Saba Montazaribarforoushi

Adelaide Medical School

Faculty of Health and Medical Sciences

Year	Citation
2025	Montazaribarforoushi, S., & Jolly, L. A. (2025). Genetic disruption of nonsense-mediated mRNA decay in neurodevelopmental disorders.. Curr Opin Genet Dev, 94, 102394. DOI
2022	Byrne, A. B., Brouillard, P., Sutton, D. L., Kazenwadel, J., Montazaribarforoushi, S., Secker, G. A., . . . Harvey, N. L. (2022). Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema. Science Translational Medicine, 14(634), eabm4869-1-eabm4869-15. DOI Scopus33 WoS7 Europe PMC20

Year	Citation
2023	Vikkula, M., Babic, M., Brautigan, P., Haan, E., White, M., Piltz, S., . . . Montazaribarforoushi, S. (2023). A new Smad4 mouse model mimicking Myhre Syndrome?. Poster session presented at the meeting of EUROPEAN JOURNAL OF HUMAN GENETICS. AUSTRIA, Vienna: SPRINGERNATURE.