6 October 2007

Hocking, Darren ORCID: 0000-0003-1143-8190, Bradshaw, John ORCID: 0000-0002-8714-5231 and Rinehart, Nicole J ORCID: 0000-0001-6109-3958 (2007) Fronto-parietal and cerebellar contributions to motor dysfunction in Williams syndrome: a review and future directions. Neuroscience and Biobehavioral Reviews, 32 (3). pp. 497-507. ISSN 0149-7634

8 October 2008

Hocking, Darren ORCID: 0000-0003-1143-8190, Rinehart, Nicole J ORCID: 0000-0001-6109-3958, McGinley, Jennifer L ORCID: 0000-0003-3775-9267 and Bradshaw, John ORCID: 0000-0002-8714-5231 (2008) Gait function in adults with Williams syndrome. Experimental Brain Research, 192. pp. 695-702. ISSN 0014-4819

15 April 2010

Hocking, Darren ORCID: 0000-0003-1143-8190, McGinley, Jennifer L ORCID: 0000-0003-3775-9267, Moss, Simon, Bradshaw, John ORCID: 0000-0002-8714-5231 and Rinehart, Nicole J ORCID: 0000-0001-6109-3958 (2010) Effects of external and internal cues on gait function in Williams syndrome. Journal of the Neurological Sciences, 291 (1-2). pp. 57-63. ISSN 0022-510X

15 May 2010

Hocking, Darren ORCID: 0000-0003-1143-8190, Fielding, Joanne ORCID: 0000-0002-1131-0587, Corben, LA, Cremer, Phillip D, Millist, Lynette, White, Owen B and Delatycki, MB (2010) Ocular motor fixation deficits in friedreich ataxia. Cerebellum, 9. pp. 411-418. ISSN 1473-4222

23 November 2010

Hocking, Darren ORCID: 0000-0003-1143-8190, Rinehart, Nicole J ORCID: 0000-0001-6109-3958, McGinley, Jennifer L ORCID: 0000-0003-3775-9267, Moss, Simon and Bradshaw, John ORCID: 0000-0002-8714-5231 (2010) A kinematic analysis of visually-guided movement in Williams syndrome. Journal of the Neurological Sciences, 301 (1-2). pp. 51-58. ISSN 0022-510X

16 August 2011

Cornish, Kim M ORCID: 0000-0003-2014-0193, Hocking, Darren ORCID: 0000-0003-1143-8190, Moss, Simon and Kogan, Cary S (2011) Selective executive markers of at-risk profiles associated with the fragile X premutation. Neurology, 77 (7). pp. 618-622. ISSN 0028-3878

1 September 2011

Cornish, Kim M ORCID: 0000-0003-2014-0193, Savage, Robert, Hocking, Darren ORCID: 0000-0003-1143-8190 and Hollis, Chris P ORCID: 0000-0003-1083-6744 (2011) Association of the dat1 genotype with inattentive behavior is mediated by reading ability in a general population sample. Brain and Cognition, 77 (3). pp. 453-458. ISSN 0278-2626

29 September 2011

Corben, LA, Georgiou-Karistianis, N, Bradshaw, John ORCID: 0000-0002-8714-5231, Hocking, Darren ORCID: 0000-0003-1143-8190, Churchyard, Andrew J and Delatycki, MB (2011) The Fitts task reveals impairments in planning and online control of movement in Friedreich ataxia: reduced cerebellar-cortico connectivity? Neuroscience, 192. pp. 382-390. ISSN 0306-4522

1 December 2011

Hocking, Darren ORCID: 0000-0003-1143-8190, Rinehart, Nicole J ORCID: 0000-0001-6109-3958, McGinley, Jennifer L ORCID: 0000-0003-3775-9267, Galna, Brook, Moss, Simon and Bradshaw, John ORCID: 0000-0002-8714-5231 (2011) Gait adaptation during obstacle crossing reveals impairments in the visual control of locomotion in Williams syndrome. Neuroscience, 197. pp. 320-329. ISSN 0306-4522

12 March 2012

Hocking, Darren ORCID: 0000-0003-1143-8190, Kogan, Cary S and Cornish, Kim M ORCID: 0000-0003-2014-0193 (2012) Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation. Brain and Cognition, 79 (1). pp. 39-44. ISSN 0278-2626

23 January 2013

Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren ORCID: 0000-0003-1143-8190, Bradshaw, John ORCID: 0000-0002-8714-5231, Fielding, Joanne ORCID: 0000-0002-1131-0587, Cohen, Jonathan, Georgiou-Karistianis, N and Cornish, Kim M ORCID: 0000-0003-2014-0193 (2013) Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndrome. Neuroscience and Biobehavioral Reviews, 37 (3). pp. 522-547. ISSN 0149-7634

