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My research group has been at the forefront of developing and using clinically relevant in vivo models (Drosophila and Mouse) and humans to address the pathophysiological basis of circadian/metabolic dysregulation linked to cardiometabolic disease, myofibrillar-myopathies, proteinopathies, neuropathies, sleep, and aging disorders.

By integrating omics with physiological, cell-molecular, genetics, genomics, and nutritional approaches, our goal is to understand how lifestyle (circadian rhythms and Time-restricted Feeding) and genetic factors act to maintain the structural integrity of cells, tissues, and organs that in turn dictate organismal physiology and Behavior. 

With sustained NIH funding, our research findings have been published in Science, Nature Communications, Aging Cells, Human Molecular Genetics, Physiology, and PLoS Genetics. See the research section for the summary of my main research projects.