2009

• Vandebona, H., Mitchell, P., Manwaring, N., Griffiths, K., Gopinath, B., Wang, J., Sue, C. Prevalence of mitochondrial 1555A-->G mutation in adults of European descent. The New England Journal of Medicine. 2009. p. 642-644. [Abstract]
• Mehta, P., Mellick, G., Rowe, D., Halliday, G., Jones, M., Manwaring, N., Vandebona, H., Silburn, P., Wang, J., Mitchell, P., Sue, C. Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community. Movement disorders : official journal of the Movement Disorder Society. 2009; 24:290-2. [Abstract]

2008

• Manwaring, N., Wang, J., Mitchell, P., Sue, C. Mitochondrial DNA disease prevalence: Still underrecognized?. Annals of neurology. 2008; 64:471; author reply 471-2. [Abstract]
• Grünewald, A., Djarmati, A., Lohmann-Hedrich, K., Farrell, K., Zeller, J., Allert, N., Papengut, F., Petersen, B., Fung, V., Sue, C., O'Sullivan, D., Mahant, N., Kupsch, A., Chuang, R., Wiegers, K., Pawlack, H., Hagenah, J., Ozelius, L., Stephani, U., Schuit, R., Lang, A., Volkmann, J., Münchau, A., Klein, C. Myoclonus-dystonia: significance of large SGCE deletions. Human mutation. 2008; 29:331-332. [Abstract]

2007

• Mehta, P., Kifley, A., Wang, J., Rochtchina, E., Mitchell, P., Sue, C. Population prevalence and incidence of Parkinson's disease in an Australian community. Internal medicine journal. 2007; 37:812-4. [Abstract]
• Manwaring, N., Jones, M., Wang, J., Rochtchina, E., Howard, C., Newall, P., Mitchell, P., Sue, C. Mitochondrial DNA haplogroups and age-related hearing loss. Archives of otolaryngology--head & neck surgery. 2007; 133:929-933. [Abstract]
• Jones, M., Manwaring, N., Wang, J., Rochtchina, E., Mitchell, P., Sue, C. Mitochondrial DNA haplogroups and age-related maculopathy. Archives of ophthalmology. 2007; 125:1235-1240. [Abstract]
• Huang, Y., Halliday, G., Vandebona, H., Mellick, G., Mastaglia, F., Stevens, J., Kwok, J., Garlepp, M., Silburn, P., Horne, M., Kotschet, K., Venn, A., Rowe, D., Rubio, J., Sue, C. Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society. 2007; 22:982-989. [Abstract]
• Manwaring, N., Jones, M., Wang, J., Rochtchina, E., Howard, C., Mitchell, P., Sue, C. Population prevalence of the MELAS A3243G mutation. Mitochondrion. 2007; 7:230-233. [Abstract]
• Sutherland, G., Mellick, G., Sue, C., Chan, D., Rowe, D., Silburn, P., Halliday, G. A functional polymorphism in the parkin gene promoter affects the age of onset of Parkinson's disease. Neuroscience letters. 2007; 414:170-173. [Abstract]
• Trenell, M., Sue, C., Thompson, C., Kemp, G. Supplemental oxygen and muscle metabolism in mitochondrial myopathy patients. European journal of applied physiology. 2007; 99:541-547. [Abstract]

2006

• Manwaring, N., Jones, M., Wang, J., Rochtchina, E., Mitchell, P., Sue, C. Prevalence of mitochondrial DNA haplogroups in an Australian population. Internal medicine journal. 2006; 36:530-3. [Abstract]
• Trenell, M., Thompson, C., Sue, C. Exercise and myotonic dystrophy: A P-31 magnetic resonance spectroscopy and magnetic resonance imaging case study. Annals of Neurology. 2006; 59:871-872. [Abstract]
• Trenell, M., Sue, C., Kemp, G., Sachinwalla, T., Thompson, C. Aerobic exercise and muscle metabolism in patients with mitochondrial myopathy. Muscle & nerve. 2006; 33:524-31. [Abstract]
• Trenell, M., Sue, C., Kemp, G., Sachinwalla, T., Thompson, C. Aerobic exercise and muscle metabolism in patients with mitochondrial myopathy. Muscle & Nerve. 2006; 33:524-531. [Abstract]
• Trenell, M., Rooney, K., Sue, C., Thompson, C. Compression garments and recovery from eccentric exercise: A P-31-MRS study. Journal of Sports Science and Medicine. 2006; 5:106-114. [Abstract]
• Shepherd, R., Checcarelli, N., Naini, A., De Vivo, D., DiMauro, S., Sue, C. Measurement of ATP production in mitochondrial disorders. Journal of inherited metabolic disease. 2006; 29:86-91. [Abstract]

2004

• Jones, M., Mitchell, P., Wang, J., Sue, C. MELAS A3243G mitochondrial DNA mutation and age related maculopathy. American journal of ophthalmology. 2004; 138:1051-3. [Abstract]