Associated Papers
Atrial fibrillation-a complex polygenetic disease.
Andersen JH et al.
European Journal of Human Genetics : Ejhg, 2021
33279945 (PubMed )
Supplement: 41431_2020_784_MOESM3_ESM.xlsx › Sheet1
Loperamide Toxicity Revealing Apical Hypertrophic Cardiomyopathy.
Khan N et al.
Methodist Debakey Cardiovascular Journal, 2021
Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note.
Weeke P et al.
Circulation. Cardiovascular Genetics, 2015
Atrial fibrillation: the role of common and rare genetic variants.
Olesen MS et al.
European Journal of Human Genetics : Ejhg, 2014
Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk.
Mann SA et al.
Journal of the American College of Cardiology, 2012
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
Hedley PL et al.
Journal of Negative Results in Biomedicine, 2011
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