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

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HLBS-PopOmics

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

What's New

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
• 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
• Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next-generation sequencing.  
  Fidalgo Teresa et al. Research and practice in thrombosis and haemostasis 2017 Jul 1(1) 69-80
• 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
• Effectiveness of a comprehensive educational programme for Accredited Social Health Activists (ASHAs) to identify individuals in the Udupi district with bleeding disorders: A community-based survey.  
  Badagabettu S et al. Haemophilia : the official journal of the World Federation of Hemophilia 2018 Aug
• Effort to Diversify Medical Research Raises Thorny Questions of Race  
  M Miller, Scientific American, August 10, 2018
• EGFR Mutation Testing of non-squamous NSCLC: Impact and Uptake during Implementation of Testing Guidelines in a Population-Based Registry Cohort from Northern New Zealand.  
  McKeage Mark et al. Targeted oncology 2017 12(5) 663-675
• Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory Experience.  
  Perez Botero Juliana et al. Seminars in thrombosis and hemostasis 2018 Apr 44(3) 287-292
• Factor XIII deficiency diagnosis: Challenges and tools.  
  Karimi M et al. International journal of laboratory hematology 2018 Feb 40(1) 3-11
• Family history of immune conditions and autism spectrum and developmental disorders: Findings from the study to explore early development.  
  Croen Lisa A et al. Autism research : official journal of the International Society for Autism Research 2018 Aug
• From Durham, The Future Of Clinical Research Looks A Lot Like Implementation Science  
  D Shaywitz, Forbes, August 9, 2018