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JAMA|December 12, 2018
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial FibrillationSeung Hoan Choi, Lu-Chen Weng, Carolina Roselli, et al.JAMA Cardiology|February 12, 2025
Arrhythmic Risk Stratification of Carriers of Filamin C Truncating Variants, Marta Gigli, Davide Stolfo, et al.Circulation|January 17, 2020
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic ConditionJason D Roberts, S Yukiko Asaki, Andrea Mazzanti, et al.Circulation. Genomic and Precision Medicine|May 28, 2024
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular ArrhythmiasLu-Chen Weng, Shaan Khurshid, Amelia Weber Hall, et al.Nature Communications|October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with heightGareth Hawkes, Robin N Beaumont, Zilin Li, et al.Nature Genetics|January 2, 2025
The impact of common and rare genetic variants on bradyarrhythmia developmentLu-Chen Weng, Joel T Rämö, Sean J Jurgens, et al.Scientific Reports|September 14, 2017
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen ConsortiumLu-Chen Weng, Kathryn L Lunetta, Martina Müller-Nurasyid, et al.Research Square|May 18, 2026
Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillationSean Jurgens, Nobuyuki Enzan, Ian Dinsmore, et al.Science Advances|May 1, 2023
The genetic determinants of recurrent somatic mutations in 43,693 blood genomesJoshua S Weinstock, Cecelia A Laurie, Jai G Broome, et al.Nature Communications|May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genesRebecca Keener, Surya B Chhetri, Carla J Connelly, et al.Pageof 72