Locomotion Controls Spatial Integration in Mouse Visual Cortex

Normalization as a canonical neural computation

Carandini, M., & Heeger, D. J. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3136 · Cited by 1,906

Modulation of visual responses by behavioral state in mouse visual cortex

Niell, C. M., & Stryker, M. P. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.033 · Cited by 1,483 · cited 7×

Is neocortex essentially multisensory?

GHAZANFAR, A., & SCHROEDER, C. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.04.008 · Cited by 1,463

The Normalization Model of Attention

Reynolds, J. H., & Heeger, D. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.002 · Cited by 1,457

Sparse Coding and Decorrelation in Primary Visual Cortex During Natural Vision

Vinje, W. E., & Gallant, J. L. (2000) · Science · doi:10.1126/science.287.5456.1273 · Cited by 1,286

Cortical state and attention

Harris, K. D., & Thiele, A. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3084 · Cited by 915

Natural signal statistics and sensory gain control

Schwartz, O., & Simoncelli, E. P. (2001) · Nature Neuroscience · doi:10.1038/90526 · Cited by 835

Nature and Interaction of Signals From the Receptive Field Center and Surround in Macaque V1 Neurons

Cavanaugh, J. R., Bair, W., & Movshon, J. A. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00692.2001 · Cited by 784

A neural circuit for spatial summation in visual cortex

Adesnik, H., Bruns, W., Taniguchi, H., Huang, Z. J., & Scanziani, M. (2012) · Nature · doi:10.1038/nature11526 · Cited by 702

Sensorimotor mismatch signals in primary visual cortex of the behaving mouse

Keller, G. B., Bonhoeffer, T., & Hübener, M. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.040 · Cited by 668

The meso-connectomes of mouse, marmoset, and macaque: network organization and the emergence of higher cognition

Magrou, L., Joyce, M. K. P., Froudist‐Walsh, S., Datta, D., Wang, X., Martínez-Trujillo, J., & Arnsten, A. F. T. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae174 · Cited by 34

Pharmaco‐electroencephalographic responses in the rat differ between active and inactive locomotor states

Hansen, I. H., Agerskov, C., Arvastson, L., Bastlund, J. F., Sørensen, H. B. D., & Herrik, K. F. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14373 · Cited by 34

Flexible neural population dynamics govern the speed and stability of sensory encoding in mouse visual cortex

Horrocks, E. A. B., Rodrigues, F. R., & Saleem, A. B. (2024) · Nature Communications · doi:10.1038/s41467-024-50563-y · Cited by 35

Unique Spatial Integration in Mouse Primary Visual Cortex and Higher Visual Areas

Murgas, K. A., Wilson, A. M., Michael, V., & Glickfeld, L. L. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1997-19.2020 · Cited by 32

Ongoing movement controls sensory integration in the dorsolateral striatum

de la Torre‐Martínez, R., Ketzef, M., & Silberberg, G. (2023) · Nature Communications · doi:10.1038/s41467-023-36648-0 · Cited by 32

Naturalistic neuroscience and virtual reality

Thurley, K. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.896251 · Cited by 39

Integration of visual and whisker signals in rat superior colliculus

Gharaei, S., Arabzadeh, E., & Solomon, S. G. (2018) · Scientific Reports · doi:10.1038/s41598-018-34661-8 · Cited by 29

Self-motion processing in visual and entorhinal cortices: inputs, integration, and implications for position coding

Campbell, M. G., & Giocomo, L. M. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00686.2017 · Cited by 29

Running modulates primate and rodent visual cortex differently

Liska, J. P., Rowley, D. P., Nguyen, T. T. K., Muthmann, J.-O., Butts, D. A., Yates, J. L., & Huk, A. C. (2024) · eLife · doi:10.7554/elife.87736.3 · Cited by 29

Locomotion-Related Population Cortical Ca2+ Transients in Freely Behaving Mice

Zhang, Q., Yao, J., Guang, Y., Liang, S., Guan, J., Qin, H., Liao, X., Jin, W., Zhang, J., Pan, J., et al. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00024 · Cited by 26

Deconstructing Interocular Suppression: Attention and Divisive Normalization

Li, H.-H., Carrasco, M., & Heeger, D. J. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004510 · Cited by 27

