Milstein Lab

Traditional Hebbian models of synaptic plasticity that require two neurons to be precisely co-active within a short time window completely fail to explain the most canonical type of learning – associating a behavioral choice with a delayed outcome! How, then, do neural circuits and synaptic plasticity mechanisms found in the brain accomplish rapid associative learning on behavioral timescales, and how are these mechanisms disrupted in neurological disorders affecting learning? While recent advances in experimental neuroscience implicate roles for i) specific neuronal circuit architectures, ii) nonlinear synaptic integration in neuronal dendrites, and iii) non-Hebbian forms of synaptic plasticity, these fundamental mechanisms have yet to be integrated into most theoretical and clinical models of learning, stalling progress. The Milstein Lab combines analysis of in vivo and ex vivo experimental data with biologically-detailed computational modeling to 1) predict and interpret the results of experimental neural circuit perturbations, 2) understand the pathophysiology of learning and memory disorders and inform mechanism-based treatments, and 3) engineer artificial learning systems that, like biological organisms, can flexibly learn new associations with or without explicit reinforcement.

Alternate Lab Website

CABM 227
Cellular and subcellular specialization enables biology-constrained deep learning
March 26, 2026
Cellular and subcellular specialization enables biology-constrained deep learning
Cell Reports

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Congratulations Michael Finch: Recipient of the The Gordon J. and Ruth M. Macdonald Foundation gift
April 16, 2025
Congratulations Michael Finch: Recipient of the The Gordon J. and Ruth M. Macdonald Foundation gift

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