PuSH - Publication Server of Helmholtz Zentrum München

37 Records found.
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1.
Gilly, A. et al.: Very low depth whole genome sequencing in complex trait association studies. Bioinformatics, accepted (2019)
2.
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)
3.
Zheng, J.* et al.: Mendelian Randomization analysis reveals a causal influence of circulating sclerostin levels on bone mineral density and fractures. J. Bone Min. Res., accepted (2019)
4.
Gilly, A.* et al.: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. Nat. Commun. 9:4674 (2018)
5.
Gilly, A.* et al.: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. Nat. Commun. 9:5460 (2018)
6.
Hackinger, S.* et al.: Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia. Transl. Psychiatry 8:252 (2018)
7.
Huckins, L.M.* et al.: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa. Mol. Psychiatry 23, 1169-1180 (2018)
8.
Huckins, L.M.* et al.: Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa. Mol. Psychiatry 23:1 (2018)
9.
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)
10.
Mahajan, A.* et al.: Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. Nat. Genet. 50, 1505-1513 (2018)
11.
Warrington, N.M.* et al.: Maternal and fetal genetic contribution to gestational weight gain. Int. J. Obes. 42, 755-784 (2018)
12.
Justice, A.E.* et al.: Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nat. Commun. 8:14977 (2017)
13.
Liu, D.J.* et al.: Exome-wide association study of plasma lipids in >300,000 individuals. Nat. Genet. 49, 1758-1766 (2017)
14.
Saleheen, D.* et al.: Loss of cardioprotective effects at the ADAMTS7 locus as a result of gene-smoking interactions. Circulation 135, 2336-2353 (2017)
15.
van den Berg, M.* et al.: Discovery of novel heart rate-associated loci using the Exome Chip. Hum. Mol. Genet. 26, 2346-2363 (2017)
16.
Barban, N.* et al.: Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat. Genet. 48, 1462-1472 (2016)
17.
Ehret, G.B.* et al.: The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat. Genet. 48, 1171-1184 (2016)
18.
Kanoni, S.* et al.: Analysis with the exome array identifies multiple new independent variants in lipid loci. Hum. Mol. Genet. 25, 4094-4106 (2016)
19.
McCarthy, S.* et al.: A reference panel of 64,976 haplotypes for genotype imputation. Nat. Genet. 48, 1279-1283 (2016)
20.
Surendran, P.* et al.: Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat. Genet. 48, 1151-1161 (2016)