Auditory cortex ensembles jointly encode sound and locomotion speed to support sound perception during movement

Vivaldo, C. A., Lee, J., Shorkey, M., Keerthy, A., & Rothschild, G. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002277 · Cited by 37

Common rules underlying optogenetic and behavioral modulation of responses in multi-cell-type V1 circuitsPreprint

Palmigiano, A., Fumarola, F., Mossing, D. P., Kraynyukova, N., Adesnik, H., & Miller, K. D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.11.378729 · Cited by 26

Stability and Plasticity of Contextual Modulation in the Mouse Visual Cortex

Ranson, A. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.12.080 · Cited by 27

Cortical circuits for integration of self-motion and visual-motion signals

Chaplin, T. A., & Margrie, T. W. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.11.013 · Cited by 24

The influence of locomotion on sensory processing and its underlying neuronal circuits

Busse, L. (2018) · e-Neuroforum · doi:10.1515/nf-2017-a046 · Cited by 24

The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of attention in head-fixed mice

Havenith, M. N., Zijderveld, P. M., van Heukelum, S., Abghari, S., Glennon, J. C., & Tiesinga, P. H. E. (2018) · Scientific Reports · doi:10.1038/s41598-018-34966-8 · Cited by 22

Low rank mechanisms underlying flexible visual representations

Ruff, D. A., Xue, C., Kramer, L. E., Baqai, F., & Cohen, M. R. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005797117 · Cited by 20

Temporally precise movement-based predictions in the mouse auditory cortexPreprint

Audette, N. J., Zhou, W., & Schneider, D. M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.13.472457 · Cited by 22

Attention Decorrelates Sensory and Motor Signals in the Mouse Visual Cortex

Abdolrahmani, M., Lyamzin, D. R., Aoki, R., & Benucci, A. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109377 · Cited by 30

Probing mechanisms of visual spatial attention in mice

Speed, A., & Haider, B. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.07.009 · Cited by 22

Walking humans and running mice: perception and neural encoding of optic flow during self-motion

Horrocks, E. A. B., Mareschal, I., & Saleem, A. B. (2022) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2021.0450 · Cited by 29

Walking modulates visual detection performance according to stride cycle phase

Davidson, M., Verstraten, F. A. J., & Alais, D. (2024) · Nature Communications · doi:10.1038/s41467-024-45780-4 · Cited by 22

Pattern identification and characterization reveal permutations of organs as a key genetically controlled property of post-meristematic phyllotaxis

Guédon, Y., Refahi, Y., Besnard, F., Farcot, E., Godin, C., & Vernoux, T. (2013) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2013.07.026 · Cited by 21

Visual Processing by Calretinin Expressing Inhibitory Neurons in Mouse Primary Visual Cortex

Camillo, D., Ahmadlou, M., Saiepour, M. H., Yasaminshirazi, M., Levelt, C. N., & Heimel, J. A. (2018) · Scientific Reports · doi:10.1038/s41598-018-30958-w · Cited by 22

Visual processing mode switching regulated by VIP cells

Lee, J. H., & Mihalaş, Ş. (2017) · Scientific Reports · doi:10.1038/s41598-017-01830-0 · Cited by 22

State-Dependent Regulation of Cortical Processing Speed via Gain Modulation

Wyrick, D. G., & Mazzucato, L. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1895-20.2021 · Cited by 27

Coarse-to-fine processing drives the efficient coding of natural scenes in mouse visual cortex

Skyberg, R. J., Tanabe, S., Chen, H., & Cang, J. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110606 · Cited by 19

Human visual processing during walking: Dissociable pre- and post-stimulus influences

Chen, X., Cao, L., & Händel, B. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119757 · Cited by 20

Cholinergic input to mouse visual cortex signals a movement state and acutely enhances layer 5 responsiveness

Yogesh, B., & Keller, G. B. (2023) · eLife · doi:10.7554/elife.89986 · Cited by 30

Hierarchical stimulus processing in rodent primary and lateral visual cortex as assessed through neuronal selectivity and repetition suppression

Kaliukhovich, D. A., & de Beeck, H. O. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00673.2017 · Cited by 20

