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A bi-directional communication paradigm between parallel NEURON and an external non-neuron process.

, , , and . EMBC, page 1413-1416. IEEE, (2016)

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A 3-D admittance-level computational model of a rat hippocampus for improving prosthetic design., , , , , and . EMBC, page 2295-2298. IEEE, (2015)Topography-dependent spatio-temporal correlations in the entorhinal-dentate-CA3 circuit in a large-scale computational model of the Rat Hippocampus., , , and . EMBC, page 3965-3968. IEEE, (2015)The contribution of relative activation levels between populations of cells to network activity in a large-scale biologically realistic model of the hippocampus., , , , and . EMBC, page 5962-5965. IEEE, (2013)The role of topography in the transformation of spatiotemporal patterns by a large-scale, biologically realistic model of the rat dentate gyrus., , , , and . EMBC, page 5950-5953. IEEE, (2013)Implementation of topographically constrained connectivity for a large-scale biologically realistic model of the hippocampus., , , , and . EMBC, page 1358-1361. IEEE, (2012)A Million-Plus Neuron Model of the Hippocampal Dentate Gyrus: Critical Role for Topography in Determining Spatiotemporal Network Dynamics., , , and . IEEE Trans. Biomed. Eng., 63 (1): 199-209 (2016)A million-plus neuron model of the hippocampal dentate gyrus: Dependency of spatio-temporal network dynamics on topography., , , and . EMBC, page 4713-4716. IEEE, (2015)Implementation of activity-dependent synaptic plasticity rules for a large-scale biologically realistic model of the hippocampus., , , , and . EMBC, page 1366-1369. IEEE, (2012)Towards a large-scale biologically realistic model of the hippocampus., , , , and . EMBC, page 4595-4598. IEEE, (2012)A bi-directional communication paradigm between parallel NEURON and an external non-neuron process., , , and . EMBC, page 1413-1416. IEEE, (2016)