- Arrhythmogenic right ventricular cardiomyopathy
- Family history of sudden cardiac death
- Hypertrophic cardiomyopathy (HCM)
- Inherited cardiomyopathy
- Genetic testing
Publications
Walsh R, Mazzarotto F, Whiffin N, Buchan R, Midwinter W, Wilk A, Li N, Felkin L, Ingold N, Govind R, Ahm,ad M, Mazaika E, Allouba M, Zhang X, de Marvao A, Day SM, Ashley E, Colan SD, Michels M, Pereira AC, Jacoby D, Ho CY, Thomson KL, Watkins H, Barton PJR, Olivotto, I, Cook SA, Ware JS. Quantitative Approaches to Variant Classification Increase the Yield and Precision of Genetic Testing for Mendelian Diseases: The Case for Hypertrophic Cardiomyopathy. , Genome Medicine, 11(1): 2019,5
Garratt M, Leander D, Pifer K, Herrera J, Day SM, Fiehn O, Brooks S, Miller RA. 17-alpha Estradiol Ameliorates Age-Associated Sarcopenia and Improves Late Life Physical Function in Male Mice But Not in Females or Castrated Males , Aging Cell, 18(2): 2019,e12920
Day SM Nonobstructive Hypertrophic Cardiomyopathy: The High Hanging Fruit. , JAMA Cardiol, 4(3): 2019,235-236
Vigneault DM, Yang E, Jensen PJ, Tee MW, Farhad H, Chu L, Noble JA, Day SM, Colan SD, Russell MW, Towbin J, Sherrid MV, Canter CE, Shi L, Ho CY, Bluemke DA Left Ventricular Strain Is Abnormal in Preclinical and Overt Hypertrophic Cardiomyopathy: Cardiac MR Feature Tracking. , Radiology, 290(3): 2019,640-48
Smith ED, Tome J, Mcgrath R, Kumar S, Concannon M, Day SM, Saberi S, Helms AS Exercise hemodynamics in hypertrophic cardiomyopathy identify risk of incident heart failure but not ventricular arrhythmias or sudden cardiac death. , Int J Cardiol, 274: 2019,226-231
O'Leary TS, Snyder J, Sadayappan S, Day SM, Previs MJ MYBPC3 truncation mutations enhance actomyosin contractile mechanics in human hypertrophic cardiomyopathy. , J Mol Cell Cardiol, 127: 2019,165-173
Glazier AA, Thompson A, Day SM Allelic imbalance and haploinsufficiency in MYBPC3-linked hypertrophic cardiomyopathy. , Pflugers Arch, 471(5): 2019,781-793
Ho CY, Day, SM, Ashley EA, Michels M, Pereira A, Jacoby D, Fox J, Caleshu C, Cirino AL, Ware J, Helms AS, Colan SD, Signorovich J, Green E, Olivotto I Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe). , Circulation, 138(14): 2018,1387-98
Lee SP, Ashley EA, Homburger J, Caleshu C, Green EM, Jacoby D, Colan SD, Arteaga-Fernández E, Day SM, Girolami F, Olivotto I, Michels M, Ho CY, Perez MV, SHaRe Investigators Incident Atrial Fibrillation Is Associated With MYH7 Sarcomeric Gene Variation in Hypertrophic Cardiomyopathy. , Circ Heart Fail, 11(9): 2018,e005191
Glazier AA, Hafeez N, Mellacheruvu D, Basrur V, Nesvizhskii AI, Lee LM, Shao H, Tang V, Yob JM, Gestwicki JE, Helms AS, Day SM HSC70 is a chaperone for wild-type and mutant cardiac myosin binding protein C. , JCI Insight, 3(11): 2018,pii: 99319