch, Eduard; Zanca, Alba; López-Querol Marta; Onieva, Irene; Benavente, Yolanda; Barahona, Marc; Fernandez Gonzalez, Sergi; De Francisco, Javier; Caño, Víctor; Vidal, August; Pijuan, Lara; Canet Hermida, Júlia; Dueñas, Nuria; Brunet, Joan; Pineda Riu, Marta; Matias-Guiu, Xavier; Ponce i Sebastià, Jordi; Bosch José, Francesc Xavier, 1947-; Sanjosé, Silvia de; Alemany i Vilches, Laia; Costas, Laura
22-Nov-2010Exploring the Link Between Germline and Somatic Genetic Alterations in Breast CarcinogenesisBonifaci Cano, Núria; Gorski, Bohdan; Masojć, Bartlomiej; Wokolorczyk, Dominika; Jakubowska, Anna; Dębniak, Tadeusz; Berenguer, Antoni; Serra-Musach, Jordi; Brunet, Joan; Dopazo, Joaquín; Narod, Steven A.; Lubinski, Jan; Lázaro García, Conxi; Cybulski, Cezary; Pujana Genestar, M. Ángel
1-Apr-2020Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer PatientsValle, Jesús del; Rofes, Paula; Moreno Cabrera, José Marcos; López Dóriga Guerra, Adriana; Belhadj, Sami; Vargas Parra, Gardenía María; Teulé-Vega, Àlex; Cuesta, Raquel; Muñoz, Xavier; Campos, Olga; Salinas Masdeu, Mònica; Cid, Rafael de; Brunet, Joan; González, Sara; Capellá, G. (Gabriel); Pineda Riu, Marta; Feliubadaló i Elorza, Maria Lídia; Lázaro García, Conxi
17-Apr-2013Functional and Structural Analysis of C-Terminal BRCA1 Missense VariantsQuiles Vidal, Francisco de Asís; Fernández-Rodríguez, Juana; Mosca, Roberto; Feliubadaló i Elorza, Maria Lídia; Tornero, Eva; Brunet, Joan; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel); Pujana Genestar, M. Ángel; Aloy, Patrick, 1972-; Monteiro, Alvaro N.; Lázaro García, Conxi
1-Jan-2023Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk SyndromesGarcia Pelaez, José; Barbosa Matos, Rita; Lobo, Silvana; Dias, Alexandre; Garrido, Luzia; Castedo, Sérgio; Sousa, Sónia; Pinheiro, Hugo; Sousa, Liliana; Monteiro, Rita; Maqueda, Joaquin J.; Fernandes, Susana; Carneiro, Fátima; Pinto, Nádia; Lemos, Carolina; Pinto, Carla; Teixeira, Manuel R.; Aretz, Stefan; Bajalica Lagercrantz, Svetlana; Balmaña, Judith; Blatnik, Ana; Benusiglio, Patrick R.; Blanluet, Maud; Bours, Vincent; Brems, Hilde; Brunet, Joan; Calistri, Daniele; Capella, Gabriel; Carrera, Sergio; Colas, Chrystelle; Dahan, Karin; Putter, Robin de; Desseignés, Camille; Domínguez Garrido, Elena; Egas, Conceição; Evans, D. Gareth; Feret, Damien; Fewings, Eleanor; Fitzgerald, Rebecca C.; Coulet, Florence; Garcia Barcina, María; Genuardi, Maurizio; Golmard, Lisa; Hackmann, Karl; Hanson, Helen; Holinski Feder, Elke; Hüneburg, Robert; Krajc, Mateja; Lagerstedt Robinson, Kristina; Lázaro, Conxi; Ligtenberg, Marjolijn J. L.; Martínez Bouzas, Cristina; Merino, Sonia; Michils, Geneviève; Novaković, Srdjan; Patiño García, Ana; Ranzani, Guglielmina Nadia; Schröck, Evelin; Silva, Inês; Silveira, Catarina; Soto, José L.; Spier, Isabel; Steinke Lange, Verena; Tedaldi, Gianluca; Tejada, María isabel; Woodward, Emma R; Tischkowitz, Marc; Hoogerbrugge, Nicoline; Oliveira, Carla
1-Dec-2022Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohortHendricks, Linda A.J.; Hoogerbrugge, Nicoline; Venselaar, Hanka; Aretz, Stefan; Spier, Isabel; Legius, Eric; Brems, Hilde; De Putter, Robin; Claes, Kathleen B.M.; Evans, D. Gareth; Woodward, Emma R.; Genuardi, Maurizio; Brugnoletti, Fulvia; Van Ierland, Yvette; Dijke, Kim; Tham, Emma; Tesi, Bianca; Schuurs Hoeijmakers, Janneke H.M.; Branchaud, Maud; Salvador, Hector; Jahn, Arne; Schnaiter, Simon; Anastasiadou, Violetta Christophidou; Brunet, Joan; Oliveira, Carla; Roht, Laura; Blatnik, Ana; Irmejs, Arvids; Mensenkamp, Arjen R.; Vos, Janet R.; Duijkers, Floor; Giltay, Jacques C.; Van Hest, Liselotte P.; Kleefstra, Tjitske; Leter, Edward M.; Nielsen, Maartje; Nijmeijer, Sebastiaan W.R.; Olderode-berends, Maran J.W.