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NPJ Genomic Medicine|October 29, 2024
SLC16A8 is a causal contributor to age-related macular degeneration riskNavid Nouri, Bailey Hannon Gussler, Amy Stockwell, et al.
Diabetologia|March 29, 2012
A gene variant near ATM is significantly associated with metformin treatment response in type 2 diabetes: a replication and meta-analysis of five cohortsN van Leeuwen, G Nijpels, M L Becker, et al.
Plos Genetics|May 17, 2012
Extent, causes, and consequences of small RNA expression variation in human adipose tissueLeopold Parts, Åsa K Hedman, Sarah Keildson, et al.
Brain Communications|March 10, 2023
Investigating genotype-phenotype relationship of extreme neuropathic pain disorders in a UK national cohortAndreas C Themistocleous, Georgios Baskozos, Iulia Blesneac, et al.
Diabetes|March 19, 2008
Common variation in the FTO gene alters diabetes-related metabolic traits to the extent expected given its effect on BMIRachel M Freathy, Nicholas J Timpson, Debbie A Lawlor, et al.
Diabetologia|September 30, 2010
A role for coding functional variants in HNF4A in type 2 diabetes susceptibilityB Jafar-Mohammadi, C J Groves, A P Gjesing, et al.
American Journal of Human Genetics|January 31, 2017
Decreased STARD10 Expression Is Associated with Defective Insulin Secretion in Humans and MiceGaelle R Carrat, Ming Hu, Marie-Sophie Nguyen-Tu, et al.
American Journal of Human Genetics|August 2, 2001
Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United KingdomJ C Evans, T M Frayling, P G Cassell, et al.
Nature Genetics|January 14, 2014
Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variantsLorenzo Pasquali, Kyle J Gaulton, Santiago A Rodríguez-Seguí, et al.
Diabetes|January 22, 2015
Association analysis of 29,956 individuals confirms that a low-frequency variant at CCND2 halves the risk of type 2 diabetes by enhancing insulin secretionHanieh Yaghootkar, Alena Stancáková, Rachel M Freathy, et al.
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