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Plos One|October 8, 2011
Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgeryAmanda A Fox, Mias Pretorius, Kuang-Yu Liu, et al.JAMA|August 29, 2013
Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetesLu Qi, Qibin Qi, Sabrina Prudente, et al.Chemical Reviews|September 7, 2019
Nanoscale Technologies for Prevention and Treatment of Heart Failure: Challenges and OpportunitiesMohammad Javad Hajipour, Mehdi Mehrani, Seyed Hesameddin Abbasi, et al.The Journal of Clinical Investigation|February 11, 2014
5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathyDanos C Christodoulou, Hiroko Wakimoto, Kenji Onoue, et al.Circulation|July 10, 2023
Multiomics of Tissue Extracellular Vesicles Identifies Unique Modulators of Atherosclerosis and Calcific Aortic Valve StenosisMark C Blaser, Fabrizio Buffolo, Arda Halu, et al.The Journal of Clinical Investigation|March 20, 2014
A common genetic variant within SCN10A modulates cardiac SCN5A expressionMalou van den Boogaard, Scott Smemo, Ozanna Burnicka-Turek, et al.Circulation. Cardiovascular Genetics|December 25, 2009
Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgerySimon C Body, Charles D Collard, Stanton K Shernan, et al.Nature|April 24, 2025
BMAL1-HIF2A heterodimer modulates circadian variations of myocardial injuryWei Ruan, Tao Li, In Hyuk Bang, et al.JAMA Cardiology|July 5, 2023
Novel Association of the NOTCH Pathway Regulator MIB1 Gene With the Development of Bicuspid Aortic ValveIdit Tessler, Juliette Albuisson, Rebeca Piñeiro-Sabarís, et al.European Heart Journal|March 4, 2022
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapseCarolina Roselli, Mengyao Yu, Victor Nauffal, et al.Pageof 9