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. Current Opinion in Genetics and Development, 94, 11 pages. 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 Scopus38 WoS29 Europe PMC28

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.