Publicacións en colaboración con investigadores/as de Hospital Universitario 12 de Octubre (17)

2024

  1. Clinical and Genetic Analysis of Patients With TK2 Deficiency

    Neurology: Genetics, Vol. 10, Núm. 2

  2. Novel risk loci for COVID-19 hospitalization among admixed American populations

    eLife, Vol. 13

2023

  1. A crowdsourcing database for the copy-number variation of the Spanish population

    Human Genomics, Vol. 17, Núm. 1

  2. A second update on mapping the human genetic architecture of COVID-19

    Nature

2022

  1. Novel genes and sex differences in COVID-19 severity

    Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806

2017

  1. The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study

    Journal of Molecular and Cellular Cardiology, Vol. 102, pp. 3-9

2014

  1. A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis

    PLoS ONE, Vol. 9, Núm. 6

2013

  1. Meta-Analysis of Mismatch Repair Polymorphisms within the Cogent Consortium for Colorectal Cancer Susceptibility

    PLoS ONE, Vol. 8, Núm. 9

  2. Risk of cancer in cases of suspected lynch syndrome without germline mutation

    Gastroenterology, Vol. 144, Núm. 5

2012

  1. COGENT (COlorectal cancer GENeTics) revisited

    Mutagenesis, Vol. 27, Núm. 2, pp. 143-151

2011

  1. Case-control study for colorectal cancer genetic susceptibility in EPICOLON: Previously identified variants and mucins

    BMC Cancer, Vol. 11

2010

  1. Susceptibility genetic variants associated with colorectal cancer risk correlate with cancer phenotype

    Gastroenterology, Vol. 139, Núm. 3

2004

  1. Association of PDCD1 with susceptibility to systemic lupus erythematosus: Evidence for population-specific effects

    TISSUE ANTIGENS

  2. Association of PDCD1 with susceptibility to systemic lupus erythematosus: Evidence of population-specific effects

    Arthritis and Rheumatism, Vol. 50, Núm. 8, pp. 2590-2597

2003

  1. CARD15/NOD2 analysis in rheumatoid arthritis susceptibility

    Rheumatology, Vol. 42, Núm. 11, pp. 1380-1382

  2. Reverse association of a regulatory polymorphism in PDCD1 with susceptibility to systemic lupus erythematosus.

    ARTHRITIS AND RHEUMATISM

  3. The three most common CARD15 mutations associated with Crohn's disease and the chromosome 16 susceptibility locus for systemic lupus erythematosus

    Rheumatology, Vol. 42, Núm. 4, pp. 570-574