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Ligthart, S.* et al.: Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders. Am. J. Hum. Genet. 103, 691-706 (2018)
Surendran, P.* et al.: Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat. Genet. 48, 1151-1161 (2016)
Huffman, J.E.* et al.: Modulation of genetic associations with serum urate levels by body-mass-index in humans. PLoS ONE 10:e0119752 (2015)
Köttgen, A.* et al.: Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat. Genet. 45, 145-154 (2013)
Assimes, T.L.* et al.: Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. J. Am. Coll. Cardiol. 56, 1552-1563 (2010)
Gudbjartsson, D.F.* et al.: Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat. Genet. 41, 342-347 (2009)
Malerba, G.* et al.: SNPs of the FADS gene cluster are associated with polyunsaturated fatty acids in a cohort of patients with cardiovascular disease. Lipids 43, 289-299 (2008)
Martinelli, N.* et al.: FADS genotypes and desaturase activity estimated by the ratio of arachidonic acid to linoleic acid are associated with inflammation and coronary artery disease. Am. J. Clin. Nutr. 88, 941-949 (2008)