Publicacions en col·laboració amb investigadors/es de Hospital Universitario Virgen de las Nieves (28)

2024

  1. Molecular subtypes explain lupus epigenomic heterogeneity unveiling new regulatory genetic risk variants

    npj Genomic Medicine, Vol. 9, Núm. 1

2022

  1. Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis

    npj Genomic Medicine, Vol. 7, Núm. 1

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

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

2021

  1. A new molecular classification to drive precision treatment strategies in primary Sjögren’s syndrome

    Nature Communications, Vol. 12, Núm. 1

  2. Integrative Analysis Reveals a Molecular Stratification of Systemic Autoimmune Diseases

    Arthritis and Rheumatology, Vol. 73, Núm. 6, pp. 1073-1085

  3. Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature

    Scientific Reports, Vol. 11, Núm. 1

2020

  1. IgM antibodies against malondialdehyde and phosphorylcholine in different systemic rheumatic diseases

    Scientific Reports, Vol. 10, Núm. 1

  2. Polymorphisms within the ARNT2 and CX3CR1 genes are associated with the risk of developing invasive aspergillosis

    Infection and Immunity, Vol. 88, Núm. 4

2017

  1. A combined large-scale meta-Analysis identifies COG6 as a novel shared risk locus for rheumatoid arthritis and systemic lupus erythematosus

    Annals of the Rheumatic Diseases, Vol. 76, Núm. 1, pp. 286-294

  2. Regulation of Fn14 receptor and NF-κB underlies inflammation in Meniere's disease

    Frontiers in Immunology, Vol. 8, Núm. DEC

  3. Transancestral mapping and genetic load in systemic lupus erythematosus

    Nature Communications, Vol. 8

2013

  1. A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci

    Human Molecular Genetics, Vol. 22, Núm. 19, pp. 4021-4029

  2. Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease

    Immunogenetics, Vol. 65, Núm. 5, pp. 345-355

2012

  1. Erratum to "Novel association of acid phosphatase locus 1 C allele with systemic lupus erythematosus" [Human Immunology 73 (2012) 107-110]

    Human Immunology

  2. Fine mapping and conditional analysis identify a new mutation in the autoimmunity susceptibility gene BLK that leads to reduced half-life of the BLK protein

    Annals of the Rheumatic Diseases, Vol. 71, Núm. 7, pp. 1219-1226

  3. Novel association of acid phosphatase locus 1*C allele with systemic lupus erythematosus

    Human Immunology, Vol. 73, Núm. 1, pp. 107-110

2011

  1. Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort

    Genes and Immunity, Vol. 12, Núm. 4, pp. 270-279

2010

  1. A 3′-untranslated region variant is associated with impaired expression of CD226 in T and natural killer T cells and is associated with susceptibility to systemic lupus erythematosus

    Arthritis and Rheumatism, Vol. 62, Núm. 11, pp. 3404-3414

  2. The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases

    Annals of the Rheumatic Diseases, Vol. 69, Núm. 4, pp. 696-699

2009

  1. Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus

    Human Molecular Genetics, Vol. 18, Núm. 19, pp. 3739-3748