Heart And Vascular Diseases - HLBS-PopOmics -

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Last Posted: Jan 20, 2019

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• Genetic factor may identify patients at risk for spontaneous coronary artery dissection  
  DL Bhatt, Healio, January 2019
• Value of genetic testing in the prevention of coronary heart disease events  
  Y Hynninen et al, PLOS One, January 2019
• A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.  
  Mosley Jonathan D et al. Nature communications 2018 9(1) 3522
• Advocating cardiovascular precision medicine with P2Y12 receptor inhibitors.  
  Winter Max-Paul et al. European heart journal. Cardiovascular pharmacotherapy 2017 3(4) 221-234
• Diagnostic performance of microRNA-133a in acute myocardial infarction: A meta-analysis.  
  Zhu Lei et al. Cardiology journal 2018 25(2) 260-267
• Genetic risk score (GRS) constructed from polymorphisms in the PON1, IL-6, ITGB3, and ALDH2 genes is associated with the risk of coronary artery disease in Pakistani subjects.  
  Shabana N A et al. Lipids in health and disease 2018 Sep 17(1) 224
• Sudden unexplained death in the young: epidemiology, aetiology and value of the clinically guided genetic screening.  
  Anastasakis Aris et al. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2018 20(3) 472-480
• The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry.  
  Roston Thomas M et al. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2018 20(3) 541-547
• Alpha 1-antitrypsin deficiency in patients with chronic obstructive pulmonary disease patients: is systematic screening necessary?  
  da Costa Cláudia Henrique et al. BMC research notes 2019 Jan 12(1) 10
• Validation of a clinical pharmacogenetic model to predict methotrexate nonresponse in rheumatoid arthritis patients.  
  Eektimmerman Frank et al. Pharmacogenomics 2019 Jan
• [Whole Exome Sequencing in daily practice: the possibilities and impossibilities of this diagnostic test].  
  Bouman Arjan et al. Nederlands tijdschrift voor geneeskunde 2018 162
• Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use  
  M Liu et al, Nature Genetics, January 14, 2019
• Place-Based Inequity in Smoking Prevalence in the Largest Cities in the United States  
  EC Leas et al, JAMA Internal Medicine, January 2019
• Cost Efficacy of ?-Galactosidase A Enzyme Screening for Fabry Disease.  
  Newman Darrell B et al. Mayo Clinic proceedings 2019 Jan 94(1) 84-88
• Early diagnosis and treatment of familial hypercholesterolemia.  
  Elkins J Casey et al. The Nurse practitioner 2019 Jan