On the public citation graph
Signals in inferotemporal and perirhinal cortex suggest an untangling of visual target information
0 signed · 167 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cne.10243openalex-snapshot
Perirhinal and parahippocampal cortices of the macaque monkey: Projections to the neocortex
inferredcites →https://doi.org/10.1002/cne.903500402openalex-snapshot
Perirhinal and parahippocampal cortices of the macaque monkey: Cortical afferents
inferredcites →https://doi.org/10.1007/3-540-36478-1_3openalex-snapshot
Matching: A Well-Solved Class of Integer Linear Programs
inferredcites →https://doi.org/10.1007/978-1-4419-0389-1_7openalex-snapshot
Gain Modulation as a Mechanism for Switching Reference Frames, Tasks, and Targets
inferredcites →https://doi.org/10.1007/978-1-4899-4541-9openalex-snapshot
An Introduction to the Bootstrap
inferredcites →https://doi.org/10.1007/bf00247569openalex-snapshot
State dependent activity in monkey visual cortex
inferredcites →https://doi.org/10.1007/bf00247570openalex-snapshot
State dependent activity in monkey visual cortex
inferredcites →https://doi.org/10.1016/j.neuron.2009.01.002openalex-snapshot
The Normalization Model of Attention
inferredcites →https://doi.org/10.1016/j.neuron.2012.01.010openalex-snapshot
How Does the Brain Solve Visual Object Recognition?
inferredcites →https://doi.org/10.1016/j.tics.2007.06.010openalex-snapshot
Untangling invariant object recognition
inferredcites →https://doi.org/10.1016/j.tins.2006.04.001openalex-snapshot
Feature-based attention in visual cortex
inferredcites →https://doi.org/10.1016/s0042-6989(97)00183-1openalex-snapshot
A model of neuronal responses in visual area MT
inferredcites →https://doi.org/10.1016/s0896-6273(02)00971-6openalex-snapshot
Banburismus and the Brain
inferredcites →https://doi.org/10.1017/s0952523800009640openalex-snapshot
Normalization of cell responses in cat striate cortex
inferredcites →https://doi.org/10.1017/s095252380001035xopenalex-snapshot
Extraretinal representations in area V4 in the macaque monkey
inferredcites →https://doi.org/10.1038/363345a0openalex-snapshot
A neural basis for visual search in inferior temporal cortex
inferredcites →https://doi.org/10.1038/44372openalex-snapshot
Top-down signal from prefrontal cortex in executive control of memory retrieval
inferredcites →https://doi.org/10.1038/nature03390openalex-snapshot
Optimal eye movement strategies in visual search
inferredcites →https://doi.org/10.1038/nn.2304openalex-snapshot
Reinforcement learning can account for associative and perceptual learning on a visual-decision task
inferredcites →https://doi.org/10.1038/nn.2439openalex-snapshot
Attention improves performance primarily by reducing interneuronal correlations
inferredcites →https://doi.org/10.1038/nn.2733openalex-snapshot
Decoding the activity of neuronal populations in macaque primary visual cortex
inferredcites →https://doi.org/10.1038/nn1786openalex-snapshot
How MT cells analyze the motion of visual patterns
inferredcites →https://doi.org/10.1093/cercor/11.8.761openalex-snapshot
Responses of Neurons in Macaque Area V4 During Memory-guided Visual Search
inferredcites →https://doi.org/10.1093/cercor/4.5.523openalex-snapshot
Inferior Temporal Mechanisms for Invariant Object Recognition
inferredcites →https://doi.org/10.1101/lm.32100openalex-snapshot
Perception and Recognition Memory in Monkeys Following Lesions of Area TE and Perirhinal Cortex
inferredcites →https://doi.org/10.1126/science.1109676openalex-snapshot
Parallel and Serial Neural Mechanisms for Visual Search in Macaque Area V4
