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Synergistic population encoding and precise coordinated variability across interlaminar ensembles in the early visual system
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jcp.1030010211openalex-snapshot
Nerve impulses from single receptors in the eye
inferredcites →https://doi.org/10.1007/bf00238900openalex-snapshot
The dependence of response amplitude and variance of cat visual cortical neurones on stimulus contrast
inferredcites →https://doi.org/10.1007/s10827-005-1739-3openalex-snapshot
Encoding Stimulus Information by Spike Numbers and Mean Response Time in Primary Auditory Cortex
inferredcites →https://doi.org/10.1016/0006-8993(74)90438-7openalex-snapshot
Neuronal variability: non-stationary responses to identical visual stimuli
inferredcites →https://doi.org/10.1016/0959-4388(94)90059-0openalex-snapshot
Noise, neural codes and cortical organization
inferredcites →https://doi.org/10.1016/j.neuron.2008.12.020openalex-snapshot
The Excitatory Neuronal Network of the C2 Barrel Column in Mouse Primary Somatosensory Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2009.03.014openalex-snapshot
Spontaneous Events Outline the Realm of Possible Sensory Responses in Neocortical Populations
inferredcites →https://doi.org/10.1016/j.neuron.2011.09.020openalex-snapshot
Primary Motor Cortex Reports Efferent Control of Vibrissa Motion on Multiple Timescales
inferredcites →https://doi.org/10.1016/j.neuron.2012.06.031openalex-snapshot
From Functional Architecture to Functional Connectomics
inferredcites →https://doi.org/10.1016/j.neuron.2012.12.036openalex-snapshot
Gamma and the Coordination of Spiking Activity in Early Visual Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2015.06.035openalex-snapshot
The Nature of Shared Cortical Variability
inferredcites →https://doi.org/10.1016/j.neuron.2015.07.026openalex-snapshot
Coordinated Neuronal Activity Enhances Corticocortical Communication
inferredcites →https://doi.org/10.1016/j.neuron.2015.10.025openalex-snapshot
Neurodata Without Borders: Creating a Common Data Format for Neurophysiology
inferredcites →https://doi.org/10.1016/j.neuron.2016.02.012openalex-snapshot
Signal, Noise, and Variation in Neural and Sensory-Motor Latency
inferredcites →https://doi.org/10.1016/j.neuron.2019.07.006openalex-snapshot
Synergistic Coding of Visual Information in Columnar Networks
inferredcites →https://doi.org/10.1016/j.neuron.2019.10.020openalex-snapshot
Discovering Precise Temporal Patterns in Large-Scale Neural Recordings through Robust and Interpretable Time Warping
inferredcites →https://doi.org/10.1016/j.visres.2012.07.007openalex-snapshot
Determining the role of correlated firing in large populations of neurons using white noise and natural scene stimuli
inferredcites →https://doi.org/10.1016/s0006-3495(67)86596-2openalex-snapshot
Neuronal Spike Trains and Stochastic Point Processes
inferredcites →https://doi.org/10.1016/s0896-6273(00)00072-6openalex-snapshot
Low Response Variability in Simultaneously Recorded Retinal, Thalamic, and Cortical Neurons
inferredcites →https://doi.org/10.1016/s0896-6273(00)80477-8openalex-snapshot
Efficient Discrimination of Temporal Patterns by Motion-Sensitive Neurons in Primate Visual Cortex
inferredcites →https://doi.org/10.1016/s0896-6273(01)00481-0openalex-snapshot
Population Coding of Stimulus Location in Rat Somatosensory Cortex
inferredcites →https://doi.org/10.1038/2217openalex-snapshot
Coding of visual information by precisely correlated spikes in the lateral geniculate nucleus
inferredcites →https://doi.org/10.1038/35079612openalex-snapshot
Retinal ganglion cells act largely as independent encoders
inferredcites →https://doi.org/10.1038/370140a0openalex-snapshot
Correlated neuronal discharge rate and its implications for psychophysical performance
inferredcites →https://doi.org/10.1038/383815a0openalex-snapshot
Precisely correlated firing in cells of the lateral geniculate nucleus
inferredcites →https://doi.org/10.1038/84032openalex-snapshot
Rapid feature selective neuronal synchronization through correlated latency shifting
inferredcites →https://doi.org/10.1038/nature03252openalex-snapshot
Excitatory cortical neurons form fine-scale functional networks
inferredcites →https://doi.org/10.1038/nature06105openalex-snapshot
Temporal precision in the neural code and the timescales of natural vision
inferredcites →https://doi.org/10.1038/nature09178openalex-snapshot
Sparse coding and high-order correlations in fine-scale cortical networks
inferredcites →https://doi.org/10.1038/nature14273openalex-snapshot
Diverse coupling of neurons to populations in sensory cortex
