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21.
Makita, N.* et al.: Novel calmodulin (CALM2) mutations associated with congenital arrhythmia susceptibility. Circ. Cardiovasc. Genet. 7, 466-474 (2014)
22.
Duchatelet, S.* et al.: Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome. Circ. Cardiovasc. Genet. 6, 354-361 (2013)
23.
Mäkelä, K.M.* et al.: Genome-wide association study pinpoints a new functional apolipoprotein B variant influencing oxidized low-density lipoprotein levels but not cardiovascular events: AtheroRemo Consortium. Circ. Cardiovasc. Genet. 6, 73-81 (2013)
24.
Chu, A.Y.* et al.: Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy. Circ. Cardiovasc. Genet. 5, 676-685 (2012)
25.
Davies, R.W.* et al.: A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. Circ. Cardiovasc. Genet. 5, 217-225 (2012)
26.
Kääb, S.* et al.: A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes. Circ. Cardiovasc. Genet. 5, 91-99 (2012)
27.
Murabito, J.M.* et al.: Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. Circ. Cardiovasc. Genet. 5, 100-112 (2012)
28.
Edmondson, A.C.* et al.: Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol. Circ. Cardiovasc. Genet. 4, 145-155 (2011)
29.
Lucas, G.* et al.: Post-genomic update on a classical candidate gene for coronary artery disease: ESR1. Circ. Cardiovasc. Genet. 4, 647-654 (2011)
30.
Meder, B.* et al.: Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies. Circ. Cardiovasc. Genet. 4, 110-122 (2011)
31.
Schnabel, R.B.* et al.: Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: The National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project. Circ. Cardiovasc. Genet. 4, 557-564 (2011)
32.
Wild, P.S.* et al.: A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circ. Cardiovasc. Genet. 4, 403-412 (2011)
33.
Teupser, D.* et al.: Genetic regulation of serum phytosterol levels and risk of coronary artery disease. Circ. Cardiovasc. Genet. 3, 331-339 (2010)
34.
Body, S.C.* et al.: Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery. Circ. Cardiovasc. Genet. 2, 499-506 (2009)
35.
Dehghan, A.* et al.: Association of novel genetic Loci with circulating fibrinogen levels: A genome-wide association study in 6 population-based cohorts. Circ. Cardiovasc. Genet. 2, 125-133 (2009)
36.
Marroni, F.* et al.: A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: The EUROSPAN project. Circ. Cardiovasc. Genet. 2, 322-328 (2009)
37.
Heid, I.M. et al.: Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. Circ. Cardiovasc. Genet. 1, 10-20 (2008)
38.
Rutsch, F.* et al.: Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy. Circ. Cardiovasc. Genet. 1, 133-40 (2008)
39.
Sedlacek, K.* et al.: Common genetic variants in ANK2 modulate QT interval: Results from the KORA study. Circ. Cardiovasc. Genet. 1, 93-99 (2008)
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