Boukhloufi, I., Baranello, G., Brusa, C., Scoto, M., Morgan, J. E., Hong, Y., . . . Zhou, H. (n.d.). Characterizing circulating endothelial cells in transgenic SMA mice. Presented at: The 3rd International Scientific Congress on Spinal Muscular Atrophy.

Morera, C., Kim, J., Paredes-Redondo, A., Nobles, M., Rybin, D., Moccia, R., . . . Lin, Y. -. Y. (2022). CRISPR-mediated correction of skeletal muscle Ca2+ handling in a novel DMD patient-derived pluripotent stem cell model. Neuromuscular Disorders. doi:10.1016/j.nmd.2022.10.007

Meng, J., Moore, M., Counsell, J., Muntoni, F., Popplewell, L., & Morgan, J. (2022). Optimized lentiviral vector for restoration of full-length dystrophin via a cell-mediated approach in a mouse model of Duchenne muscular dystrophy. Molecular Therapy: Methods & Clinical Development. doi:10.1016/j.omtm.2022.04.015

Morgan, J., & Muntoni, F. (2021). Changes in Myonuclear Number During Postnatal Growth – Implications for AAV Gene Therapy for Muscular Dystrophy. Journal of Neuromuscular Diseases. doi:10.3233/JND-210683

Betts, C. A., Jagannath, A., van Westering, T. L. E., Bowerman, M., Banerjee, S., Meng, J., . . . Wood, M. J. A. (2021). Dystrophin involvement in peripheral circadian SRF signalling. Life Science Alliance, 4 (10), e202101014. doi:10.26508/lsa.202101014

Betts, C., Jagannath, A., van Westering, T. L. E., Bowerman, M., Banerjee, S., Meng, J., . . . Wood, M. J. A. (2021). Dystrophin regulates peripheral circadian SRF signalling. doi:10.1101/2021.06.23.449492

Torelli, S., Scaglioni, D., Sardone, V., Ellis, M. J., Domingos, J., Jones, A., . . . Muntoni, F. (2021). High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients. Journal of Neuropathology & Experimental Neurology, nlab088. doi:10.1093/jnen/nlab088

Jaiswal, J. K., Nagaraju, K., & Morgan, J. (2021). Terence A Partridge: A career dedicated to pursuit of curiosity, mentorship, and secrets of skeletal muscle stem cells. Journal of neuromuscular diseases, 8 (s2), S173-S179. doi:10.3233/JND-219010

Scaglioni, D., Catapano, F., Ellis, M., Torelli, S., Chambers, D., Feng, L., . . . Muntoni, F. (2021). The administration of antisense oligonucleotide golodirsen reduces pathological regeneration in patients with Duchenne muscular dystrophy. Acta Neuropathol Commun, 9 (1), 7. doi:10.1186/s40478-020-01106-1

Spicer, C., Lu, C. H., Catapano, F., Scoto, M., Zaharieva, I., Malaspina, A., . . . Zhou, H. (2021). The altered expression of neurofilament in mouse models and patients with spinal muscular atrophy. Annals of Clinical and Translational Neurology. doi:10.1002/acn3.51336