Publicaciones en colaboración con investigadores/as de Universidad del Rosario (31)

2023

  1. Author Correction: Genome-wide association study identifies Sjögren’s risk loci with functional implications in immune and glandular cells (Nature Communications, (2022), 13, 1, (4287), 10.1038/s41467-022-30773-y)

    Nature Communications

2022

  1. Erratum: Author Correction: Genome-wide association study identifies Sjögren's risk loci with functional implications in immune and glandular cells (Nature communications (2022) 13 1 (4287))

    Nature communications

  2. Genome-wide association study identifies Sjögren’s risk loci with functional implications in immune and glandular cells

    Nature Communications, Vol. 13, Núm. 1

2018

  1. A plausibly causal functional lupus-associated risk variant in the STAT1-STAT4 locus

    Human Molecular Genetics, Vol. 27, Núm. 13, pp. 2392-2404

  2. Corrigendum to “Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome” [Clin. Immunol. 168 (2016) 25–29](S1521661616300614)(10.1016/j.clim.2016.04.002)

    Clinical Immunology

2017

  1. Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome

    Arthritis and Rheumatology, Vol. 69, Núm. 11, pp. 2187-2192

2016

  1. Decreased SMG7 expression associates with lupus-risk variants and elevated antinuclear antibody production

    Annals of the Rheumatic Diseases, Vol. 75, Núm. 11, pp. 2007-2013

  2. Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome

    Clinical Immunology, Vol. 168, pp. 25-29

  3. Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA

    Annals of the Rheumatic Diseases, Vol. 75, Núm. 1, pp. 242-252

  4. X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome

    Arthritis and Rheumatology, Vol. 68, Núm. 5, pp. 1290-1300

2015

  1. Genetic association of CD247 (CD3ζ) with SLE in a large-scale multiethnic study

    Genes and Immunity, Vol. 16, Núm. 2, pp. 142-150

  2. Genetic associations of leptin-related polymorphisms with systemic lupus erythematosus

    Clinical Immunology, Vol. 161, Núm. 2, pp. 157-162

  3. Lupus risk variant increases pSTAT1 binding and decreases ETS1 expression

    American Journal of Human Genetics, Vol. 96, Núm. 5, pp. 731-739

  4. The IRF5-TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share

    Human Molecular Genetics, Vol. 24, Núm. 2, pp. 582-596

2014

  1. Lupus risk variants in the PXK locus alter B-cell receptor internalization

    Frontiers in Genetics, Vol. 5, Núm. DEC

2013

  1. ABIN1 dysfunction as a genetic basis for lupus nephritis

    Journal of the American Society of Nephrology, Vol. 24, Núm. 11, pp. 1743-1754

  2. Fine mapping of Xq28: Both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups

    Annals of the Rheumatic Diseases, Vol. 72, Núm. 3, pp. 437-444

  3. PTPN22 Association in Systemic Lupus Erythematosus (SLE) with Respect to Individual Ancestry and Clinical Sub-Phenotypes

    PLoS ONE, Vol. 8, Núm. 8

  4. Trans-Ancestral Studies Fine Map the SLE-Susceptibility Locus TNFSF4

    PLoS Genetics, Vol. 9, Núm. 7

2012

  1. A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus

    Genes and Immunity, Vol. 13, Núm. 5, pp. 380-387