Contact Details
University Links
- Position
- PhD student
- Department
- Department of Paediatrics and Child Health (Dunedin)
- Qualifications
- BMedSc(Hons), MBChB (Otago)
- Research summary
- Genetics of non-syndromic biliary atresia
Publications
Fukushima, K., Avery, N., Desjardins, J., Halliday, B. J., Jenkins, Z. A., Porteous, R., Morgan, T., Parthasarathy, P., Lau, M., Vincent, M. W., … Robertson, S. P. (2026). Impaired retinoic acid receptor-γ signaling underlies a heritable form of urothelial keratinizing squamous metaplasia. Human Genetics & Genomic Advances, 7(2), 100590. doi: 10.1016/j.xhgg.2026.100590 Journal - Research Other
Avery, N., Fukushima, K., Guan, G., Praganta, J., Rich, A., Vincent, M., & Robertson, S. (2024). Familial aggregation of keratinising desquamative squamous metaplasia in the urinary tract. BJU International, 133(Suppl. 3), 15-17. doi: 10.1111/bju.16160 Journal - Research Article
Fukushima, K., Parthasarathy, P., Wade, E. M., Morgan, T., Gowrishankar, K., Markie, D. M., & Robertson, S. P. (2021). Intragenic deletions in FLNB are part of the mutational spectrum causing spondylocarpotarsal synostosis syndrome. Genes, 12(4), 528. doi: 10.3390/genes12040528 Journal - Research Other