Author
Serra E. Favila
New York UniversityORCID 0000-0003-1528-2875Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
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2017-2026 · peak 1/yrCo-Author Collaboration Network
10 top collaborators · 11 mutual co-author links6 papers
Recent·Most cited
- NeurosciencebioRxivPreprint
Early visual cortex supports one-shot episodic memory via spatially tuned reactivation
Robert Woodry, Jonathan A. Winawer, Serra E. Favila
This study shows that early visual cortex reactivates spatially tuned representations during one-shot episodic memory retrieval, linking neural activity to memory performance.
- NeuroscienceNature CommunicationsPeer-reviewed
Perception and memory have distinct spatial tuning properties in human visual cortex
Serra E. Favila, Brice A. Kuhl, Jonathan A. Winawer
This study shows that spatial tuning properties differ between perceptual activity and memory retrieval in human visual cortex, with reduced spatial precision in memory that cannot be explained by noise or performance.
- NeurosciencebioRxivPreprint
Abrupt remapping in human CA3/dentate gyrus signals resolution of memory interference
Wanjia Guo, Serra E. Favila, Ghootae Kim…·Brice A. Kuhl
This study shows that abrupt remapping in human CA3/dentate gyrus correlates with successful learning and resolves memory interference by decorrelating similar memory representations.
- NeuroscienceJournal of NeurosciencePeer-reviewed
Parietal representations of stimulus features are amplified during memory retrieval and flexibly aligned with top-down goals
Serra E. Favila, Rosalie Samide, Sarah C. Sweigart, Brice A. Kuhl
The paper shows that lateral parietal cortex (LPC) amplifies stimulus feature information during memory retrieval compared to perception, with dorsal LPC reflecting top-down goals and ventral LPC being goal-independent.
92 citations - NeuroscienceCurrent BiologyPeer-reviewed
Overlap among spatial memories triggers repulsion of hippocampal representations
Avi J. H. Chanales, Ashima Oza, Serra E. Favila, Brice A. Kuhl
The paper shows that hippocampal representations of overlapping routes diverge with learning, becoming less similar than non-overlapping events, indicating overlap triggers repulsion.