Reference health

Coarse-to-Fine Processing Drives the Efficient Coding of Natural Scenes in Mouse Visual Cortex

https://doi.org/10.2139/ssrn.3933995
CiteStamped reference-health badge
52/52 checkable references clean · checked 2026-08-07

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

12 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 52 checked references that resolve
resolves10.1523/JNEUROSCI.3297-06.2006
Dynamic Spatial Processing Originates in Early Visual Pathways
resolves10.1016/j.neuron.2011.11.013
Functional Specialization of Mouse Higher Visual Cortical Areas
resolves10.1037/h0054663
Some informational aspects of visual perception.
resolves10.1523/JNEUROSCI.1920-16.2016
Cortical Control of Spatial Resolution by VIP<sup>+</sup>Interneurons
resolves10.1163/156856897X00357
The Psychophysics Toolbox
resolves10.1523/JNEUROSCI.22-05-01976.2002
Dynamics of Spatial Frequency Tuning in Macaque V1
resolves10.1152/jn.1997.78.2.1045
Spatiotemporal Receptive Field Organization in the Lateral Geniculate Nucleus of Cats and Kittens
resolves10.1152/jn.00320.2014
Subtype-dependent postnatal development of direction- and orientation-selective retinal ganglion cells in mice
resolves10.1523/JNEUROSCI.1155-20.2020
Lack of Evidence for Stereotypical Direction Columns in the Mouse Superior Colliculus
resolves10.1016/j.neuron.2017.08.030
A Fully Automated Approach to Spike Sorting
resolves10.1038/nature11129
Neural population dynamics during reaching
resolves10.1523/JNEUROSCI.16-10-03351.1996
Efficient Coding of Natural Scenes in the Lateral Geniculate Nucleus: Experimental Test of a Computational Theory
resolves10.1016/j.neuron.2012.01.010
How Does the Brain Solve Visual Object Recognition?
resolves10.2307/2986986
An Investigation into the Results of Principal Component Analysis of Data Derived from Random Numbers
resolves10.1152/jn.00858.2003
Visual Cortex Neurons of Monkeys and Cats: Temporal Dynamics of the Spatial Frequency Response Function
resolves10.1523/JNEUROSCI.6456-09.2010
Parallel Input Channels to Mouse Primary Visual Cortex
resolves10.1523/JNEUROSCI.1032-14.2014
Benefits of Pathway Splitting in Sensory Coding
resolves10.1152/jn.00699.2003
Quantitative Characterization of Visual Response Properties in the Mouse Dorsal Lateral Geniculate Nucleus
resolves10.1007/BF02289447
A Rationale and Test for the Number of Factors in Factor Analysis
resolves10.1523/JNEUROSCI.3174-14.2015
Layer-Specific Refinement of Visual Cortex Function after Eye Opening in the Awake Mouse
resolves10.1038/nature07481
Emergence of complex cell properties by learning to generalize in natural scenes
resolves10.1038/nature12015
The emergence of functional microcircuits in visual cortex
resolves10.1016/j.neuron.2011.12.004
Functional Specialization of Seven Mouse Visual Cortical Areas
resolves10.1093/cercor/bhh209
Population Dynamics of Face-responsive Neurons in the Inferior Temporal Cortex
resolves10.1073/pnas.022638499
Spatial frequency and orientation tuning dynamics in area V1
resolves10.1038/nn986
Stereoscopic depth processing in the visual cortex: a coarse-to-fine mechanism
resolves10.1038/s41593-021-00846-0
Efficient and adaptive sensory codes
resolves10.1523/JNEUROSCI.0623-08.2008
Highly Selective Receptive Fields in Mouse Visual Cortex
resolves10.1016/j.neuron.2010.01.033
Modulation of Visual Responses by Behavioral State in Mouse Visual Cortex
resolves10.1038/35079612
Retinal ganglion cells act largely as independent encoders
resolves10.1038/381607a0
Emergence of simple-cell receptive field properties by learning a sparse code for natural images
resolves10.1088/0954-898X_7_2_014
Natural image statistics and efficient coding
resolves10.1016/j.csda.2004.06.015