19 March 2013

Hocking, Darren ORCID: 0000-0003-1143-8190, Thomas, Daniel, Menant, Jasmine C, Porter, Melanie A, Smith, Stuart, Lord, Stephen R ORCID: 0000-0002-7111-8802 and Cornish, Kim M ORCID: 0000-0003-2014-0193 (2013) The interplay between executive control and motor functioning in Williams syndrome. Developmental Science, 16 (3). pp. 428-442. ISSN 1363-755X

27 July 2013

Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren ORCID: 0000-0003-1143-8190, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Fielding, Joanne ORCID: 0000-0002-1131-0587, Trollor, Julian N ORCID: 0000-0002-7685-2977, Bradshaw, John ORCID: 0000-0002-8714-5231, Cohen, Jonathan and Cornish, Kim M ORCID: 0000-0003-2014-0193 (2013) Cognitive-motor interference during postural control indicates at-risk cerebellar profiles in females with the FMR1 premutation. Behavioural Brain Research, 253. pp. 329-336. ISSN 0166-4328

24 October 2013

Kirk, Hannah, Hocking, Darren ORCID: 0000-0003-1143-8190, Riby, Deborah M and Cornish, Kim M ORCID: 0000-0003-2014-0193 (2013) Linking social behaviour and anxiety to attention to emotional faces in Williams syndrome. Research in Developmental Disabilities, 34 (12). pp. 4608-4616. ISSN 0891-4222

26 October 2013

Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren ORCID: 0000-0003-1143-8190, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Fielding, Joanne ORCID: 0000-0002-1131-0587, Trollor, Julian N ORCID: 0000-0002-7685-2977, Bradshaw, John ORCID: 0000-0002-8714-5231, Cohen, Jonathan and Cornish, Kim M ORCID: 0000-0003-2014-0193 (2013) 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). pp. 41-51. ISSN 1552-4841

28 October 2013

Hocking, Darren ORCID: 0000-0003-1143-8190, Menant, Jasmine C, Kirk, Hannah, Lord, Stephen R ORCID: 0000-0002-7111-8802 and Porter, Melanie A (2013) Gait profiles as indicators of domain-specific impairments in executive control across neurodevelopmental disorders. Research in Developmental Disabilities, 35 (1). pp. 203-214. ISSN 0891-4222

7 November 2013

Riby, Deborah M, Hanley, Mary, Kirk, Hannah, Clark, Fiona, Little, Katie, Fleck, Ruth, Janes, Emily, Kelso, Linzi, O'Kane, Fionnuala, Cole-Fletcher, Rachel, Allday, Marianne Hvistendahl, Hocking, Darren ORCID: 0000-0003-1143-8190, Cornish, Kim M ORCID: 0000-0003-2014-0193 and Rodgers, Jacqui (2013) The interplay between anxiety and social functioning in Williams syndrome. Journal of Autism and Developmental Disorders, 44. pp. 1220-1229. ISSN 0162-3257

11 January 2014

Shelton, Annie L, Cornish, Kim M ORCID: 0000-0003-2014-0193, Kraan, Claudine M ORCID: 0000-0003-1805-6339, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Bradshaw, John ORCID: 0000-0002-8714-5231, Hocking, Darren ORCID: 0000-0003-1143-8190, Archibald, Alison D, Cohen, Jonathan, Trollor, Julian N ORCID: 0000-0002-7685-2977 and Fielding, Joanne ORCID: 0000-0002-1131-0587 (2014) Exploring inhibitory deficits in female premutation carriers of fragile X syndrome: through eye movements. Brain and Cognition, 85. pp. 201-208. ISSN 0278-2626

13 February 2014

Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren ORCID: 0000-0003-1143-8190, Bradshaw, John ORCID: 0000-0002-8714-5231, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Fielding, Joanne ORCID: 0000-0002-1131-0587, Trollor, Julian N ORCID: 0000-0002-7685-2977, Cohen, Jonathan and Cornish, Kim M ORCID: 0000-0003-2014-0193 (2014) Symbolic sequence learning is associated with cognitive-affective profiles in female FMR1 premutation carriers. Genes, Brain and Behavior, 13 (4). pp. 385-393. ISSN 1601-1848

20 March 2014

Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren ORCID: 0000-0003-1143-8190, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Fielding, Joanne ORCID: 0000-0002-1131-0587, Trollor, Julian N ORCID: 0000-0002-7685-2977, Bradshaw, John ORCID: 0000-0002-8714-5231, Cohen, Jonathan and Cornish, Kim M ORCID: 0000-0003-2014-0193 (2014) Age and CGG-repeat length are associated with neuromotor impairments in at-risk females with the FMR1 premutation. Neurobiology of Aging, 35 (9). pp. 7-13. ISSN 0197-4580

