Bart Loeys

Congenital glucose–galactose malabsorption: a novel deletion within the SLC5A1 gene

B. Loeys, A. Móring, L. Vallaeys, 2013, European Journal of Pediatrics.

Genetics of sudden cardiac death in the young

B. Loeys, F. Marchau, E. V. Van Craenenbroeck, 2015, Clinical genetics.

Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome Running title: Genome-wide association study in long QT syndrome

T. Werge, P. Ellinor, S. Priori, 2020 .

Circulating MicroRNA as Biomarkers of Anthracycline-Induced Cardiotoxicity

E. V. Van Craenenbroeck, M. Alaerts, A. Gevaert, 2024, JACC. CardioOncology.