Skip to main content

  • PhD in Computer Science UC Santa Barbara·2022–2027 (expected)
  • MS in Computer Science University of Colorado, Boulder·2020
  • BS in Computer Science University of Colorado, Boulder·2018
  • Research Fellowship MATS Program (2026)
  • Community Fellowship College of Creative Studies, UC Santa Barbara (2026)
  • Summer Internship Meta (2024, 2026)
  • Outstanding TA Award Computer Science, UC Santa Barbara (2024)

Research Areas

We compare representations in biological and artificial visual systems to understand what makes them similar, where they differ, and which biological constraints matter for learning and behavior.

Lucas Nadolskis Galen Pogoncheff

Affiliated Research Areas

We develop methods for choosing stimulation patterns that produce a desired percept or neural response, using predictive models, optimization, and feedback from the user or the brain.


Publications

We present a percept-aware framework for surgical planning of cortical visual prostheses that formulates electrode placement as a constrained optimization problem in anatomical space.

We show that apparent differences in what neural activity represents can reverse when language inputs are better matched, meaning that model design can strongly shape representational conclusions.

We introduce BIRD (Behavior Induction via Representation-structure Distillation), a flexible framework for transferring aligned behavior by matching the internal representation structure of a student model to that of a teacher.

Spotlight Talk

We present a series of analyses on the shared representations between evoked neural activity in the primary visual cortex of a blind human with an intracortical visual prosthesis, and latent visual representations computed in deep neural networks.

We present explainable artificial intelligence (XAI) models fit on a large longitudinal dataset that can predict perceptual thresholds on individual Argus II electrodes over time.

We systematically incorporated neuroscience-derived architectural components into CNNs to identify a set of mechanisms and architectures that comprehensively explain neural activity in V1.