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Inference of Nonlinear Spatial Subunits in Primate Retina with Spike-Triggered Clustering
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Diffuse bipolar cells provide input to OFF parasol ganglion cells in the macaque retina
inferredcites →https://doi.org/10.1007/978-1-4613-9940-7_3openalex-snapshot
A Method for Finding Projections onto the Intersection of Convex Sets in Hilbert Spaces
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Constraints for joint angle control of the human arm
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The identification of nonlinear biological systems: LNL cascade models
inferredcites →https://doi.org/10.1007/bf00341929openalex-snapshot
The identification of nonlinear biological systems: Wiener and Hammerstein cascade models
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Fast inference in generalized linear models via expected log-likelihoods
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Directionally selective complex cells and the computation of motion energy in cat visual cortex
inferredcites →https://doi.org/10.1016/j.cub.2016.11.040openalex-snapshot
Neural Circuit Inference from Function to Structure
inferredcites →https://doi.org/10.1016/j.neuron.2005.05.021openalex-snapshot
Spatiotemporal Elements of Macaque V1 Receptive Fields
inferredcites →https://doi.org/10.1016/j.neuron.2011.10.039openalex-snapshot
Closed-Loop Measurements of Iso-Response Stimuli Reveal Dynamic Nonlinear Stimulus Integration in the Retina
inferredcites →https://doi.org/10.1016/j.neuron.2016.03.012openalex-snapshot
Nonlinear Spatiotemporal Integration by Electrical and Chemical Synapses in the Retina
inferredcites →https://doi.org/10.1016/j.neuron.2016.05.006openalex-snapshot
Synaptic Rectification Controls Nonlinear Spatial Integration of Natural Visual Inputs
inferredcites →https://doi.org/10.1016/s0042-6989(00)00039-0openalex-snapshot
Center surround receptive field structure of cone bipolar cells in primate retina
inferredcites →https://doi.org/10.1016/s0896-6273(00)80304-9openalex-snapshot
The Light Response of Retinal Ganglion Cells Is Truncated by a Displaced Amacrine Circuit
inferredcites →https://doi.org/10.1016/s0896-6273(02)01050-4openalex-snapshot
Fast and Slow Contrast Adaptation in Retinal Circuitry
inferredcites →https://doi.org/10.1017/s0952523800009640openalex-snapshot
Normalization of cell responses in cat striate cortex
inferredcites →https://doi.org/10.1017/s0952523803201012openalex-snapshot
Center-surround organization in bipolar cells: Symmetry for opposing contrasts
inferredcites →https://doi.org/10.1038/226458a0openalex-snapshot
Algebraic Summation of Centre and Surround Inputs to Retinal Ganglion Cells of the Cat
inferredcites →https://doi.org/10.1038/nature01652openalex-snapshot
Segregation of object and background motion in the retina
inferredcites →https://doi.org/10.1038/nature07140openalex-snapshot
Spatio-temporal correlations and visual signalling in a complete neuronal population
inferredcites →https://doi.org/10.1038/nature09424openalex-snapshot
Functional connectivity in the retina at the resolution of photoreceptors
inferredcites →https://doi.org/10.1038/nn.3225openalex-snapshot
The spatial structure of a nonlinear receptive field
inferredcites →https://doi.org/10.1038/nn.3534openalex-snapshot
Origin and effect of phototransduction noise in primate cone photoreceptors
inferredcites →https://doi.org/10.1038/nrc3398openalex-snapshot
Ceramide-orchestrated signalling in cancer cells
inferredcites →https://doi.org/10.1038/nrn3136openalex-snapshot
Normalization as a canonical neural computation
inferredcites →https://doi.org/10.1038/s41467-017-00156-9openalex-snapshot
Inference of neuronal functional circuitry with spike-triggered non-negative matrix factorization
inferredcites →https://doi.org/10.1080/713663221openalex-snapshot
A simple white noise analysis of neuronal light responses
inferredcites →https://doi.org/10.1080/net.12.2.199.213openalex-snapshot
A simple white noise analysis of neuronal light responses
inferredcites →https://doi.org/10.1085/jgp.201110629openalex-snapshot
Nonlinear spatial encoding by retinal ganglion cells: when 1 + 1 ≠ 2
inferredcites →https://doi.org/10.1088/0954-898x_14_3_304openalex-snapshot
Convergence properties of three spike-triggered analysis techniques
inferredcites →https://doi.org/10.1098/rspb.1998.0303openalex-snapshot
Independent component filters of natural images compared with simple cells in primary visual cortex
inferredcites →https://doi.org/10.1101/045336openalex-snapshot
Testing pseudo-linear models of responses to natural scenes in primate retina
inferredcites →https://doi.org/10.1109/cdc.2012.6426698openalex-snapshot
Randomized smoothing for (parallel) stochastic optimization
inferredcites →https://doi.org/10.1109/tns.2004.832706openalex-snapshot
What does the eye tell the brain?: Development of a system for the large-scale recording of retinal output activity
inferredcites →https://doi.org/10.1113/jphysiol.1959.sp006308openalex-snapshot
Receptive fields of single neurones in the cat's striate cortex
inferredcites →https://doi.org/10.1113/jphysiol.1962.sp006837openalex-snapshot
Receptive fields, binocular interaction and functional architecture in the cat's visual cortex
inferredcites →https://doi.org/10.1113/jphysiol.1966.sp008107openalex-snapshot
The contrast sensitivity of retinal ganglion cells of the cat
inferredcites →https://doi.org/10.1113/jphysiol.1976.sp011595openalex-snapshot
Linear and nonlinear spatial subunits in Y cat retinal ganglion cells.
inferredcites →https://doi.org/10.1113/jphysiol.1978.sp012488openalex-snapshot
Spatial summation in the receptive fields of simple cells in the cat's striate cortex.
inferredcites →https://doi.org/10.1113/jphysiol.1990.sp018193openalex-snapshot
Visual transduction in cones of the monkey Macaca fascicularis.
