Peter Weeke

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 · 546 citations

Life Sciences, Genetics, Molecular Genetics +13

Semaglutide versus placebo in patients with heart failure and mildly reduced or preserved ejection fraction: a pooled analysis of the SELECT, FLOW, STEP-HFpEF, and STEP-HFpEF DM randomised trials

Mikhail Kosiborod, John Deanfield, Richard Pratley et al. · The Lancet · 2024 · 264 citations

Medicine, Cardiology, Pharmacology +9

Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study

Elijah R. Behr, Eleonora Savio‐Galimberti, Julien Barc et al. · Cardiovascular Research · 2015 · 107 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation

Eleonora Savio‐Galimberti, Peter Weeke, Raafia Muhammad et al. · Cardiovascular Research · 2014 · 80 citations · Full text

Medicine, Cardiology, Genetics +17

Exome Sequencing Implicates an Increased Burden of Rare Potassium Channel Variants in the Risk of Drug-Induced Long QT Interval Syndrome

Peter Weeke, Jonathan D. Mosley, D. Hanna et al. · Journal of the American College of Cardiology · 2014 · 76 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16