inferredcites →https://doi.org/10.1126/science.1117593openalex-snapshot
Fast Readout of Object Identity from Macaque Inferior Temporal Cortex
inferredcites →https://doi.org/10.1126/science.7233192openalex-snapshot
Inferotemporal Neurons Distinguish and Retain Behaviorally Relevant Features of Visual Stimuli
inferredcites →https://doi.org/10.1126/science.8290960openalex-snapshot
Parallel Neuronal Mechanisms for Short-Term Memory
inferredcites →https://doi.org/10.1152/jn.00919.2005openalex-snapshot
Effects of Noise Correlations on Information Encoding and Decoding
inferredcites →https://doi.org/10.1152/jn.1992.68.4.1277openalex-snapshot
Role of inferior temporal neurons in visual memory. I. Temporal encoding of information about visual images, recalled images, and behavioral context
inferredcites →https://doi.org/10.1152/jn.1997.78.3.1263openalex-snapshot
Sensory Modality Specificity of Neural Activity Related to Memory in Visual Cortex
inferredcites →https://doi.org/10.1152/jn.2000.83.3.1677openalex-snapshot
Response Differences in Monkey TE and Perirhinal Cortex: Stimulus Association Related to Reward Schedules
inferredcites →https://doi.org/10.1152/jn.2001.86.4.1916openalex-snapshot
Neural Basis of a Perceptual Decision in the Parietal Cortex (Area LIP) of the Rhesus Monkey
inferredcites →https://doi.org/10.1364/josaa.2.000284openalex-snapshot
Spatiotemporal energy models for the perception of motion
inferredcites →https://doi.org/10.1371/journal.pcbi.1000073openalex-snapshot
Short-Term Memory Trace in Rapidly Adapting Synapses of Inferior Temporal Cortex
inferredcites →https://doi.org/10.1523/jneurosci.0179-10.2010openalex-snapshot
Selectivity and Tolerance (“Invariance”) Both Increase as Visual Information Propagates from Cortical Area V4 to IT
inferredcites →https://doi.org/10.1523/jneurosci.13-12-05418.1993openalex-snapshot
Effects on visual recognition of combined and separate ablations of the entorhinal and perirhinal cortex in rhesus monkeys
inferredcites →https://doi.org/10.1523/jneurosci.16-16-05154.1996openalex-snapshot
Neural Mechanisms of Visual Working Memory in Prefrontal Cortex of the Macaque
inferredcites →https://doi.org/10.1523/jneurosci.4569-03.2004openalex-snapshot
Fast Remapping of Sensory Stimuli onto Motor Actions on the Basis of Contextual Modulation
inferredcites →https://doi.org/10.1523/jneurosci.4906-06.2007openalex-snapshot
Comparison of Recordings from Microelectrode Arrays and Single Electrodes in the Visual Cortex
inferredcites →https://doi.org/10.1523/jneurosci.6150-10.2011openalex-snapshot
Same or Different? A Neural Circuit Mechanism of Similarity-Based Pattern Match Decision Making
inferredcites →https://doi.org/10.3389/fncom.2010.00024openalex-snapshot
Internal representation of task rules by recurrent dynamics: the importance of the diversity of neural responses
inferredcites →https://doi.org/10.3389/fnhum.2011.00085openalex-snapshot
An LCD monitor with sufficiently precise timing for research in vision
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4808933openalex-extracted
Geometric Structure of Features Underlies Human Vtc Object Recognition
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.21078-xopenalex-snapshot
Perirhinal Cortex: Neural Representations ☆
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115461openalex-snapshot
Neural correlates of visual object recognition in rats
inferred← citeshttps://doi.org/10.1016/j.conb.2014.01.002openalex-snapshot
Emerging principles of population coding: in search for the neural code
inferred← citeshttps://doi.org/10.1016/j.conb.2014.01.016openalex-snapshot
Do we understand high-level vision?
