I. Moskowitz

An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy.

James O. Mudd, J. Seidman, D. Fatkin, 2000, The Journal of clinical investigation.

An abnormal Ca2+ response in mutant sarcomere protein–mediated familial hypertrophic cardiomyopathy

James O. Mudd, J. Seidman, D. Fatkin, 2000 .

Complex genomic rearrangement in CCS‐LacZ transgenic mice

J. Seidman, G. Fishman, S. Rentschler, 2007, Genesis.

Comparison of Two Murine Models of Familial Hypertrophic Cardiomyopathy

F J Schoen, James O. Mudd, D. Kass, 2001, Circulation research.

Cardiac electrophysiological phenotypes in postnatal expression of Nkx2.5 transgenic mice

C. Berul, H. Wakimoto, S. Izumo, 2003, Genesis.

Ventricular Arrhythmia Vulnerability in Cardiomyopathic Mice With Homozygous Mutant Myosin-Binding Protein C Gene

J. Seidman, C. Seidman, C. Berul, 2001, Circulation.

Tetralogy of Fallot with Congenital Aortic Valvar Stenosis: The Tetralogy–Truncus Interrelationship

A. Juraszek, I. Moskowitz, R. Praagh, 2006, Pediatric Cardiology.

Tbx5 maintains atrial identity in postnatal cardiomyocytes by regulating an atrial-specific enhancer network

Vassilios J. Bezzerides, H. Wakimoto, Carlos Perez-Cervantes, 2023, Nature Cardiovascular Research.