What's New

Last Posted: Dec 21, 2020

• Genetic Association between Hypoplastic Left Heart Syndrome and Cardiomyopathies.
  Theis Jeanne L et al. Circulation. Genomic and precision medicine 2020 Dec
• Assessing the Role of Rare Genetic Variation in Patients With Heart Failure.
  Povysil Gundula et al. JAMA cardiology 2020 Dec
• Performance and clinical utility of supervised machine-learning approaches in detecting familial hypercholesterolaemia in primary care.
  Akyea Ralph K et al. NPJ digital medicine 2020 Oct 3(1) 142
• Sex Differences in the Risk of Coronary Heart Disease Associated With Type 2 Diabetes: A Mendelian Randomization Analysis.
  Peters Tricia M et al. Diabetes care 2020 Dec
• Machine learning algorithm for early detection of end-stage renal disease.
  Segal Zvi et al. BMC nephrology 2020 Nov 21(1) 518
• [Artificial intelligence technology in cardiac auscultation screening for congenital heart disease: present and future].
  Xu Weize et al. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2020 Oct 49(5) 548-555
• Role of Non-Coding Variants in Brugada Syndrome.
  Pérez-Agustín Adrian et al. International journal of molecular sciences 2020 Nov 21(22)
• Sex differences in cardiovascular morbidity associated with familial hypercholesterolaemia: A retrospective cohort study of the UK Simon Broome register linked to national hospital records.
  Iyen Barbara et al. Atherosclerosis 2020 Oct
• Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets.
  Berger Mark J et al. Database : the journal of biological databases and curation 2020 Jan 2020
• Prediction of metabolic syndrome based on sleep and work-related risk factors using an artificial neural network.
  Eyvazlou Meysam et al. BMC endocrine disorders 2020 Nov 20(1) 169
• Identifying familial hypercholesterolaemia in primary care: Validation and optimisation of a clinical tool (FAMCAT).
  Akyea Ralph Kwame et al. BJGP open 2020 Nov
• Prevalence of Familial Hypercholesterolaemia in Acute Coronary Syndrome Patients in a Large Regional Coronary Care Unit.
  Samuel Rohit et al. Heart, lung & circulation 2020 Oct
• A simple, rapid, interpretable, actionable and implementable digital PCR based mortality index.
  Philibert Robert et al. Epigenetics 2020 Nov 1-15
• Genetic variant affecting the myosin light chain 2 related to familial hypertrophic cardiomyopathy.
  Gil Wilmar Saldarriaga et al. Intractable & rare diseases research 2020 Nov 9(4) 229-232
• Identification of risk factors of 30-day readmission and 180-day in-hospital mortality, and its corresponding relative importance in patients with Ischemic heart disease: a machine learning approach.
  Okere Arinze Nkemdirim et al. Expert review of pharmacoeconomics & outcomes research 2020 Oct