Coronary Heart Disease
- HLBS-PopOmics -
What's New
Last Posted: Mar 08, 2018
- A large electronic-health-record-based genome-wide study of serum lipids.
Hoffmann Thomas J et al. Nature genetics 2018 Mar - Molecular diagnosis of familial hypercholesterolaemia.
Graham Colin A et al. Current opinion in lipidology 2017 Aug 28(4) 313-320 - A nation-wide survey of patients with homozygous familial hypercholesterolemia phenotype undergoing LDL-apheresis in Turkey (A-HIT 1 registry).
Kayikcioglu Meral et al. Atherosclerosis 2018 Jan 27042-48 - Application of Single-Nucleotide Polymorphism-Related Risk Estimates in Identification of Increased Genetic Susceptibility to Cardiovascular Diseases: A Literature Review.
Fiatal Szilvia et al. Frontiers in public health 2017 5358 - Effect of polymorphisms in the CD36 and STAT3 genes on different dietary interventions among patients with coronary artery disease: study protocol for a randomized controlled trial.
Portal Vera Lucia et al. Trials 2016 17(1) 437 - CYP2C19 and ABCB1 genetic polymorphisms correlate with the recurrence of ischemic cardiovascular adverse events after clopidogrel treatment.
Hou Xumin et al. Journal of clinical laboratory analysis 2018 Feb - The cost-effectiveness of screening strategies for familial hypercholesterolaemia in Poland.
Pelczarska Aleksandra et al. Atherosclerosis 2018 Jan 270132-138 - Effect of Disclosing Genetic Risk for Coronary Heart Disease on Information Seeking and Sharing: The MI-GENES Study (Myocardial Infarction Genes).
Brown Sherry-Ann N et al. Circulation. Cardiovascular genetics 2017 Aug 10(4) - Genetics of familial hypercholesterolemia: a tool for development of novel lipid lowering pharmaceuticals?
Volta Andrea et al. Current opinion in lipidology 2018 Jan - A Cluster Randomized Trial of a Personalized Multi-Condition Risk Assessment in Primary Care.
Haas Jennifer S et al. American journal of preventive medicine 2017 Jan 52(1) 100-105
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