Theresa V. Strong

The paper introduces PCAN, a resource integrating high-throughput phenotyping of mouse models for Prader-Willi syndrome to evaluate phenotypes and therapeutic strategies.

This study analyzes hospitalization outcomes for COVID-19 in patients with Prader-Willi syndrome compared to those without, finding increased severity and costs.

This study generates and characterizes a rat model with a truncating Magel2 mutation, revealing altered behavioral and physiological traits consistent with human neurodevelopmental disorders.