Works by Ordóñez, R.

Results: 39
    1

    Algebraic Formulation of Quantum Decoherence.

    Published in:
    International Journal of Theoretical Physics, 2004, v. 43, n. 3, p. 695, doi. 10.1023/B:IJTP.0000048170.55598.05
    By:
    • Castagnino, M. A.;
    • Ordóñez, A. R.
    Publication type:
    Article
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    Comprehensive genomic diagnosis of inherited retinal and optical nerve disorders reveals hidden syndromes and personalized therapeutic options.

    Published in:
    Acta Ophthalmologica (1755375X), 2020, v. 98, n. 8, p. e1034, doi. 10.1111/aos.14479
    By:
    • Diñeiro, Marta;
    • Capín, Raquel;
    • Cifuentes, Guadalupe Á.;
    • Fernández‐Vega, Beatriz;
    • Villota, Eva;
    • Otero, Andrea;
    • Santiago, Adrián;
    • Pruneda, Patricia C.;
    • Castillo, David;
    • Viejo‐Díaz, Mónica;
    • Hernando, Inés;
    • Durán, Noelia S.;
    • Álvarez, Rebeca;
    • Lago, Claudia G.;
    • Ordóñez, Gonzalo R.;
    • Fernández‐Vega, Álvaro;
    • Cabanillas, Rubén;
    • Cadiñanos, Juan
    Publication type:
    Article
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    Peritonitis por Mycoplasma?

    Published in:
    Nefrologia, 2010, v. 30, n. 4, p. 484, doi. 10.3265/Nefrologia.pre2010.May.10414
    By:
    • López, A. Sastre;
    • Velasco, M. A. Prieto;
    • Ordóñez, R.;
    • de León, B.;
    • Stefan, G.;
    • Granda, M.
    Publication type:
    Article
    9

    Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 47, doi. 10.1038/ng.1032
    By:
    • Quesada, Víctor;
    • Conde, Laura;
    • Villamor, Neus;
    • Ordóñez, Gonzalo R;
    • Jares, Pedro;
    • Bassaganyas, Laia;
    • Ramsay, Andrew J;
    • Beà, Sílvia;
    • Pinyol, Magda;
    • Martínez-Trillos, Alejandra;
    • López-Guerra, Mónica;
    • Colomer, Dolors;
    • Navarro, Alba;
    • Baumann, Tycho;
    • Aymerich, Marta;
    • Rozman, María;
    • Delgado, Julio;
    • Giné, Eva;
    • Hernández, Jesús M;
    • González-Díaz, Marcos
    Publication type:
    Article
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    Hereditary Spastic Paraplegia and Intellectual Disability: Clinicogenetic Lessons From a Family Suggesting a Dual Genetics Diagnosis.

    Published in:
    Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00041
    By:
    • Aguilera-Albesa, Sergio;
    • de la Hoz, Ana Belén;
    • Ibarluzea, Nekane;
    • Ordóñez-Castillo, Andrés R.;
    • Busto-Crespo, Olivia;
    • Villate, Olatz;
    • Ibiricu-Yanguas, María Asunción;
    • Yoldi-Petri, María E.;
    • García de Gurtubay, Iñaki;
    • Perez de Nanclares, Guiomar;
    • Pereda, Arrate;
    • Tejada, María Isabel
    Publication type:
    Article
    34

    Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia.

    Published in:
    Nature, 2011, v. 475, n. 7354, p. 101, doi. 10.1038/nature10113
    By:
    • Puente, Xose S.;
    • Pinyol, Magda;
    • Quesada, Víctor;
    • Conde, Laura;
    • Ordóñez, Gonzalo R.;
    • Villamor, Neus;
    • Escaramis, Georgia;
    • Jares, Pedro;
    • Beà, Sílvia;
    • González-Díaz, Marcos;
    • Bassaganyas, Laia;
    • Baumann, Tycho;
    • Juan, Manel;
    • López-Guerra, Mónica;
    • Colomer, Dolors;
    • Tubío, José M. C.;
    • López, Cristina;
    • Navarro, Alba;
    • Tornador, Cristian;
    • Aymerich, Marta
    Publication type:
    Article
    35

    A small-cell lung cancer genome with complex signatures of tobacco exposure.

    Published in:
    Nature, 2010, v. 463, n. 7278, p. 184, doi. 10.1038/nature08629
    By:
    • Pleasance, Erin D.;
    • Cheetham, R. Keira;
    • Stephens, Philip J.;
    • McBride, David J.;
    • Humphray, Sean J.;
    • Greenman, Chris D.;
    • Varela, Ignacio;
    • Meng-Lay Lin;
    • Ordóñez, Gonzalo R.;
    • Bignell, Graham R.;
    • Kai Ye;
    • Alipaz, Julie;
    • Bauer, Markus J.;
    • Beare, David;
    • Butler, Adam;
    • Carter, Richard J.;
    • Chen, Lina;
    • Cox, Anthony J.;
    • Edkins, Sarah;
    • Kokko-Gonzales, Paula I.
    Publication type:
    Article
    36

    A comprehensive catalogue of somatic mutations from a human cancer genome.

    Published in:
    Nature, 2010, v. 463, n. 7278, p. 191, doi. 10.1038/nature08658
    By:
    • Pleasance, Erin D.;
    • Cheetham, R. Keira;
    • Stephens, Philip J.;
    • McBride, David J.;
    • Humphray, Sean J.;
    • Greenman, Chris D.;
    • Varela, Ignacio;
    • Lin, Meng-Lay;
    • Ordóñez, Gonzalo R.;
    • Bignell, Graham R.;
    • Ye, Kai;
    • Alipaz, Julie;
    • Bauer, Markus J.;
    • Beare, David;
    • Butler, Adam;
    • Carter, Richard J.;
    • Chen, Lina;
    • Cox, Anthony J.;
    • Edkins, Sarah;
    • Kokko-Gonzales, Paula I.
    Publication type:
    Article
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