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- 2022
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Mark
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
- 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
Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk
- 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
-
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
-
Mark
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
- Contribution to journal › Article
- 2018
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Mark
Genetic predisposition to infection in a case of atypical hemolytic uremic syndrome
- Contribution to journal › Article
-
Mark
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
- 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
-
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