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.175.4027.1276openalex-snapshot
White-Noise Analysis of a Neuron Chain: An Application of the Wiener Theory
inferredcites →https://doi.org/10.1152/jn.01175.2004openalex-snapshot
Fidelity of the Ensemble Code for Visual Motion in Primate Retina
inferredcites →https://doi.org/10.1152/jn.1987.58.6.1187openalex-snapshot
The two-dimensional spatial structure of simple receptive fields in cat striate cortex
inferredcites →https://doi.org/10.1152/jn.1989.61.6.1110openalex-snapshot
Dissection of the neuron network in the catfish inner retina. III. Interpretation of spike kernels
inferredcites →https://doi.org/10.1152/physrev.1992.72.2.491openalex-snapshot
White-noise analysis in neurophysiology
inferredcites →https://doi.org/10.1162/08997660360675044openalex-snapshot
What Causes a Neuron to Spike?
inferredcites →https://doi.org/10.1162/089976604322742010openalex-snapshot
Analyzing Neural Responses to Natural Signals: Maximally Informative Dimensions
inferredcites →https://doi.org/10.1167/6.11.13openalex-snapshot
Spatial four-alternative forced-choice method is the preferred psychophysical method for naive observers
inferredcites →https://doi.org/10.1167/6.4.13openalex-snapshot
Spike-triggered neural characterization
inferredcites →https://doi.org/10.1167/6.4.9openalex-snapshot
Dimensionality reduction in neural models: An information-theoretic generalization of spike-triggered average and covariance analysis
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.pbio.1000063openalex-snapshot
Receptive Fields in Primate Retina Are Coordinated to Sample Visual Space More Uniformly
inferredcites →https://doi.org/10.1371/journal.pcbi.1003143openalex-snapshot
Inferring Nonlinear Neuronal Computation Based on Physiologically Plausible Inputs
inferredcites →https://doi.org/10.1371/journal.pcbi.1003356openalex-snapshot
Beyond GLMs: A Generative Mixture Modeling Approach to Neural System Identification
inferredcites →https://doi.org/10.1371/journal.pone.0071959openalex-snapshot
Maximally Informative “Stimulus Energies” in the Analysis of Neural Responses to Natural Signals
inferredcites →https://doi.org/10.1523/jneurosci.19-22-09756.1999openalex-snapshot
Functional Circuitry of the Retinal Ganglion Cell's Nonlinear Receptive Field
inferredcites →https://doi.org/10.1523/jneurosci.21-19-07447.2001openalex-snapshot
Bipolar Cells Contribute to Nonlinear Spatial Summation in the Brisk-Transient (Y) Ganglion Cell in Mammalian Retina
inferredcites →https://doi.org/10.1523/jneurosci.21-24-09904.2001openalex-snapshot
Adaptation to Temporal Contrast in Primate and Salamander Retina
inferredcites →https://doi.org/10.1523/jneurosci.22-07-02737.2002openalex-snapshot
Functional Asymmetries in ON and OFF Ganglion Cells of Primate Retina
inferredcites →https://doi.org/10.1523/jneurosci.2815-13.2015openalex-snapshot
A Convolutional Subunit Model for Neuronal Responses in Macaque V1
inferredcites →https://doi.org/10.1523/jneurosci.3437-07.2007openalex-snapshot
Spatial Properties and Functional Organization of Small Bistratified Ganglion Cells in Primate Retina
inferredcites →https://doi.org/10.3389/fnana.2015.00122openalex-snapshot
OFF bipolar cells in macaque retina: type-specific connectivity in the outer and inner synaptic layers
inferredcites →https://doi.org/10.48550/arxiv.1412.6980openalex-snapshot
Adam: A Method for Stochastic Optimization
inferredcites →https://doi.org/10.48550/arxiv.1702.01825openalex-snapshot
Deep Learning Models of the Retinal Response to Natural Scenes
inferredcites →https://doi.org/10.7554/elife.05241openalex-snapshot
Mapping nonlinear receptive field structure in primate retina at single cone resolution
inferredcites →https://doi.org/10.7554/elife.38841openalex-snapshot
Receptive field center-surround interactions mediate context-dependent spatial contrast encoding in the retina
inferredcites →https://doi.org/10.7554/elife.38841.025openalex-snapshot
Author response: Receptive field center-surround interactions mediate context-dependent spatial contrast encoding in the retina
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.neuron.2019.05.036openalex-snapshot
Unusual Physiological Properties of Smooth Monostratified Ganglion Cell Types in Primate Retina
inferred← citeshttps://doi.org/10.1038/s41583-019-0242-1openalex-snapshot
Understanding the retinal basis of vision across species
inferred← citeshttps://doi.org/10.1038/s41598-020-61899-yopenalex-snapshot
Probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina
inferred← citeshttps://doi.org/10.1523/eneuro.0191-21.2021openalex-snapshot
Identification of Multiple Noise Sources Improves Estimation of Neural Responses across Stimulus Conditions
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