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Sequential sampling of visual objects during sustained attention

https://doi.org/10.1371/journal.pbio.2001903
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What this work says

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

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EEG alpha oscillations: The inhibition–timing hypothesis
inferredcites →https://doi.org/10.1016/j.cub.2012.03.050openalex-snapshot
Perceptual Echoes at 10 Hz in the Human Brain
inferredcites →https://doi.org/10.1016/j.cub.2012.03.054openalex-snapshot
Attention Samples Stimuli Rhythmically
inferredcites →https://doi.org/10.1016/j.cub.2013.10.063openalex-snapshot
Rhythmic Sampling within and between Objects despite Sustained Attention at a Cued Location
inferredcites →https://doi.org/10.1016/j.cub.2015.07.048openalex-snapshot
Distributed Attention Is Implemented through Theta-Rhythmic Gamma Modulation
inferredcites →https://doi.org/10.1016/j.cub.2015.10.007openalex-snapshot
The Speed of Alpha-Band Oscillations Predicts the Temporal Resolution of Visual Perception
inferredcites →https://doi.org/10.1016/j.cub.2016.04.046openalex-snapshot
Attention Reorients Periodically
inferredcites →https://doi.org/10.1016/j.cub.2016.04.070openalex-snapshot
Temporal Integration Windows in Neural Processing and Perception Aligned to Saccadic Eye Movements
inferredcites →https://doi.org/10.1016/j.neuroimage.2006.05.054openalex-snapshot
The VESPA: A method for the rapid estimation of a visual evoked potential
inferredcites →https://doi.org/10.1016/j.neuroimage.2014.04.012openalex-snapshot
Towards obtaining spatiotemporally precise responses to continuous sensory stimuli in humans: A general linear modeling approach to EEG
inferredcites →https://doi.org/10.1016/j.neuron.2015.09.017openalex-snapshot
From Behavior to Neural Dynamics: An Integrated Theory of Attention
inferredcites →https://doi.org/10.1016/j.tics.2005.04.010openalex-snapshot
Capacity limits of information processing in the brain
inferredcites →https://doi.org/10.1016/j.tics.2005.05.009openalex-snapshot
Tracking multiple targets with multifocal attention
inferredcites →https://doi.org/10.1016/j.tics.2012.03.002openalex-snapshot
An oscillatory mechanism for prioritizing salient unattended stimuli
inferredcites →https://doi.org/10.1016/j.tics.2012.10.007openalex-snapshot
Alpha-band oscillations, attention, and controlled access to stored information
inferredcites →https://doi.org/10.1016/j.tics.2016.07.006openalex-snapshot
Perceptual Cycles
inferredcites →https://doi.org/10.1016/j.tins.2008.09.012openalex-snapshot
Low-frequency neuronal oscillations as instruments of sensory selection
inferredcites →https://doi.org/10.1016/j.tins.2014.04.001openalex-snapshot
Temporal coding organized by coupled alpha and gamma oscillations prioritize visual processing
inferredcites →https://doi.org/10.1016/j.visres.2011.04.012openalex-snapshot
Visual attention: The past 25 years
inferredcites →https://doi.org/10.1016/s0896-6273(00)81206-4openalex-snapshot
Attention Increases Sensitivity of V4 Neurons
inferredcites →https://doi.org/10.1016/s0959-4388(02)00309-4openalex-snapshot
The dark side of visual attention
inferredcites →https://doi.org/10.1016/s1364-6613(00)01452-2openalex-snapshot
Inhibition of return
inferredcites →https://doi.org/10.1017/s0140525x00079577openalex-snapshot
Analyzing vision at the complexity level
inferredcites →https://doi.org/10.1038/383334a0openalex-snapshot
Attentional resolution and the locus of visual awareness
inferredcites →https://doi.org/10.1038/nature06860openalex-snapshot
Discrete fixed-resolution representations in visual working memory
inferredcites →https://doi.org/10.1038/nn.3063openalex-snapshot
Cortical oscillations and speech processing: emerging computational principles and operations
inferredcites →https://doi.org/10.1038/nn.3689openalex-snapshot
Serial dependence in visual perception
inferredcites →https://doi.org/10.1038/srep16290openalex-snapshot
Dense sampling reveals behavioral oscillations in rapid visual categorization
inferredcites →https://doi.org/10.1073/pnas.0707316104openalex-snapshot
The blinking spotlight of attention
inferredcites →https://doi.org/10.1073/pnas.1511331112openalex-snapshot
Attention searches nonuniformly in space and in time
inferredcites →https://doi.org/10.1080/00335558008248231openalex-snapshot
