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Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Exome wide association study for blood lipids in 1,158,017 individuals from diverse populationsSatoshi Koyama, Zhi Yu, Seung Hoan Choi, et al.
Nature Genetics|May 25, 2026
Exome-wide association study of blood lipids in 1,158,017 individuals from diverse populationsSatoshi Koyama, Zhi Yu, Seung Hoan Choi, et al.
Circulation|August 25, 2010
Independent susceptibility markers for atrial fibrillation on chromosome 4q25Steven A Lubitz, Moritz F Sinner, Kathryn L Lunetta, et al.
Medrxiv : the Preprint Server for Health Sciences|November 25, 2020
Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancerSeyedeh M Zekavat, Shu-Hong Lin, Alexander G Bick, et al.
Nature Cardiovascular Research|August 29, 2022
Neutrophils incite and macrophages avert electrical storm after myocardial infarctionJana Grune, Andrew J M Lewis, Masahiro Yamazoe, et al.
Circulation. Genomic and Precision Medicine|March 16, 2018
Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human SubjectsRay Hu, Michael P Morley, Jeffrey Brandimarto, et al.
Nature Genetics|November 27, 2021
Deep learning enables genetic analysis of the human thoracic aortaJames P Pirruccello, Mark D Chaffin, Elizabeth L Chou, et al.
Biorxiv : the Preprint Server for Biology|December 3, 2025
The <i>9p21.3</i> Coronary Artery Disease Risk Locus Modulates Vascular Cell-State Transitions via Enhancer-Driven Regulation of <i>MTAP</i>Timothy N Audam, Benjamin Schmandt, Yi Huang, et al.
Science Translational Medicine|April 17, 2024
Placental senescence pathophysiology is shared between peripartum cardiomyopathy and preeclampsia in mouse and humanJason D Roh, Claire Castro, Andy Yu, et al.
Plos Genetics|October 30, 2016
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of InheritanceSoto Romuald Kiando, Nathan R Tucker, Luis-Jaime Castro-Vega, et al.
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