Variants conferring risk of atrial fibrillation on chromosome 4q25

By Daniel Fannar Gudbjartsson, D. Arnar, A. Helgadóttir, S. Gretarsdottir, H. Hólm, A. Sigurdsson, Adalbjorg Jonasdottir, A. Baker, G. Thorleifsson, K. Kristjánsson and 30 more. Nature, 2007

983 citations recorded by the source corpus.

Subfields: Genetics, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/28369b1ddacb34ca93be5bbdd2faea45fd90a2ae

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Citations in the corpus

• 2017 HRS/EHRA/ECAS/APHRS/SOLAECE expert consensus statement on catheter and surgical ablation of atrial fibrillation (2017, positive): “Therefore, population-based or genome-wide studies have been used to identify many AF risk loci.(25,26,27,28,29,30) The genes at these loci encode transcription factors and ion channels, and many are without a clear relation to AF at the present time.”