Works by Aznarez, Francisco


Results: 16
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    Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.

    Published in:
    Nature Genetics, 2011, v. 43, n. 7, p. 663, doi. 10.1038/ng.861
    By:
    • Comino-Méndez, Iñaki;
    • Gracia-Aznárez, Francisco J.;
    • Schiavi, Francesca;
    • Landa, Iñigo;
    • Leandro-García, Luis J.;
    • Letón, Rocío;
    • Honrado, Emiliano;
    • Ramos-Medina, Rocío;
    • Caronia, Daniela;
    • Pita, Guillermo;
    • Gómez-Graña, Álvaro;
    • de Cubas, Aguirre A.;
    • Inglada-Pérez, Lucía;
    • Maliszewska, Agnieszka;
    • Taschin, Elisa;
    • Bobisse, Sara;
    • Pica, Giuseppe;
    • Loli, Paola;
    • Hernández-Lavado, Rafael;
    • Díaz, José A.
    Publication type:
    Article
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    Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles.

    Published in:
    PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0055681
    By:
    • Gracia-Aznarez, Francisco Javier;
    • Fernandez, Victoria;
    • Pita, Guillermo;
    • Peterlongo, Paolo;
    • Dominguez, Orlando;
    • de la Hoya, Miguel;
    • Duran, Mercedes;
    • Osorio, Ana;
    • Moreno, Leticia;
    • Gonzalez-Neira, Anna;
    • Rosa-Rosa, Juan Manuel;
    • Sinilnikova, Olga;
    • Mazoyer, Sylvie;
    • Hopper, John;
    • Lazaro, Conchi;
    • Southey, Melissa;
    • Odefrey, Fabrice;
    • Manoukian, Siranoush;
    • Catucci, Irene;
    • Caldes, Trinidad
    Publication type:
    Article
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