Ronald J. Trent
Affiliations: | University of Sydney, Camperdown, New South Wales, Australia |
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| Fukuda Y, Cheong PL, Lynch J, et al. (2016) The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6. Nature Communications. 7: 12353 |
| Yu B, O'Toole SA, Trent RJ. (2015) Somatic DNA mutation analysis in targeted therapy of solid tumours. Translational Pediatrics. 4: 125-38 |
| Hinchcliffe M, Le H, Fimmel A, et al. (2014) Diagnostic validation of a familial hypercholesterolaemia cohort provides a model for using targeted next generation DNA sequencing in the clinical setting. Pathology. 46: 60-8 |
| Pamphlett R, Cheong PL, Trent RJ, et al. (2013) Can ALS-Associated C9orf72 Repeat Expansions Be Diagnosed on a Blood DNA Test Alone? Plos One. 8 |
| Ramos EM, Latourelle JC, Gillis T, et al. (2013) Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset. Neurogenetics. 14: 173-9 |
| Cooper C, Selinger C, Ng CC, et al. (2013) 6. Patterns of somatic mutations in nine cases of metaplastic carcinoma of the breast Pathology. 45 |
| Cheong PL, Yu B, Bojovic J, et al. (2013) Hepatic complications of erythropoietic protoporphyria Pathology. 45 |
| Ramos EM, Latourelle JC, Lee JH, et al. (2012) Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset. Human Genetics. 131: 1833-40 |
| Lee JH, Lee JM, Ramos EM, et al. (2012) TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. Biochemical and Biophysical Research Communications. 424: 404-8 |
| Lee JM, Gillis T, Mysore JS, et al. (2012) Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics. 90: 434-44 |