19 April 2014

Hocking, Darren ORCID: 0000-0003-1143-8190, Corben, LA, Fielding, Joanne ORCID: 0000-0002-1131-0587, Cremer, Phillip D, Millist, Lynette, White, Owen B and Delatycki, MB (2014) Saccade reprogramming in Friedreich ataxia reveals impairments in the cognitive control of saccadic eye movement. Brain and Cognition, 87. pp. 161-167. ISSN 0278-2626

15 May 2014

Birch, Rachael C ORCID: 0000-0001-8026-2155, Cornish, Kim M ORCID: 0000-0003-2014-0193, Hocking, Darren ORCID: 0000-0003-1143-8190 and Trollor, Julian N ORCID: 0000-0002-7685-2977 (2014) Understanding the neuropsychiatric phenotype of fragile X-associated tremor ataxia syndrome: a systematic review. Neuropsychology Review, 24. pp. 491-513. ISSN 1040-7308

16 July 2014

Milne, Sarah C, Hocking, Darren ORCID: 0000-0003-1143-8190, Georgiou-Karistianis, N, Murphy, Anna, Delatycki, MB and Corben, LA (2014) Sensitivity of spatiotemporal gait parameters in measuring disease severity in Friedreich ataxia. Cerebellum, 13. pp. 677-688. ISSN 1473-4222

30 July 2014

Grigsby, Jim, Cornish, Kim M ORCID: 0000-0003-2014-0193, Hocking, Darren ORCID: 0000-0003-1143-8190, Kraan, Claudine M ORCID: 0000-0003-1805-6339, Olichney, John M, Rivera, Susan M, Schneider, Andrea, Sherman, Stephanie, Wang, Jun Yi and Yang, Jin-Chen (2014) The cognitive neuropsychological phenotype of carriers of the FMR1 premutation. Journal of Neurodevelopmental Disorders, 6. ISSN 1866-1947

1 September 2014

Ternes, A-M, Fielding, Joanne ORCID: 0000-0002-1131-0587, Corben, LA, White, Owen B, Bradshaw, John ORCID: 0000-0002-8714-5231, Hocking, Darren ORCID: 0000-0003-1143-8190 and Georgiou-Karistianis, N (2014) Movement planning and online control in multiple sclerosis: assessment using a fitts law reciprocal aiming task. Cognitive and Behavioral Neurology, 27 (3). pp. 139-147. ISSN 1543-3633

26 November 2014

Hocking, Darren ORCID: 0000-0003-1143-8190, Kraan, Claudine M ORCID: 0000-0003-1805-6339, Godler, David E ORCID: 0000-0002-6405-269X, Bui, Quang M, Li, Xin, Bradshaw, John ORCID: 0000-0002-8714-5231, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Turbitt, Erin ORCID: 0000-0002-6650-9702, Fielding, Joanne ORCID: 0000-0002-1131-0587, Trollor, Julian N ORCID: 0000-0002-7685-2977, Cohen, Jonathan and Cornish, Kim M ORCID: 0000-0003-2014-0193 (2014) Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation. Neurobiology of Aging, 36 (3). pp. 1400-1408. ISSN 0197-4580

16 February 2015

Birch, Rachael C ORCID: 0000-0001-8026-2155, Hocking, Darren ORCID: 0000-0003-1143-8190, Cornish, Kim M, Menant, Jasmine C, Georgiou-Karistianis, N, Godler, David E ORCID: 0000-0002-6405-269X, Wen, Wei, Hackett, Anna, Rogers, Carolyn and Trollor, Julian N ORCID: 0000-0002-7685-2977 (2015) Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males. Genes, Brain and Behavior, 14 (3). pp. 251-259. ISSN 1601-1848

25 March 2015

Cornish, Kim M, Kraan, Claudine M, Bui, Quang M, Bellgrove, M, Metcalfe, Sylvia A, Trollor, Julian N ORCID: 0000-0002-7685-2977, Hocking, Darren ORCID: 0000-0003-1143-8190, Slater, Howard R, Inaba, Yoshimi, Li, Xin, Archibald, Alison D, Turbitt, Erin, Cohen, Jonathan and Godler, David E ORCID: 0000-0002-6405-269X (2015) Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women. Neurology, 84 (16). pp. 1631-1638. ISSN 0028-3878

10 September 2015

Hocking, Darren ORCID: 0000-0003-1143-8190, Reeve, Jessica and Porter, Melanie A (2015) 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? PLoS ONE, 10 (9). ISSN 1932-6203

