A great first step, but a long way to go
Author:
Affiliation:
1. Cardiovascular Division, Free University of Brussels (UZ Brussel), Brussel, Belgium
Publisher
Oxford University Press (OUP)
Subject
Cardiology and Cardiovascular Medicine
Link
http://academic.oup.com/eurheartj/advance-article-pdf/doi/10.1093/eurheartj/ehz596/29603459/ehz596.pdf
Reference6 articles.
1. Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores,2019
2. Common genetic variant risk score is associated with drug-induced QT prolongation and torsade de pointes risk;Strauss;Circulation,2017
3. A new initiative on precision medicine;Collins;N Engl J Med,2015
4. Common variants at SCN5A–SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death;Bezzina;Nat Genet,2013
5. Evaluation of gene panels for inherited cardiac disease—is less more?;Dooijes;Neth Heart J,2019
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Outcome after tailored catheter ablation of atrial tachycardia using ultra‐high‐density mapping;Journal of Cardiovascular Electrophysiology;2020-08-11
2. A rare case of narrow QRS tachycardia with “hidden” concealed left-sided accessory pathway;Herzschrittmachertherapie + Elektrophysiologie;2020-06-29
3. Channelopathies and sudden cardiac death: genetics and pharmacological triggers;European Heart Journal;2019-10-01
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