ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017
Visual Sampling Predicts Hippocampal Activity.
Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.
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Who cites it
53 citing papers in PubMed, 115 citations in OpenAlex.
- Age-related changes to oscillatory dynamics during maintenance and retrieval in a relational memory task.PloS one · 2019Trial
- Eye movements reflect capacity-dependent organization of working memory.PLoS biology · 2026Article
- Positive and Negative Retinotopic Codes in the Human Hippocampus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026Article
- Rethinking category-selectivity in human visual cortex.Cognitive neuroscience · 2026Review
- Tracking the eyes to track decline: Global eye movement similarity as a novel neuropsychological marker of mild cognitive impairment.GeroScience · 2026Article
- The relationship between category-level neural differentiation and exploratory eye movements in healthy young and older adults.Neurobiology of aging · 2025Article
- Immersive, Open-World Virtual Reality for Dementia Care: NeuroVRX Pilot Study.Journal of clinical medicine · 2025Article
- Dynamic face-related eye movement representations in the human ventral pathway.Communications biology · 2025Article
- Entorhinal grid-like codes for visual space during memory formation.Nature communications · 2025Article
- Frontal, temporal, cerebellar changes link to sepsis survivors' cognitive issues: A resting state functional magnetic resonance imaging study.World journal of psychiatry · 2025Article
- Binocular cues to 3D face structure increase activation in depth-selective visual cortex with negligible effects in face-selective areas.Journal of vision · 2025Article
- Neural and behavioral reinstatement jointly reflect retrieval of narrative events.Nature communications · 2025Article
- Anticipatory eye gaze as a marker of memory.Communications psychology · 2025Article
- Effective connectivity between the medial temporal lobes and early visual cortex modulated by unrestricted viewing predicts memory retrieval and gaze reinstatement.Imaging neuroscience (Cambridge, Mass.) · 2025Article
- Organizing space through saccades and fixations between primate posterior parietal cortex and hippocampus.Nature communications · 2024Article
- Identifying the bioimaging features of Alzheimer's disease based on pupillary light response-driven brain-wide fMRI in awake mice.Nature communications · 2024Article
- Peering into the future: Eye movements predict neural repetition effects during episodic simulation.Neuropsychologia · 2024Article
- Gender and cytoarchitecture differences: Functional connectivity of the hippocampal sub-regions.Heliyon · 2023Article
- Dynamic interactions between memory and viewing behaviors: Insights from dyadic modeling of eye movements.Journal of experimental psychology. Human perception and performance · 2023Article
- Computational cross-species views of the hippocampal formation.Hippocampus · 2023Review
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
Abstract
Eye movements serve to accumulate information from the visual world, contributing to the formation of coherent memory representations that support cognition and behavior. The hippocampus and the oculomotor network are well connected anatomically through an extensive set of polysynaptic pathways. However, the extent to which visual sampling behavior is related to functional responses in the hippocampus during encoding has not been studied directly in human neuroimaging. In the current study, participants engaged in a face processing task while brain responses were recorded with fMRI and eye movements were monitored simultaneously. The number of gaze fixations that a participant made on a given trial was correlated significantly with hippocampal activation such that more fixations were associated with stronger hippocampal activation. Similar results were also found in the fusiform face area, a face-selective perceptual processing region. Notably, the number of fixations was associated with stronger hippocampal activation when the presented faces were novel, but not when the faces were repeated. Increases in fixations during viewing of novel faces also led to larger repetition-related suppression in the hippocampus, indicating that this fixation-hippocampal relationship may reflect the ongoing development of lasting representations. Together, these results provide novel empirical support for the idea that visual exploration and hippocampal binding processes are inherently linked. SIGNIFICANCE STATEMENT: The hippocampal and oculomotor networks have each been studied extensively for their roles in the binding of information and gaze function, respectively. Despite the evidence that individuals with amnesia whose damage includes the hippocampus show alterations in their eye movement patterns and recent findings that the two systems are anatomically connected, it has not been demonstrated whether visual exploration is related to hippocampal activity in neurologically intact adults. In this combined fMRI-eye-tracking study, we show how hippocampal responses scale with the number of gaze fixations made during viewing of novel, but not repeated, faces. These findings provide new evidence suggesting that the hippocampus plays an important role in the binding of information, as sampled by gaze fixations, during visual exploration.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.