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Issue Date | Title | Author(s) |
---|---|---|
23-Jan-2021 | BARD1 Pathogenic Variants are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer Cohort | Rofes, 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 |
1-May-2018 | Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations | Feliubadaló i Elorza, Maria Lídia; Teulé-Vega, Àlex; CIMBA Consortium |
1-Apr-2020 | Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients | Valle, 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 |
1-Apr-2015 | Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers | Blanco Guillermo, Ignacio; Cuadras, Daniel; Ruiz de Garibay, Gorka; Librado Sanz, Pablo; Sánchez-Gracia, Alejandro; Rozas Liras, Julio A.; Bonifaci Cano, Núria; Mateo González, Francesca; Berenguer, Antoni; Petit, Anna; Català, Isabel; Feliubadaló i Elorza, Maria Lídia; Tornero, Eva; Lázaro García, Conxi; Pujana Genestar, M. Ángel; Esteller, Manel; Gómez, Antonio; Sayols, Sergi; Vidal, Enrique; Heyn, Holger |
1-Sep-2016 | Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus | Feliubadaló i Elorza, Maria Lídia; Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers (GEMO); Epidemiological study of BRCA1 & BRCA2 Mutation Carriers (EMBRACE); Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON); KConFab Investigators; Australian Ovarian Cancer Study Group |
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