inferred← citeshttps://doi.org/10.1016/j.conb.2015.06.008openalex-snapshot
Visual recognition memory: a view from V1
inferred← citeshttps://doi.org/10.1016/j.conb.2016.01.010openalex-snapshot
Why neurons mix: high dimensionality for higher cognition
inferred← citeshttps://doi.org/10.1016/j.conb.2016.02.001openalex-snapshot
Eight open questions in the computational modeling of higher sensory cortex
inferred← citeshttps://doi.org/10.1016/j.conb.2022.102644openalex-snapshot
The implications of categorical and category-free mixed selectivity on representational geometries
inferred← citeshttps://doi.org/10.1016/j.conb.2026.103243openalex-snapshot
Population codes for context-dependent decision-making
inferred← citeshttps://doi.org/10.1016/j.cub.2018.04.092openalex-snapshot
Encoding of Target Detection during Visual Search by Single Neurons in the Human Brain
inferred← citeshttps://doi.org/10.1016/j.cub.2026.08.016openalex-snapshot
Compression as a neural mechanism of mnemonic chunking in prefrontal cortex
inferred← citeshttps://doi.org/10.1016/j.jmp.2015.11.004openalex-snapshot
Similarity, kernels, and the fundamental constraints on cognition
inferred← citeshttps://doi.org/10.1016/j.neures.2019.08.002openalex-snapshot
Recency memory effects in Macaques during sequential delayed match-to-sample task with visual noise
inferred← citeshttps://doi.org/10.1016/j.neuron.2015.05.007openalex-snapshot
Neuronal Modulations in Visual Cortex Are Associated with Only One of Multiple Components of Attention
inferred← citeshttps://doi.org/10.1016/j.neuron.2016.07.032openalex-snapshot
Hunger-Dependent Enhancement of Food Cue Responses in Mouse Postrhinal Cortex and Lateral Amygdala
inferred← citeshttps://doi.org/10.1016/j.neuron.2018.01.004openalex-snapshot
Motor Cortex Embeds Muscle-like Commands in an Untangled Population Response
inferred← citeshttps://doi.org/10.1016/j.neuron.2018.06.038openalex-snapshot
Economic Choice as an Untangling of Options into Actions
inferred← citeshttps://doi.org/10.1016/j.neuron.2020.05.020openalex-snapshot
Neural Trajectories in the Supplementary Motor Area and Motor Cortex Exhibit Distinct Geometries, Compatible with Different Classes of Computation
inferred← citeshttps://doi.org/10.1016/j.neuron.2021.07.011openalex-snapshot
The population doctrine in cognitive neuroscience
inferred← citeshttps://doi.org/10.1016/j.tics.2015.08.008openalex-snapshot
Understanding What We See: How We Derive Meaning From Vision
inferred← citeshttps://doi.org/10.1038/ncomms12554openalex-snapshot
A dynamic code for economic object valuation in prefrontal cortex neurons
inferred← citeshttps://doi.org/10.1038/nn.3865openalex-snapshot
A category-free neural population supports evolving demands during decision-making
inferred← citeshttps://doi.org/10.1038/nn.4244openalex-snapshot
Using goal-driven deep learning models to understand sensory cortex
inferred← citeshttps://doi.org/10.1038/nn.4255openalex-snapshot
Conceptual and technical advances define a key moment for theoretical neuroscience
inferred← citeshttps://doi.org/10.1038/s41467-017-01912-7openalex-snapshot
The representation of colored objects in macaque color patches
inferred← citeshttps://doi.org/10.1038/s41467-018-05873-3openalex-snapshot
Reconciling persistent and dynamic hypotheses of working memory coding in prefrontal cortex
inferred← citeshttps://doi.org/10.1038/s41467-020-14578-5openalex-snapshot
Separability and geometry of object manifolds in deep neural networks
inferred← citeshttps://doi.org/10.1038/s41467-021-24456-3openalex-snapshot
Temporal stability of stimulus representation increases along rodent visual cortical hierarchies
inferred← citeshttps://doi.org/10.1038/s41467-021-26793-9openalex-snapshot
Revealing nonlinear neural decoding by analyzing choices
inferred← citeshttps://doi.org/10.1038/s41467-023-37400-4openalex-snapshot
Dynamical latent state computation in the male macaque posterior parietal cortex
inferred← citeshttps://doi.org/10.1038/s41467-023-37804-2openalex-snapshot
A distributed and efficient population code of mixed selectivity neurons for flexible navigation decisions
inferred← citeshttps://doi.org/10.1038/s41467-026-77421-3openalex-snapshot
Repeatable, low-drift recordings in behaving nonhuman primates using flexible microelectrodes
inferred← citeshttps://doi.org/10.1038/s41583-022-00582-9openalex-snapshot
Priority coding in the visual system
inferred← citeshttps://doi.org/10.1038/s41586-021-03184-0openalex-snapshot
