C. Wulf

Epidemiological evidence for a hereditary contribution to myasthenia gravis: a retrospective cohort study of patients from North America

A. Pestronk, B. Traynor, M. Benatar, 2020, BMJ Open.

A genome-wide association study of myasthenia gravis.

Michael Benatar, Sonja W. Scholz, Adriano Chiò, 2015, JAMA neurology.

Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network

J. Miller, J. Mendell, A. Nicorici, 2013, Neuromuscular Disorders.

Development of a model‐based clinical trial simulation platform to optimize the design of clinical trials for Duchenne muscular dystrophy

A. Pestronk, A. Nicorici, J. Florence, 2021, CPT: pharmacometrics & systems pharmacology.

AGenome-Wide Association Study ofMyasthenia Gravis

Sonja W. Scholz, Hannah A. Pliner, Janel O. Johnson, 2015 .

A genome-wide association study of myasthenia gravis.

Sonja W. Scholz, Hannah A. Pliner, Janel O. Johnson, 2015, JAMA neurology.