PuSH - Publication Server of Helmholtz Zentrum München

135 Records found.
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1.
Bentley, A.R.* et al.: Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nat. Genet. 51, 636-648 (2019)
2.
de Vries, P.S.* et al.: Multi-ancestry genome-wide association study of lipid levels incorporating gene-alcohol interactions. Am. J. Epidemiol., accepted (2019)
3.
Erzurumluoglu, A.M.* et al.: Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. Mol. Psychiatry, accepted (2019)
4.
Ji, Y.* et al.: Genome-wide and abdominal MRI data provide evidence that a genetically determined favorable adiposity phenotype is characterized by lower ectopic liver fat and lower risk of type 2 diabetes, heart disease, and hypertension. Diabetes 68, 207-219 (2019)
5.
Justice, A.E.* et al.: Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nat. Genet. 51, 452–469 (2019)
6.
Karasik, D.* et al.: Disentangling the genetics of lean mass. Am. J. Clin. Nutr. 109, 276-287 (2019)
7.
Kilpeläinen, T.O.* et al.: Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nat. Commun. 10:376 (2019)
8.
Shrine, N.* et al.: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nat. Genet. 51, 481-493 (2019)
9.
Shrine, N.* et al.: Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nat. Genet., accepted (2019)
10.
Benedetti, E. et al.: Erratum: Publisher Correction: Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway (Nature communications (2017) 8 1 (1483)). Nat. Commun. 9:706 (2018)
11.
Bihlmeyer, N.A.* et al.: ExomeChip-wide analysis of 95 626 individuals identifies 10 novel loci associated with QT and JT intervals. Circ. Genom. Precis. Med. 11:e001758 (2018)
12.
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)
13.
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)
14.
Jiang, X.* et al.: Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Nat. Commun. 9:260 (2018)
15.
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)
16.
Lin, H.* et al.: Common and rare coding genetic variation underlying the electrocardiographic PR interval. Circ. Genom. Precis. Med. 11:e002037 (2018)
17.
Mahajan, A.* et al.: Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nat. Genet. 50, 559-571 (2018)
18.
Prins, B.P.* et al.: Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Genome Biol. 19:87 (2018)
19.
Roselli, C.* et al.: Multi-ethnic genome-wide association study for atrial fibrillation. Nat. Genet. 50, 1225–1233 (2018)
20.
Sung, Y.J.* et al.: A large-scale multi-ancestry genome-wide study accounting for smoking behavior identifies multiple significant loci for blood pressure. Am. J. Hum. Genet. 102, 375-400 (2018)