Christodoulou, J. GENE DISCOVERY FOR ORPHAN DISEASES.
Armani, R, Archer, H, Clarke, A, Vasudevan, P, Zweier, C, Ho, G, Williamson, S, Cloosterman, D, Yang, N, Christodoulou, J. Transcription Factor 4 and Myocyte Enhancer Factor 2C mutations are not common causes of Rett syndrome.
American Journal of Medical Genetics Part A
Ho, G, Walter, JH, Christodoulou, J. Costeff optic atrophy syndrome: New clinical case and novel molecular findings.
Journal of Inherited Metabolic Disease
Schindeler, S, Ghosh-Jerath, S, Thompson, S, Rocca, A, Joy, P, Kemp, A, Rae, C, Green, K, Wilcken, B, Christodoulou, J. The effects of large neutral amino acid supplements in PKU: An MRS and neuropsychological study.
Molecular Genetics and Metabolism
Pelka, GJ, Watson, CM, Radziewic, T, Hayward, M, Lahooti, H, Christodoulou, J, Tam, PPL. Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice.