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23
Initial sequencing and comparative analysis of the mouse genome
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns
High Grade Gliomas and DIPG
Single-cell transcriptomics from human pancreatic islets: sample preparation matters
Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample
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