HelgadottirA, ManolescuA, HelgasonA, et al. (2006) A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction. Nat Genet, 38:68-74.
3.
HoferT, RayN, WegmannD, et al. (2009) Large allele frequency differences between human continental groups are more likely to have occurred by drift during range expansions than by selection. Ann Hum Genet, 73:95-108.
4.
KongSW, LeeIH, LeshchinerI, et al. (2015) Summarizing polygenic risks for complex diseases in a clinical whole-genome report. Genet Med, 17:536-544.
5.
MylesS, DavisonD, BarrettJ, et al. (2008) Worldwide population differentiation at disease-associated SNPs. BMC Med Genomics, 1:22.
6.
PrescottNJ, DominyKM, KuboM, et al. (2010) Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease. Hum Mol Genet, 19:1828-1839.
7.
SaxenaR, SaleheenD, BeenLF, et al. (2013) Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. Diabetes, 62:1746-1755.
8.
SmithTD, VihinenM (2015) Human Variome Project. Standard development at the Human Variome Project. Database (Oxford) Vol. 2015: article ID bav024; DOI: 10.1093.