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Timothy J Edwards - Publications

Affiliations: 
University of Queensland, Saint Lucia, Queensland, Australia 
Area:
Neuroscience
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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Edwards TJ, Fenlon LR, Dean RJ, Bunt J, Sherr EH, Richards LJ. Altered structural connectivity networks in a mouse model of complete and partial dysgenesis of the corpus callosum. Neuroimage. 116868. PMID 32360691 DOI: 10.1016/J.Neuroimage.2020.116868  0.359
2018 Schanze I, Bunt J, Lim JWC, Schanze D, Dean RJ, Alders M, Blanchet P, Attié-Bitach T, Berland S, Boogert S, Boppudi S, Bridges CJ, Cho MT, Dobyns WB, Donnai D, ... ... Edwards TJ, et al. NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. American Journal of Human Genetics. 103: 752-768. PMID 30388402 DOI: 10.1016/J.Ajhg.2018.10.006  0.414
2018 Edwards TJ, Marsh APL, Lockhart PJ, Richards LJ, Leventer RJ. Teaching NeuroImages: Imaging features of -mediated mirror movements and isolated agenesis of the corpus callosum. Neurology. 91: e886-e887. PMID 30150274 DOI: 10.1212/Wnl.0000000000006085  0.344
2017 Marsh AP, Edwards TJ, Galea C, Cooper HM, Engle EC, Jamuar SS, Méneret A, Moutard ML, Nava C, Rastetter A, Robinson G, Rouleau G, Roze E, Spencer-Smith M, Trouillard O, et al. DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum and developmental split brain syndrome. Human Mutation. PMID 29068161 DOI: 10.1002/Humu.23361  0.407
2017 Gobius I, Suárez R, Morcom L, Paolino A, Edwards TJ, Kozulin P, Richards LJ. Astroglial-mediated remodeling of the interhemispheric midline during telencephalic development is exclusive to eutherian mammals. Neural Development. 12: 9. PMID 28558801 DOI: 10.1186/S13064-017-0086-1  0.38
2017 Marsh AP, Heron D, Edwards TJ, Quartier A, Galea C, Nava C, Rastetter A, Moutard ML, Anderson V, Bitoun P, Bunt J, Faudet A, Garel C, Gillies G, Gobius I, et al. Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance. Nature Genetics. PMID 28250454 DOI: 10.1038/Ng.3794  0.362
2014 Edwards TJ, Sherr EH, Barkovich AJ, Richards LJ. Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes. Brain : a Journal of Neurology. 137: 1579-613. PMID 24477430 DOI: 10.1093/Brain/Awt358  0.414
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