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Nature Communications|November 14, 2022
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failureMichael G Levin, Noah L Tsao, Pankhuri Singhal, et al.
JACC. Clinical Electrophysiology|September 7, 2024
Ablation for Atrial Fibrillation in Patients With Rare Pathogenic Variants in Cardiomyopathy and Arrhythmia GenesMajd A El-Harasis, Zachary T Yoneda, Katherine C Anderson, et al.
Science (New York, N.Y.)|August 13, 2021
Population sequencing data reveal a compendium of mutational processes in the human germ lineVladimir B Seplyarskiy, Ruslan A Soldatov, Evan Koch, 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.
Nature Genetics|November 1, 2025
An African ancestry-specific nonsense variant in CD36 is associated with a higher risk of dilated cardiomyopathyJennifer E Huffman, Liam Gaziano, Zeina R Al Sayed, et al.
Science Translational Medicine|May 24, 2019
Primary cilia defects causing mitral valve prolapseKatelynn A Toomer, Mengyao Yu, Diana Fulmer, et al.
Nature Genetics|November 21, 2018
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysmRussell A Gould, Hamza Aziz, Courtney E Woods, et al.
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|July 20, 2014
B-type natriuretic peptide and C-reactive protein in the prediction of atrial fibrillation risk: the CHARGE-AF Consortium of community-based cohort studiesMoritz F Sinner, Katherine A Stepas, Carlee B Moser, et al.
Genetics|March 15, 2021
Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestriesAlan M Kwong, Thomas W Blackwell, Jonathon LeFaive, et al.
Nature Communications|August 30, 2022
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genesJennifer L Halford, Valerie N Morrill, Seung Hoan Choi, et al.
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