Megan A. Waldrop

Gene Therapy for Spinal Muscular Atrophy: Safety and Early Outcomes

Megan A. Waldrop, Cassandra Karingada, Mike A. Storey et al. · PEDIATRICS · 2020 · 127 citations

Expression of Neurexin, Neuroligin, and Their Cytoplasmic Binding Partners in the Pancreatic β-Cells and the Involvement of Neuroligin in Insulin Secretion

Arthur T. Suckow, Davide Comoletti, Megan A. Waldrop et al. · Endocrinology · 2008 · 77 citations · Full text

Synapse Formation, Synapse-inducing Adhesion Molecules, Synaptic Transmission +22

Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy

Megan A. Waldrop, Steven A. Moore, Katherine D. Mathews et al. · Human Mutation · 2022 · 47 citations · Full text

Diagnostic Utility of Whole Exome Sequencing in the Neuromuscular Clinic

Matthew Pastore, Rachel Schrader, Emily Sites et al. · Neuropediatrics · 2019 · 40 citations

Variants in MED12L, encoding a subunit of the mediator kinase module, are responsible for intellectual disability associated with transcriptional defect

Mathilde Nizon, Vincent Laugel, Kevin M. Flanigan et al. · Genetics in Medicine · 2019 · 40 citations · Full text

Transcriptional Regulation, Mendelian Disorder, Mediator Kinase Module +9