Default image

Findlay Lab

Andrew Findlay, MD

Developing therapeutic strategies for hereditary muscle disorders such as muscular dystrophy and age-related conditions like sarcopenia by translating disease mechanisms into targeted treatments.

Research profile

Default image

Knox Lab

Renatta Knox, MD, PhD

Focused on inherited neuromuscular disorders, including facioscapulohumeral muscular dystrophy and congenital myopathies, aiming to develop targeted therapies through molecular and translational research.

Research profile

Default image

Ly Lab

Cindy Ly, MD, PhD

Investigates the molecular mechanisms of amyotrophic lateral sclerosis and related neuromuscular disorders, aiming to translate genetic discoveries into targeted therapies.

Research profile

Default image

Weihl Lab

Conrad Weihl, MD, PhD

Investigating how disruptions in protein quality control contribute to muscle and neurodegenerative diseases. Using biochemistry, cell culture, animal models and patient tissue, the lab studies conditions like inclusion body myopathy, Paget’s disease, frontotemporal dementia and limb-girdle muscular dystrophy to uncover mechanisms of protein aggregation and cellular degeneration. [weihllab.wustl.edu]

Research profile