Publications

Book chapters

2017

Hocking, D.R. (2017). Williams syndrome. In N.J. Rinehart, J.L. Bradshaw, & P.G. Enticott (Eds.), Developmental Disorders of the Brain. Psychology Press, New York: Taylor Francis Group.

Hocking, D.R. (2017). Cerebellar-frontal-parietal axis in developmental disorders. In N.J. Rinehart, J.L. Bradshaw, & P.G. Enticott (Eds.), Developmental Disorders of the Brain. Psychology Press, New York: Taylor Francis Group.

Refereed journal articles

*Note the first two authors shared first authorship and contributed equally to this work.

Vivanti, G., Fanning, P.A.J., Hocking, D.R., Sievers, S., & Dissanayake, C. (accepted 14/3/17). Social attention, joint attention and sustained attention in Autism Spectrum Disorder and Williams syndrome: Convergences and divergences. Journal of Autism and Developmental Disorders.

Fanning, P.A.J., Hocking, D.R., Dissanayake, C., Vivanti, G. (2017). Delineation of a spatial working memory profile using a non-verbal eye tracking paradigm in young children with autism and Williams syndrome. Child Neuropsychology, DOI: 10.1080/09297049.2017.1284776.

Vivanti, G., Hocking, D.R., Fanning, P., Uljarevic, M., Postorino, V., Mazzone, L., Dissanayake, C. (2017). Attention to novelty versus repetition: contrasting habituation profiles in autism and Williams syndrome. Developmental Cognitive Neuroscience, DOI: 10.1016/j.dcn.2017.01.006.

Vivanti, G., Hocking, D.R., Fanning, P.A.J, Dissanayake, C. (2017). The social nature of overimitation: Insights from autism and Williams syndrome. Cognition, 161, 10-18.

Hocking, D.R., Birch, R.C., Bui, Q.M., Menant, J.C., Lord, S.R., Georgiou-Karistianis, N., Godler, D.E., Wen, W., Hackett, A., Rogers, C., Trollor, J.N. (2017). Cerebellar volume mediates the relationship between FMR1 mRNA levels and voluntary step initiation in males with the premutation. Neurobiology of Aging, 50, 5-12.

Birch, R.C., Hocking, D.R., Cornish, K.M., Menant, J.C., Lord, S.R., Georgiou-Karistianis, N., Godler, D.E., Wen, W., Rogers, C., Trollor, J.N. (2017). Selective subcortical contributions to gait impairments in males with the FMR1 premutation. Journal of Neurology, Neurosurgery, and Psychiatry, 88(2), 188-190.

2016

Vivanti, G., Hocking, D.R., Fanning, P., Dissanayake, C. (2016). Verbal labels increase the salience of novel objects for preschoolers with typical development and Williams syndrome, but not in autism. Journal of Neurodevelopmental Disorders, 8:46, doi: 10.1186/s11689-016-9180-7.

Vivanti, G., Hocking, D.R., Fanning, P., Dissanayake, C. (2016). Social affiliation motives modulate spontaneous learning in Williams syndrome but not autism. Molecular Autism, 7;40, doi: 10.1186/s13229-016-0101-0.

Birch, R.C., Hocking, D.R., & Trollor, J.N. (2016). Prevalence and predictors of subjective memory complaints in adult male carriers of the FMR1 premutation. The Clinical Neuropsychologist, 30(6), 834-48.

2015

Hocking, D.R. Reeve, J., & Porter, M.A. (2015). Characterising the profile of everyday executive functioning and relation to IQ in adults with Williams syndrome. PLoS One, 10(9):e0137628.

Birch, R.C., Hocking, D.R., Cornish, K.M., Menant, J.C., Georgiou-Karistianis, N., Godler, D.E., Wen, W., Hackett, A., Rogers, C., Trollor, J.N. (2015). Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males. Genes, Brain and Behavior, 14(3), 251-259.

Hocking, D.R., Kraan, C.M., Godler, D.E., Bui, Q.M., Li X., Bradshaw, J.L., Georgiou-Karistianis, N., Melcalfe, S.A., Archibald, A.D., Turbitt, E., Fielding, J., Trollor, J., Cohen, J., Cornish, K.M. (2015). Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation. Neurobiology of Aging, 36(3), 1400-1408.

