D. Hocking

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The Fitts task reveals impairments in planning and online control of movement in Friedreich ataxia: reduced cerebellar-cortico connectivity?

J. Bradshaw, L. Corben, N. Georgiou-Karistianis, 2011, Neuroscience.

Fragile X-associated tremor ataxia syndrome

J. Trollor, D. Hocking, Rachael C. Cvejic, 2019, Degenerative Disorders of the Brain.

Gait function in adults with Williams syndrome

John L. Bradshaw, Jennifer L. McGinley, N. Rinehart, 2009, Experimental Brain Research.

Cognitive-motor interference during postural control indicates at-risk cerebellar profiles in females with the FMR1 premutation

Jonathan Cohen, John L. Bradshaw, Nellie Georgiou-Karistianis, 2013, Behavioural Brain Research.

Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation

K. Cornish, C. Kogan, D. Hocking, 2012, Brain and Cognition.

Motor functioning in developmental psychopathology: A review of autism as an example context.

K. Hudry, D. Hocking, Lacey Chetcuti, 2020, Research in developmental disabilities.

Movement Planning and Online Control in Multiple Sclerosis: Assessment Using a Fitts Law Reciprocal Aiming Task

J. Bradshaw, L. Corben, N. Georgiou-Karistianis, 2014, Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology.

Evidence for Training-Dependent Structural Neuroplasticity in Brain-Injured Patients: A Critical Review

Derek K. Jones, G. Egan, A. Leemans, 2018, Neurorehabilitation and neural repair.

The development of the size-weight illusion in children coincides with the development of nonverbal cognition rather than motor skills.

Elizabeth J. Saccone, Philippe A. Chouinard, Elizabeth J Saccone, 2019, Journal of experimental child psychology.

Fronto-parietal and cerebellar contributions to motor dysfunction in Williams syndrome: A review and future directions

N. Rinehart, J. Bradshaw, D. Hocking, 2008, Neuroscience & Biobehavioral Reviews.

Symbolic sequence learning is associated with cognitive–affective profiles in female FMR1 premutation carriers

J. Bradshaw, J. Trollor, N. Georgiou-Karistianis, 2014, Genes, brain, and behavior.

Saccade reprogramming in Friedreich ataxia reveals impairments in the cognitive control of saccadic eye movement

L. Corben, M. Delatycki, J. Fielding, 2014, Brain and Cognition.

Gait adaptation during obstacle crossing reveals impairments in the visual control of locomotion in Williams syndrome

B. Galna, N. Rinehart, J. Bradshaw, 2011, Neuroscience.

Gait profiles as indicators of domain-specific impairments in executive control across neurodevelopmental disorders.

S. Lord, M. Porter, J. Menant, 2014, Research in developmental disabilities.

Cerebellar volume mediates the relationship between FMR1 mRNA levels and voluntary step initiation in males with the premutation

S. Lord, J. Trollor, W. Wen, 2017, Neurobiology of Aging.

Graduate-entry medical students: older and wiser but not less distressed

Susan J. Thomas, D. Hocking, A. Kemp-Casey, 2016, Australasian psychiatry : bulletin of Royal Australian and New Zealand College of Psychiatrists.

Reduced Motor Interference in Preschoolers with Autism Spectrum Disorder and Williams Syndrome

C. Dissanayake, G. Vivanti, D. Hocking, 2018, Developmental neuropsychology.

Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women

M. Bellgrove, J. Trollor, Q. Bui, 2015, Neurology.

A 12‐week exercise programme has a positive effect on everyday executive function in young people with Down syndrome: a pilot non‐randomised controlled trial

N. Shields, D. Hocking, L. Prendergast, 2022, Journal of intellectual disability research : JIDR.

Assessing IQ in adolescents with mild to moderate cerebral palsy using the WISC-V

Hisham M. Abu-Rayya, D. Reddihough, H. Abu-Rayya, 2021, The Clinical neuropsychologist.

Ten‐year follow‐up study found that motor‐free intelligence quotient declined in children with mild‐to‐moderate cerebral palsy

Hisham M. Abu-Rayya, D. Reddihough, H. Abu-Rayya, 2022, Acta paediatrica.

