PuSH - Publication Server of Helmholtz Zentrum München

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41.
Berndt, S.I.* et al.: Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat. Genet. 45, 501-512 (2013)
42.
Codd, V.* et al.: Identification of seven loci affecting mean telomere length and their association with disease. Nat. Genet. 45, 422-427 (2013)
43.
Deloukas, P.* et al.: Large-scale association analysis identifies new risk loci for coronary artery disease. Nat. Genet. 45, 25-35 (2013)
44.
den Hoed, M.* et al.: Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat. Genet. 45, 621-631 (2013)
45.
Erdmann, J.* et al.: Dysfunctional nitric oxide signalling increases risk of myocardial infarction. Nature 504, 432-436 (2013)
46.
Ho, J.E.* et al.: Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. J. Clin. Invest. 123, 4208-4218 (2013)
47.
Lieb, W.* et al.: Genetic predisposition to higher blood pressure increases coronary artery disease risk. Hypertension 61, 995-1001 (2013)
48.
Randall, J.C.* et al.: Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genet. 9:e1003500 (2013)
49.
Reiner, A.P.* et al.: Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Hum. Mol. Genet. 22, 3381-3393 (2013)
50.
Sabater-Lleal, M.* et al.: Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. Circulation 128, 1310-1324 (2013)
51.
Boraska, V.* et al.: Genome-wide meta-analysis of common variant differences between men and women. Hum. Mol. Genet. 21, 4805-4815 (2012)
52.
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)
53.
Hughes, M.F.* et al.: Genetic markers enhance coronary risk prediction in men: The MORGAM prospective cohorts. PLoS ONE 7:e40922 (2012)
54.
Lu, X.* et al.: Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. Nat. Genet. 44, 890-894 (2012)
55.
Voight, B.F.* et al.: The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet. 8:e1002793 (2012)
56.
Yang, J.* et al.: FTO genotype is associated with phenotypic variability of body mass index. Nature 490, 267-272 (2012)
57.
Erdmann, J.* et al.: Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. Eur. Heart J. 32, 158-168 (2011)
58.
Gieger, C. et al.: New gene functions in megakaryopoiesis and platelet formation. Nature 480, 201-208 (2011)
59.
Reilly, M.P.* et al.: Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: Two genome-wide association studies. Lancet 377, 383-392 (2011)
60.
Schunkert, H.* et al.: Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat. Genet. 43, 333-340 (2011)