Dr. Matthew Wheeler is a physician scientist with interests in cardiomyopathies, rare and undiagnosed diseases, therapeutics and genomics. Dr. Wheeler has research training in both myocardial and skeletal muscle biology and genetics, genomics, and multi-scale networks and is a physician with interest and experience treating patients with hypertrophic cardiomyopathy and other inherited cardiomyopathies. I have clinical training in medicine, cardiology, cardiovascular genetics, and advanced heart failure. He has extensive translational science efforts, participating in several ongoing clinical trials for hypertrophic cardiomyopathy, dilated cardiomyopathy, ATTR cardiac amyloidosis, and mechanical circulatory support. Dr. Wheeler is also the Co-PI of Stanford’s NIH-funded Center for Undiagnosed Diseases a clinical site of the Undiagnosed Diseases Network and a co-Investigator of the Bioinformatics Center of the Molecular Transducers of Physical Activity Consortium. He pursues projects and collaborations at the intersection of striated muscle genetics, genomics, and clinical investigation