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1.
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)
2.
Wain, L.V.* et al.: Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): A genetic association study in UK Biobank. Lancet Resp. Med. 3, 769-781 (2015)
3.
Budin-Ljosne, I.* et al.: Data sharing in large research consortia: Experiences and recommendations from ENGAGE. Eur. J. Hum. Genet. 22, 317-321 (2014)
4.
Lange, L.A.* et al.: Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am. J. Hum. Genet. 94, 233-245 (2014)
5.
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)
6.
Demirkan, A.* et al.: Genetic architecture of circulating lipid levels. Eur. J. Hum. Genet. 19, 813-819 (2011)
7.
Nalls, M.A.* et al.: Failure to validate association between 12p13 variants and ischemic stroke. N. Engl. J. Med. 362, 1547-1550 (2010)