Orienting of Attention
inferredcites →https://doi.org/10.1111/1467-9868.00346openalex-snapshot
A Direct Approach to False Discovery Rates
inferredcites →https://doi.org/10.1111/j.1467-9280.2005.01587.xopenalex-snapshot
Independent Resources for Attentional Tracking in the Left and Right Visual Hemifields
inferredcites →https://doi.org/10.1126/science.1055465openalex-snapshot
Modulation of Oscillatory Neuronal Synchronization by Selective Visual Attention
inferredcites →https://doi.org/10.1126/science.7878473openalex-snapshot
Storage of 7 ± 2 Short-Term Memories in Oscillatory Subcycles
inferredcites →https://doi.org/10.1146/annurev-psych-120710-100422openalex-snapshot
Working Memory: Theories, Models, and Controversies
inferredcites →https://doi.org/10.1146/annurev.ne.18.030195.001205openalex-snapshot
Neural Mechanisms of Selective Visual Attention
inferredcites →https://doi.org/10.1146/annurev.neuro.051508.135603openalex-snapshot
Neuronal Gamma-Band Synchronization as a Fundamental Process in Cortical Computation
inferredcites →https://doi.org/10.1146/annurev.neuro.26.041002.131039openalex-snapshot
ATTENTIONAL MODULATION OF VISUAL PROCESSING
inferredcites →https://doi.org/10.1152/jn.00297.2011openalex-snapshot
Neural coding of continuous speech in auditory cortex during monaural and dichotic listening
inferredcites →https://doi.org/10.1155/2011/156869openalex-snapshot
FieldTrip: Open Source Software for Advanced Analysis of MEG, EEG, and Invasive Electrophysiological Data
inferredcites →https://doi.org/10.1155/2011/720971openalex-snapshot
Unveiling the Biometric Potential of Finger-Based ECG Signals
inferredcites →https://doi.org/10.1162/jocn.2010.21557openalex-snapshot
Alpha Oscillations Correlate with the Successful Inhibition of Unattended Stimuli
inferredcites →https://doi.org/10.1162/jocn_a_00164openalex-snapshot
Somatosensory Anticipatory Alpha Activity Increases to Suppress Distracting Input
inferredcites →https://doi.org/10.1371/journal.pbio.1001965openalex-snapshot
Occipital Alpha Activity during Stimulus Processing Gates the Information Flow to Object-Selective Cortex
inferredcites →https://doi.org/10.1523/jneurosci.0113-09.2009openalex-snapshot
The Phase of Ongoing EEG Oscillations Predicts Visual Perception
inferredcites →https://doi.org/10.1523/jneurosci.1140-14.2014openalex-snapshot
Attention-Dependent Early Cortical Suppression Contributes to Crowding
inferredcites →https://doi.org/10.1523/jneurosci.4294-14.2015openalex-snapshot
Behavioral Oscillation in Priming: Competing Perceptual Predictions Conveyed in Alternating Theta-Band Rhythms
inferredcites →https://doi.org/10.1523/jneurosci.4568-14.2015openalex-snapshot
Rhythmic Oscillations of Visual Contrast Sensitivity Synchronized with Action
inferredcites →https://doi.org/10.1523/jneurosci.4856-13.2014openalex-snapshot
Behavioral Oscillations in Attention: Rhythmic α Pulses Mediated through θ Band
inferredcites →https://doi.org/10.7554/elife.14320openalex-snapshot
Serial grouping of 2D-image regions with object-based attention in humans

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Neural Representation of Multi-Object Attention: Evidence from Magnetoencephalography
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Attentional Rhythms Are Sensitive to Binocular Visual Pathway
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Training the attentional blink: subclinical depression decreases learning potential
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Cognitive preference for ordered structures in visual attention
inferred← citeshttps://doi.org/10.1007/s12264-024-01289-wopenalex-snapshot
Rhythm Facilitates Auditory Working Memory via Beta-Band Encoding and Theta-Band Maintenance
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Behavioral oscillation in face priming: Prediction about face identity is updated at a theta-band rhythm
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The dynamics of microsaccade amplitude reflect shifting of covert attention
inferred← citeshttps://doi.org/10.1016/j.cub.2018.05.086openalex-snapshot
Theta Rhythmic Neuronal Activity and Reaction Times Arising from Cortical Receptive Field Interactions during Distributed Attention
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Predictive visuo-motor communication through neural oscillations
inferred← citeshttps://doi.org/10.1016/j.cub.2023.09.065openalex-snapshot
