Publicaciones en colaboración con investigadores/as de Instituto de Parasitología y Biomedicina López Neyra (24)

2024

  1. Genome-Wide Association Study Identifies the First Germline Genetic Variant Associated With Erdheim-Chester Disease

    Arthritis and Rheumatology, Vol. 76, Núm. 1, pp. 141-145

2023

  1. A Summary on the Genetics of Systemic Lupus Erythematosus, Rheumatoid Arthritis, Systemic Sclerosis, and Sjögren’s Syndrome

    Clinical Reviews in Allergy and Immunology, Vol. 64, Núm. 3, pp. 392-411

  2. FLT3 functional low-frequency variant rs76428106-C is associated with susceptibility to systemic sclerosis

    Rheumatology (Oxford, England), Vol. 62, Núm. SI, pp. SI138-SI142

  3. Identification of new risk loci shared across systemic vasculitides points towards potential target genes for drug repurposing

    Annals of the Rheumatic Diseases, Vol. 82, Núm. 6, pp. 837-847

2022

  1. Methylome and transcriptome profiling of giant cell arteritis monocytes reveals novel pathways involved in disease pathogenesis and molecular response to glucocorticoids

    Annals of the Rheumatic Diseases, Vol. 81, Núm. 9, pp. 1290-1300

2021

  1. Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet’s Disease

    Arthritis and Rheumatology, Vol. 73, Núm. 7, pp. 1244-1252

2020

  1. Epigenomics and transcriptomics of systemic sclerosis CD4+ T cells reveal long-range dysregulation of key inflammatory pathways mediated by disease-associated susceptibility loci

    Genome Medicine, Vol. 12, Núm. 1

  2. The role of a functional variant of TYK2 in vasculitides and infections

    Clinical and Experimental Rheumatology, Vol. 38, Núm. 5, pp. 949-955

2019

  1. Behçet’s Disease

    Rare Diseases of the Immune System (Springer Nature), pp. 37-51

2018

  1. Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus

    Scientific Reports, Vol. 8, Núm. 1

  2. Cross-phenotype analysis of Immunochip data identifies KDM4C as a relevant locus for the development of systemic vasculitis

    Annals of the Rheumatic Diseases, Vol. 77, Núm. 4, pp. 589-595

2017

  1. Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach

    Scientific Reports, Vol. 7, Núm. 1

2016

  1. Genetic analysis with the immunochip platform in Behçet disease. Identification of residues associated in the HLA class I region and new susceptibility loci

    PLoS ONE, Vol. 11, Núm. 8

  2. PTPN22 is not associated with Behçet's disease. Study spanning the complete gene region in the Spanish population and meta-analysis of the functional variant R620W

    Clinical and Experimental Rheumatology, Vol. 34, pp. 41-45

2015

  1. A large-scale genetic analysis reveals a strong contribution of the HLA class II region to giant cell arteritis susceptibility

    American Journal of Human Genetics, Vol. 96, Núm. 4, pp. 565-580

  2. Association of CCR5Δ32 and Behçet's disease: New data from a case-control study in the Spanish population and meta-analysis

    Clinical and Experimental Rheumatology, Vol. 33, pp. 96-100

  3. Association of HLA-B*41:02 with Henoch-Schönlein Purpura (IgA Vasculitis) in Spanish individuals irrespective of the HLA-DRB1 status

    Arthritis Research and Therapy, Vol. 17, Núm. 1

  4. Association of haplotypes of the TLR8 locus with susceptibility to Crohn's and Behçet's diseases

    Clinical and Experimental Rheumatology, Vol. 33, pp. 117-122

  5. Brief report: Association of HLA-DRB101 with IgA vasculitis (henoch-schönlein)

    Arthritis and Rheumatology, Vol. 67, Núm. 3, pp. 823-827

  6. Lack of association of TNFAIP3 and JAK1 with Behçet's disease in the European population

    Clinical and Experimental Rheumatology, Vol. 33, pp. 36-39