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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.
Wuttke, M.* et al.: A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nat. Genet. 51, 957-972 (2019)
3.
Turcot, V.* et al.: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat. Genet. 50, 26-41 (2018)
4.
Turcot, V.* et al.: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 765, 2017). Nat. Genet. 50, 764-768 (2018)
5.
Böger, C.A.* et al.: NFAT5 and SLC4A10 loci associate with plasma osmolality. J. Am. Soc. Nephrol. 28, 2311-2321 (2017)
6.
Gorski, M.* et al.: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci. Rep. 7:45040 (2017)
7.
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)
8.
Marouli, E.* et al.: Rare and low-frequency coding variants alter human adult height. Nature 542, 186-190 (2017)
9.
Pattaro, C.* et al.: Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat. Commun. 7:10023 (2016)
10.
Teumer, A.* et al.: Genome-wide association studies identify genetic loci associated with albuminuria in diabetes. Diabetes 65, 803-817 (2016)
11.
Winkler, T.W.* et al.: Correction: The influence of age and sex on genetic associations with adult body size and shape: A large-scale genome-wide interaction study. PLoS Genet. 12:e1006166 (2016)
12.
Gorski, M.* et al.: Genome-wide association study of kidney function decline in individuals of European descent. Kidney Int. 87, 1017–1029 (2015)
13.
Stangl, S.* et al.: Association between apolipoprotein A-IV concentrations and chronic kidney disease in two large population-based cohorts: Results from the KORA studies. J. Intern. Med. 278, 410-423 (2015)
14.
Winkler, T.W.* et al.: The influence of age and sex on genetic associations with adult body size and shape: A large-scale genome-wide interaction study. PLoS Genet. 11:e1005378 (2015)
15.
Dumann, K.* et al.: Association of cutaneous Advanced Glycation End Products (AGES) with Chronic Kidney Disease (CKD) in Diabetes Mellitus type 2 (DM2): A subgroup analysis of the diacore study baseline visit. Nephrol. Dial. Transplant. 29, iii419 (2014)
16.
Laschkolnig, A.* et al.: Lipoprotein (a) concentrations, apolipoprotein (a) phenotypes, and peripheral arterial disease in three independent cohorts. Cardiovasc. Res. 103, 28-36 (2014)
17.
Rheinberger, M.* et al.: Chronic Kidney Disease (CKD) and obesity in Diabetes Mellitus type 2 (DM2): Baseline characteristics of the Diabetes Cohorte study (DIACORE). Nephrol. Dial. Transplant. 29, 424 (2014)
18.
Burghardt, T.* et al.: LMX1B is essential for the maintenance of differentiated podocytes in adult kidneys. J. Am. Soc. Nephrol. 24, 1830-1848 (2013)
19.
Dörhöfer, L.* et al.: Study design of DIACORE (DIAbetes COhoRtE) - a cohort study of patients with diabetes mellitus type 2. BMC Med. Genet. 14:25 (2013)
20.
Parsa, A.* et al.: Common variants in mendelian kidney disease genes and their association with renal function. J. Am. Soc. Nephrol. 24, 2105-2117 (2013)