Book Chapter
Morcom, Laura R., Edwards, Timothy J. and Richards, Linda J. (2016). Cortical architecture, midline guidance, and tractography of 3D white matter tracts. Axons and brain architecture. (pp. 289-313) edited by Kathleen S. Rockland. Cambridge, United Kingdom: Academic Press. doi: 10.1016/B978-0-12-801393-9.00014-1
Journal Articles
Edwards, Timothy J., Marsh, Ashley P. L., Lockhart, Paul J., Richards, Linda J. and Leventer, Richard J. (2018). Teaching NeuroImages: imaging features of DCC-mediated mirror movements and isolated agenesis of the corpus callosum. Neurology, 91 (9), E886-E887. doi: 10.1212/WNL.0000000000006085
Gobius, Ilan, Suarez, Rodrigo, Morcom, Laura, Paolino, Annalisa, Edwards, Timothy J., Kozulin, Peter and Richards, Linda J. (2017). Astroglial-mediated remodeling of the interhemispheric midline during telencephalic development is exclusive to eutherian mammals. Neural Development, 12 (1) 9, 9. doi: 10.1186/s13064-017-0086-1
Edwards, Timothy J., Sherr, Elliott H., Barkovich, A. James and Richards, Linda J. (2016). Reply: ARID 1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability. Brain, 139 (11), e65. doi: 10.1093/brain/aww171
Lim, Jonathan W. C., Donahoo, Amber-Lee S., Bunt, Jens, Edwards, Timothy J., Fenlon, Laura R., Liu, Ying, Zhou, Jing, Moldrich, Randal X., Piper, Michael, Gobius, Ilan, Bailey, Timothy L., Wray, Naomi R., Kessaris, Nicoletta, Poo, Mu-Ming, Rubenstein, John L. R. and Richards, Linda J. (2015). EMX1 regulates NRP1-mediated wiring of the mouse anterior cingulate cortex. Development, 142 (21), 3746-3757. doi: 10.1242/dev.119909
Edwards, Timothy J., Sherr, Elliott H., Barkovich, A. James and Richards, Linda J. (2014). Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes. Brain, 137 (6), 1579-1613. doi: 10.1093/brain/awt358
Conference Paper
Marsh, A., Edwards, T., Raabus, M., Stephenson, S., Richards, L., Galea, C., Heng, J., Farlie, P., Leventer, R. and Lockhart, P. (2017). Identification and characterisation of a novel mirror movement gene. ISN-ESN 2017 Meeting, Paris, France, 20-24 August, 2017. HOBOKEN: Wiley.