Relationships of Motor Changes with Cognitive and Neuropsychiatric Features in FMR1 Male Carriers Affected with Fragile X-Associated Tremor/Ataxia Syndrome

D. Loesch, E. Storey, F. Tassone, 2022, Brain sciences.

Brief Report: The Impact of Sensory Hypersensitivity and Intolerance of Uncertainty on Anxiety in Williams Syndrome

I. Labuschagne, D. Hocking, M. Uljarević, 2018, Journal of Autism and Developmental Disorders.

The Interplay Between Anxiety and Social Functioning in Williams Syndrome

D. Riby, K. Cornish, D. Hocking, 2013, Journal of Autism and Developmental Disorders.

Understanding the Neuropsychiatric Phenotype of Fragile X-Associated Tremor Ataxia Syndrome: a Systematic Review

J. Trollor, K. Cornish, D. Hocking, 2014, Neuropsychology Review.

Social Attention, Joint Attention and Sustained Attention in Autism Spectrum Disorder and Williams Syndrome: Convergences and Divergences

C. Dissanayake, G. Vivanti, D. Hocking, 2017, Journal of Autism and Developmental Disorders.

Verbal labels increase the salience of novel objects for preschoolers with typical development and Williams syndrome, but not in autism

C. Dissanayake, G. Vivanti, D. Hocking, 2016, Journal of Neurodevelopmental Disorders.

Delineating the Relationships Between Motor, Cognitive-Executive and Psychiatric Symptoms in Female FMR1 Premutation Carriers

D. Loesch, E. Storey, F. Tassone, 2021, Frontiers in Psychiatry.

Total and Regional White Matter Lesions Are Correlated With Motor and Cognitive Impairments in Carriers of the FMR1 Premutation

D. Loesch, E. Storey, F. Tassone, 2019, Front. Neurol..

Delineation of a spatial working memory profile using a non-verbal eye-tracking paradigm in young children with autism and Williams syndrome

C. Dissanayake, G. Vivanti, D. Hocking, 2018, Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.

Brief Report: The Impact of Sensory Hypersensitivity and Intolerance of Uncertainty on Anxiety in Williams Syndrome

I. Labuschagne, D. Hocking, M. Uljarević, 2018, Journal of autism and developmental disorders.

Shared and syndrome-specific adaptive difficulties in preschoolers with Williams syndrome and autism spectrum disorder: a cross-syndrome study.

N. Lee, G. Vivanti, D. Hocking, 2019, Journal of intellectual disability research : JIDR.

A kinematic analysis of visually-guided movement in Williams syndrome

Simon A. Moss, John L. Bradshaw, Jennifer L. McGinley, 2011, Journal of the Neurological Sciences.

Effects of external and internal cues on gait function in Williams syndrome

N. Rinehart, J. Bradshaw, S. Moss, 2010, Journal of the Neurological Sciences.

Intranasal oxytocin, social cognition and neurodevelopmental disorders: A meta-analysis

S. Crowe, D. Hocking, B. Keech, 2018, Psychoneuroendocrinology.

Ocular Motor Fixation Deficits in Friedreich Ataxia

L. Corben, M. Delatycki, J. Fielding, 2010, The Cerebellum.

Delineating Visual Habituation Profiles in Preschoolers with Neurofibromatosis Type 1 and Autism Spectrum Disorder: A Cross-Syndrome Study

Hayley Darke, K. North, G. Vivanti, 2023, Journal of autism and developmental disorders.

Functional play in young children with autism and Williams syndrome: A cross-syndrome comparison

C. Dissanayake, G. Vivanti, Laura Sparaci, 2020, Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.

Social affiliation motives modulate spontaneous learning in Williams syndrome but not in autism

C. Dissanayake, G. Vivanti, D. Hocking, 2016, Molecular Autism.

Social Attention, Joint Attention and Sustained Attention in Autism Spectrum Disorder and Williams Syndrome: Convergences and Divergences

C. Dissanayake, G. Vivanti, D. Hocking, 2017, Journal of Autism and Developmental Disorders.

Impaired response inhibition is associated with self‐reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers

J. Bradshaw, J. Trollor, N. Georgiou-Karistianis, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The cognitive neuropsychological phenotype of carriers of the FMR1 premutation

S. Rivera, J. Olichney, Jin-Chen Yang, 2014, Journal of Neurodevelopmental Disorders.

Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndrome

J. Bradshaw, N. Georgiou-Karistianis, J. Fielding, 2013, Neuroscience & Biobehavioral Reviews.

Attention to novelty versus repetition: Contrasting habituation profiles in Autism and Williams syndrome

Giacomo Vivanti, C. Dissanayake, G. Vivanti, 2017, Developmental Cognitive Neuroscience.

WISC-V motor-free cognitive profile and predictive factors in adolescents with cerebral palsy.

Hisham M. Abu-Rayya, D. Reddihough, H. Abu-Rayya, 2021, Research in developmental disabilities.

Feasibility of a virtual reality-based exercise intervention and low-cost motion tracking method for estimation of motor proficiency in youth with autism spectrum disorder

R. Lenroot, H. Abu-Rayya, S. Kachnowski, 2022, Journal of neuroengineering and rehabilitation.

Do Active Video Games Improve Motor Function in People With Developmental Disabilities? A Meta-analysis of Randomized Controlled Trials.

