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Memory Guides Attention: Evidence from Eye Movements and Encoding Strength

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Outgoing claims: the papers this work cites, builds on, or argues with.

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A comparison and evaluation of the predictions of relational and conjunctive accounts of hippocampal function
inferredcites →https://doi.org/10.1002/hipo.22023openalex-snapshot
Aerobic fitness enhances relational memory in preadolescent children: The FITKids randomized control trial
inferredcites →https://doi.org/10.1002/hipo.22256openalex-snapshot
Memory‐related eye movements challenge behavioral measures of pattern completion and pattern separation
inferredcites →https://doi.org/10.1007/3-540-36181-2_45openalex-snapshot
A Goal Oriented Attention Guidance Model
inferredcites →https://doi.org/10.1007/978-1-4899-5379-7openalex-snapshot
Eye Movements and Vision
inferredcites →https://doi.org/10.1007/978-3-319-50406-3_12openalex-snapshot
How Hippocampal Memory Shapes, and Is Shaped by, Attention
inferredcites →https://doi.org/10.1007/s00221-008-1548-9openalex-snapshot
Episodic memory for spatial context biases spatial attention
inferredcites →https://doi.org/10.1016/0010-0285(72)90021-7openalex-snapshot
Eye fixations and recognition memory for pictures
inferredcites →https://doi.org/10.1016/0042-6989(71)90213-6openalex-snapshot
Scanpaths in saccadic eye movements while viewing and recognizing patterns
inferredcites →https://doi.org/10.1016/0042-6989(86)90164-1openalex-snapshot
Human visual suppression
inferredcites →https://doi.org/10.1016/0749-596x(91)90025-fopenalex-snapshot
A process dissociation framework: Separating automatic from intentional uses of memory
inferredcites →https://doi.org/10.1016/j.cognition.2018.12.014openalex-snapshot
Distinct roles of eye movements during memory encoding and retrieval
inferredcites →https://doi.org/10.1016/j.cognition.2020.104312openalex-snapshot
Attention capture by episodic long-term memory
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Eyetracking and selective attention in category learning
inferredcites →https://doi.org/10.1016/j.cub.2019.01.030openalex-snapshot
Dissociable Components of Experience-Driven Attention
inferredcites →https://doi.org/10.1016/j.neubiorev.2009.11.001openalex-snapshot
Neural binding mechanisms in learning and memory
inferredcites →https://doi.org/10.1016/j.neuron.2006.01.021openalex-snapshot
Orienting Attention Based on Long-Term Memory Experience
inferredcites →https://doi.org/10.1016/j.neuropsychologia.2015.06.026openalex-snapshot
Contributions of attention and elaboration to associative encoding in young and older adults
inferredcites →https://doi.org/10.1016/j.tics.2023.01.007openalex-snapshot
Good-enough attentional guidance
inferredcites →https://doi.org/10.1016/j.visres.2005.12.005openalex-snapshot
The long and the short of it: Spatial statistics at fixation vary with saccade amplitude and task
inferredcites →https://doi.org/10.1016/s0042-6989(99)00163-7openalex-snapshot
A saliency-based search mechanism for overt and covert shifts of visual attention
inferredcites →https://doi.org/10.1016/s0079-7421(08)60162-0openalex-snapshot
SAM: A Theory of Probabilistic Search of Associative Memory
inferredcites →https://doi.org/10.1016/s1364-6613(00)01534-5openalex-snapshot
Escape from illusion: reducing false memories
inferredcites →https://doi.org/10.1017/s0140525x00035391openalex-snapshot
Two functional components of the hippocampal memory system
inferredcites →https://doi.org/10.1017/s1355617711000683openalex-snapshot
Memory Transformation and Systems Consolidation
inferredcites →https://doi.org/10.1037//0033-295x.89.6.609openalex-snapshot
A theory for the storage and retrieval of item and associative information.
inferredcites →https://doi.org/10.1037/0033-295x.88.2.93openalex-snapshot
Search of associative memory.
inferredcites →https://doi.org/10.1037/0033-295x.90.4.316openalex-snapshot
A distributed memory model for serial-order information.
inferredcites →https://doi.org/10.1037/h0037368openalex-snapshot
Saccadic suppression: A review and an analysis.
inferredcites →https://doi.org/10.1037/h0081031openalex-snapshot
Towards a model of the mind's eye's movement.
