Publications dans lesquelles il/elle collabore avec MARTA EUGENIA ALARCON RIQUELME (23)

2024

  1. Response to the letter 'testing the effectiveness of MyPROSLE in classifying patients with lupus nephritis'

    Briefings in Bioinformatics

2023

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

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

  2. Scoring personalized molecular portraits identify Systemic Lupus Erythematosus subtypes and predict individualized drug responses, symptomatology and disease progression

    Briefings in bioinformatics, Vol. 23, Núm. 5

  3. Whole blood DNA methylation analysis reveals respiratory environmental traits involved in COVID-19 severity following SARS-CoV-2 infection

    Nature Communications, Vol. 13, Núm. 1

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. 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

  4. Mapping the human genetic architecture of COVID-19

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

  5. Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility

    PLoS ONE, Vol. 16, Núm. 8

2020

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

    Infection and Immunity, Vol. 88, Núm. 4

2019

  1. An update on the genetics of systemic lupus erythematosus

    Current Opinion in Rheumatology, Vol. 31, Núm. 6, pp. 659-668

  2. Epigenome-wide comparative study reveals key differences between mixed connective tissue disease and related systemic autoimmune diseases

    Frontiers in Immunology, Vol. 10, Núm. AUG

  3. Exploring impacts of rare variation in systemic lupus erythematosus by a genome wide imputation approach

    Frontiers in Immunology, Vol. 10, Núm. FEB

2018

  1. Trans-ethnic mapping of BANK1 identifies two independent SLE-Risk linkage groups enriched for co-transcriptional splicing marks

    International Journal of Molecular Sciences, Vol. 19, Núm. 8

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

    Frontiers in Immunology, Vol. 8, Núm. DEC

2016

  1. Single nucleotide polymorphism clustering in systemic autoimmune diseases

    PLoS ONE, Vol. 11, Núm. 8

2015

  1. Defective removal of ribonucleotides from DNA promotes systemic autoimmunity

    Journal of Clinical Investigation, Vol. 125, Núm. 1, pp. 413-424

  2. Defective removal of ribonucleotides from DNA promotes systemic lupus erythematosus

    Pediatric Rheumatology, Vol. 13, Núm. 1