Rachel Bastiaenen

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Connie R. Bezzina, Julien Barc, Yuka Mizusawa et al. · Nature Genetics · 2013 · 540 citations · Full text

Cardiomyopathy, Genetic Disorder, Genetics +9

Clinical Usefulness, Angiographic Characteristics, and Safety Evaluation of Intracoronary Acetylcholine Provocation Testing Among 921 Consecutive White Patients With Unobstructed Coronary Arteries

Peter Ong, Anastasios Athanasiadis, Gábor Borgulya et al. · Circulation · 2014 · 350 citations · Full text

Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia

Yalda Jamshidi, Ilja M. Nolte, Chrysoula Dalageorgou et al. · Journal of the American College of Cardiology · 2012 · 119 citations · Full text

Molecular Pharmacology, Nos1ap Gene Is, Cardiomyopathy +9

Anterior T-Wave Inversion in Young White Athletes and Nonathletes

Aneil Malhotra, Harshil Dhutia, Sabiha Gati et al. · Journal of the American College of Cardiology · 2017 · 114 citations

Kinesiology, Exercise Physiology, Applied Physiology +5

The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy

Michael Papadakis, Efstathios Papatheodorou, Greg Mellor et al. · Journal of the American College of Cardiology · 2018 · 110 citations · Full text

Brugada Syndrome, Sudden Death, Normal Autopsy