Periodic attention deficits after frontoparietal lesions provide causal evidence for rhythmic attentional sampling
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2025.112582openalex-snapshot
Neural responses to global and local visual information processing provide neural signatures of ADHD symptoms
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104096openalex-snapshot
Interpersonal synchronization of movement intermittency
inferred← citeshttps://doi.org/10.1016/j.isci.2023.107988openalex-snapshot
Nonadditive integration of visual information in ensemble processing
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Rhythmic facilitation of sensory processing: A critical review
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Brain state model: A novel method to represent the rhythmicity of object-specific selective attention from magnetoencephalography data
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Selective spatial attention involves two alpha-band components associated with distinct spatiotemporal and functional characteristics
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.116870openalex-snapshot
Visual target detection in a distracting background relies on neural encoding of both visual targets and background
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2022.119182openalex-snapshot
Asymmetrical cross-modal influence on neural encoding of auditory and visual features in natural scenes
inferred← citeshttps://doi.org/10.1016/j.neuron.2018.07.032openalex-snapshot
Neural Mechanisms of Sustained Attention Are Rhythmic
inferred← citeshttps://doi.org/10.1016/j.neuropsychologia.2022.108290openalex-snapshot
Ensemble size perception: Its neural signature and the role of global interaction over individual items
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Temporally coherent perturbation of neural dynamics during retention alters human multi-item working memory
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The flickering spotlight of visual attention: Characterizing abnormal object-based attention in schizophrenia
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Signal switching may enhance processing power of the brain
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A neuro-computational model of visual attention with multiple attentional control sets
inferred← citeshttps://doi.org/10.1038/s41467-019-13282-3openalex-snapshot
Competing rhythmic neural representations of orientations during concurrent attention to multiple orientation features
inferred← citeshttps://doi.org/10.1038/s41467-025-64987-7openalex-snapshot
Visual awareness sharpens and accelerates attentional sampling through enhancing inhibitory neural modulation in the attention network
inferred← citeshttps://doi.org/10.1038/s41598-022-25264-5openalex-snapshot
Frequency modulation of cortical rhythmicity governs behavioral variability, excitability and synchrony of neurons in the visual cortex
inferred← citeshttps://doi.org/10.1073/pnas.1719433115openalex-snapshot
A theta rhythm in macaque visual cortex and its attentional modulation
inferred← citeshttps://doi.org/10.1073/pnas.1904160116openalex-snapshot
The causal role of α-oscillations in feature binding
inferred← citeshttps://doi.org/10.1073/pnas.2530939123openalex-snapshot
Sensitivity suppression during attention shifts
inferred← citeshttps://doi.org/10.1093/cercor/bhab291openalex-snapshot
Alpha-Band Phase Modulates Bottom-up Feature Processing
inferred← citeshttps://doi.org/10.1093/cercor/bhad347openalex-snapshot
EEG-based speaker–listener neural coupling reflects speech-selective attentional mechanisms beyond the speech stimulus
inferred← citeshttps://doi.org/10.1101/117804openalex-snapshot
A theta rhythm in macaque visual cortex and its attentional modulation
inferred← citeshttps://doi.org/10.1101/2020.08.14.250514openalex-snapshot
Propagation and update of auditory perceptual priors through alpha and theta rhythms
inferred← citeshttps://doi.org/10.1101/2021.01.11.426257openalex-snapshot
The visual cortex produces gamma band echo in response to broadband visual flicker
inferred← citeshttps://doi.org/10.1101/2022.04.05.487107openalex-snapshot
Attentional rhythms are generated in binocular cells
inferred← citeshttps://doi.org/10.1101/2022.11.07.515418openalex-snapshot
Periodic neglect after frontoparietal lesions provides causal evidence for rhythmic attention sampling
