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21.
Pattaro, C.* et al.: Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat. Commun. 7:10023 (2016)
22.
Teumer, A.* et al.: Genome-wide association studies identify genetic loci associated with albuminuria in diabetes. Diabetes 65, 803-817 (2016)
23.
Gaulton, K.J.* et al.: Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nat. Genet. 47, 1415-1425 (2015)
24.
Gorski, M.* et al.: Genome-wide association study of kidney function decline in individuals of European descent. Kidney Int. 87, 1017–1029 (2015)
25.
Huffman, J.E.* et al.: Modulation of genetic associations with serum urate levels by body-mass-index in humans. PLoS ONE 10:e0119752 (2015)
26.
Lin, S.* et al.: Hippocampal metabolomics using ultrahigh-resolution mass spectrometry reveals neuroinflammation from Alzheimer's disease in CRND8 mice. Anal. Bioanal. Chem. 405, 5105-5117 (2013)
27.
Lin, S.* et al.: Ultrahigh resolution mass spectrometry-based metabolic characterization reveals cerebellum as a disturbed region in two animal models. Talanta 118, 45-53 (2013)
28.
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)
29.
Chasman, D.I.* et al.: Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum. Mol. Genet. 21, 5329-5343 (2012)
30.
Morris, A.P.* et al.: Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat. Genet. 44, 981-990 (2012)
31.
Pattaro, C.* et al.: Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet. 8:e1002584 (2012)
32.
Perry, J.R.* et al.: Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. PLoS Genet. 8:e1002741 (2012)
33.
Saxena, R.* et al.: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. Am. J. Hum. Genet. 90, 410-425 (2012)
34.
Böger, C.A.* et al.: Association of eGFR-related loci identified by GWAS with incident CKD and ESRD. PLoS Genet. 7:e1002292 (2011)
35.
Böger, C.A.* et al.: CUBN is a gene locus for albuminuria. J. Am. Soc. Nephrol. 22, 555-570 (2011)
36.
Edmondson, A.C.* et al.: Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol. Circ. Cardiovasc. Genet. 4, 145-155 (2011)
37.
Lanktree, M.B.* et al.: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height. Am. J. Hum. Genet. 88, 6-18 (2011)
38.
Peng, C. et al.: Pitx3 is a critical mediator of GDNF-induced BDNF expression in nigrostriatal dopaminergic neurons. J. Neurosci. 31, 12802-12815 (2011)
39.
Reilly, M.P.* et al.: Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: Two genome-wide association studies. Lancet 377, 383-392 (2011)
40.
Wild, P.S.* et al.: A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circ. Cardiovasc. Genet. 4, 403-412 (2011)