Cornish, K.M., Kraan, C.M., Bui, Q.M., Bellgrove, M.A., Metcalfe, S.A., Trollor, T., Hocking, D.R., Slater, H.R., Inaba, Y., Li X., Archibald, A.D., Turbitt, E., Cohen, J., Godler, D.E. (2015). Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation females. Neurology, 84(16), 1631-1638.

2014

Kraan, C., Hocking, D.R., Georgiou-Karistianis, N., Metcalfe, S., Archibald, A., Fielding, J., Trollor, J., Bradshaw, J.L., Cohen, J., Cornish, K.M. (2014). Impaired response inhibition is associated with self-reported symptoms of depression, anxiety and ADHD in female FMR1 premutation carriers. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 165B(1), 41-51.

*Milne, S., *Hocking, D.R., Murphy, A., Georgiou-Karistianis, N., Delatycki, M., Corben, L.A. (2014) Sensitivity of spatiotemporal gait parameters in measuring disease severity in Friedreich ataxia. Cerebellum, 13(6), 677-688.

Birch, R.C., Cornish, K.M., Hocking, D.R., Trollor, J.N. (2014). Understanding the neuropsychiatric phenotype of fragile X-associated tremor ataxia syndrome: A systematic review.Neuropsychology Review, 24(4), 491-513.

Hocking, D.R., Corben, L.A., Fielding, J., Cremer, P.D., Millist, L., White, O.B., Delatycki, M.B. (2014). Saccade repogramming in Friedreich ataxia reveals impairments in the cognitive control of saccadic eye movement. Brain and Cognition, 87, 161-167.

*Kraan, C., *Hocking, D.R., Bradshaw, J.L., Georgiou-Karistianis, N., Metcalfe, S., Archibald, A., Fielding, J., Trollor, J., Cohen, J., Cornish, K.M. (2014). Age and CGG-repeat length are associated with neuromotor impairments in at-risk females with the FMR1 premutation. Neurobiology of Aging, 35(9), 2179 e7-13.

Kraan, C., Hocking, D.R.,  Bradshaw, J.L., Georgiou-Karistianis, N., Metcalfe, S., Archibald, A., Fielding, J., Trollor, J., Cohen, J., Cornish, K.M. (2014). Symbolic sequence learning is associated with cognitive-affective profiles in female FMR1 premutation carriers. Genes, Brain and Behavior, 13(4), 385-393.

Grigsby, J., Cornish, K., Hocking, D., Kraan, C., Olichney, J.M., Rivera, S.M., Schneider, A., Sherman, S., Wang, J.Y., Yang, J-C. (2014). The cognitive neuropsychological phenotype of carriers of the FMR1 premutation. Journal of Neurodevelopmental Disorders, 6(1), 28.

Shelton, A., Cornish, K., Kraan, C., Georgiou-Karistianis, N., Metcalfe, S., Bradshaw J., Hocking, D.R., Archibald, A., Cohen, J., Trollor, J., Fielding, J. (2014), Exploring inhibitory deficits in female premutation carriers of fragile X syndrome through eye movements. Brain and Cognition, 85, 201-208.

Hocking, D.R., Menant, J.C. Kirk, H.E., Lord, S., Porter, M.A. (2014). Gait profiles as indicators of domain-specific impairments in executive control across neurodevelopmental disorders. Research in Developmental Disabilities, 35(1), 203-14.

Riby, D.M., Hanley, M., Kirk, H., Clark, F., Little, K., Fleck, R., Janes, E., Kelso, L., O'Kane, F., Cole-Fletcher, R., Allday, M.H., Hocking, D., Cornish, K., Rodgers, J. (2014). The Interplay Between Anxiety and Social Functioning in Williams Syndrome. Journal of Autism and Developmental Disorders, 44(5), 1220-1229.

Ternes, A-M., Fielding, J., Corben. L., White. O., Bradshaw, J.L., Hocking. D., Georgiou-Karistianis, N. (2014). Analysis of planning and online control of movement in Multiple Sclerosis using a Fitts' law reciprocal aiming paradigm. Cognitive and Behavioral Neurology, 27(3), 139-47.

