J. Cotney

Generation of isogenic models of Angelman syndrome and Prader-Willi syndrome in CRISPR/Cas9-engineered human embryonic stem cells

Stormy J. Chamberlain, S. Chamberlain, Rachel B. Gilmore, 2023, bioRxiv.

Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes

S. Weinberg, M. Marazita, E. Leslie, 2023, Human Genetics.

Ube3a unsilencer for the potential treatment of Angelman syndrome

Rachel B. Gilmore, Hyeong-Min Lee, Benjamin D. Philpot, 2024, Nature communications.

Multimodal spatiotemporal transcriptomic resolution of embryonic palate osteogenesis

F. Faucz, Apratim Mitra, Caroline Esnault, 2023, Nature communications.

Identifying key underlying regulatory networks and predicting targets of orphan C/D box SNORD116 snoRNAs in Prader-Willi syndrome

Rachel B. Gilmore, Christopher E. Stoddard, Justin L. Cotney, 2023, bioRxiv.