Xenética
Servizo
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Institut d'Investigació Biomèdica Girona
Girona, EspañaPublicacións en colaboración con investigadores/as de Institut d'Investigació Biomèdica Girona (11)
2022
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2021
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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
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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
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Shared heritability and functional enrichment across six solid cancers
Nature Communications, Vol. 10, Núm. 1
2015
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A Genetically Vulnerable Myocardium May Predispose to Myocarditis
Journal of the American College of Cardiology
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Erratum: Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant (Seizure (2015) 25 (65-67))
Seizure
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Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant
Seizure, Vol. 25, pp. 65-67
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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
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Negative autopsy and sudden cardiac death
International Journal of Legal Medicine, Vol. 128, Núm. 4, pp. 599-606
2013
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Nuevas herramientas diagnósticas en la genética de la muerte súbita
Revista Espanola de Cardiologia Suplementos, Vol. 13, Núm. SUPPL.1, pp. 24-29