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Evangelou, E.* et al.: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat. Genet. 50, 1412-1425 (2018)
Evangelou, E.* et al.: Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x). Nat. Genet., accepted (2018)
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)
Gorski, M.* et al.: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci. Rep. 7:45040 (2017)
Malik, R.* et al.: Common coding variant in SERPINA1 increases the risk for large artery stroke. Proc. Natl. Acad. Sci. U.S.A. 114, 3613-3618 (2017)
Wain, L.V.* et al.: Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney. Hypertension 70, e4-e19 (2017)
Barban, N.* et al.: Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat. Genet. 48, 1462-1472 (2016)
Cheng, Y.C.* et al.: Genome-wide association analysis of young onset stroke identifies a locus on chromosome 10q25 near HABP2. Stroke 47, 307-316 (2016)
de Vries, P.S.* et al.: A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Hum. Mol. Genet. 25, 358-370 (2016)
Malik, R.* et al.: Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. Neurology 86, 1217-1226 (2016)
Okbay, A.* et al.: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat. Genet. 48, 624-633 (2016)
Okbay, A.* et al.: Genome-wide association study identifies 74 loci associated with educational attainment. Nature 533, 539-542 (2016)
Pattaro, C.* et al.: Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat. Commun. 7:10023 (2016)
Bluher, A.* et al.: Heritability of young- and old-onset ischaemic stroke. Eur. J. Neurol. 22, 1488-1491 (2015)
Gorski, M.* et al.: Genome-wide association study of kidney function decline in individuals of European descent. Kidney Int. 87, 1017–1029 (2015)
Loth, D.W.* et al.: Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nat. Genet. 46, 669-677 (2014)
Köttgen, A.* et al.: Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat. Genet. 45, 145-154 (2013)
Parsa, A.* et al.: Common variants in mendelian kidney disease genes and their association with renal function. J. Am. Soc. Nephrol. 24, 2105-2117 (2013)
Rietveld, C.A.* et al.: GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science 340, 1467-1471 (2013)
Sim, X.* et al.: Genetic loci for retinal arteriolar microcirculation. PLoS ONE 8:e65804 (2013)