Barbara Voraberger

Bi-allelic mutation in SEC16B alters collagen trafficking and increases ER stress
El-Gazzar, A., Voraberger, B., Rauch, F., Mairhofer, M., Schmidt, K., Guillemyn, B., Mitulović, G., Reiterer, V., Haun, M., Mayr, M. M., Mayr, J. A., Kimeswenger, S., Drews, O., Saraff, V., Shaw, N., Fratzl-Zelman, N., Symoens, S., Farhan, H. & Högler, W., 11 Apr 2023, In: EMBO Molecular Medicine. 15, 4, 20 p., e16834.
Research output: Contribution to journal › Article › peer-review

Open Access
Investigating the role of ASCC1 in the causation of bone fragility
Voraberger, B., Mayr, J. A., Fratzl-Zelman, N., Blouin, S., Uday, S., Kopajtich, R., Koedam, M., Hödlmayr, H., Csillag, B., Högler, W. & et al., Jun 2023, In: Frontiers in Endocrinology. 14, 15 p., 1137573.
Research output: Contribution to journal › Article › peer-review

Open Access
A novel cryptic splice site mutation in COL1A2 as a cause of osteogenesis imperfecta
El-Gazzar, A., Mayr, J. A., Voraberger, B., Brugger, K., Blouin, S., Tischlinger, K., Duba, H.-C., Prokisch, H., Fratzl-Zelman, N. & Högler, W., 2021, In: Bone Reports. 7 p., 101110.
Research output: Contribution to journal › Article › peer-review

Novel gene mutations in children with Osteogenesis imperfecta
El-Gazzar, A. (Researcher), Högler, W. (Researcher) & Voraberger, B. (PI)
30.09.2021 → 30.09.2022
Project: Other › PhD thesis project

Investigating the effect of a novel ASCC1 deletion mutation on human bone fragility
Voraberger, B. (Speaker), Schaberl, H. (Speaker), Fratzl-Zelman, N. (Speaker), Mayr, J. A. (Speaker), Wortmann, S. B. (Speaker), Csillag, B. (Speaker), Kopajtich, R. (Speaker), Prokisch, H. (Speaker), El-Gazzar, A. (Speaker) & Högler, W. (Speaker)
05 Jul 2022
Activity: Talk or presentation › Poster presentation › science-to-science

Research output