European ancestry samples in this dataset are included in the "DIAMANTE (European) T2D GWAS" dataset.
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
Gaulton KJ, et al.
Nat Genet. 2015 Dec;47(12):1415-25. doi: 10.1038/ng.3437.
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.
Lu Y, et al.
Nat Commun. 2016 Feb 1;7:10495. doi: 10.1038/ncomms10495
Summary statistics are available for download from the Japanese ENcyclopedia of GEnetic associations by Riken.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Kanai M, et al.
Nat Genet. 2018 Mar;50(3):390-400. doi: 10.1038/s41588-018-0047-6.
PMID: 29403010
Summary statistics are available for download from the Japanese ENcyclopedia of GEnetic associations by Riken.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Kanai M, et al.
Nat Genet. 2018 Mar;50(3):390-400. doi: 10.1038/s41588-018-0047-6.
PMID: 29403010
Summary statistics are available for download from the Japanese ENcyclopedia of GEnetic associations by Riken.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Kanai M, et al.
Nat Genet. 2018 Mar;50(3):390-400. doi: 10.1038/s41588-018-0047-6.
PMID: 29403010
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
Dastani Z, et al.
PLoS Genet. 2012;8(3):e1002607. doi: 10.1371/journal.pgen.1002607
Note that samples from the European cohorts of AAGILE GWAS are included in the MAGIC Metabochip GWAS dataset.
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.
Liu CT, et al.
Am J Hum Genet. 2016 Jul 7;99(1):56-75. doi: 10.1016/j.ajhg.2016.05.006
This dataset is a subset of the FinnMetSeq exome sequence analysis dataset.
Exome sequencing of Finnish isolates enhances rare-variant association power.
Locke A, Meltz Steinberg K, Chiang, CWK, Service S, et al.
Nature. 2019 Jul 31. doi: 10.1038/s41586-019-1457-z
The 13k exome sequence analysis dataset is a subset of the AMP T2D-GENES exome sequence analysis dataset.