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Heart And Vascular Diseases

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Last Posted: Aug 17, 2018

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• Genetic testing pushed for hereditary high cholesterol disease,  
• Clinical Course and Management of Hypertrophic Cardiomyopathy.  
  Maron Barry J et al. The New England journal of medicine 2018 Aug (7) 655-668
• A Harvard Scientist Thinks He Has a Gene Test for Heart Attack Risk. He Wants to Give It Away Free.  
  M Herper, Forbes, August 13, 2018
• Association of Broad-Based Genomic Sequencing With Survival Among Patients With Advanced Non-Small Cell Lung Cancer in the Community Oncology Setting. 
  Presley Carolyn J et al. JAMA 2018 Aug 320(5) 469-477
• Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California.  
  Gallant N M et al. Molecular genetics and metabolism 2017 Nov 122(3) 76-84
• Challenges in the Diagnosis of Anderson-Fabry Disease: A Deceptively Simple and Yet Complicated Genetic Disease.  
  Marian Ali J et al. Journal of the American College of Cardiology 2016 68(10) 1051-3
• Clues to Your Health Are Hidden at 6.6 Million Spots in Your DNA With a sophisticated new algorithm, scientists have found a way to forecast an individual’s risks for five deadly diseases.  
  G Kolata, New York Times, August 13, 2018
• Cost Effectiveness of Genotype-Guided Warfarin Dosing in Patients with Mechanical Heart Valve Replacement Under the Fee-for-Service System.  
  Kim Dong-Jin et al. Applied health economics and health policy 2017 Oct 15(5) 657-667
• From Durham, The Future Of Clinical Research Looks A Lot Like Implementation Science  
  D Shaywitz, Forbes, August 9, 2018
• Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers. 
  Nishiuchi Suguru et al. Circulation. Cardiovascular genetics 2017 Dec 10(6)
• Genetics of Dilated Cardiomyopathy: Clinical Implications.  
  Paldino A et al. Current cardiology reports 2018 Aug 20(10) 83
• Genetics of hypertrophic cardiomyopathy: A review of current state.  
  Sabater-Molina M et al. Clinical genetics 2018 Jan 93(1) 3-14
• Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.  
  Khera Amit V et al. Nature genetics 2018 Aug
• Guidance on the management of familial hypercholesterolaemia in Hong Kong: an expert panel consensus viewpoin.  
  Tomlinson B et al. Hong Kong medical journal = Xianggang yi xue za zhi 2018 Aug 24(4) 408-415
• Hypertrophic Cardiomyopathy Genotype Prediction Models in a Pediatric Population.  
  Newman Randa et al. Pediatric cardiology 2018 Apr 39(4) 709-717