How many principal components? stopping rules for determining the number of non-trivial axes revisited
resolves10.1152/jn.00601.2004
Temporal Dynamics of Direction Tuning in Motion-Sensitive Macaque Area MT
resolves10.1162/jocn.2010.21424
The Neural Substrates and Timing of Top–Down Processes during Coarse-to-Fine Categorization of Visual Scenes: A Combined fMRI and ERP Study
resolves10.1523/JNEUROSCI.5187-12.2013
Diverse Visual Features Encoded in Mouse Lateral Geniculate Nucleus
resolves10.1038/nn.3064
Decorrelation and efficient coding by retinal ganglion cells
resolves10.1046/j.1460-9568.2003.02420.x
Developmental plasticity of mouse visual acuity
resolves10.1073/pnas.1005846107
Retina is structured to process an excess of darkness in natural scenes
resolves10.1038/387281a0
Dynamics of orientation tuning in macaque primary visual cortex
resolves10.1016/j.neuron.2011.06.013
Development of Direction Selectivity in Mouse Cortical Neurons
resolves10.1038/s41586-021-03317-5
Inter-mosaic coordination of retinal receptive fields
resolves10.1103/PhysRevLett.73.814
Statistics of natural images: Scaling in the woods
resolves10.1038/nn.4498
Retinal origin of direction selectivity in the superior colliculus
resolves10.1038/s41586-019-1346-5
High-dimensional geometry of population responses in visual cortex
resolves10.1038/23703
Global and fine information coded by single neurons in the temporal visual cortex
resolves10.1523/JNEUROSCI.2857-17.2018
Refinement of Spatial Receptive Fields in the Developing Mouse Lateral Geniculate Nucleus Is Coordinated with Excitatory and Inhibitory Remodeling
resolves10.1126/science.287.5456.1273
Sparse Coding and Decorrelation in Primary Visual Cortex During Natural Vision
resolves10.1152/jn.00022.2012
Dynamics of spatial frequency tuning in mouse visual cortex
resolves10.1016/j.neuron.2013.07.023
Environmental Enrichment Rescues Binocular Matching of Orientation Preference in Mice that Have a Precocious Critical Period
resolves10.1088/1741-2552/ab581a
Open source silicon microprobes for high throughput neural recording
resolves10.1152/jn.90941.2008
Gaussian-Process Factor Analysis for Low-Dimensional Single-Trial Analysis of Neural Population Activity
The 12 references without a DOI — listed, not checked
no DOI — not checkedref3
no DOI — not checkedref6
no DOI — not checkedSpatial frequency sensitivity in macaque midbrain
no DOI — not checkedref14
no DOI — not checkedref25
no DOI — not checkedEfficient coding of natural images with a population of noisy Linear-Nonlinear neurons
no DOI — not checkedref28
no DOI — not checkedDevelopment of Natural Scene Representation in Primary Visual Cortex Requires Early Postnatal Experience
no DOI — not checkedThe role of early visual experience in the development of spatial-frequency preference in the primary visual cortex
no DOI — not checkedTransformation of Feature Selectivity From Membrane Potential to Spikes in the Mouse Superior Colliculus
no DOI — not checkedDistinct Circuits for Recovery of Eye Dominance and Acuity in Murine Amblyopia
no DOI — not checkedref63
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

checked 2026-08-07 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record

Embed this badge

Both snippets point at the live badge image and link back to this page. The badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.

<a href="https://citestamp.com/citestamped/10.2139/ssrn.3933995"><img src="https://citestamp.com/citestamped/10.2139/ssrn.3933995/badge.svg" alt="CiteStamped reference-health badge" width="460" height="64"></a>
[![CiteStamped reference-health badge](https://citestamp.com/citestamped/10.2139/ssrn.3933995/badge.svg)](https://citestamp.com/citestamped/10.2139/ssrn.3933995)