Ms Saba Montazaribarforoushi
NHMRC Grant-Funded Researcher A
School of Medicine
College of Health
| Year | Citation |
|---|---|
| 2026 | Nawaz, U., Nicolas-Martinez, E., Montazaribarforoushi, S., Carroll, R., Voineagu, I., Gecz, J., & Jolly, L. A. (2026). UPF3A and UPF3B shape the transcriptome cooperatively yet oppose cell function.. Journal of molecular biology, 169918. |
| 2025 | Montazaribarforoushi, S., & Jolly, L. A. (2025). Genetic disruption of nonsense-mediated mRNA decay in neurodevelopmental disorders. Current Opinion in Genetics and Development, 94, 102394-1-102394-11. Scopus2 WoS2 Europe PMC1 |
| 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. Scopus44 WoS36 Europe PMC37 |
| Year | Citation |
|---|---|
| 2025 | Tan, N. B., Jolly, L., Nawaz, U., Zhao, S. F., Gyurkovska, V., Silk, M., . . . White, S. M. (2025). UPF1 variants cause syndromic intellectual disability with a transcriptome profile convergent with fragile X syndrome (Award Candidate). Poster session presented at the meeting of Abstracts from the 58th European Society of Human Genetics (ESHG) Conference as published in European Journal of Human Genetics. United Kingdom: Nature Publishing Group. |
| 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. |
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