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- 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
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Pharmacological targeting of MTHFD2 suppresses acute myeloid leukemia by inducing thymidine depletion and replication stress
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- Contribution to journal › Article
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Mark
Rare germline copy number variants (CNVs) and breast cancer risk
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- Contribution to journal › Article
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Mark
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease
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- Contribution to journal › Article
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Mark
Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization
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- Contribution to journal › Article
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Mark
Small-molecule activation of OGG1 increases oxidative DNA damage repair by gaining a new function
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- Contribution to journal › Article
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Mark
SELNET clinical practice guidelines for bone sarcoma
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- Contribution to journal › Article
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Genetic Landscape of the ACE2 Coronavirus Receptor
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- Contribution to journal › Article
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Mark
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
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Birthweight, BMI in adulthood and latent autoimmune diabetes in adults : a Mendelian randomisation study
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- Contribution to journal › Article