The brain during free movement – What can we learn from the animal model

Händel, B., & Schölvinck, M. L. (2017) · Brain Research · doi:10.1016/j.brainres.2017.09.003 · Cited by 18

High-yield methods for accurate two-alternative visual psychophysics in head-fixed micePreprint

Burgess, C., Lak, A., Steinmetz, N. A., Zatka-Haas, P., Reddy, C. B., Jacobs, E. A. K., Linden, J. F., Paton, J. J., Ranson, A., Soares, S., et al. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/051912 · Cited by 18

Existing function in primary visual cortex is not perturbed by new skill acquisition of a non-matched sensory task

Jeon, B. B., Fuchs, T. A. E., Chase, S. M., & Kuhlman, S. J. (2022) · Nature Communications · doi:10.1038/s41467-022-31440-y · Cited by 18

Astrocyte Calcium Responses to Sensory Input: Influence of Circuit Organization and Experimental Factors

López-Hidalgo, M. A., Kellner, V., & Schummers, J. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00016 · Cited by 16

The validity and consistency of continuous joystick response in perceptual decision-making

Szul, M. J., Bompas, A., Sumner, P., & Zhang, J. (2019) · Behavior Research Methods · doi:10.3758/s13428-019-01269-3 · Cited by 16

V1 as an egocentric cognitive map

Linton, P. (2021) · Neuroscience of Consciousness · doi:10.1093/nc/niab017 · Cited by 18

A passive, camera-based head-tracking system for real-time, three-dimensional estimation of head position and orientation in rodents

Vanzella, W., Grion, N., Bertolini, D., Perissinotto, A., Gigante, M., & Zoccolan, D. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00301.2019 · Cited by 16

Antagonistic inhibitory subnetworks control cooperation and competition across cortical spacePreprint

Mossing, D. P., Veit, J., Palmigiano, A., Miller, K. D., & Adesnik, H. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.31.437953 · Cited by 16

Wide-field calcium imaging of cortical activation and functional connectivity in externally- and internally-driven locomotion

West, S. L., Gerhart, M. L., & Ebner, T. J. (2024) · Nature Communications · doi:10.1038/s41467-024-51816-6 · Cited by 17

Moderate physical activity alters the estimation of time, but not space

Tonelli, A., Lunghi, C., & Gori, M. (2022) · Frontiers in Psychology · doi:10.3389/fpsyg.2022.1004504 · Cited by 12

Aerobic Exercise and Human Visual Cortex Neuroplasticity: A Narrative Review

Abuleil, D., Thompson, B. S., & Dalton, K. (2022) · Neural Plasticity · doi:10.1155/2022/6771999 · Cited by 15

Preserving inhibition with a disinhibitory microcircuit in the retina

Chen, Q., Smith, R. G., Huang, X., & Wei, W. (2020) · eLife · doi:10.7554/elife.62618 · Cited by 13

Noise-Robust Modes of the Retinal Population Code Have the Geometry of “Ridges” and Correspond to Neuronal Communities

Loback, A., Prentice, J., Ioffe, M. L., & Berry, M. J. (2017) · Neural Computation · doi:10.1162/neco_a_01011 · Cited by 14

Tracking the Contents of Spatial Working Memory during an Acute Bout of Aerobic Exercise

Garrett, J., Bullock, T., & Giesbrecht, B. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01714 · Cited by 11

Spatiotemporal patterns of population response in the visual cortex under isoflurane: from wakefulness to loss of consciousness

Margalit, S. N., Golomb, N. G., Tsur, O., Yehoshua, E. B., Raz, A., & Slovin, H. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac031 · Cited by 13

Correction of z ‐motion artefacts to allow population imaging of synaptic activity in behaving mice

Ryan, T. M., Hinojosa, A. J., Vroman, R., Papasavvas, C., & Lagnado, L. (2020) · The Journal of Physiology · doi:10.1113/jp278957 · Cited by 12

Running modulates primate and rodent visual cortex differentlyPreprint

Liska, J. P., Rowley, D. P., Nguyen, T. T. K., Muthmann, J.-O., Butts, D. A., Yates, J. L., & Huk, A. C. (2023) · eLife · doi:10.7554/elife.87736 · Cited by 15

