Timothy J Edwards
Affiliations: | University of Queensland, Saint Lucia, Queensland, Australia |
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| Edwards TJ, Fenlon LR, Dean RJ, et al. (2020) Altered structural connectivity networks in a mouse model of complete and partial dysgenesis of the corpus callosum. Neuroimage. 116868 |
| Schanze I, Bunt J, Lim JWC, et al. (2018) NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. American Journal of Human Genetics. 103: 752-768 |
| Edwards TJ, Marsh APL, Lockhart PJ, et al. (2018) Teaching NeuroImages: Imaging features of -mediated mirror movements and isolated agenesis of the corpus callosum. Neurology. 91: e886-e887 |
| Marsh AP, Edwards TJ, Galea C, et al. (2017) DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum and developmental split brain syndrome. Human Mutation |
| Gobius I, Suárez R, Morcom L, et al. (2017) Astroglial-mediated remodeling of the interhemispheric midline during telencephalic development is exclusive to eutherian mammals. Neural Development. 12: 9 |
| Marsh AP, Heron D, Edwards TJ, et al. (2017) Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance. Nature Genetics |
| Lim JW, Donahoo AL, Bunt J, et al. (2015) EMX1 regulates NRP1-mediated wiring of the mouse anterior cingulate cortex. Development (Cambridge, England). 142: 3746-57 |
| Edwards TJ, Sherr EH, Barkovich AJ, et al. (2014) Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes. Brain : a Journal of Neurology. 137: 1579-613 |