Toward Precision Policy — The Case of Cardiovascular Care

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HLBS-PopOmics

- Heart, Lung, Blood, and Sleep Disorders Knowledge Base in Population Genomics -

What's New

Last Posted: Dec 08, 2018

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• 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
• Gene therapy for sickle cell disease.  
  Olowoyeye Abiola et al. The Cochrane database of systematic reviews 2018 Nov 11CD007652
• 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
• Genomics, microbiomics, proteomics, and metabolomics in bronchopulmonary dysplasia.  
  Lal Charitharth Vivek et al. Seminars in perinatology 2018 Nov 42(7) 425-431
• Implementing Genomics-Based Screening Programs for Healthy Adults: A Proposed Evidence-based Approach from the Genomics and Population Health Action Collaborative
  Khoury MJ et al, Blog Post, December 3, 2018
• Prevalence of nonfounder BRCA1/2 mutations in Ashkenazi Jewish patients presenting for genetic testing at a hereditary breast and ovarian cancer center.  
  Frey Melissa K et al. Cancer 2018 Nov
• The current state of sickle-cell trait: implications for reproductive and genetic counseling.  
  Pecker Lydia H et al. Blood 2018 Nov
• The diagnosis of hereditary angioedema with C1 inhibitor deficiency: a survey of Canadian physicians and laboratories.  
  Charest-Morin Xavier et al. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2018 1483
• 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
• Genetic Modifiers of Fetal Haemoglobin in Sickle Cell Disease.  
  Menzel Stephan et al. Molecular diagnosis & therapy 2018 Nov