inferred← citeshttps://doi.org/10.1109/tii.2026.3668360openalex-snapshot
D2TriPO-DETR: Dual-Decoder Triple-Parallel-Output Detection Transformer
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EEG Correlates of Sustained Attention Variability during Discrete Multi-finger Force Control Tasks
inferred← citeshttps://doi.org/10.1111/ejn.14401openalex-snapshot
Visual crowding involves delayed frontoparietal response and enhanced top‐down modulation
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Propagation and update of auditory perceptual priors through alpha and theta rhythms
inferred← citeshttps://doi.org/10.1111/ejn.15353openalex-snapshot
No evidence of rhythmic visuospatial attention at cued locations in a spatial cuing paradigm, regardless of their behavioural relevance
inferred← citeshttps://doi.org/10.1111/ejn.15489openalex-snapshot
Rhythmic sampling revisited: Experimental paradigms and neural mechanisms
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Attentional sampling of visual and auditory objects is captured by theta‐modulated neural activity
inferred← citeshttps://doi.org/10.1111/ejn.15790openalex-snapshot
Evidence for a theta‐band behavioural oscillation in rapid face detection
inferred← citeshttps://doi.org/10.1111/psyp.13827openalex-snapshot
New methods for oscillation analyses push new theories of discrete cognition
inferred← citeshttps://doi.org/10.1111/psyp.14494openalex-snapshot
Concurrent attention to hetero‐depth surfaces in 3‐D visual space is governed by theta rhythm
inferred← citeshttps://doi.org/10.1111/psyp.14755openalex-snapshot
Aperiodic Pupil Fluctuations at Rest Predict Orienting of Visual Attention
inferred← citeshttps://doi.org/10.1146/annurev-psych-010418-103429openalex-snapshot
Functional Specialization in the Attention Network
inferred← citeshttps://doi.org/10.1152/jn.00810.2017openalex-snapshot
The rhythmic nature of visual perception
inferred← citeshttps://doi.org/10.1162/imag_a_00223openalex-snapshot
Frequency tagging of spatial attention using periliminal flickers
inferred← citeshttps://doi.org/10.1162/jocn_a_01371openalex-snapshot
Saliency-based Rhythmic Coordination of Perceptual Predictions
inferred← citeshttps://doi.org/10.1162/jocn_a_01436openalex-snapshot
The Common Rhythm of Action and Perception
inferred← citeshttps://doi.org/10.1167/19.5.22openalex-snapshot
Attention explores space periodically at the theta frequency
inferred← citeshttps://doi.org/10.1360/n972018-00566openalex-snapshot
Behavioral oscillations and their performance in attention and perception
inferred← citeshttps://doi.org/10.1371/journal.pbio.2003230openalex-snapshot
Multiple visual objects are sampled sequentially
inferred← citeshttps://doi.org/10.1371/journal.pbio.2003646openalex-snapshot
Perceptual integration rapidly activates dorsal visual pathway to guide local processing in early visual areas
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1009046openalex-snapshot
The visual cortex produces gamma band echo in response to broadband visual flicker
inferred← citeshttps://doi.org/10.1523/eneuro.0282-24.2024openalex-snapshot
Visual Processing by Hierarchical and Dynamic Multiplexing
inferred← citeshttps://doi.org/10.1523/eneuro.0472-22.2023openalex-snapshot
“Leader–Follower” Dynamic Perturbation Manipulates Multi-Item Working Memory in Humans
inferred← citeshttps://doi.org/10.1523/jneurosci.0231-20.2020openalex-snapshot
Oscillatory Bursts in Parietal Cortex Reflect Dynamic Attention between Multiple Objects and Ensembles
inferred← citeshttps://doi.org/10.1523/jneurosci.0325-26.2026openalex-snapshot
Location-Specific and Location-Invariant Neural Representations of Visual Summary Statistics
inferred← citeshttps://doi.org/10.1523/jneurosci.2006-20.2021openalex-snapshot
Automatic and Fast Encoding of Representational Uncertainty Underlies the Distortion of Relative Frequency
inferred← citeshttps://doi.org/10.1523/jneurosci.3633-17.2018openalex-snapshot
Alpha-Band Oscillation Mediates the Temporal Organization of Serially Presented Flashes
inferred← citeshttps://doi.org/10.17605/osf.io/cagh8openalex-snapshot
Interpersonal synchronization of movement intermittency
inferred← citeshttps://doi.org/10.22624/aims/digital/v4n4p62openalex-snapshot
The Role of Working Memory in Eliciting Users Cognitive Requirements
inferred← citeshttps://doi.org/10.26599/bsa.2018.9050008openalex-snapshot
Do Brain Oscillations Orchestrate Memory?
