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Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia
Fulminant Myocarditis with Combination Immune Checkpoint Blockade
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
CYP2C19 Phenotype and Risk of Proton Pump Inhibitor-Associated Infections
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study
The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
