McKenna, R., Rushe, T. M. & Woodcock, K. A (2017) Informing the structure of executive function in children: a 1 meta-analysis of functional neuroimaging data. Frontiers in Human Neuroscience, 11:154. doi: 10.3389/fnhum.2017.00154
Haig, E. L. & Woodcock, K. A. (2017). Rigidity in routines and the development of resistance to change in individuals with Prader-Willi syndrome. Journal of Intellectual Disability Research, 61(5), 488-500. doi: 10.1111/jir.12368
Bull, L. E., Oliver, C. & Woodcock, K. A. (2017) Signalling changes to individuals who show resistance to change can reduce challenging behaviour. Journal of Behavioral Therapy and Experimental Psychiatry (Epub 2016 Jun 22), 54, 58-70. doi: 10.1016/j.jbtep.2016.06.006
Bull, L. E., Oliver, C., Callaghan, E., & Woodcock, K. A. (2015). Increased exposure to rigid routines can lead to increased challenging behavior following changes to those routines. Journal of Autism and Developmental Disorders, 45(6), 1569-1578. doi:10.1007/s10803-014-2308-2
Bull, L. E., Oliver, C., Tunnicliffe, P. L., & Woodcock, K. A. (2015). An informant report behavior diary for measuring temper outbursts in an intervention setting. Journal of Developmental and Physical Disabilities, 27(4), 489-504. doi:10.1007/s10882-015-9429-1
Waite, J., Heald, M., Wilde, L., Woodcock, K., Welham, A., Adams, D. & Oliver, C. (2014). The importance of understanding the behavioural phenotypes of genetic syndromes associated with intellectual disability. Paediatrics and Child Health, 24(10), 468-472. doi:10.1016/j.paed.2014.05.002
Tunnicliffe, P. L., Woodcock, K. A., Bull, L.E, Penhallow, J. & Oliver, C. (2014). Temper outbursts in Prader-Willi syndrome: Causes, behavioural and emotional sequence and responses by carers. Journal of Intellectual Disability Research. 58, 134-150. doi: 10.1111/jir.12010
Liu, Y., Sheng, F., Woodcock, K. A. & Han, S. (2013). Oxytocin effects on neural correlates of self-referential processing. Biological Psychology, 94, 380-387. doi:10.1016/j.biopsycho.2013.08.003
Woodcock, K. A., Yu, D. Yi, L. & Han, S. (2013). The presence of a culturally similar or dissimilar social partner affects neural responses to emotional stimuli. Socioaffective Neuroscience and Psychology, 3, 20500. doi:10.3402/snp.v3i0.20500
Oliver, C., Adams, D.… & Woodcock, K. (2013) Causal models of clinically significant behaviours in Angelman, Cornelia de Lange, Prader-Willi and Smith-Magenis syndromes. International Review of Research in Developmental Disabilities, Challenging Behaviour, Elsevier, 44, 169-211. doi:10.1016/b978-0-12-401662-0.00006-3
Hoddell, J., Moss, J., Woodcock, K. & Oliver, C. (2011). Further refinement of the nature of the communication impairment in Cornelia de Lange syndrome. Advances in Mental Health and Intellectual Disabilities, 5(4), 15-25. doi:10.1108/20441281111165562
Sloneem, J., Oliver, C. Udwin, O. & Woodcock, K. A. (2011). Prevalence, phenomenology, aetiology and predictors of challenging behaviour in Smith-Magenis syndrome. Journal of Intellectual Disability Research, 55, 138-151. doi:10.1111/j.1365-2788.2010.01371.x
Woodcock, K. A., Oliver, C., & Humphreys, G, W. (2011). The relationship between specific cognitive impairment and behaviour in Prader-Willi syndrome. Journal of Intellectual Disability Research. 55, 152-171. doi:10.1111/j.1365-2788.2010.01368.x
Woodcock, K. A., Humphreys, G, W., Oliver, C. & Hansen, P. (2010). Neural correlates of task-switching in paternal 15q11-q13 deletion Prader-Willi syndrome. Brain Research, 1363, 128-142. doi:10.1016/j.brainres.2010.09.093
Burbidge, C., Oliver, C., Moss, J…& Woodcock, K. A. (2010). The association between repetitive behaviours, impulsivity and hyperactivity in people with intellectual disability. Journal of Intellectual Disability Research, 54, 1078-1092. doi: doi:10.1111/j.1365-2788.2011.01387.x
Woodcock, K. A., Oliver, C., & Humphreys, G, W. (2009). Hypothesis: A specific pathway can be identified between genetic characteristics and behaviour profiles in Prader-Willi syndrome via cognitive, environmental and physiological mechanisms. Journal of Intellectual Disability Research, 53, 493-500. doi:10.1111/j.1365-2788.2009.01167.x
Woodcock, K. A., Humphreys, G, W. & Oliver, C. (2009). Dorsal and ventral stream mediated visual processing in genetic subtypes of Prader-Willi syndrome. Neuropsychologia, 47, 2367-2373. doi:10.1016/j.neuropsychologia.2008.09.019
Woodcock, K. A., Oliver, C., & Humphreys, G, W. (2009). Task switching deficits and repetitive behaviour in genetic neurodevelopmental disorders: Data from children with Prader-Willi syndrome chromosome 15 q11-q13 deletion and boys with Fragile-X syndrome. Cognitive Neuropsychology, 26, 172-194. doi:10.1080/02643290802685921
Woodcock, K. A., Oliver, C., & Humphreys, G, W (2009). Associations between repetitive questioning, resistance to change, temper outbursts and anxiety in Prader-Willi and Fragile-X syndromes. Journal of Intellectual Disability Research, 53, 265-278. doi:10.1111/j.1365-2788.2008.01122.x
Oliver, C., Woodcock, K. A. & Humphreys, G. W. (2009). The relationship between components of the behavioural phenotype in Prader-Willi syndrome: Brief Report. Journal of Applied Research in Intellectual Disabilities, 22, 403-407. doi:10.1111/j.1468-3148.2008.00475.x
Woodcock, K. A., & Rose, J (2007). The relationship between the recognition of facial expressions and self-reported anger in people with intellectual disabilities. Journal of Applied Research in Intellectual Disabilities, 20, 279-284. doi:10.1111/j.1468-3148.2006.00326.x
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