Publicaciones en colaboración con investigadores/as de Uppsala University (81)

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

  2. Erratum to: Mapping the human genetic architecture of COVID-19 (Nature, (2021), 600, 7889, (472-477), 10.1038/s41586-021-03767-x)

    Nature

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

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

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

2021

  1. Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

    Journal of Clinical Investigation, Vol. 131, Núm. 23

  2. Mapping the human genetic architecture of COVID-19

    Nature, Vol. 600, Núm. 7889, pp. 472-477

  3. The trans-ancestral genomic architecture of glycemic traits

    Nature Genetics, Vol. 53, Núm. 6, pp. 840-860

2018

  1. 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

  2. Whole Exome Sequencing of Patients from Multicase Families with Systemic Lupus Erythematosus Identifies Multiple Rare Variants

    Scientific Reports, Vol. 8, Núm. 1

2017

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

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

  2. Transancestral mapping and genetic load in systemic lupus erythematosus

    Nature Communications, Vol. 8

2016

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

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

  2. The SLE variant Ala71Thr of BLK severely decreases protein abundance and binding to BANK1 through impairment of the SH3 domain function

    Genes and Immunity, Vol. 17, Núm. 2, pp. 128-138

  3. 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 analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus

    Nature Genetics, Vol. 47, Núm. 12, pp. 1457-1464

  2. PXK locus in systemic lupus erythematosus: Fine mapping and functional analysis reveals novel susceptibility gene ABHD6

    Annals of the Rheumatic Diseases, Vol. 74, Núm. 3

  3. 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

2012

  1. Evaluation of TRAF6 in a large multiancestral lupus cohort

    Arthritis and Rheumatism, Vol. 64, Núm. 6, pp. 1960-1969

  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