inferredcites →https://doi.org/10.1038/nature24636openalex-snapshot
Fully integrated silicon probes for high-density recording of neural activity
inferredcites →https://doi.org/10.1038/nn.4242openalex-snapshot
The mechanics of state-dependent neural correlations
inferredcites →https://doi.org/10.1038/nrn2315openalex-snapshot
Regulation of spike timing in visual cortical circuits
inferredcites →https://doi.org/10.1038/nrn2634openalex-snapshot
The probability of neurotransmitter release: variability and feedback control at single synapses
inferredcites →https://doi.org/10.1038/nrn2886openalex-snapshot
Spiking activity propagation in neuronal networks: reconciling different perspectives on neural coding
inferredcites →https://doi.org/10.1038/nrn4026openalex-snapshot
Packet-based communication in the cortex
inferredcites →https://doi.org/10.1038/s41586-019-1716-zopenalex-snapshot
Hierarchical organization of cortical and thalamic connectivity
inferredcites →https://doi.org/10.1038/s41593-018-0089-1openalex-snapshot
Feedback determines the structure of correlated variability in primary visual cortex
inferredcites →https://doi.org/10.1038/s41593-018-0091-7openalex-snapshot
Nontoxic, double-deletion-mutant rabies viral vectors for retrograde targeting of projection neurons
inferredcites →https://doi.org/10.1038/s41593-019-0550-9openalex-snapshot
A large-scale standardized physiological survey reveals functional organization of the mouse visual cortex
inferredcites →https://doi.org/10.1073/pnas.0605643104openalex-snapshot
Sequential structure of neocortical spontaneous activity in vivo
inferredcites →https://doi.org/10.1093/cercor/1.1.1openalex-snapshot
Distributed Hierarchical Processing in the Primate Cerebral Cortex
inferredcites →https://doi.org/10.1093/cercor/1.1.1-aopenalex-snapshot
Preface: Cerebral Cortex Has Come of Age
inferredcites →https://doi.org/10.1093/cercor/13.1.5openalex-snapshot
Interlaminar Connections in the Neocortex
inferredcites →https://doi.org/10.1093/cercor/bhy001openalex-snapshot
Training and Spontaneous Reinforcement of Neuronal Assemblies by Spike Timing Plasticity
inferredcites →https://doi.org/10.1098/rstb.2012.0467openalex-snapshot
Reading spike timing without a clock: intrinsic decoding of spike trains
inferredcites →https://doi.org/10.1103/physreve.99.052414openalex-snapshot
Correlated states in balanced neuronal networks
inferredcites →https://doi.org/10.1103/physrevlett.80.197openalex-snapshot
Entropy and Information in Neural Spike Trains
inferredcites →https://doi.org/10.1113/jphysiol.1926.sp002308openalex-snapshot
The impulses produced by sensory nerve endings
inferredcites →https://doi.org/10.1126/science.1065839openalex-snapshot
Independent and Redundant Information in Nearby Cortical Neurons
inferredcites →https://doi.org/10.1126/science.1149639openalex-snapshot
Rapid Neural Coding in the Retina with Relative Spike Latencies
inferredcites →https://doi.org/10.1126/science.1179850openalex-snapshot
The Asynchronous State in Cortical Circuits
inferredcites →https://doi.org/10.1126/science.270.5239.1207openalex-snapshot
Concerted Signaling by Retinal Ganglion Cells
inferredcites →https://doi.org/10.1126/science.7770778openalex-snapshot
Reliability of Spike Timing in Neocortical Neurons
inferredcites →https://doi.org/10.1126/science.aar7186openalex-snapshot
The threshold for conscious report: Signal loss and response bias in visual and frontal cortex
inferredcites →https://doi.org/10.1126/science.aav7893openalex-snapshot
Spontaneous behaviors drive multidimensional, brainwide activity
inferredcites →https://doi.org/10.1146/annurev-neuro-070815-013851openalex-snapshot
Correlations and Neuronal Population Information
inferredcites →https://doi.org/10.1152/jn.00031.2004openalex-snapshot
Precise Temporal Responses in Whisker Trigeminal Neurons
inferredcites →https://doi.org/10.1152/jn.00900.2006openalex-snapshot
Precision, Reliability, and Information-Theoretic Analysis of Visual Thalamocortical Neurons
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.00951.2016openalex-snapshot
Systems-based analysis of dendritic nonlinearities reveals temporal feature extraction in mouse L5 cortical neurons
inferredcites →https://doi.org/10.1152/jn.2001.86.4.1700openalex-snapshot
Excess Synchrony in Motor Cortical Neurons Provides Redundant Direction Information With That From Coarse Temporal Measures
inferredcites →https://doi.org/10.1162/089976698300017089openalex-snapshot
Ion Channel Stochasticity May Be Critical in Determining the Reliability and Precision of Spike Timing
inferredcites →https://doi.org/10.1162/089976699300015981openalex-snapshot