1 March 2016

Cheng, Lesley ORCID: 0000-0002-8075-6144, Quek, Camelia YJ, Hung, Lin W, Sharples, Robyn A, Sherratt, Nicki A, Barnham, Kevin J ORCID: 0000-0003-1164-9465 and Hill, Andrew F ORCID: 0000-0001-5581-2354 (2016) Gene dysregulation is restored in the Parkinson's disease MPTP neurotoxic mice model upon treatment of the therapeutic drug CuII (atsm). Scientific Reports, 6. ISSN 2045-2322

29 June 2016

Birch, Rachael C ORCID: 0000-0001-8026-2155, Hocking, Darren ORCID: 0000-0003-1143-8190 and Trollor, Julian N ORCID: 0000-0002-7685-2977 (2016) Prevalence and predictors of subjective memory complaints in adult male carriers of the FMR1 premutation. Clinical Neuropsychologist, 30 (6). pp. 834-848. ISSN 1385-4046

7 September 2016

Vivanti, Giacomo ORCID: 0000-0002-4034-9157, Hocking, Darren ORCID: 0000-0003-1143-8190, Fanning, Peter AJ ORCID: 0000-0002-6074-5130 and Dissanayake, Cheryl (2016) Social affiliation motives modulate spontaneous learning in Williams syndrome but not in autism. Molecular Autism, 7. ISSN 2040-2392

3 November 2016

Hocking, Darren ORCID: 0000-0003-1143-8190 (2016) Cerebellar-frontal-parietal axis in developmental disorders. In: Developmental Disorders of the Brain: Second Edition. (2nd ed.) Psychology Press, London, UK, pp. 333-352.

Hocking, Darren ORCID: 0000-0003-1143-8190 (2016) Williams syndrome. In: Developmental Disorders of the Brain: Second Edition. (2nd ed.) Psychology Press, London, UK, pp. 271-290.

9 November 2016

Hocking, Darren ORCID: 0000-0003-1143-8190, Birch, Rachael C ORCID: 0000-0001-8026-2155, Bui, Quang M, Menant, Jasmine C, Lord, Stephen R ORCID: 0000-0002-7111-8802, Georgiou-Karistianis, N, Godler, David E ORCID: 0000-0002-6405-269X, Wen, Wei, Hackett, Anna, Rogers, Carolyn and Trollor, Julian N ORCID: 0000-0002-7685-2977 (2016) Cerebellar volume mediates the relationship between FMR1 mRNA levels and voluntary step initiation in males with the premutation. Neurobiology of Aging, 50. pp. 5-12. ISSN 0197-4580

10 December 2016

Bellingham, Shayne A ORCID: 0000-0001-5657-7413, Shambrook, Mitch and Hill, Andrew F ORCID: 0000-0001-5581-2354 (2016) Quantitative analysis of exosomal miRNA via qPCR and digital PCR. In: Exomes and Microvesicles: Methods and Protocols. Hill, Andrew F, ed. Methods in Molecular Biology, 1545 . Springer, New York, USA, pp. 55-70.

Cheng, Lesley ORCID: 0000-0002-8075-6144 and Hill, Andrew F ORCID: 0000-0001-5581-2354 (2016) Small RNA library construction for exosomal RNA from biological samples for the ion torrent PGM™ and ion S5™ system. In: Exosomes and Microvesicles: Methods and Protocols. Hill, Andrew F, ed. Methods in Molecular Biology, 1545 . Springer, New York, USA, pp. 71-90.

30 December 2016

Vivanti, Giacomo ORCID: 0000-0002-4034-9157, Hocking, Darren ORCID: 0000-0003-1143-8190, Fanning, Peter AJ ORCID: 0000-0002-6074-5130 and Dissanayake, Cheryl (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. ISSN 1866-1947

9 February 2017

Fanning, Peter AJ ORCID: 0000-0002-6074-5130, Hocking, Darren ORCID: 0000-0003-1143-8190, Dissanayake, Cheryl and Vivanti, Giacomo ORCID: 0000-0002-4034-9157 (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, 24 (4). pp. 469-489. ISSN 0929-7049

16 May 2017

Hocking, Darren ORCID: 0000-0003-1143-8190 and Caeyenberghs, K (2017) What is the nature of motor impairments in autism, are they diagnostically useful, and what are the implications for intervention? Current Developmental Disorders Reports, 4. pp. 19-27. ISSN 2196-2987

2 September 2017

Bellingham, Shayne A ORCID: 0000-0001-5657-7413 and Hill, Andrew F ORCID: 0000-0001-5581-2354 (2017) Analysis of miRNA signatures in neurodegenerative prion disease. In: Prions: Methods and Protocols. Lawson, Victoria A, ed. Methods in Molecular Biology, 1658 . Humana Press, Inc, New York, USA, pp. 67-80.

