GIANT 2012 GWAS
Download summary statistics at the GIANT Consortium website
Publications
FTO genotype is associated with phenotypic variability of body mass index.
Yang J, et al.
Nature. 2012 Oct 11;490(7419):267-72. doi: 10.1038/nature11401
Download summary statistics at the GIANT Consortium website
FTO genotype is associated with phenotypic variability of body mass index.
Yang J, et al.
Nature. 2012 Oct 11;490(7419):267-72. doi: 10.1038/nature11401
Nat1 Deficiency Is Associated with Mitochondrial Dysfunction and Exercise Intolerance in Mice.
Chennamsetty I, et al.
Cell Rep. 2016 Oct 4;17(2):527-540. doi: 10.1016/j.celrep.2016.09.005
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene.
Knowles JW, et al.
J Clin Invest. 2015 Apr;125(4):1739-51. doi: 10.1172/JCI74692
All samples in this dataset are included in the "DIAMANTE (European) T2D GWAS" dataset.
All samples in this dataset are included in the "DIAMANTE (European) T2D GWAS" dataset.
A genome-wide association meta-analysis identifies new childhood obesity loci.
Bradfield JP, et al.
Nat Genet. 2012 May;44(5):526-31. doi: 10.1038/ng.2247
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Salem RM, et al.
J Am Soc Nephrol. 2019 Oct;30(10):2000-2016. doi: 10.1681/ASN.2019030218
The "DIAMANTE (European) T2D GWAS" dataset includes samples from other datasets in the T2DKP:
Download URL: http://diagram-consortium.org/downloads.html
Download date: January 2018
An expanded genome-wide association study of type 2 diabetes in Europeans.
Scott RA, et al.
Diabetes. 2017 Nov;66(11):2888-2902. doi: 10.2337/db16-1253
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Mahajan A, et al.
Nat Genet. 2014 Mar;46(3):234-44. doi: 10.1038/ng.2897.
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.
Ligthart S, et al.
Am J Hum Genet. 2018 Nov 1;103(5):691-706. doi: 10.1016/j.ajhg.2018.09.009