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Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.Circulation|February 4, 2009
Prevention of atrial fibrillation: report from a national heart, lung, and blood institute workshopEmelia J Benjamin, Peng-Sheng Chen, Diane E Bild, et al.Plos One|June 29, 2019
GWAS of QRS duration identifies new loci specific to Hispanic/Latino populationsBrenton R Swenson, Tin Louie, Henry J Lin, et al.Circulation. Genomic and Precision Medicine|July 1, 2020
Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex TraitsAntoine R Baldassari, Colleen M Sitlani, Heather M Highland, et al.Communications Biology|October 2, 2018
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.Circulation|October 30, 2016
Genetic Risk Prediction of Atrial FibrillationSteven A Lubitz, Xiaoyan Yin, Henry J Lin, et al.Nature Genetics|July 15, 2009
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic strokeDaniel F Gudbjartsson, Hilma Holm, Solveig Gretarsdottir, et al.Nature Genetics|May 1, 2012
Meta-analysis identifies six new susceptibility loci for atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Christine M Albert, et al.Circulation. Arrhythmia and Electrophysiology|February 21, 2020
Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation AblationM Benjamin Shoemaker, Daniela Husser, Carolina Roselli, et al.Frontiers in Endocrinology|May 20, 2022
The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry PopulationsZhe Wang, Shing Wan Choi, Nathalie Chami, et al.Pageof 18