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: 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
• Clinical Classification, Screening and Diagnosis for Thalassemia.  
  Viprakasit Vip et al. Hematology/oncology clinics of North America 2018 32(2) 193-211
• 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
• Incidence of hemoglobinopathies and thalassemias in Northern Alberta. Establishment of reference intervals for HbF and HbA2.  
  Rodriguez-Capote Karina et al. Clinical biochemistry 2015 Jul 48(10-11) 698-702
• 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
• Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank  
  LC Pilling et al, BMJ, January 16, 2019
• Common gene disorder causes serious “stealth” disease, but could be easily treated  
  UK Biobank, January 17,. 2019
• 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
• Burden of Sickle Cell Disease in Ghana: The Korle-Bu Experience.  
  Asare Eugenia V et al. Advances in hematology 2018 20186161270
• Self-management recommendations for sickle cell disease: A Ghanaian health professionals' perspective.  
  Druye Andrews et al. Health science reports 2018 Nov 1(11) e88