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Multi-national assessment of clinical factors, genetic scores, and electrocardiogram-based artificial intelligence for atrial fibrillation prediction
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Clinical impact of cardiomyopathy-associated rare variants and cardiovascular comorbidities in multi-ancestry populations
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Effects of SGLT2 inhibition on incident heart failure in carriers of cardiomyopathy-associated genetic variants
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Clinical trajectories and prognostic implications of incident heart failure versus atrial fibrillation in cardiomyopathy variant carriers
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Genetically mediated differences in LDL cholesterol were not consistently associated with venous thromboembolism: rare variant analyses in over 700,000 participants
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Associations of catch-up sleep pattern with cardiovascular outcomes and incident disease risk across the phenome
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Exome sequencing in over 63,000 patients in TIMI trials uncovers pathogenic cardiomyopathy variant carriers with high risk for heart failure and cardiovascular death
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