Doctor of Philosophy The University of Adelaide
Bachelor of Science (Honours) The University of Adelaide
Bachelor of Science The University of Adelaide
Excludes commercial-in-confidence projects.
Open access indicates that an output is open access.
Pham, D, Tan, C, Homan, C, Jolly, L & Gecz, J 2016, 'Protocadherin Mutations in Neurodevelopmental Disorders', in C Sala & C Verpelli (eds), Neuronal and synaptic dysfunction in autism spectrum disorder and intellectual disability, Elsevier, UK, ch. 14, pp. 221-231.
Homan, CC, Pederson, S, To, T-H, Tan, C, Piltz, S, Corbett, MA, Wolvetang, E, Thomas, PQ, Jolly, LA & Gecz, J 2018, 'PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering Epilepsy', Neurobiology of Disease, vol. 116, pp. 106-119.
Kumar, R, Gardner, A, Homan, CC, Douglas, E & Gecz, J and 26 other authors and 1 consortium 2018, 'Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery', Human Mutation, vol. 39, no. 8, pp. 1126-1138.
Pham, DH, Tan, CC, Homan, CC, Kolc, KL, Corbett, MA, McAninch, D, Fox, AH, Thomas, PQ, Kumar, R & Gecz, J 2017, 'Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα)', Human Molecular Genetics.
Open access 7 7 3
Pederick, DT, Homan, CC, Jaehne, EJ, Piltz, SG, Haines, BP, Baune, BT, Jolly, LA, Hughes, JN, Gecz, J & Thomas, PQ 2016, 'Pcdh19 Loss-of-Function Increases Neuronal Migration In Vitro but is Dispensable for Brain Development in Mice', Scientific Reports, vol. 6, article no. 26765, pp. 1-10.
Open access 14 14 6
Hamon, R, Homan, CC, Tran, HB, Mukaro, VR, Lester, SE, Roscioli, E, Bosco, MD, Murgia, CM, Ackland, ML, Jersmann, HP, Lang, C, Zalewski, PD & Hodge, SJ 2014, 'Zinc and zinc transporters in macrophages and their roles in efferocytosis in COPD', PLoS One, vol. 9, no. 10, article no. e110056, pp. 1-9.
Open access 19 17 1
Homan, CC, Kumar, R, Nguyen, LS, Haan, E, Raymond, FL, Abidi, F, Raynaud, M, Schwartz, CE, Wood, SA, Gecz, J & Jolly, LA 2014, 'Mutations in USP9X are associated with x-linked intellectual disability and disrupt neuronal cell migration and growth', American Journal of Human Genetics, vol. 94, no. 3, pp. 470-478.
Open access 44 42 139
Jolly, LA, Homan, CC, Jacob, R, Barry, S & Gecz, J 2013, 'The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth', Human Molecular Genetics, vol. 22, no. 23, pp. 4673-4687.
Open access 50 50 1
|CREA - Research Center for Food and Nutrition||ITALY|
|Greenwood Genetics Center||UNITED STATES|
|Queen Elizabeth Hospital||AUSTRALIA|
|Regional University Hospital of Tours||FRANCE|
|Royal Adelaide Hospital||AUSTRALIA|
|University of Adelaide||AUSTRALIA|
|University of Cambridge||UNITED KINGDOM|
|University of Queensland||AUSTRALIA|
|University of Western Australia||AUSTRALIA|
|Women's and Children's Hospital||AUSTRALIA|
1st Annual Adelaide Stem Cell Network meeting -collaborators day
Best Oral Presentation Award
2nd Annual Collaborative Conference of Cell Reprogramming Australia - The Making of Reprogramming, Melbourne
National Stem Cell Foundation of Australia Conference