8 October 2017

Keech, Britney, Crowe, Simon and Hocking, Darren ORCID: 0000-0003-1143-8190 (2017) Intranasal oxytocin, social cognition and neurodevelopmental disorders: a meta-analysis. Psychoneuroendocrinology, 87. pp. 9-19. ISSN 0306-4530

9 April 2018

Vivanti, Giacomo ORCID: 0000-0002-4034-9157, Hocking, Darren ORCID: 0000-0003-1143-8190, Fanning, Peter AJ ORCID: 0000-0002-6074-5130, Uljarević, Mirko ORCID: 0000-0002-7481-3923, Postorino, Valentina ORCID: 0000-0003-0142-4625, Mazzone, Luigi ORCID: 0000-0002-5287-3386 and Dissanayake, Cheryl (2018) Attention to novelty versus repetition: contrasting habituation profiles in Autism and Williams syndrome. Developmental Cognitive Neuroscience, 29. pp. 54-60. ISSN 1878-9293

13 June 2018

Uljarević, Mirko, Labuschagne, Izelle, Bobin, Rebecca, Atkinson, Anna and Hocking, Darren ORCID: 0000-0003-1143-8190 (2018) Brief report: the impact of sensory hypersensitivity and intolerance of uncertainty on anxiety in Williams syndrome. Journal of Autism and Developmental Disorders, 48. pp. 3958-3964. ISSN 0162-3257

25 July 2018

Cvejic, Rachael C, Hocking, Darren ORCID: 0000-0003-1143-8190, Wen, Wei, Georgiou-Karistianis, N, Cornish, Kim M, Godler, David E, Rogers, Carolyn and Trollor, Julian N ORCID: 0000-0002-7685-2977 (2018) Reduced caudate volume and cognitive slowing in men at risk of fragile X-associated tremor ataxia syndrome. Brain Imaging and Behavior, 13. pp. 1128-1134. ISSN 1931-7557

24 October 2018

Soekmadji, Carolina ORCID: 0000-0002-6920-6627, Hill, Andrew F ORCID: 0000-0001-5581-2354, Wauben, Marca HM, Buzas, Edit, Di Vizio, Dolores, Gardiner, Chris, Lötvall, Jan ORCID: 0000-0001-9195-9249, Sahoo, Susmita and Witwer, Kenneth W ORCID: 0000-0003-1664-4233 (2018) Towards mechanisms and standardization in extracellular vesicle and extracellular RNA studies: results of a worldwide survey. Journal of Extracellular Vesicles, 7 (1). ISSN 2001-3078

20 December 2018

Jacques, Macsue ORCID: 0000-0002-4337-7022, Landen, Shanie, Voisin, Sarah ORCID: 0000-0002-4074-7083, Lamon, Séverine and Eynon, Nir ORCID: 0000-0003-4046-8276 (2018) Nurture vs. nature: the genetics and epigenetics of exercise. In: Research Methods in Physical Activity and Health. Bird, SR, ed. Routledge, London, pp. 21-27.

2019

Voisin, Sarah ORCID: 0000-0002-4074-7083 (2019) Bioinformatic and Biostatistic Methods for DNA Methylome Analysis of Obesity. In: Computational Epigenetics and Diseases. Wei, LK, ed. Translational Epigenetics, 9 . Academic Press, pp. 165-179.

22 April 2019

Cvejic, Rachael C, Trollor, Julian N ORCID: 0000-0002-7685-2977 and Hocking, Darren ORCID: 0000-0003-1143-8190 (2019) Fragile X-associated tremor ataxia syndrome. In: Degenerative Disorders of the Brain. Taylor & Francis, London, UK, pp. 143-162.

Hocking, Darren ORCID: 0000-0003-1143-8190, Bradshaw, John and Fielding, Joanne (2019) Degenerative disorders of the brain. Hocking, Darren ORCID: 0000-0003-1143-8190, Bradshaw, John and Fielding, Joanne, eds. Routledge, London, UK, pp. 1-266.