Detecting and Estimating Signals in Noisy Cable Structures, II: Information Theoretical Analysis
inferredcites →https://doi.org/10.1371/journal.pbio.0060220openalex-snapshot
Whisker-Mediated Texture Discrimination
inferredcites →https://doi.org/10.1371/journal.pcbi.1002536openalex-snapshot
Fast Coding of Orientation in Primary Visual Cortex
inferredcites →https://doi.org/10.1371/journal.pcbi.1003418openalex-snapshot
The Role of Thalamic Population Synchrony in the Emergence of Cortical Feature Selectivity
inferredcites →https://doi.org/10.1371/journal.pone.0086314openalex-snapshot
Comparison of Classifiers for Decoding Sensory and Cognitive Information from Prefrontal Neuronal Populations
inferredcites →https://doi.org/10.1523/jneurosci.17-08-02914.1997openalex-snapshot
Response Variability of Neurons in Primary Visual Cortex (V1) of Alert Monkeys
inferredcites →https://doi.org/10.1523/jneurosci.1742-16.2016openalex-snapshot
Spatial Organization of Chromatic Pathways in the Mouse Dorsal Lateral Geniculate Nucleus
inferredcites →https://doi.org/10.1523/jneurosci.20-14-05392.2000openalex-snapshot
Temporal Coding of Visual Information in the Thalamus
inferredcites →https://doi.org/10.1523/jneurosci.21-05-01676.2001openalex-snapshot
Correlated Firing in Macaque Visual Area MT: Time Scales and Relationship to Behavior
inferredcites →https://doi.org/10.1523/jneurosci.2929-08.2008openalex-snapshot
Spatial and Temporal Scales of Neuronal Correlation in Primary Visual Cortex
inferredcites →https://doi.org/10.1523/jneurosci.3417-06.2007openalex-snapshot
The Role of Correlations in Direction and Contrast Coding in the Primary Visual Cortex
inferredcites →https://doi.org/10.1523/jneurosci.4536-14.2015openalex-snapshot
Role of Input Correlations in Shaping the Variability and Noise Correlations of Evoked Activity in the Neocortex
inferredcites →https://doi.org/10.1523/jneurosci.5106-04.2005openalex-snapshot
Stimulus Dependence of Neuronal Correlation in Primary Visual Cortex of the Macaque
inferredcites →https://doi.org/10.1523/jneurosci.5279-09.2010openalex-snapshot
Cellular Mechanisms of Temporal Sensitivity in Visual Cortex Neurons
inferredcites →https://doi.org/10.1523/jneurosci.5435-11.2012openalex-snapshot
Neurons with Stereotyped and Rapid Responses Provide a Reference Frame for Relative Temporal Coding in Primate Auditory Cortex
inferredcites →https://doi.org/10.3389/fncir.2016.00020openalex-snapshot
On Parallel Streams through the Mouse Dorsal Lateral Geniculate Nucleus
inferredcites →https://doi.org/10.3389/fncom.2014.00058openalex-snapshot
Population coding in mouse visual cortex: response reliability and dissociability of stimulus tuning and noise correlation
inferredcites →https://doi.org/10.3389/fncom.2014.00171openalex-snapshot
Correlated activity supports efficient cortical processing
inferredcites →https://doi.org/10.3389/fncom.2016.00107openalex-snapshot
A Readout Mechanism for Latency Codes
inferredcites →https://doi.org/10.3389/fncom.2017.00034openalex-snapshot
The Influence of Mexican Hat Recurrent Connectivity on Noise Correlations and Stimulus Encoding
inferredcites →https://doi.org/10.3389/fnins.2011.00090openalex-snapshot
Estimating the Amount of Information Conveyed by a Population of Neurons
inferredcites →https://doi.org/10.7554/elife.06619openalex-snapshot
Low-noise encoding of active touch by layer 4 in the somatosensory cortex
inferredcites →https://doi.org/10.7554/elife.37349openalex-snapshot
Sparse recurrent excitatory connectivity in the microcircuit of the adult mouse and human cortex
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.csbj.2020.09.007openalex-snapshot
Inferring neural information flow from spiking data
inferred← citeshttps://doi.org/10.1038/s41467-020-20722-yopenalex-snapshot
Scaling of sensory information in large neural populations shows signatures of information-limiting correlations
inferred← citeshttps://doi.org/10.1038/s41467-025-56092-6openalex-snapshot
Incomplete remyelination via therapeutically enhanced oligodendrogenesis is sufficient to recover visual cortical function
inferred← citeshttps://doi.org/10.1038/s41467-025-56733-wopenalex-snapshot
Deciphering neuronal variability across states reveals dynamic sensory encoding
inferred← citeshttps://doi.org/10.1088/1741-2552/ad647dopenalex-snapshot
A fully automatic multichannel neural spike sorting algorithm with spike reduction and positional feature
inferred← citeshttps://doi.org/10.1101/2022.09.02.506385openalex-snapshot
Multichannel neural spike sorting with spike reduction and positional feature
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