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Dr Claire Homan

Research Associate Centre for Cancer Biology

email Claire.Homan@unisa.edu.au

Research

Research focus

Biological Sciences
Clinical Sciences
Medical and Health Sciences
Biochemistry and Cell Biology
Genetics

Research

Outputs

Research since 2008 is shown below. To see earlier years visit ORCID, ResearcherID or Scopus

Open access indicates that an output is open access.

Chapters

Year	Output
2016	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. 2

Journal Articles

Year	Output
2021	Homan, CC, Venugopal, P, Arts, P, Shahrin, NH, Feurstein, S, Rawlings, L, Lawrence, DM, Andrews, J, King-Smith, SL, Harvey, NL, Brown, AL, Scott, HS & Hahn, CN 2021, 'GATA2 deficiency syndrome: a decade of discovery', Human Mutation, online, pp. 1-23. Open access 1 1
2020	Brown, AL, Arts, P, Babic, M, Dobbins, J, Feng, J, Ha, T, Homan, CC, King-Smith, SL, Li, X-C, Brautigan, P, Butcher, C, D'Andrea, RJ, Hahn, CN & Scott, HS and 46 other authors 2020, 'RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML', Blood Advances, vol. 4, no. 6, pp. pp. 1131-1144. Open access 32 29 3
2019	Jackson, MR, Loring, KE, Homan, CC, Thai, MH, Määttänen, L, Arvio, M, Jarvela, I, Shaw, M, Gardner, A, Gecz, J & Shoubridge, C 2019, 'Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females', Life Science Alliance, vol. 2, no. 4, pp. 1-18. Open access 10 9 3
2018	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. Open access 20 19
2018	Jolly, LA, Sun, Y, Carroll, R, Homan, CC & Gecz, J 2018, 'Robust imaging and gene delivery to study human lymphoblastoid cell lines', Journal of Human Genetics, vol. 63, no. 9, pp. 945-955. 1 1 1
2018	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. Open access 6 6 1
2017	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 19 18 3
2016	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 34 31 6
2014	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 34 34 2
2014	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 69 70 142
2013	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 67 65 1

External engagement & recognition

Collaborations

External engagement & recognition

Collaborations

Organisation	Country
CREA - Research Center for Food and Nutrition	ITALY
Deakin University	AUSTRALIA
Greenwood Genetics Center	UNITED STATES
Griffith University	AUSTRALIA
Queen Elizabeth Hospital	AUSTRALIA
Regional University Hospital of Tours	FRANCE
Royal Adelaide Hospital	AUSTRALIA
SA Pathology	AUSTRALIA
Turku University Hospital	FINLAND
University of Adelaide	AUSTRALIA
University of Cambridge	UNITED KINGDOM
University of Chicago	UNITED STATES
University of Helsinki	FINLAND
University of Queensland	AUSTRALIA
University of South Australia	AUSTRALIA
University of Western Australia	AUSTRALIA
Women's and Children's Hospital	AUSTRALIA

External engagement & recognition

External engagement & recognition

Engagement/recognition	Year
Founding Committee Member BLiSS Science and Innovation Inc	2021
Invited Speaker 2nd National Symposium on BMFS, Maddie Riewoldt's Vision	2021
Founding Committee Member BLiSS Science and Innovation Inc	2020
Founding Committee Member BLiSS Science and Innovation Inc	2019
Organiser 1st Annual Adelaide Stem Cell Network meeting -collaborators day	2017
Best Oral Presentation Award 2nd Annual Collaborative Conference of Cell Reprogramming Australia - The Making of Reprogramming, Melbourne	2014
Education Award National Stem Cell Foundation of Australia Conference	2013

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