18 July 2019

Hamner, Taralee ORCID: 0000-0001-7672-7669, Raitano Lee, N, Hocking, Darren ORCID: 0000-0003-1143-8190 and Vivanti, Giacomo ORCID: 0000-0002-4034-9157 (2019) Shared and syndrome-specific adaptive difficulties in preschoolers with Williams syndrome and autism spectrum disorder: a cross-syndrome study. Journal of Intellectual Disability Research, 63 (11). pp. 1305-1311. ISSN 0964-2633

13 August 2019

Hocking, Darren ORCID: 0000-0003-1143-8190, Loesch, Danuta Z, Trost, Nicholas, Bui, Minh Q, Hammersley, Eleanor, Francis, David, Tassone, Flora ORCID: 0000-0002-6388-9180 and Storey, Elsdon (2019) Total and regional white matter lesions are correlated with motor and cognitive impairments in carriers of the FMR1 premutation. Frontiers in Neurology, 10. ISSN 1664-2295

25 November 2019

Zhao, Wenting, Cheng, Lesley ORCID: 0000-0002-8075-6144, Quek, Camelia ORCID: 0000-0002-1244-961X, Bellingham, Shayne A ORCID: 0000-0001-5657-7413 and Hill, Andrew F ORCID: 0000-0001-5581-2354 (2019) Novel miR-29b target regulation patterns are revealed in two different cell lines. Scientific Reports, 9. ISSN 2045-2322

2020

Jacques, Macsue (2020) The epigenetic basis of variable response to exercise training. PhD thesis, Victoria University.

18 May 2020

Jones, Patrice ORCID: 0000-0002-4948-1445, Lucock, Mark, Martin, Charlotte, Thota, Rohith, Garg, Manohar, Yates, Zoe, Scarlett, Christopher J, Veysey, Martin and Beckett, Emma (2020) Independent and Interactive Influences of Environmental UVR, Vitamin D Levels, and Folate Variant MTHFD1-rs2236225 on Homocysteine Levels. Nutrients, 12 (5). ISSN 2072-6643

23 July 2020

Hudry, Kristelle ORCID: 0000-0002-2752-8345, Chetcuti, Lacey and Hocking, Darren ORCID: 0000-0003-1143-8190 (2020) Motor functioning in developmental psychopathology: a review of autism as an example context. Research in Developmental Disabilities, 105. ISSN 0891-4222

20 August 2020

Fanning, Peter AJ, Sparaci, Laura, Dissanayake, Cheryl, Hocking, Darren ORCID: 0000-0003-1143-8190 and Vivanti, Giacomo (2020) Functional play in young children with autism and Williams syndrome: a cross-syndrome comparison. Child Neuropsychology, 27 (1). pp. 125-149. ISSN 0929-7049

21 September 2020

Turner, DC, Gorski, PP, Maasar, MF, Seaborne, RA, Baumert, P, Brown, AD, Kitchen, MO, Erskine, Robert M, Dos-Remedios, I, Voisin, Sarah ORCID: 0000-0002-4074-7083, Eynon, Nir ORCID: 0000-0003-4046-8276, Sultanov, RI, Borisov, OV, Larin, AK, Semenova, EA, Popov, DV, Generozov, EV, Stewart, CE, Drust, B, Owens, DJ, Ahmetov, Ildus I and Sharples, AP (2020) DNA methylation across the genome in aged human skeletal muscle tissue and muscle-derived cells: the role of HOX genes and physical activity. Scientific Reports, 10. ISSN 2045-2322

2021

Jacques, Macsue ORCID: 0000-0002-4337-7022, Landen, Shanie ORCID: 0000-0002-7658-030X, Palmer, Andrew and Eynon, Nir ORCID: 0000-0003-4046-8276 (2021) Epigenetic Effects of Exercise on Human Skeletal Muscle. In: Stress: Genetics, Epigenetics and Genomics. Fink, G, ed. Handbook of Stress, 4 . Academic Press, pp. 269-273.

Landen, Shanie (2021) Sex-Specific Epigenetic Adaptations to Exercise Training. PhD thesis, Victoria University.

Voisin, Sarah ORCID: 0000-0002-4074-7083 (2021) Exercise and/or Stress Effects on the Epigenetic Clock. In: Stress: Genetics, Epigenetics and Genomics. Handbook of Stress Series, 4 . Academic Press, pp. 275-278.

16 March 2021

Coceski, Monika ORCID: 0000-0001-7705-6350, Hocking, Darren ORCID: 0000-0003-1143-8190, Abu-Rayya, Hisham M, Sherwell, Sarah, Reid, Susan, Reddihough, Dinah, Wrennall, Jacquie and Stargatt, Robyn (2021) WISC-V motor-free cognitive profile and predictive factors in adolescents with cerebral palsy. Research in Developmental Disabilities, 113. ISSN 0891-4222

25 March 2021

Cheng, Lesley ORCID: 0000-0002-8075-6144, Quek, Camelia ORCID: 0000-0002-1244-961X, Li, Xia, Bellingham, Shayne A ORCID: 0000-0001-5657-7413, Ellett, Laura, Shambrook, Mitch, Zafar, Saima, Zerr, Inga, Lawson, Victoria A ORCID: 0000-0002-7362-7176 and Hill, Andrew F ORCID: 0000-0001-5581-2354 (2021) Distribution of microRNA profiles in pre-clinical and clinical forms of murine and human prion disease. Communications Biology, 4 (1). ISSN 2399-3642

