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Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes.
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Sex differences in stroke: Challenges and opportunities.
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Identification of TNFSF13, SPATC1L, SLC22A25 and SALL4 as novel susceptibility loci for atrial fibrillation by an exome‑wide association study.
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Impact of genetic variants on the upstream efficacy of renin-angiotensin system inhibitors for the prevention of atrial fibrillation.
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Common variants in KCNN3 are associated with lone atrial fibrillation.
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Impact of genetic discoveries on the classification of lone atrial fibrillation.
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Comparative performance of gene-based warfarin dosing algorithms in a multiethnic population.
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Several common variants modulate heart rate, PR interval and QRS duration.
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Genome-wide association study of PR interval.
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Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery.
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Angiotensinogen polymorphisms and acquired atrial fibrillation in Chinese.
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From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.
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Familial aggregation of atrial fibrillation: a study in Danish twins.
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Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population.
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