References (Supplied by CrossRef)
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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
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Nat Genet 2013
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
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Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndrome
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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
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Including known covariates can reduce power to detect genetic effects in case-control studies
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Nat Genet 2012
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