Urbanowicz A, Ciccone N, Girdler S, Leonard H, Downs J. Choice making in Rett syndrome: A descriptive study using video data. Disability and Rehabilitation. Forthcoming 2017.
Downs J, Leonard H, Wong K, Newton N, Hill K. Quantification of walking-based physical activity and sedentary time in individuals with Rett syndrome. Developmental Medicine & Child Neurology. Forthcoming 2017.
Urbanowicz A, Downs J, Girdler S, Ciccone N, Leonard H. An exploration of the use of eye gaze and gestures in females with Rett syndrome. Journal of Speech Language and Hearing Research. Forthcoming 2015.
Downs J, Leonard H. Longitudinal approaches to populations with childhood onset neurodevelopmental conditions: Australian experience with Rett syndrome. In: Ronen GM, Rosenbaum PL, editors. Life Quality Outcomes in Children and Young People with Neurological and Developmental Conditions: Concepts, Evidence and Practice. London: MacKeith Press; 2013.
Archer HL, Evans JC, Millar DS, Thompson PW, Kerr AM, Leonard H, Christodoulou J, Ravine D, Lazarou L, Grove L, Verity C, Whatley SD, Pitz DT, Sampson JR, Clarke AJ. NTNG1 mutations are a rare cause of Rett syndrome. American Journal of Medical Genetics Part A. 2006; 140A(7):691-694.
Leonard H, Fyfe S, Ellaway C. Possible link between skeletal and electrocardiographic abnormalities and autonomic dysfunction in Rett syndrome. In: Kerr AM, Engerström IW, editors. Rett Disorder and the developing Brain. Oxford: Oxford University Press; 2001. p. 265-267.
Gill HK, Cheadle JP, Maynard J, Fleming N, Kerr A, Leonard H, Thompson EM, Hanefeld F, Skjeldal O, Sampson J, Clarke A. MECP2 analysis in possible familial Rett syndrome. American Journal of Human Genetics. 2000; 67(4):706.