Publicacións en colaboración con investigadores/as de Institut d'Investigació Biomèdica Girona (11)

2023

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

    Nature

2022

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

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

2021

  1. Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants

    Cell Reports Medicine, Vol. 2, Núm. 4

2019

  1. Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4)

    Nature Communications

  2. Shared heritability and functional enrichment across six solid cancers

    Nature Communications, Vol. 10, Núm. 1

2015

  1. A Genetically Vulnerable Myocardium May Predispose to Myocarditis

    Journal of the American College of Cardiology

  2. Erratum: Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant (Seizure (2015) 25 (65-67))

    Seizure

  3. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant

    Seizure, Vol. 25, pp. 65-67

  4. Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series

    International Journal of Legal Medicine, Vol. 129, Núm. 3, pp. 495-504

2014

  1. Negative autopsy and sudden cardiac death

    International Journal of Legal Medicine, Vol. 128, Núm. 4, pp. 599-606

2013

  1. Nuevas herramientas diagnósticas en la genética de la muerte súbita

    Revista Espanola de Cardiologia Suplementos, Vol. 13, Núm. SUPPL.1, pp. 24-29