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- 2015
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Mark
Mendelian randomization of blood lipids for coronary heart disease
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- Contribution to journal › Article
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Mark
Rare coding variants and X-linked loci associated with age at menarche
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- Contribution to journal › Article
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Mark
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis
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- Contribution to journal › Article
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Mark
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
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- Contribution to journal › Article
- 2014
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Mark
Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations
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- Contribution to journal › Article
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Mark
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
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- Contribution to journal › Article
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Mark
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
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- Contribution to journal › Article
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Mark
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
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- Contribution to journal › Article
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Mark
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data.
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- Contribution to journal › Article
- 2013
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Mark
Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia.
(
- Contribution to journal › Article