Single-neuronal predictions of others’ beliefs in humans
inferred← citeshttps://doi.org/10.1038/s41593-021-00865-xopenalex-snapshot
Collicular circuits for flexible sensorimotor routing
inferred← citeshttps://doi.org/10.1038/s41593-021-00888-4openalex-snapshot
Reduced sociability and social agency encoding in adult Shank3-mutant mice are restored through gene re-expression in real time
inferred← citeshttps://doi.org/10.1038/s41598-025-88910-8openalex-snapshot
Orthogonal neural representations support perceptual judgments of natural stimuli
inferred← citeshttps://doi.org/10.1038/s42003-022-04335-3openalex-snapshot
Magnetoencephalography recordings reveal the neural mechanisms of auditory contributions to improved visual detection
inferred← citeshttps://doi.org/10.1038/s42256-023-00772-9openalex-snapshot
Inversion dynamics of class manifolds in deep learning reveals tradeoffs underlying generalization
inferred← citeshttps://doi.org/10.1038/srep30808openalex-snapshot
A neural substrate for object permanence in monkey inferotemporal cortex
inferred← citeshttps://doi.org/10.1088/1741-2552/ab9986openalex-snapshot
A modular high-density μ ECoG system on macaque vlPFC for auditory cognitive decoding
inferred← citeshttps://doi.org/10.1098/rsif.2022.0677openalex-snapshot
Geometry of spiking patterns in early visual cortex: a topological data analytic approach
inferred← citeshttps://doi.org/10.1098/rstb.2015.0257openalex-snapshot
Weighted parallel contributions of binocular correlation and match signals to conscious perception of depth
inferred← citeshttps://doi.org/10.1101/049718openalex-snapshot
Two frequency bands contain the most stimulus-related information in visual cortex
inferred← citeshttps://doi.org/10.1101/152181openalex-snapshot
Inferotemporal cortex multiplexes behaviorally-relevant target match signals and visual representations in a manner that minimizes their interference
inferred← citeshttps://doi.org/10.1101/2021.03.12.435023openalex-snapshot
The neural code for face memory
inferred← citeshttps://doi.org/10.1101/2021.10.08.463709openalex-snapshot
Feature-based gating of cortical information transmission
inferred← citeshttps://doi.org/10.1101/2022.01.19.476187openalex-snapshot
Seeing sounds: Neural mechanisms underlying auditory contributions to visual detection
inferred← citeshttps://doi.org/10.1101/2022.11.13.515644openalex-snapshot
Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.1101/2022.12.10.519901openalex-snapshot
Abstraction of reward context facilitates relative reward coding in neural populations of the anterior cingulate cortex
inferred← citeshttps://doi.org/10.1101/2024.12.27.630539openalex-snapshot
Hierarchical Optimization predicts Plasticity in the Macaque Inferior Temporal Cortex following Object Training
inferred← citeshttps://doi.org/10.1101/2025.03.27.645288openalex-snapshot
Functional populations in prefrontal cortex related to working memory encoding and maintenance
inferred← citeshttps://doi.org/10.1101/2025.10.18.683207openalex-snapshot
The neural basis of emotional generalization in empathy
inferred← citeshttps://doi.org/10.1101/341792openalex-snapshot
Nonlinear processing of shape information in rat lateral extrastriate cortex
inferred← citeshttps://doi.org/10.1101/535724openalex-snapshot
The development, recognition, and learning mechanisms of animal-like neural network
inferred← citeshttps://doi.org/10.1101/lm.041764.116openalex-snapshot
Humans and monkeys use different strategies to solve the same short-term memory tasks
inferred← citeshttps://doi.org/10.1103/physreve.103.012315openalex-snapshot
Weakly correlated synapses promote dimension reduction in deep neural networks
inferred← citeshttps://doi.org/10.1103/physreve.93.060301openalex-snapshot
Linear readout of object manifolds
inferred← citeshttps://doi.org/10.1103/physreve.98.062313openalex-snapshot
Mechanisms of dimensionality reduction and decorrelation in deep neural networks
inferred← citeshttps://doi.org/10.1146/annurev-neuro-080317-061936openalex-snapshot
Cognition as a Window into Neuronal Population Space
inferred← citeshttps://doi.org/10.1152/jn.00015.2019openalex-snapshot
Human frontoparietal cortex represents behaviorally relevant target status based on abstract object features
inferred← citeshttps://doi.org/10.1152/jn.00024.2019openalex-snapshot
The integration of visual and target signals in V4 and IT during visual object search
inferred← citeshttps://doi.org/10.1152/jn.00260.2014openalex-snapshot
