| human | Q5 |
| P496 | ORCID iD | 0000-0002-1529-9872 |
| P106 | occupation | researcher | Q1650915 |
| Q35783016 | A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes |
| Q28254872 | Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family |
| Q92740969 | Automated external defibrillator use in a previously healthy 31-day-old infant with out-of-hospital cardiac arrest due to ventricular fibrillation |
| Q36628071 | Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation |
| Q96434246 | Catheter Ablation of Orthodromic Reciprocating Tachycardia and Atrioventricular Nodal Reentrant Tachycardia in Children with Hypoplastic Left Heart Syndrome |
| Q92974067 | Chronotropic incompetence as a risk predictor in children and young adults with catecholaminergic polymorphic ventricular tachycardia |
| Q28534878 | Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes |
| Q35647717 | Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy |
| Q37146274 | Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation |
| Q24322712 | Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation |
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