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- 2024
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Mark
The Gly82Ser polymorphism in the receptor for advanced glycation endproducts increases the risk for coronary events in the general population
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- Contribution to journal › Article
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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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Mark
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
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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
- 2021
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Mark
Plasma Vitamin C and type 2 diabetes : Genome-wide association study and mendelian randomization analysis in European populations
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- Contribution to journal › Article
- 2020
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Mark
The effect of LRRK2 loss-of-function variants in humans
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- Contribution to journal › Article
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Mark
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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Mark
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes
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- Contribution to journal › Article
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Mark
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
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- Contribution to journal › Article
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Mark
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
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- Contribution to journal › Article