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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
- Contribution to journal › Article
- 2022
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Mark
Genetic Landscape of the ACE2 Coronavirus Receptor
- Contribution to journal › Article
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
- Contribution to journal › Article
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Mark
A saturated map of common genetic variants associated with human height
- Contribution to journal › Article
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Mark
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease
- Contribution to journal › Article
- 2021
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Mark
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
- Contribution to journal › Article
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Mark
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
- 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
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
- Contribution to journal › Article
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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
- Contribution to journal › Article