13 May 2021

Williams, Camilla J, Li, Zhixiu, Harvey, Nicholas, Lea, Rodney A, Gurd, Brendon J, Bonafiglia, Jacob T, Papadimitriou, Ioannis D, Jacques, Macsue ORCID: 0000-0002-4337-7022, Croci, I, Stensvold, D, Wisloff, U, Taylor, JL, Gajanand, T, Cox, Emily R, Ramos, JS, Fassett, RG, Little, JP, Francois, ME, Hearon, CM, Sarma, S, Janssen, SLJE, Van Craenenbroeck, EM, Beckers, P, Cornelissen, VA, Howden, EJ, Keating, SE, Yan, Xu ORCID: 0000-0001-8547-4210, Bishop, David ORCID: 0000-0002-6956-9188, Bye, A, Haupt, LM, Griffiths, LR, Ashton, KJ, Brown, Matthew, Torquati, Luciana, Eynon, Nir ORCID: 0000-0003-4046-8276 and Coombes, JS (2021) Genome wide association study of response to interval and continuous exercise training: the Predict-HIIT study. Journal of Biomedical Science, 28. ISSN 1021-7770

14 June 2021

Coceski, Monika ORCID: 0000-0001-7705-6350, Hocking, Darren ORCID: 0000-0003-1143-8190, Reid, Susan, Abu-Rayya, Hisham M, Reddihough, Dinah, Wrennall, Jacquie and Stargatt, Robyn (2021) Assessing IQ in adolescents with mild to moderate cerebral palsy using the WISC-V. Clinical Neuropsychologist, 36 (7). pp. 1767-1786. ISSN 1385-4046

21 August 2021

Lucock, Mark, Jones, Patrice ORCID: 0000-0002-4948-1445, Veysey, Martin, Thota, Rohith, Garg, Manohar, Furst, John, Martin, Charlotte, Yates, Zoe, Scarlett, Christopher J, Jablonski, Nina G, Chaplin, George and Beckett, Emma (2021) Biophysical evidence to support and extend the vitamin D-folate hypothesis as a paradigm for the evolution of human skin pigmentation. American Journal of Human Biology, 34 (4). ISSN 1042-0533

18 October 2021

Feldmann, Daniel C, Rahim, Masouda, Suijkerbuijk, Mathjis A M ORCID: 0000-0002-2732-9856, Laguette, Mary-Jessica N ORCID: 0000-0001-9979-117X, Cieszczyk, Pawel, Ficek, K, Huminska-Lisowska, Kinga, Häger, Charlotte K, Stattin, Evalena, Nilsson, Kjell G, Alvarez-Romero, Javier, Eynon, Nir ORCID: 0000-0003-4046-8276, Feller, Julian A, Tirosh, Oren, Posthumus, Michael, Chimusa, Emile R, Collins, M and September, Alison V ORCID: 0000-0003-0950-286X (2021) Investigation of multiple populations highlight VEGFA polymorphisms to modulate anterior cruciate ligament injury. Journal of Orthopaedic Research, 40 (7). pp. 1604-1612. ISSN 0736-0266

3 November 2021

Landen, Shanie, Jacques, Macsue, Hiam, Danielle ORCID: 0000-0003-0135-329X, Alvarez-Romero, Javier, Harvey, NR, Haupt, LM, Griffiths, LR, Ashton, KJ, Lamon, Séverine, Voisin, Sarah ORCID: 0000-0002-4074-7083 and Eynon, Nir ORCID: 0000-0003-4046-8276 (2021) Skeletal muscle methylome and transcriptome integration reveals profound sex differences related to muscle function and substrate metabolism. Clinical Epigenetics, 13. ISSN 1868-7075

3 December 2021

Hocking, Darren ORCID: 0000-0003-1143-8190, Loesch, Danuta Z, Stimpson, Paige, Tassone, Flora ORCID: 0000-0002-6388-9180, Atkinson, Anna and Storey, Elsdon (2021) Delineating the relationships between motor, cognitive-executive and psychiatric symptoms in female FMR1 premutation carriers. Frontiers in Psychiatry, 12. ISSN 1664-0640

30 December 2021

Alvarez-Romero, Javier, Laguette, Mary-Jessica N ORCID: 0000-0001-9979-117X, Seale, Kirsten, Jacques, Macsue ORCID: 0000-0002-4337-7022, Voisin, Sarah ORCID: 0000-0002-4074-7083, Hiam, Danielle ORCID: 0000-0003-0135-329X, Feller, Julian A, Tirosh, Oren, Miyamoto-Mikami, E, Kumagai, Hiroshi, Kikuchi, N, Kamiya, Nobuhiro, Fuku, N, Collins, M, September, Alison V ORCID: 0000-0003-0950-286X and Eynon, Nir ORCID: 0000-0003-4046-8276 (2021) Genetic variants within the COL5A1 gene are associated with ligament injuries in physically active populations from Australia, South Africa, and Japan. European Journal of Sport Science. ISSN 1746-1391

