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DSM staff profile

Dr Adam O’Neill

PositionResearch Fellow
DepartmentDepartment of Women's and Children's Health (Dunedin)
Research summaryNeurodevelopmental conditions

Publications

Buchsbaum, I. Y., Kielkowski, P., Giorgio, G., O'Neill, A. C., Di Giaimo, R., Kyrousi, C., … Robertson, S. P., & Cappello, S. (2020). ECE2 regulates neurogenesis and neuronal migration during human cortical development. EMBO Reports, 21, e48204. doi: 10.15252/embr.201948204

Wade, E. M., Halliday, B. J., Jenkins, Z. A., O'Neill, A. C., & Robertson, S. P. (2020). The X-linked filaminopathies: Synergistic insights from clinical and molecular analysis. Human Mutation, 41, 865-883. doi: 10.1002/humu.24002

Heinzen, E. L., O'Neill, A. C., Zhu, X., Allen, A. S., Bahlo, M., Chelly, J., … Robertson, S. P., … for the Epi4K Consortium, Epilepsy Phenome/Genome Project. (2018). De novo and inherited private variants in MAP1B in periventricular nodular heterotopia. PLoS Genetics, 14(5), e1007281. doi: 10.1371/journal.pgen.1007281

O'Neill, A. C., Kyrousi, C., Klaus, J., Leventer, R. J., Kirk, E. P., Fry, A., … Markie, D. M., … Robertson, S. P. (2018). A primate-specific Isoform of PLEKHG6 regulates neurogenesis and neuronal migration. Cell Reports, 25(10), 2729-2741. doi: 10.1016/j.celrep.2018.11.029

O'Neill, A. C., Kyrousi, C., Einsiedler, M., Burtscher, I., Drukker, M., Markie, D. M., … Robertson, S. P., & Cappello, S. (2018). Mob2 insufficiency disrupts neuronal migration in the developing cortex. Frontiers in Cellular Neuroscience, 12, 57. doi: 10.3389/fncel.2018.00057

Journal - Research Article

Buchsbaum, I. Y., Kielkowski, P., Giorgio, G., O'Neill, A. C., Di Giaimo, R., Kyrousi, C., … Robertson, S. P., & Cappello, S. (2020). ECE2 regulates neurogenesis and neuronal migration during human cortical development. EMBO Reports, 21, e48204. doi: 10.15252/embr.201948204

Heinzen, E. L., O'Neill, A. C., Zhu, X., Allen, A. S., Bahlo, M., Chelly, J., … Robertson, S. P., … for the Epi4K Consortium, Epilepsy Phenome/Genome Project. (2018). De novo and inherited private variants in MAP1B in periventricular nodular heterotopia. PLoS Genetics, 14(5), e1007281. doi: 10.1371/journal.pgen.1007281

O'Neill, A. C., Kyrousi, C., Einsiedler, M., Burtscher, I., Drukker, M., Markie, D. M., … Robertson, S. P., & Cappello, S. (2018). Mob2 insufficiency disrupts neuronal migration in the developing cortex. Frontiers in Cellular Neuroscience, 12, 57. doi: 10.3389/fncel.2018.00057

O'Neill, A. C., Kyrousi, C., Klaus, J., Leventer, R. J., Kirk, E. P., Fry, A., … Markie, D. M., … Robertson, S. P. (2018). A primate-specific Isoform of PLEKHG6 regulates neurogenesis and neuronal migration. Cell Reports, 25(10), 2729-2741. doi: 10.1016/j.celrep.2018.11.029

Bunn, K. J., Daniel, P., Rösken, H. S., O'Neill, A. C., Cameron-Christie, S. R., Morgan, T., … Markie, D. M., & Robertson, S. P. (2015). Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome. American Journal of Human Genetics, 96(4), 623-630. doi: 10.1016/j.ajhg.2015.02.010

Marsman, J., O'Neill, A. C., Kao, B. R.-Y., Rhodes, J. M., Meier, M., Antony, J., Mönnich, M., & Horsfield, J. A. (2014). Cohesin and CTCF differentially regulate spatiotemporal runx1 expression during zebrafish development. Biochimica et Biophysica Acta: Gene Regulatory Mechanisms, 1839(1), 50-61. doi: 10.1016/j.bbagrm.2013.11.007

O'Neill, A. C., & Ricardo, S. D. (2013). Human kidney cell reprogramming: Applications for disease modeling and personalized medicine. Journal of the American Society of Nephrology, 24(9), 1347-1356. doi: 10.1681/ASN.2012121199

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Journal - Research Other

Wade, E. M., Halliday, B. J., Jenkins, Z. A., O'Neill, A. C., & Robertson, S. P. (2020). The X-linked filaminopathies: Synergistic insights from clinical and molecular analysis. Human Mutation, 41, 865-883. doi: 10.1002/humu.24002

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