Publicaciones en colaboración con investigadores/as de Broad Institute (14)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

  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. A first update on mapping the human genetic architecture of COVID-19

    Nature

  2. Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (Nature, (2022), 611, 7934, (115-123), 10.1038/s41586-022-05165-3)

    Nature

  3. Stroke genetics informs drug discovery and risk prediction across ancestries

    Nature, Vol. 611, Núm. 7934, pp. 115-123

  4. Whole-genome sequencing reveals host factors underlying critical COVID-19

    Nature, Vol. 607, Núm. 7917, pp. 97-103

2021

  1. Mapping the human genetic architecture of COVID-19

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

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

    PLoS ONE, Vol. 16, Núm. 8

2020

  1. The urgent need for integrated science to fight COVID-19 pandemic and beyond

    Journal of Translational Medicine, Vol. 18, Núm. 1

2018

  1. A community approach to mortality prediction in sepsis via gene expression analysis

    Nature Communications, Vol. 9, Núm. 1

  2. Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density

    Annals of the rheumatic diseases, Vol. 77, Núm. 3, pp. 378-385

2017

  1. The FASTK family of proteins: Emerging regulators of mitochondrial RNA biology

    Nucleic Acids Research, Vol. 45, Núm. 19, pp. 10941-10947

2013

  1. Coreceptor affinity for MHC defines peptide specificity requirements for TCR interaction with coagonist peptide-MHC

    Journal of Experimental Medicine, Vol. 210, Núm. 9, pp. 1807-1821

  2. MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: Functional andtherapeutic implications forgeneexpressionand the pathogenesis of hypertension

    Human Molecular Genetics, Vol. 22, Núm. 18, pp. 3624-3640