inferredcites →https://doi.org/10.1038/72999openalex-snapshot
The neural mechanisms of top-down attentional control
inferredcites →https://doi.org/10.1038/73009openalex-snapshot
Voluntary orienting is dissociated from target detection in human posterior parietal cortex
inferredcites →https://doi.org/10.1038/nn.2693openalex-snapshot
Hippocampal brain-network coordination during volitional exploratory behavior enhances learning
inferredcites →https://doi.org/10.1038/nrn755openalex-snapshot
Control of goal-directed and stimulus-driven attention in the brain
inferredcites →https://doi.org/10.1068/p6142openalex-snapshot
Visual Memory for Fixated Regions of Natural Images Dissociates Attraction and Recognition
inferredcites →https://doi.org/10.1073/pnas.1104047108openalex-snapshot
Value-driven attentional capture
inferredcites →https://doi.org/10.1080/00335558008248231openalex-snapshot
Orienting of Attention
inferredcites →https://doi.org/10.1080/13506280500347992openalex-snapshot
Gaze control and recollective experience in face recognition
inferredcites →https://doi.org/10.1080/13506285.2013.800931openalex-snapshot
Gaze and informativeness during category learning: Evidence for an inverse relation
inferredcites →https://doi.org/10.1080/17470218.2011.588335openalex-snapshot
Recognition Memory Strength is Predicted by Pupillary Responses at Encoding While Fixation Patterns Distinguish Recollection from Familiarity
inferredcites →https://doi.org/10.1093/acprof:oso/9780195178043.001.0001openalex-snapshot
From Conditioning to Conscious Recollection
inferredcites →https://doi.org/10.1093/cercor/bhv028openalex-snapshot
Cognitive Control Network Contributions to Memory-Guided Visual Attention
inferredcites →https://doi.org/10.1111/1467-8721.ep10768973openalex-snapshot
Stimulus-Driven Attentional Capture
inferredcites →https://doi.org/10.1111/1467-9280.00288openalex-snapshot
Amnesia is a Deficit in Relational Memory
inferredcites →https://doi.org/10.1111/1467-9280.00290openalex-snapshot
Interactions Between Visual Working Memory and Selective Attention
inferredcites →https://doi.org/10.1126/science.1068788openalex-snapshot
Neural Mechanisms of Saccadic Suppression
inferredcites →https://doi.org/10.1146/annurev-psych-113011-143733openalex-snapshot
Episodic Memory and Beyond: The Hippocampus and Neocortex in Transformation
inferredcites →https://doi.org/10.1146/annurev.neuro.23.1.315openalex-snapshot
Mechanisms of Visual Attention in the Human Cortex
inferredcites →https://doi.org/10.1146/annurev.psych.50.1.243openalex-snapshot
HIGH-LEVEL SCENE PERCEPTION
inferredcites →https://doi.org/10.1162/jocn.2007.19.10.1690openalex-snapshot
Rapid Onset Relational Memory Effects Are Evident in Eye Movement Behavior, but Not in Hippocampal Amnesia
inferredcites →https://doi.org/10.1162/jocn_a_00667openalex-snapshot
Aerobic Fitness Predicts Relational Memory but Not Item Memory Performance in Healthy Young Adults
inferredcites →https://doi.org/10.1162/jocn_a_01336openalex-snapshot
The Hippocampus Promotes Effective Saccadic Information Gathering in Humans
inferredcites →https://doi.org/10.1162/jocn_a_01761openalex-snapshot
Neural Correlates of Subsequent Memory-Related Gaze Reinstatement
inferredcites →https://doi.org/10.1167/11.5.5openalex-snapshot
Eye guidance in natural vision: Reinterpreting salience
inferredcites →https://doi.org/10.1167/11.8.17openalex-snapshot
Examining the influence of task set on eye movements and fixations
inferredcites →https://doi.org/10.1167/13.3.1openalex-snapshot
Where do we store the memory representations that guide attention?
inferredcites →https://doi.org/10.1167/3.11.15openalex-snapshot
Task demands and binocular eye movements
inferredcites →https://doi.org/10.1167/9.10.2openalex-snapshot
Accumulation of visual information across multiple fixations
inferredcites →https://doi.org/10.1167/9.3.6openalex-snapshot
Viewing task influences eye movement control during active scene perception
inferredcites →https://doi.org/10.1371/journal.pone.0002884openalex-snapshot
Eye Movements Predict Recollective Experience
inferredcites →https://doi.org/10.1371/journal.pone.0027926openalex-snapshot
Learned Value Magnifies Salience-Based Attentional Capture
inferredcites →https://doi.org/10.1523/jneurosci.1055-15.2015openalex-snapshot
Influences of Long-Term Memory-Guided Attention and Stimulus-Guided Attention on Visuospatial Representations within Human Intraparietal Sulcus
inferredcites →https://doi.org/10.1523/jneurosci.4542-08.2008openalex-snapshot
Experience-Dependent Eye Movements Reflect Hippocampus-Dependent (Aware) Memory
inferredcites →https://doi.org/10.3389/fncom.2020.00029openalex-snapshot
Attention in Psychology, Neuroscience, and Machine Learning
inferredcites →https://doi.org/10.3389/fnhum.2012.00146openalex-snapshot
The hippocampus supports multiple cognitive processes through relational binding and comparison
inferredcites →https://doi.org/10.3758/bf03193500openalex-snapshot
Memory for scenes: Refixations reflect retrieval
inferredcites →https://doi.org/10.3758/bf03206442openalex-snapshot
Faces retain attention
inferredcites →https://doi.org/10.3758/bf03209391openalex-snapshot
A model for recognition memory: REM—retrieving effectively from memory
inferredcites →https://doi.org/10.3758/bf03211559openalex-snapshot
Familiarity and recollection in item and associative recognition
inferredcites →https://doi.org/10.3758/brm.42.3.671openalex-snapshot
Controlling low-level image properties: The SHINE toolbox
inferredcites →https://doi.org/10.3758/s13414-012-0348-2openalex-snapshot
Value-driven attentional and oculomotor capture during goal-directed, unconstrained viewing
inferredcites →https://doi.org/10.3758/s13423-023-02285-3openalex-snapshot
Selection history contributes to suboptimal attention strategies
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