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- 2023
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Mark
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
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- Contribution to journal › Article
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Mark
Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
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- Contribution to journal › Article
- 2022
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
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- Contribution to journal › Article
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Mark
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
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- Contribution to journal › Article
- 2021
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Mark
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
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- Contribution to journal › Article
- 2018
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Mark
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
(
- Contribution to journal › Article
- 2017
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Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
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- Contribution to journal › Article
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Mark
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
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- Contribution to journal › Article
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Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
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- Contribution to journal › Article
- 2016
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Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article