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- 2024
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A genomic mutational constraint map using variation in 76,156 human genomes
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- Contribution to journal › Article
- 2023
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Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
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- Contribution to journal › Article
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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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Genetic insights into resting heart rate and its role in cardiovascular disease
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- Contribution to journal › Article
- 2022
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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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The role of circulating galectin-1 in type 2 diabetes and chronic kidney disease : evidence from cross-sectional, longitudinal and Mendelian randomisation analyses
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- Contribution to journal › Article
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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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HLA class I genes modulate disease risk and age at onset together with DR-DQ in Chinese patients with insulin-requiring type 1 diabetes
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- Contribution to journal › Article
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The trans-ancestral genomic architecture of glycemic traits
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- Contribution to journal › Article
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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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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
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- Contribution to journal › Article
- 2017
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Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
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- Contribution to journal › Article
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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
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- Contribution to journal › Article
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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
- 2016
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The genetic architecture of type 2 diabetes
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- Contribution to journal › Article
- 2002
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Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
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- Contribution to journal › Article
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Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels.
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- Contribution to journal › Article
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Down-regulation of insulin receptor substrates (IRS)-1 and IRS-2 and Src homologous and collagen-like protein Shc gene expression by insulin in skeletal muscle is not associated with insulin resistance or type 2 diabetes.
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- Contribution to journal › Article
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Mark
Screening for MODY mutations, GAD antibodies, and type 1 diabetes--associated HLA genotypes in women with gestational diabetes mellitus.
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- Contribution to journal › Article
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Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
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- Contribution to journal › Article
- 1999
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Polymorphism in the angiotensin converting enzyme but not in the angiotensinogen gene is associated with hypertension and type 2 diabetes: the Skaraborg Hypertension and diabetes project
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- Contribution to journal › Article