Heart And Vascular Diseases
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What's New
Last Posted: Dec 13, 2018
- Advancing FH Care at NHLBI Workshop on Implementation Science and FH
The FH Foundation, December 10, 2018 - Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield.
Thomson Kate L et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Dec - Polygenic risk score identifies associations between sleep duration and diseases determined from an electronic medical record biobank.
Dashti Hassan S et al. Sleep 2018 Dec - Prevalence of pharmacogenomic variants affecting the efficacy of clopidogrel therapy in the Hispanic Community Health Study/Study of Latinos cohort.
Melin Kyle et al. Pharmacogenomics 2018 Dec - Medical management of haemorrhagic hereditary telangiectasia in adult patients.
Riera-Mestre Antoni et al. Medicina clinica 2018 Nov - Personalised organs-on-chips: functional testing for precision medicine.
van den Berg Albert et al. Lab on a chip 2018 Dec - Can You Inherit Pulmonary Hypertension? Here’s What You Should Know
Cleveland Clinic, December 10, 2018 - New 2018 Guideline on the Management of Blood Cholesterol from the American College of Cardiology / American Heart Association Task Force on Clinical Practice Guidelines
What does it mean for FH, the FH Foundation, December 6, 2018 - Toward Precision Policy — The Case of Cardiovascular Care
RK Wadhera et al, NEJM, December 5, 2018 - A Proposed Approach for Implementing Genomics-Based Screening Programs for Healthy Adults
M. Murray and the Genomics and Population Health Action Collaborative, National Academies of Medicine, December 3, 2018 - Cardiac MRI biomarkers for Duchenne muscular dystrophy.
Magrath Patrick et al. Biomarkers in medicine 2018 Nov - FDA takes new action to advance the development of reliable and beneficial genetic tests that can improve patient care
FDA Press Release, December 4, 2018 - Genetic associations in community context: a mixed model approach identifies a functional variant in the RBP4 gene associated with HDL-C dyslipidemia.
Aref-Eshghi Erfan et al. BMC medical genetics 2018 Nov 19(1) 205 - Analytical validity of a genotyping assay for use with personalized antihypertensive and chronic kidney disease therapy.
Collins Kimberly S et al. Pharmacogenetics and genomics 2018 Nov - Application of the Japanese Guidelines for the Diagnosis of Familial Hypercholesterolemia in General Practice: It is to be Validated in International Harmonization.
Tanaka Nobukiyo et al. Journal of atherosclerosis and thrombosis 2018 Nov
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