NHLBI TOPMed: The Vanderbilt Atrial Fibrillation Registry (VU_AF)

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Meta-analysis identifies six new susceptibility loci for atrial fibrillation

P. Ellinor, K. Lunetta, Christine M. Albert, et al.. (2012). Nature Genetics. Cited 576 times. https://doi.org/10.1038/ng.2261

Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation.

Babar Parvez, J. Vaglio, S. Rowan, et al.. (2010). Journal of the American College of Cardiology. Cited 139 times. https://doi.org/10.1016/j.jacc.2012.01.070

Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation.

M. Ritchie, S. Rowan, Gayle Kucera, et al.. (2012). Journal of the American College of Cardiology. Cited 87 times. https://doi.org/10.1016/j.jacc.2012.04.030

Whole-exome sequencing in familial atrial fibrillation.

P. Weeke, Raafia Muhammad, J. Delaney, et al.. (2014). European heart journal. Cited 41 times. https://doi.org/10.1093/eurheartj/ehu156

Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation.

J. Delaney, Raafia Muhammad, Yaping Shi, et al.. (2014). 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. Cited 25 times. https://doi.org/10.1093/europace/eut278

A common variant on chromosome 4q25 is associated with prolonged PR interval in subjects with and without atrial fibrillation.

Matthew J. Kolek, Babar Parvez, Raafia Muhammad, et al.. (2014). The American journal of cardiology. Cited 18 times. https://doi.org/10.1016/j.amjcard.2013.08.045

A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation.

Matthew J. Kolek, Todd L. Edwards, Raafia Muhammad, et al.. (2014). The American journal of cardiology. Cited 12 times. https://doi.org/10.1016/j.amjcard.2014.05.040
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