High-throughput genetic clustering of type 2 diabetes loci reveals heterogeneous mechanistic pathways of metabolic disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00125-022-05848-6.pdf
Reference49 articles.
1. Redondo MJ, Hagopian WA, Oram R et al (2020) The clinical consequences of heterogeneity within and between different diabetes types. Diabetologia 63(10):2040–2048. https://doi.org/10.1007/s00125-020-05211-7
2. Mahajan A, Taliun D, Thurner M et al (2018) Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. Nat Genet 50(11):1505–1513. https://doi.org/10.1038/s41588-018-0241-6
3. Goodarzi MO, Palmer ND, Cui J et al (2020) Classification of type 2 diabetes genetic variants and a novel genetic risk score association with insulin clearance. J Clin Endocrinol Metab 105(4):1251–1260. https://doi.org/10.1210/clinem/dgz198
4. Mahajan A, Wessel J, Willems SM et al (2018) Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nat Genet 50(4):559–571. https://doi.org/10.1038/s41588-018-0084-1
5. Udler MS, Kim J, von Grotthuss M et al (2018) Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: a soft clustering analysis. PLoS Med 15(9):e1002654. https://doi.org/10.1371/journal.pmed.1002654
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