PuSH - Publication Server of Helmholtz Zentrum München

22 Records found.
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1.
Ashar, F.N.* et al.: A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. Eur. Heart J. 39, 3961-3969 (2018)
2.
Joshi, P.K.* et al.: Directional dominance on stature and cognition in diverse human populations. Nature 523, 459-462 (2015)
3.
Baumert, J.J. et al.: No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: Results from meta-analyses of 80,607 subjects. PLoS ONE 9:e111156 (2014)
4.
Lange, L.A.* et al.: Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am. J. Hum. Genet. 94, 233-245 (2014)
5.
Loth, D.W.* et al.: Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nat. Genet. 46, 669-677 (2014)
6.
Tang, W.* et al.: Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function. PLoS ONE 9:e100776 (2014)
7.
Hancock, D.B.* et al.: Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. PLoS Genet. 8:e1003098 (2013)
8.
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)
9.
Sim, X.* et al.: Genetic loci for retinal arteriolar microcirculation. PLoS ONE 8:e65804 (2013)
10.
Westra, H.J.* et al.: Systematic identification of trans eQTLs as putative drivers of known disease associations. Nat. Genet. 45, 1238-1243 (2013)
11.
Artigas, M.S.* et al.: Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat. Genet. 43, 1082-1090 (2011)
12.
Böger, C.A.* et al.: CUBN is a gene locus for albuminuria. J. Am. Soc. Nephrol. 22, 555-570 (2011)
13.
Gieger, C. et al.: New gene functions in megakaryopoiesis and platelet formation. Nature 480, 201-208 (2011)
14.
Nalls, M.A.* et al.: Multiple loci are associated with white blood cell phenotypes. PLoS Genet. 7:e1002113 (2011)
15.
Smith, N.L.* et al.: Genetic predictors of fibrin D-dimer levels in healthy adults. Circulation 123, 1864-1872 (2011)
16.
Ikram, M.K.* et al.: Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genet. 6:e1001184 (2010)
17.
Köttgen, A.* et al.: New loci associated with kidney function and chronic kidney disease. Nat. Genet. 42, 376-384 (2010)
18.
Smith, N.L.* et al.: Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) consortium. Circulation 121, 1382-1392 (2010)
19.
Benjamin, E.J.* et al.: Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat. Genet. 41, 879-81 (2009)
20.
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)