Insights into metabolic disease from studying genetics in isolated populations: stories from Greece to Greenland
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00125-016-3926-3.pdf
Reference21 articles.
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2. Zuk O, Schaffner SF, Samocha K et al (2014) Searching for missing heritability: designing rare variant association studies. Proc Natl Acad Sci U S A 111:E455–E464
3. Gudmundsson J, Sulem P, Gudbjartsson DF et al (2012) A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer. Nat Genet 44:1326–1329
4. Huyghe JR, Jackson AU, Fogarty MP et al (2013) Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Nat Genet 45:197–201
5. Li AH, Morrison AC, Kovar C et al (2015) Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease. Nat Genet 47:640–642
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