PuSH - Publication Server of Helmholtz Zentrum München

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1.
Mitry, P. et al.: Associations between usual food intake and fecal sterols and bile acids: Results from the KORA FF4 study. Br. J. Nutr., accepted (2019)
2.
Spracklen, C.N.* et al.: Exome-derived adiponectin-associated variants implicate obesity and lipid biology. Am. J. Hum. Genet., accepted (2019)
3.
Wittenbecher, C.* et al.: Insulin-like growth factor binding protein 2 (IGFBP-2) and the risk of developing type 2 diabetes. Diabetes 68, 188-197 (2019)
4.
Elhadad, M.A. et al.: Using the plasma proteome to decipher metabolic syndrome pathophysiology and discover a diagnostic biomarker panel. Eur. Heart J. 39, 998-998 (2018)
5.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 5:180002 (2018)
6.
Frey, S.* et al.: Prenatal alcohol exposure is associated with adverse cognitive effects and distinct whole-genome DNA methylation patterns in primary school children. Front. Behav. Neurosci. 12:125 (2018)
7.
Machiela, M.J.* et al.: Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility. Nat. Commun. 9:3184 (2018)
8.
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)
9.
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)
10.
Pulit, S.L.* et al.: Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. Neurol. Genet. 4:e293 (2018)
11.
Stonawski, V.* et al.: Associations of prenatal depressive symptoms with DNA methylation of HPA axis-related genes and diurnal cortisol profiles in primary school-aged children. Dev. Psychopathol., 1-13 (2018)
12.
Tönjes, A.* et al.: Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin. Hum. Mol. Genet. 27, 546-558 (2018)
13.
Christophersen, I.E.* et al.: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat. Genet. 49, 946-952 (2017)
14.
Esslinger, U.B.* et al.: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy. PLoS ONE 12:e0172995 (2017)
15.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 4:170179 (2017)
16.
Li, M.* et al.: SOS2 and ACP1 loci identified through large-scale exome chip analysis regulate kidney development and function. J. Am. Soc. Nephrol. 28, 981-994 (2017)
17.
Macé, A.* et al.: CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. Nat. Commun. 8:744 (2017)
18.
Malik, R.* et al.: Common coding variant in SERPINA1 increases the risk for large artery stroke. Proc. Natl. Acad. Sci. U.S.A. 114, 3613-3618 (2017)
19.
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)
20.
Marouli, E.* et al.: Rare and low-frequency coding variants alter human adult height. Nature 542, 186-190 (2017)