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Reincke, M.* et al.: Mutations in the deubiquitinase gene USP8 cause Cushing's disease. Nat. Genet. 47, 31-38 (2015)
Surakka, I.* et al.: The impact of low-frequency and rare variants on lipid levels. Nat. Genet. 47, 589-597 (2015)
Arking, D.E.* et al.: Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat. Genet. 46, 826-836 (2014)
Flannick, J.* et al.: Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nat. Genet. 46, 357-363 (2014)
DIAGRAM Consortium (Gieger, C. ; Grallert, H. ; Illig, T. ; Klopp, N. ; Müller-Nurasyid, M. ; Peters, A.) et al.: Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat. Genet. 46, 234-244 (2014)
Loth, D.W.* et al.: Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nat. Genet. 46, 669-677 (2014)
Shin, S.Y.* et al.: An atlas of genetic influences on human blood metabolites. Nat. Genet. 46, 543-550 (2014)
Walsh, K.M.* et al.: Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. Nat. Genet. 46, 731-735 (2014)
Wang, M.* et al.: The genome sequence of African rice (Oryza glaberrima) and evidence for independent domestication. Nat. Genet. 46, 982-988 (2014)
Wood, A.R.* et al.: Defining the role of common variation in the genomic and biological architecture of adult human height. Nat. Genet. 46, 1173-1186 (2014)
AMD Gene Consortium et al.: Seven new loci associated with age-related macular degeneration. Nat. Genet. 45, 433-439 (2013)
Global Lipids Genetics Consortium et al.: Discovery and refinement of loci associated with lipid levels. Nat. Genet. 45, 1274-1283 (2013)
Agarwala, V.* ; Flannick, J.* ; Sunyaev, S.R.* ; GoT2D Consortium (Gieger, C. ; Grallert, H. ; Hrabě de Angelis, M. ; Huth, C. ; Kriebel, J. ; Meisinger, C. ; Meitinger, T. ; Müller-Nurasyid, M. ; Peters, A. ; Rathmann, W. ; Ried, J.S. ; Strauch, K. ; Strom, T.M.) & Altshuler, D.*: Evaluating empirical bounds on complex disease genetic architecture. Nat. Genet. 45, 1418-1427 (2013)
Anttila, V.* et al.: Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nat. Genet. 45, 912-917 (2013)
Berndt, S.I.* et al.: Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat. Genet. 45, 501-512 (2013)
Beuschlein, F.* et al.: Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension. Nat. Genet. 45, 440-444 (2013)
Bezzina, C.R.* et al.: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Nat. Genet. 45, 1044-1049 (2013)
Bønnelykke, K.* et al.: Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization. Nat. Genet. 45, 902-906 (2013)
Cappello, S. et al.: Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development. Nat. Genet. 45, 1300-1308 (2013)
Codd, V.* et al.: Identification of seven loci affecting mean telomere length and their association with disease. Nat. Genet. 45, 422-427 (2013)