inferred← citeshttps://doi.org/10.33612/diss.242384451openalex-snapshot
Ups and downs: Individual Differences in the Temporal Dynamics of Attention
inferred← citeshttps://doi.org/10.3389/fninf.2019.00022openalex-snapshot
Transcranial Magnetic Stimulation to the Middle Frontal Gyrus During Attention Modes Induced Dynamic Module Reconfiguration in Brain Networks
inferred← citeshttps://doi.org/10.3389/fnins.2023.1282869openalex-snapshot
Electrophysiological hallmarks for event relations and event roles in working memory
inferred← citeshttps://doi.org/10.3389/fpsyg.2020.541085openalex-snapshot
Cortical Distance but Not Physical Distance Modulates Attentional Rhythms
inferred← citeshttps://doi.org/10.3758/s13414-023-02745-xopenalex-snapshot
No evidence for rhythmic sampling in inhibition of return
inferred← citeshttps://doi.org/10.3758/s13414-023-02825-yopenalex-snapshot
Non-spatial inhibition of return attenuates audiovisual integration owing to modality disparities
inferred← citeshttps://doi.org/10.64898/2026.03.24.713943openalex-snapshot
Event-Related Warping: A Toolbox for Temporal Alignment and Jitter Correction in Sequential Experimental Paradigms
inferred← citeshttps://doi.org/10.7287/peerj.16139v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Different patterns of foreground and background processing contribute to texture segregation in humans: an electrophysiological study (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.16139v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Different patterns of foreground and background processing contribute to texture segregation in humans: an electrophysiological study (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.16139v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Different patterns of foreground and background processing contribute to texture segregation in humans: an electrophysiological study (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.16139v0.3/reviews/1openalex-snapshot
Peer Review #1 of "Different patterns of foreground and background processing contribute to texture segregation in humans: an electrophysiological study (v0.3)"
inferred← citeshttps://doi.org/10.7554/elife.108017openalex-snapshot
Visual working memory guides attention rhythmically in humans
inferred← citeshttps://doi.org/10.7554/elife.108017.1openalex-snapshot
Visual Working Memory Guides Attention Rhythmically
inferred← citeshttps://doi.org/10.7554/elife.108017.2openalex-snapshot
Visual Working Memory Guides Attention Rhythmically
inferred← citeshttps://doi.org/10.7554/elife.108017.3openalex-snapshot
Visual Working Memory Guides Attention Rhythmically
inferred← citeshttps://doi.org/10.7554/elife.35164openalex-snapshot
Fast-backward replay of sequentially memorized items in humans
inferred← citeshttps://doi.org/10.7717/peerj.16139openalex-snapshot
Different patterns of foreground and background processing contribute to texture segregation in humans: an electrophysiological study
inferred← citeshttps://doi.org/10.7717/peerj.4585openalex-snapshot
Selective attention on representations in working memory: cognitive and neural mechanisms
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