PuSH - Publication Server of Helmholtz Zentrum München

33 Records found.
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1.
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)
2.
van Setten, J.* et al.: Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. Eur. J. Hum. Genet. 27, 952-962 (2019)
3.
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)
4.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 5:180002 (2018)
5.
Lin, H.* et al.: Common and rare coding genetic variation underlying the electrocardiographic PR interval. Circ. Genom. Precis. Med. 11:e002037 (2018)
6.
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)
7.
Böger, C.A.* et al.: NFAT5 and SLC4A10 loci associate with plasma osmolality. J. Am. Soc. Nephrol. 28, 2311-2321 (2017)
8.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 4:170179 (2017)
9.
Holzinger, E.R.* et al.: Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals. BioData Min. 10:25 (2017)
10.
Manning, A.* et al.: A low-frequency inactivating Akt2 variant enriched in the Finnish population is associated with fasting insulin levels and type 2 diabetes risk. Diabetes 66, 2019-2032 (2017)
11.
Wheeler, E.* et al.: Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. PLoS Med. 14:e1002383 (2017)
12.
Fuchsberger, C.* et al.: The genetic architecture of type 2 diabetes. Nature 536, 41-47 (2016)
13.
Holmes, M.V.* et al.: Mendelian randomization of blood lipids for coronary heart disease. Eur. Heart J. 36, 539-550 (2015)
14.
Joshi, P.K.* et al.: Directional dominance on stature and cognition in diverse human populations. Nature 523, 459-462 (2015)
15.
Lieb, W.* et al.: Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes. Circ. Cardiovasc. Genet. 8, 131-140 (2015)
16.
Lunetta, K.L.* et al.: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:7756 (2015)
17.
Lunetta, K.L.* et al.: Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:10257 (2015)
18.
Mahajan, A.* et al.: Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. PLoS Genet. 11:e1004876 (2015)
19.
Swerdlow, D.I.* et al.: HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: Evidence from genetic analysis and randomised trials. Lancet 385, 351-361 (2015)
20.
Ellis, J.* et al.: Large multiethnic candidate gene study for C-reactive protein levels: Identification of a novel association at CD36 in African Americans. Hum. Genet. 133, 985-995 (2014)