Quantifying the signals contained in heterogeneous neural responses and determining their relationships with task performance
inferred← citeshttps://doi.org/10.1152/jn.00503.2018openalex-snapshot
Rethinking assumptions about how trial and nuisance variability impact neural task performance in a fast-processing regime
inferred← citeshttps://doi.org/10.1152/jn.00521.2017openalex-snapshot
Contribution of spiking activity in the primary auditory cortex to detection in noise
inferred← citeshttps://doi.org/10.1152/jn.00906.2017openalex-snapshot
Neuronal population mechanisms of lightness perception
inferred← citeshttps://doi.org/10.1162/neco_a_00890openalex-snapshot
Neural Quadratic Discriminant Analysis: Nonlinear Decoding with V1-Like Computation
inferred← citeshttps://doi.org/10.1162/neco_a_01119openalex-snapshot
Learning Data Manifolds with a Cutting Plane Method
inferred← citeshttps://doi.org/10.1162/neco_a_01216openalex-snapshot
Hidden Markov Models Predict the Future Choice Better Than a PSTH-Based Method
inferred← citeshttps://doi.org/10.1167/17.3.13openalex-snapshot
Behavioral and neural constraints on hierarchical representations
inferred← citeshttps://doi.org/10.1177/2398212818766675openalex-snapshot
A neuronal theory of sequential economic choice
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1004533openalex-snapshot
A Functional Cartography of Cognitive Systems
inferred← citeshttps://doi.org/10.1371/journal.pone.0200528openalex-snapshot
Inferotemporal cortex multiplexes behaviorally-relevant target match signals and visual representations in a manner that minimizes their interference
inferred← citeshttps://doi.org/10.1371/journal.pone.0297148openalex-snapshot
Neural processing of prototypicality and simplicity of product design in forming design preferences
inferred← citeshttps://doi.org/10.1523/eneuro.0361-21.2022openalex-snapshot
Neurophysiological Evidence for Cognitive Map Formation during Sequence Learning
inferred← citeshttps://doi.org/10.1523/jneurosci.0292-23.2023openalex-snapshot
Abstraction of Reward Context Facilitates Relative Reward Coding in Neural Populations of the Macaque Anterior Cingulate Cortex
inferred← citeshttps://doi.org/10.1523/jneurosci.1222-17.2017openalex-snapshot
Hebbian Learning in a Random Network Captures Selectivity Properties of the Prefrontal Cortex
inferred← citeshttps://doi.org/10.1523/jneurosci.1666-22.2023openalex-snapshot
Neuronal Spiking Responses to Direct Electrical Microstimulation in the Human Cortex
inferred← citeshttps://doi.org/10.1523/jneurosci.3169-16.2017openalex-snapshot
Feature-Selective Attention Adaptively Shifts Noise Correlations in Primary Auditory Cortex
inferred← citeshttps://doi.org/10.1523/jneurosci.3781-13.2014openalex-snapshot
Neural Dynamics Underlying Target Detection in the Human Brain
inferred← citeshttps://doi.org/10.1523/jneurosci.4040-13.2014openalex-snapshot
Dynamic Target Match Signals in Perirhinal Cortex Can Be Explained by Instantaneous Computations That Act on Dynamic Input from Inferotemporal Cortex
inferred← citeshttps://doi.org/10.1523/jneurosci.5181-14.2015openalex-snapshot
Simple Learned Weighted Sums of Inferior Temporal Neuronal Firing Rates Accurately Predict Human Core Object Recognition Performance
inferred← citeshttps://doi.org/10.3389/fncir.2018.00115openalex-snapshot
Understanding Sensory Information Processing Through Simultaneous Multi-area Population Recordings
inferred← citeshttps://doi.org/10.3389/fncom.2014.00058openalex-snapshot
Population coding in mouse visual cortex: response reliability and dissociability of stimulus tuning and noise correlation
inferred← citeshttps://doi.org/10.3389/fncom.2020.00046openalex-snapshot
Object Recognition at Higher Regions of the Ventral Visual Stream via Dynamic Inference
inferred← citeshttps://doi.org/10.3389/fncom.2023.1197031openalex-snapshot
Toward a computational theory of manifold untangling: from global embedding to local flattening
inferred← citeshttps://doi.org/10.3389/fnint.2016.00043openalex-snapshot
Information Accumulation over Time in Monkey Inferior Temporal Cortex Neurons Explains Pattern Recognition Reaction Time under Visual Noise
inferred← citeshttps://doi.org/10.3389/fnsys.2013.00104openalex-snapshot
The visual corticostriatal loop through the tail of the caudate: circuitry and function
inferred← citeshttps://doi.org/10.3410/f.732604736.793560110openalex-snapshot
Faculty Opinions recommendation of Motor Cortex Embeds Muscle-like Commands in an Untangled Population Response.
