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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 insights into resting heart rate and its role in cardiovascular disease
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- Contribution to journal › Article
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Identification of biomarkers for glycaemic deterioration in type 2 diabetes
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- Contribution to journal › Article
- 2022
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Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes
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- Contribution to journal › Article
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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
- 2021
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Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
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- Contribution to journal › Article
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Glucose-Dependent Insulinotropic Peptide in the High-Normal Range Is Associated With Increased Carotid Intima-Media Thickness
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- Contribution to journal › Article
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Elevated circulating follistatin associates with an increased risk of type 2 diabetes
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- Contribution to journal › Article
- 2020
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Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC
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- Contribution to journal › Article
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Glucose-dependent insulinotropic peptide and risk of cardiovascular events and mortality : a prospective study
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- Contribution to journal › Article
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Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
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- Contribution to journal › Article
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The effect of LRRK2 loss-of-function variants in humans
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- Contribution to journal › Article
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Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals
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- Contribution to journal › Article
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Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes
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- Contribution to journal › Article
- 2019
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A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
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- Contribution to journal › Article