Kraan, C., Hocking, D.R., Georgiou-Karistianis, N., Metcalfe, S., Archibald, A., Fielding, J., Trollor, J., Bradshaw, J.L., Cohen, J., Cornish, K.M. (2014). Impaired response inhibition is associated with self-reported symptoms of depression, anxiety and ADHD in female FMR1 premutation carriers. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 165(1), 41-51.

2013

Kirk, H.E., Hocking, D.R., Riby, D., & Cornish, K.M. (2013). Linking Social Behaviour and Anxiety to Attention to Emotional Faces in Williams syndrome. Research in Developmental Disabilities, 34, 4608-4616.

Kraan, C., Hocking, D.R., Georgiou-Karistianis, N., Metcalfe, S., Archibald, A., Fielding, J., Trollor, J., Bradshaw, J.L., Cohen, J., Cornish, K.M.  (2013) Cognitive-motor interference during postural control indicates at-risk cerebellar profiles in females with the FMR1 premutation. Behavioural Brain Research, 253, 329-336.

Hocking, D.R., Thomas, D., Menant, J., Porter, M.A., Smith, S., Lord, S., Cornish, K.M. (2013). The interplay between executive control and motor functioning in Williams syndrome.Developmental Science, 16(3), 428-442.

Kraan, C.M., Hocking, D.R., Bradshaw, J.L., Fielding, J., Cohen, J., Georgiou-Karistianis, N., & Cornish, K.M. (2013). Neurobehavioral evidence for the involvement of theFMR1gene in female carriers of fragile X syndrome. Neuroscience and Biobehavioral Reviews, 37(3), 522-547.

2011 - 2012

Hocking, D.R., Kogan, C.S., & Cornish, K.M. (2012). Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation. Brain and Cognition, 79(1), 39-44.

Hocking, D.R., Rinehart, N.J., McGinley, J.L., Galna, B., Moss, S.A., & Bradshaw, J.L. (2011). Gait adaptation during obstacle crossing reveals impairments in the visual control of locomotion in Williams syndrome. Neuroscience, 197, 320-329.

Cornish, K.M., Savage, R., Hocking, D.R., Hollis, C.P. (2011). Association of the DAT1 genotype with inattentive behaviour is mediated by reading ability in a general population sample. Brain and Cognition, 77(3), 453-458.

Corben, L.A., Georgiou-Karistianis, N., Bradshaw, J.L., Hocking, D.R., Churchyard, A.J., Delatycki, M.B. (2011). The Fitts task reveals impairments in planning and online control of movement in Friedreich ataxia: reduced cerebellar-cortico-connectivity? Neuroscience, 192, 382-90.

*Cornish, K.M., *Hocking, D.R., Moss, S.A., & Kogan, C.S. (2011). Selective executive markers of at-risk profiles associated with the fragile X premutation. Neurology, 77, 618-622.

Hocking, D.R., Rinehart, N.J., McGinley, J.L., Moss, S.A., & Bradshaw, J.L. (2011). A kinematic analysis of visually-guided movement in Williams syndrome. Journal of the Neurological Sciences, 301, 51-58.

2008 - 2010

Hocking, D.R., Fielding, J., Corben, L.A., Cremer, P.D., Millist, L., White, O.B., & Delatycki, M.B. (2010). Ocular motor fixation deficits in Friedreich ataxia. Cerebellum, 9(3), 411-418.

Hocking, D.R., McGinley, J.L., Moss, S.A., & Bradshaw, J.L. (2010) Effects of external and internal cues on gait function in Williams syndrome. Journal of the Neurological Sciences, 291(1-2), 57-63.

Hocking, D.R., Rinehart, N.J., McGinley, J.L., & Bradshaw, J.L. (2009). Gait function in adults with Williams syndrome. Experimental Brain Research, 192(4), 695-702.

Hocking, D.R., Bradshaw, J.L., & Rinehart, N.J. (2008). Fronto-parietal and cerebellar contributions to motor dysfunction in Williams syndrome: A review and future directions.Neuroscience and Biobehavioral Reviews, 32(3),497-507.