7 January 2022

Hocking, Darren ORCID: 0000-0003-1143-8190, Ardalan, Adel, Abu-Rayya, Hisham M, Farhat, Hassan, Andoni, Anna, Lenroot, Rhoshel and Kachnowski, Stan (2022) 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. Journal of NeuroEngineering and Rehabilitation, 19 (1). ISSN 1743-0003

2 May 2022

Seale, Kirsten, Horvath, Steve ORCID: 0000-0002-4110-3589, Teschendorff, Andrew ORCID: 0000-0001-7410-6527, Eynon, Nir ORCID: 0000-0003-4046-8276 and Voisin, Sarah ORCID: 0000-0002-4074-7083 (2022) Making sense of the ageing methylome. Nature Reviews Genetics, 23. pp. 585-605. ISSN 1471-0056

23 June 2022

Coceski, Monika ORCID: 0000-0001-7705-6350, Stargatt, Robyn, Sherwell, Sarah, Abu-Rayya, Hisham M, Reid, Susan, Reddihough, Dinah S, Wrennall, Jacquie and Hocking, Darren ORCID: 0000-0003-1143-8190 (2022) Ten-year follow-up study found that motor-free intelligence quotient declined in children with mild-to-moderate cerebral palsy. Acta Paediatrica, International Journal of Paediatrics, 111 (10). pp. 1899-1906. ISSN 0803-5253

24 June 2022

Hocking, Darren ORCID: 0000-0003-1143-8190, Ardalan, Adel, Abu-Rayya, Hisham M, Farhat, Hassan, Andoni, Anna, Lenroot, Rhoshel and Kachnowski, Stan (2022) Correction to: 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 (Journal of NeuroEngineering and Rehabilitation, (2022), 19, 1, (1), 10.1186/s12984-021-00978-1). Journal of NeuroEngineering and Rehabilitation, 19 (62). ISSN 1743-0003

13 September 2022

Shields, Nora ORCID: 0000-0002-6840-2378, Mizzi, N, Buhlert-Smith, K, Strydom, A ORCID: 0000-0002-2502-6704, Prendergast, L and Hocking, Darren ORCID: 0000-0003-1143-8190 (2022) 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. Journal of Intellectual Disability Research, 66 (12). pp. 924-938. ISSN 0964-2633

15 November 2022

Hocking, Darren ORCID: 0000-0003-1143-8190, Loesch, Danuta Z, Stimpson, Paige, Tassone, Flora ORCID: 0000-0002-6388-9180, Atkinson, Anna and Storey, Elsdon (2022) Relationships of motor changes with cognitive and neuropsychiatric features in FMR1 male carriers affected with Fragile X-Associated Tremor/Ataxia Syndrome. Brain Sciences, 12 (11). ISSN 2076-3425

2023

Alvarez Romero, Javier (2023) The molecular architecture of trainability explained by genetics. PhD thesis, Victoria University.

Seale, Kirsten (2023) Quantifying the ageing methylome: a multi-tissue map in humans. PhD thesis, Victoria University.

6 March 2023

Hocking, Darren ORCID: 0000-0003-1143-8190, Sun, Xiaoyun, Haebich, Kristina, Darke, Hayley, North, Kathryn N, Vivanti, Giacomo ORCID: 0000-0002-4034-9157 and Payne, Jonathan M (2023) Delineating visual habituation profiles in preschoolers with neurofibromatosis type 1 and autism spectrum disorder: a cross-syndrome study. Journal of autism and developmental disorders. ISSN 0162-3257

31 July 2023

Luo, Qi, Dwaraka, Varun B, Chen, Qingwen, Tong, Huige, Zhu, Tianyu, Seale, Kirsten, Raffaele, Joseph M, Zheng, Shijie C, Mendez, Tavis L, Chen, Yulu, Carreras, Natalia, Begum, Sofina, Mendez, Kevin, Voisin, Sarah ORCID: 0000-0002-4074-7083, Eynon, Nir ORCID: 0000-0003-4046-8276, Lasky-Su, Jessica A, Smith, Ryan and Teschendorff, Andrew ORCID: 0000-0001-7410-6527 (2023) A meta-analysis of immune-cell fractions at high resolution reveals novel associations with common phenotypes and health outcomes. Genome Medicine, 15. ISSN 1756-994X