inferred← citeshttps://doi.org/10.3410/f.733821237.793560118openalex-snapshot
Faculty Opinions recommendation of Constraints on neural redundancy.
inferred← citeshttps://doi.org/10.3758/s13414-013-0532-zopenalex-snapshot
Informative cues can slow search: The cost of matching a specific template
inferred← citeshttps://doi.org/10.3758/s13423-026-02979-4openalex-snapshot
Memory recall errors reflect interacting sensory and mnemonic representations
inferred← citeshttps://doi.org/10.48550/arxiv.2006.11413openalex-snapshot
Visualizing and Understanding Vision System
inferred← citeshttps://doi.org/10.48550/arxiv.2106.00790openalex-snapshot
Statistical Mechanics of Neural Processing of Object Manifolds
inferred← citeshttps://doi.org/10.53846/goediss-6058openalex-snapshot
Towards population coding principles in the primate premotor and parietal grasping network
inferred← citeshttps://doi.org/10.64898/2026.01.22.696490openalex-snapshot
The geometric structure of features underlies human VTC object recognition
inferred← citeshttps://doi.org/10.7554/elife.22794openalex-snapshot
Emergence of transformation-tolerant representations of visual objects in rat lateral extrastriate cortex
inferred← citeshttps://doi.org/10.7554/elife.22794.030openalex-snapshot
Author response: Emergence of transformation-tolerant representations of visual objects in rat lateral extrastriate cortex
inferred← citeshttps://doi.org/10.7554/elife.32259openalex-snapshot
Single-exposure visual memory judgments are reflected in inferotemporal cortex
inferred← citeshttps://doi.org/10.7554/elife.33891openalex-snapshot
Developmental deprivation-induced perceptual and cortical processing deficits in awake-behaving animals
inferred← citeshttps://doi.org/10.7554/elife.36310openalex-snapshot
Perceptual processing in the ventral visual stream requires area TE but not rhinal cortex
inferred← citeshttps://doi.org/10.7554/elife.38105openalex-snapshot
How biological attention mechanisms improve task performance in a large-scale visual system model
inferred← citeshttps://doi.org/10.7554/elife.43625openalex-snapshot
Representational untangling by the firing rate nonlinearity in V1 simple cells
inferred← citeshttps://doi.org/10.7554/elife.44526openalex-snapshot
State-dependent geometry of population activity in rat auditory cortex
inferred← citeshttps://doi.org/10.7554/elife.44838openalex-snapshot
Primate prefrontal neurons signal economic risk derived from the statistics of recent reward experience
inferred← citeshttps://doi.org/10.7554/elife.83382openalex-snapshot
Experience transforms crossmodal object representations in the anterior temporal lobes
inferred← citeshttps://doi.org/10.7554/elife.87881openalex-snapshot
Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.87881.1openalex-snapshot
Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.87881.2openalex-snapshot
Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.87881.3openalex-snapshot
Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.87881.3.sa0openalex-snapshot
Author response: Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.87881.3.sa1openalex-snapshot
Reviewer #4 (Public Review): Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.87881.3.sa2openalex-snapshot
Reviewer #2 (Public Review): Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.87881.3.sa3openalex-snapshot
Reviewer #1 (Public Review): Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.87881.3.sa4openalex-snapshot
eLife Assessment: Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.87881.4openalex-snapshot
Revealing unexpected complex encoding but simple decoding mechanisms in motor cortex via separating behaviorally relevant neural signals
inferred← citeshttps://doi.org/10.7554/elife.98351openalex-snapshot
An image-computable model of speeded decision-making
inferred← citeshttps://doi.org/10.7554/elife.98351.1openalex-snapshot
An image-computable model of speeded decision-making
inferred← citeshttps://doi.org/10.7554/elife.98351.2openalex-snapshot
An image-computable model of speeded decision-making
inferred← citeshttps://doi.org/10.7554/elife.98351.3openalex-snapshot
An image-computable model of speeded decision-making
inferred← citeshttps://doi.org/10.7907/wd1d-w918openalex-snapshot
Dissecting Neural Circuits for Vision in Nonhuman Primates using fMRI-Guided Electrophysiology and Optogenetics
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.