K. Caeyenberghs, N. Shields, D. Hocking, 2019, Archives of physical medicine and rehabilitation.

Association of the DAT1 genotype with inattentive behavior is mediated by reading ability in a general population sample

C. Hollis, K. Cornish, R. Savage, 2011, Brain and Cognition.

Intercomparison of clumping index estimates from POLDER, MODIS, and MISR satellite data over reference sites

Hongliang Fang, Jan Pisek, Tim Wardlaw, 2015 .

SPECIAL—Savanna Patterns of Energy and Carbon Integrated across the Landscape

U. KyawThaPaw, L. Hutley, J. Beringer, 2011 .

Reduced caudate volume and cognitive slowing in men at risk of fragile X-associated tremor ataxia syndrome

J. Trollor, W. Wen, N. Georgiou-Karistianis, 2018, Brain Imaging and Behavior.

Reduced caudate volume and cognitive slowing in men at risk of fragile X-associated tremor ataxia syndrome

J. Trollor, W. Wen, N. Georgiou-Karistianis, 2018, Brain Imaging and Behavior.

Selective subcortical contributions to gait impairments in males with the FMR1 premutation

S. Lord, J. Trollor, W. Wen, 2016, Journal of Neurology, Neurosurgery & Psychiatry.

Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males

J. Trollor, W. Wen, N. Georgiou-Karistianis, 2015, Genes, brain, and behavior.

Selective executive markers of at-risk profiles associated with the fragile X premutation

S. Moss, K. Cornish, C. Kogan, 2011, Neurology.

Working memory is a core executive function supporting dual-task locomotor performance across childhood and adolescence.

J. Menant, D. Hocking, Heba Bendak, 2020, Journal of experimental child psychology.

Exploring inhibitory deficits in female premutation carriers of fragile X syndrome: Through eye movements

J. Bradshaw, J. Trollor, N. Georgiou-Karistianis, 2014, Brain and Cognition.

Linking social behaviour and anxiety to attention to emotional faces in Williams syndrome.

D. Riby, K. Cornish, D. Hocking, 2013, Research in developmental disabilities.

Running Head : Anxiety and Emotional Faces in WS 2

D. Riby, K. Cornish, D. Hocking, 2014 .

The Interplay Between Anxiety and Social Functioning in Williams Syndrome

D. Riby, K. Cornish, D. Hocking, 2014, Journal of autism and developmental disorders.

Age and CGG-repeat length are associated with neuromotor impairments in at-risk females with the FMR1 premutation

J. Bradshaw, J. Trollor, N. Georgiou-Karistianis, 2014, Neurobiology of Aging.

What is the Nature of Motor Impairments in Autism, Are They Diagnostically Useful, and What Are the Implications for Intervention?

K. Caeyenberghs, D. Hocking, 2017, Current Developmental Disorders Reports.

Running Head : WS ANXIETY AND SOCIAL BEHAVIOUR 1 The Interplay between Social Functioning in Anxiety in Williams Syndrome

D. Riby, K. Cornish, D. Hocking, 2017 .

The social nature of overimitation: Insights from Autism and Williams syndrome

C. Dissanayake, G. Vivanti, D. Hocking, 2017, Cognition.

Sensitivity of Spatiotemporal Gait Parameters in Measuring Disease Severity in Friedreich Ataxia

Sarah C. Milne, L. Corben, N. Georgiou-Karistianis, 2014, The Cerebellum.

Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation

J. Bradshaw, J. Trollor, Q. Bui, 2015, Neurobiology of Aging.

Characterising the Profile of Everyday Executive Functioning and Relation to IQ in Adults with Williams Syndrome: Is the BRIEF Adult Version a Valid Rating Scale?

M. Porter, D. Hocking, J. Reeve, 2015, PloS one.

Attention to novelty versus repetition : contrasting habituation profiles in Autism and Williams syndrome

C. Dissanayake, G. Vivanti, L. Mazzone, 2017 .

Verbal labels increase the salience of novel objects for preschoolers with typical development and Williams syndrome, but not in autism

C. Dissanayake, G. Vivanti, D. Hocking, 2016, Journal of Neurodevelopmental Disorders.

The interplay between executive control and motor functioning in Williams syndrome.

S. Lord, M. Porter, Stuart T. Smith, 2013, Developmental science.

Prevalence and predictors of subjective memory complaints in adult male carriers of the FMR1 premutation

J. Trollor, D. Hocking, R. Birch, 2016, The Clinical neuropsychologist.