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Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.Circulation|September 26, 2022
Cross-Ancestry Investigation of Venous Thromboembolism Genomic PredictorsFlorian Thibord, Derek Klarin, Jennifer A Brody, et al.Nature Genetics|June 2, 2022
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validationMarijana Vujkovic, Shweta Ramdas, Kim M Lorenz, et al.Lancet (London, England)|March 17, 2012
Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies, Nadeem Sarwar, Adam S Butterworth, et al.Nature Genetics|July 13, 2010
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysmSolveig Gretarsdottir, Annette F Baas, Gudmar Thorleifsson, et al.American Journal of Human Genetics|February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksGina M Peloso, Paul L Auer, Joshua C Bis, et al.Nature Human Behaviour|August 4, 2022
Rare genetic variants explain missing heritability in smokingSeon-Kyeong Jang, Luke Evans, Allison Fialkowski, et al.Nature Genetics|December 19, 2025
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease predictionAeron M Small, Ta-Yu Yang, Shinsuke Itoh, et al.Nature Genetics|March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation riskSeung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.Circulation. Cardiovascular Genetics|November 23, 2016
Multiethnic Exome-Wide Association Study of Subclinical AtherosclerosisPradeep Natarajan, Joshua C Bis, Lawrence F Bielak, et al.Pageof 81