March 2010

Delatycki, Martin B, Wolthuizen, Michelle, Collins, Veronica, Varley, E, Craven, Joanna, Allen, Katrina J, Aitken, Maryanne, Bond, Lyndal ORCID: 0000-0003-1693-5508, Lockhart, Paul J, Wilson, Gabrielle R, Macciocca, Ivan and Metcalfe, Sylvia A (2010) Implementation of ironXS: A study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schools. Clinical Genetics, 77 (3). 241 - 248. ISSN 0009-9163

May 2012

Delatycki, Martin B, Wolthuizen, Michelle, Collins, Veronica, Varley, Elizabeth, Craven, Joanna, Allen, Katrina J, Gurrin, Lyle, Aitken, Maryanne, Trembath, M Kaye, Bond, Lyndal ORCID: 0000-0003-1693-5508, Wilson, Gabrielle R, Stephenson, Sarah EM, Macciocca, Ivan, Hickerton, Chriselle, Lockhart, Paul J and Metcalfe, Sylvia A (2012) ironXS: High-school screening for hereditary haemochromatosis is acceptable and feasible. European Journal of Human Genetics, 20 (5). 505 - 509. ISSN 1018-4813

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

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

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

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

2015

Pitt, Penelope ORCID: 0000-0002-4869-836X, Metcalfe, Sylvia A, Halliday, Jane, Fisher, Jane L, Hickerton, Chriselle, Petersen, Kerry, Menezes, Melody, McClaren, Belinda and Hodgson, Jan (2015) Women’s and men’s experiences of disclosure of a fetal abnormality. Journal of Paediatrics and Child Health, 51 (S1). A228 - A228. ISSN 1440-1754

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

12 July 2016

Hodgson, Jan, Pitt, Penelope ORCID: 0000-0002-4869-836X, Metcalfe, Sylvia A, Halliday, Jane, Menezes, Melody, Fisher, Jane L, Hickerton, Chriselle, Petersen, Kerry and McClaren, Belinda (2016) Experiences of prenatal diagnosis and decision-making about termination of pregnancy: a qualitative study. The Australian and New Zealand Journal of Obstetrics and Gynaecology. ISSN 1479-828X