Publications

Bikoff, J.B. (2019). Interneuron diversity and function in the spinal motor system. Curr. Opin. Physiol. 8, 36-43.

Hoang, P., Chalif, J.I., Bikoff, J.B., Jessell, T.M., Mentis, G.Z., and Wichterle, H. (2018). Subtype diversification and synaptic specificity of stem cell-derived spinal interneurons.. Neuron, 100, 135-149.
 
Sweeney, L.B., Bikoff, J.B.*, Gabitto, M.I.*, Brenner-Morton, Baek, M., Yang, J.H., Tabak, E., S., Dasen, J.S., Kintner, C.R., and Jessell, T.M. (2018). Origin and segmental diversity of spinal inhibitory interneurons. Neuron, 97, 341-355. *equal contribution
 
Gosgnach, S., Bikoff, J.B., Dougherty, K., El Manira, A., Lanuza, G., and Zhang, Y. (2017). Delineating the diversity of spinal interneurons in locomotor circuits. J. Neurosci., 37 (45), 10835-10841.

Bikoff, J.B., Gabitto, M.I., Rivard, A.F., Drobac, E., Machado, T.A., Miri, A., Brenner-Morton, S., Famojure, E., Diaz, C., Alvarez, F.J., Mentis, G.Z., and Jessell, T.M. (2016). Spinal inhibitory interneuron diversity delineates variant motor microcircuits. Cell, 165, 207-219.

Gabitto, M.I.*, Pakman, A.*, Bikoff, J.B.*, Abbott, L.F., Jessell, T.M., and Paninski, L. (2016). Bayesian sparse regression analysis documents the diversity of spinal inhibitory interneurons. Cell, 165, 220-233. *equal contribution

Ho H.Y., Susman M.W., Bikoff J.B., Ryu Y.K., Jonas A.M., Hu L., Kuruvilla R., and Greenberg M.E. (2012). Wnt5a-Ror- Dishevelled signaling constitutes a core developmental pathway that controls tissue morphogenesis. Proc. Natl. Acad. Sci., 13, 4044-4051.

Margolis, S.S., Salogiannis, J., Lipton, D.M., Mandel-Brehm, C., Wills, Z.P., Mardinly, A.R., Hu, L., Greer, P.L., Bikoff, J.B., Ho, H.Y., Soskis,M.J., Sahin, M., and Greenberg, M.E. (2010). EphB-mediated degredation of the RhoA GEF Ephexin5 relieves a developmental brake on excitatory synapse formation. Cell, 143, 442-455.

Zhou, P., Porcionatto, M., Pilapil, M., Chen, Y., Choi, Y., Tolias, K.F., Bikoff, J.B., Hong, E.J., Greenberg, M.E., and Segal, R.A. (2007). Polarized signaling endosomes coordinate BDNF- induced chemotaxis of cerebellar precursors. Neuron, 55, 53-68.

Tolias, K.F., Bikoff, J.B., Kane, C.G., Tolias, C.S., Hu, L., and Greenberg, M.E. (2007). The Rac1 guanine nucleotide exchange factor Tiam1 mediates EphB receptor-dependent dendritic spine development. Proc. Natl. Acad. Sci., 104, 7265-7270.

Fu, W.Y., Chen, Y., Sahin, M., Zhao, S.S., Shi, L., Bikoff, J.B., Lai, K.O., Yung, W.H., Fu, A.K.Y., Greenberg, M.E., and Ip, N.Y. (2007). Cdk5 regulates EphA4-mediated dendritic spine retraction through an ephexin1-dependent mechanism. Nat. Neurosci., 10, 67-76.

Tolias, K.F.*, Bikoff, J.B.*, Burette, A., Paradis, S., Harrar, D., Tavazoie, S., Weinberg, R.J., and Greenberg, M.E. (2005). The Rac1-GEF Tiam1 couples the NMDA receptor to the activity-dependent development of dendritic arbors and spines. Neuron, 45, 525-538. *equal contribution

Wills, Z., Emerson, M., Rusch, J., Bikoff, J., Baum, B., Perrimon, N., and Van Vactor, D. (2002). A Drosophila homolog of cyclase-associated proteins collaborates with the Abl tyrosine kinase to control midline axon pathfinding. Neuron, 36, 611-622.