Evaluating Visual Cues Modulates Their Representation in Mouse Visual and Cingulate Cortex

Wal, A., Klein, F. J., Born, G., Busse, L., & Katzner, S. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1828-20.2021 · Cited by 12

Coherent mapping of position and head direction across auditory and visual cortex

Mertens, P. E. C., Marchesi, P., Ruikes, T. R., Lohuis, M. N. O., Krijger, Q., Pennartz, C. M. A., & Lansink, C. S. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad045 · Cited by 13

Controlling Brain States

Bennett, C., Arroyo, S., & Hestrin, S. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.007 · Cited by 12

Did you even see that? visual sensory processing of single stimuli under different locomotor loads

Reiser, J. E., Arnau, S., Rinkenauer, G., & Wascher, E. (2022) · PLoS ONE · doi:10.1371/journal.pone.0267896 · Cited by 9

Octopaminergic modulation of temporal frequency tuning of a fly visual motion-sensitive neuron depends on adaptation level

ders, J. L. ⁄., & Kurtz, R. (2015) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2015.00036 · Cited by 10

The neural circuitry supporting successful spatial navigation despite variable movement speeds

Sheeran, W. M., & Ahmed, O. J. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.11.013 · Cited by 12

Cannabinoids modulate associative cerebellar learning via alterations in behavioral state

Albergaria, C., Silva, N. T., Darmohray, D. M., & Carey, M. R. (2020) · eLife · doi:10.7554/elife.61821 · Cited by 12

Moculus: an immersive virtual reality system for mice incorporating stereo vision

Judák, L., Dobos, G., Ócsai, K., Báthory, E., Szebik, H., Tarján, B., Maák, P. A., Szadai, Z., Takács, I., Chiovini, B., et al. (2024) · Nature Methods · doi:10.1038/s41592-024-02554-6 · Cited by 11

Is the impact of spontaneous movements on early visual cortex species specific?

Kang, I., Talluri, B. C., Yates, J. L., Niell, C. M., & Nienborg, H. (2024) · Trends in Neurosciences · doi:10.1016/j.tins.2024.11.006 · Cited by 12

Feedforward and disinhibitory circuits differentially control activity of cortical somatostatin interneurons during behavioral state transitions

van Velze, M. D. B., Dhanasobhon, D., Martinez, M., Morabito, A., Berthaux, E., Pinho, C. M., Zerlaut, Y., & Rebola, N. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114197 · Cited by 9

Running reduces firing but improves coding in rodent higher-order visual cortexPreprint

Christensen, A. J., & Pillow, J. W. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/214007 · Cited by 9

Motor and vestibular signals in the visual cortex permit the separation of self versus externally generated visual motion

Vélez‐Fort, M., Cossell, L., Porta, L., Clopath, C., & Margrie, T. W. (2025) · Cell · doi:10.1016/j.cell.2025.01.032 · Cited by 9

Locomotion-dependent auditory gating to the parietal cortex guides multisensory decisions

Choi, I., & Lee, S. (2025) · Nature Communications · doi:10.1038/s41467-025-57347-y · Cited by 12

Attention Decorrelates Sensory and Motor Signals in the Mouse Visual CortexPreprint

Abdolrahmani, M., Lyamzin, D. R., Aoki, R., & Benucci, A. (2021) · SSRN Electronic Journal · doi:10.1101/615229 · Cited by 8

Recruitment of frontal sensory circuits during visual discrimination

Broom, E., Imbriotis, V., Sengpiel, F., Connelly, W. M., & Ranson, A. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110932 · Cited by 7

Continuous peripersonal tracking accuracy is limited by the speed and phase of locomotion

Davidson, M., Keys, R. T., Szekely, B. J., MacNeilage, P. R., Verstraten, F. A. J., & Alais, D. (2023) · Scientific Reports · doi:10.1038/s41598-023-40655-y · Cited by 7

Truly pattern: Nonlinear integration of motion signals is required to account for the responses of pattern cells in rat visual cortex

Matteucci, G., Marotti, R. B., Zattera, B., & Zoccolan, D. (2023) · Science Advances · doi:10.1126/sciadv.adh4690 · Cited by 7

Lack of functional specialization of neurons in the mouse primary visual cortex that have expressed calretinin

