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The in vivo endothelial cell translatome is highly heterogeneous across vascular beds

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Rare Loss-of-Function Mutations of PTGIR identified in Fibromuscular Dysplasia and Spontaneous Coronary Artery Dissection

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Genetic association studies of fibromuscular dysplasia identify new risk loci and shared genetic basis with more common vascular diseases

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A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

genetics more details view paper

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