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1.
Flannick, J.* et al.: Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. Nature 570, 71-76 (2019)
2.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 5:180002 (2018)
3.
Rivas, M.A.* et al.: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. PLoS Genet. 14:e1007329 (2018)
4.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 4:170179 (2017)
5.
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)
6.
Fuchsberger, C.* et al.: The genetic architecture of type 2 diabetes. Nature 536, 41-47 (2016)
7.
Flannick, J.* et al.: Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nat. Genet. 46, 357-363 (2014)
8.
Jentsch, A.* et al.: Climate extremes initiate ecosystem-regulating functions while maintaining productivity. J. Ecol. 99, 689-702 (2011)
9.
Freathy, R.M.* et al.: Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nat. Genet. 42, 430-435 (2010)
10.
Heid, I.M. et al.: Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: Results of genome-wide association analyses including 4659 European individuals. Atherosclerosis 208, 412-420 (2010)
11.
Richards, J.B.* et al.: A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. PLoS Genet. 5:e1000768 (2009)
12.
Glaser, B.* ; Klopp, N. & Illig, T.: No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biol. Psychiatry 58, 78-80 (2005)
13.
Glaser, B.* et al.: Molecular cytogenetic analysis of a de novo balanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations. Am. J. Med. Genet. A 126A, 229-236 (2004)