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Implementation of topographically constrained connectivity for a large-scale biologically realistic model of the hippocampus.

, , , , and . EMBC, page 1358-1361. IEEE, (2012)

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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)Generalized volterra kernel model identification of spike-timing-dependent plasticity from simulated spiking activity., , and . EMBC, page 6585-6588. IEEE, (2014)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)A sparse null code emerges in deep neural networks., , , and . UniReps, volume 243 of Proceedings of Machine Learning Research, page 302-314. PMLR, (2023)Nonlinear dynamical modeling of human hippocampal CA3-CA1 functional connectivity for memory prostheses., , , , , , and . NER, page 316-319. IEEE, (2015)Laguerre-volterra identification of spike-timing-dependent plasticity from spiking activity: A simulation study., , and . EMBC, page 5578-5581. IEEE, (2013)Implementation of topographically constrained connectivity for a large-scale biologically realistic model of the hippocampus., , , , and . EMBC, page 1358-1361. IEEE, (2012)Monte Carlo validation of spike-timing-dependent plasticity identification from spiking activity., , and . EMBC, page 1624-1627. IEEE, (2016)Decoding memory features from hippocampal spiking activities using sparse classification models., , , , , and . EMBC, page 1620-1623. IEEE, (2016)Implementation of activity-dependent synaptic plasticity rules for a large-scale biologically realistic model of the hippocampus., , , , and . EMBC, page 1366-1369. IEEE, (2012)