Camillo, D., Levelt, C. N., & Heimel, J. A. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00089 · Cited by 7

On the Influence of Walking on Hazard Detection for Prospective User-Centered Design of an Assistance System for Older Pedestrians

Protzak, J., & Wiczorek, R. (2017) · i-com · doi:10.1515/icom-2017-0007 · Cited by 7

Layer 3 Dynamically Coordinates Columnar Activity According to Spatial Context

Plomp, G., Larderet, I., Fiorini, M., & Busse, L. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1568-18.2018 · Cited by 6

Excitatory/inhibitory ratio disruption modulates neural synchrony and flow directions in a cortical microcircuit

Wagatsuma, N., Nobukawa, S., & Kurikawa, T. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013306 · Cited by 6

Behavioral modulations can alter the visual tuning of neurons in the mouse thalamocortical pathway

Socha, K. Z., Couto, J., Whiteway, M. R., Hosseinjany, S., Butts, D. A., & Bonin, V. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114947 · Cited by 6

Large scale in vivo recordings to study neuronal biophysics

Giocomo, L. M. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.09.009 · Cited by 6

Long-range recruitment of Martinotti cells causes surround suppression and promotes saliency in an attractor network model

Krishnamurthy, P., Silberberg, G., & Lansner, A. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00060 · Cited by 7

Active learning of cortical connectivity from two-photon imaging data

Bertrán, M., Martínez, N., Wang, Y., Dunson, D. B., Sapiro, G., & Ringach, D. L. (2018) · PLoS ONE · doi:10.1371/journal.pone.0196527 · Cited by 6

Robust representation of natural images by sparse and variable population of active neurons in visual cortexPreprint

Yoshida, T., & Ohki, K. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/300863 · Cited by 5

Motor state changes escape behavior of crickets

Kiuchi, K., Shidara, H., Iwatani, Y., & Ogawa, H. (2023) · iScience · doi:10.1016/j.isci.2023.107345 · Cited by 6

Sensory input to cortex encoded on low-dimensional periphery-correlated subspaces

Barreiro, A. K., Fontenele, A. J., Ly, C., Raju, P. C., Gautam, S. H., & Shew, W. L. (2023) · PNAS Nexus · doi:10.1093/pnasnexus/pgae010 · Cited by 5

Context flexibly modulates cue representations in visual cortex

Faulkner, A. D., Chiu, A. S., Sarabi, A., Karthik, S., Li, Y. S., & Burgess, C. R. (2025) · Nature Communications · doi:10.1038/s41467-025-61314-y · Cited by 5

Switching Operation Modes in the Neocortex via Cholinergic Neuromodulation

Puigbò, J.-Y., Arsiwalla, X. D., González‐Ballester, M. Á., & Verschure, P. F. M. J. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-01764-w · Cited by 5

Running modulates primate and rodent visual cortex differentlyPreprint

Liska, J. P., Rowley, D. P., Nguyen, T. T. K., Muthmann, J.-O., Butts, D. A., Yates, J. L., & Huk, A. C. (2023) · eLife · doi:10.7554/elife.87736.1 · Cited by 5

Traceable teleportation: Improving spatial learning in virtual locomotion

Jia, Y., Sin, Z. P. T., Li, C., Ng, P. H. F., Huang, X. X., Baciu, G., Cao, J., & Li, Q. (2024) · International Journal of Human-Computer Studies · doi:10.1016/j.ijhcs.2024.103399 · Cited by 5

Modulation of cortical representations of sensory and contextual information underlies aversive associative learning

Dai, J., & Sun, Q. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114672 · Cited by 3

Measuring contrast processing in the visual system using the steady state visually evoked potential (SSVEP)

Wade, A. R., & Baker, D. H. (2025) · Vision Research · doi:10.1016/j.visres.2025.108614 · Cited by 5

Modeling circuit mechanisms of opposing cortical responses to visual flow perturbations

Fraile, J. G., Scherr, F., Ramasco, J. J., Arkhipov, A. S., Maass, W., & Mirasso, C. R. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011921 · Cited by 5

Visual acuity performance level is independent of locomotionPreprint

Swain, A. D., Park, E., Cheng, Z., Kowalewski, N. N., Sun, A., Allen, T., & Kuhlman, S. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/750844 · Cited by 4

