Matthew Taylor MD, PhD

Matthew Taylor MD, PhD received his undergraduate degree in Genetics from the University of California at Berkeley.

After completing medical school at the University of Southern California, he moved to Colorado for residency training programs in Internal Medicine and Clinical Genetics. In 2005 he received a PhD degree from the University of Colorado Denver for work related to the genetic basis of dilated cardiomyopathy.

Clinically, he directs the Adult Medical Genetics clinic that serves adults and families with genetic conditions in the Denver and Rocky Mountain region. The clinic services include genetic diagnosis, testing, and counseling. Additionally, the clinic serves as a regional hub for recruitment of patients with rare genetic diseases as well as for clinical trials in genetic diseases where novel therapies are now coming online in the trial arena.

Many of his research subjects are initially identified through this clinic and feed into his laboratory’s research on inherited cardiomyopathies, major causes of heart failure and heart transplantation. While the initial focus was on a nearest-neighbor approach in candidate gene studies, the current work involves whole Exome studies in multi-generational cardiomyopathy families. This work has been funded through the NIH (both R01 and CCTSI funding) and most recently the laboratory was informed of successful funding from the Leducq Foundation as part of a multi-center trans-Atlantic partnership to study mechanisms of arrhythmias in cardiomyopathies. In addition to descriptive and mechanistic studies in cardiomyopathies, his group is just initiating two clinical trials in rare forms of hereditary cardiomyopathy where specific mutational sub-classes of disease are targeted with therapies designed to benefit those individuals with mutations in key subsets of cardiomyopathy genes.

Beyond cardiomyopathies, Dr. Taylor is involved in therapeutic studies in rare inborn errors of metabolism including past and ongoing treatment trials in Gaucher, Fabry, and Pompe diseases. The rapid advances from genetic discovery to and understanding of pathophysiology to treatment development ensures that additional studies in rare genetic conditions will shortly be arriving on the scene.

In 2014, he became Associate Director of Personalized Medicine within the newly minted Biomedical Informatics and Personalized Medicine Center. The Center is designed to stimulate and enable translational research that promotes the goals of personalized medicine (also referred to as ‘precision medicine’).

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Rachael Rzasa Lynn, MD

President

Joshua Blum, MD

Vice President

Drew Trainor, MD

Secretary

Ellen Price, DO

Treasurer

Scott Bainbridge, MD

Immediate Past President

Jonathan Clapp, MD, MS

Past President

Brent Van Dorsten, PhD

Past President

Giancarlo Barolat, MD

Past President

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