Integration of sound and locomotion information by auditory cortical neuronal ensemblesPreprint

Vivaldo, C. A., Lee, J., Shorkey, M., Keerthy, A., & Rothschild, G. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.16.492071 · Cited by 4

Walking Modulates Active Auditory Sensing

Chen, X., Cao, L., Wieske, R. E., Prada, J. P., Gramann, K., & Händel, B. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0489-25.2025 · Cited by 3

Environmental context influences visual processing in thalamus

Peelman, K., & Haider, B. (2024) · Current Biology · doi:10.1016/j.cub.2025.02.009 · Cited by 4

Motor-Driven Modulation in Visual Neural Circuits

Fujiwara, T., & Chiappe, M. E. (2017) · Springer eBooks · doi:10.1007/978-3-319-57363-2_10 · Cited by 3

A spherical treadmill system to train head-fixed adult rats

Fernández, A. M. M. M., Burman, A., Cáceres, A. I. M., Mininni, C. J., Zanutto, B. S., & Lew, S. E. (2017) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2017.12.018 · Cited by 3

Subcortical source and modulation of the narrowband gamma oscillation in mouse visual cortexPreprint

Saleem, A. B., Lien, A. D., Krumin, M., Haider, B., Rosón, M. R., Ayaz, A., Reinhold, K., Busse, L., Carandini, M., & Harris, K. D. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/050245 · Cited by 3

Behavioral response to visual motion impacts population coding in the mouse visual thalamusPreprint

Socha, K. Z., Whiteway, M. R., Butts, D. A., & Bonin, V. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/382671 · Cited by 3

Interneuron subtypes enable independent modulation of excitatory and inhibitory firing rates after sensory deprivationPreprint

Richter, L. M. A., & Gjorgjieva, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.25.445562 · Cited by 3

Stimulus-Effector Associations Modulate Activity in Early Visual Cortex of MonkeysPreprint

Zubair, M., Arsenault, J. T., & Vanduffel, W. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3985609 · Cited by 3

Behavioral decomposition reveals rich encoding structure employed across neocortexPreprint

Mimica, B., Tombaz, T., Battistin, C., Fuglstad, J. G., Dunn, B. A., & Whitlock, J. R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.08.479515 · Cited by 3

Visuomotor processing in the superior colliculus

Lezama, E., & Treviño, M. (2025) · Academia Neuroscience and Brain Research · doi:10.20935/acadneurosci8046 · Cited by 2

Single Circuit in V1 Capable of Switching Contexts During Movement Using an Inhibitory Population as a Switch

Voina, D., Recanatesi, S., Hu, B., Shea‐Brown, E., & Mihalaş, Ş. (2022) · Neural Computation · doi:10.1162/neco_a_01472 · Cited by 3

Acute exercise has specific effects on the formation process and pathway of visual perception in healthy young men

Komiyama, T., Takedomi, H., Aoyama, C., Goya, R., & Shimegi, S. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.16082 · Cited by 2

Speed modulations in grid cell information geometry

Ye, Z., & Weßel, R. (2025) · Nature Communications · doi:10.1038/s41467-025-62856-x · Cited by 3

Network States Classification based on Local Field Potential Recordings in the Awake Mouse Neocortex

Zerlaut, Y., Zucca, S., Fellin, T., & Panzeri, S. (2022) · eNeuro · doi:10.1523/eneuro.0073-22.2022 · Cited by 2

Precision multidimensional neural population code recovered from single intracellular recordings

Johnson, J. K., Geng, S., Hoffman, M. W., Adesnik, H., & Weßel, R. (2020) · Scientific Reports · doi:10.1038/s41598-020-72936-1 · Cited by 2

Effects of locomotion extend throughout the mouse early visual system

Erisken, S., Vaiceliunaite, A., Jurjut, O., Fiorini, M., Katzner, S., & Busse, L. (2014) · Current Biology · doi:10.1016/j.cub.2014.10.045 · Cited by 256

Looking at vision and behavior in mouse visual cortex

Carandini, M. (2014) · Journal of Vision · doi:10.1167/14.15.6

Spatial integration in mouse primary visual cortex

Vaičeliūnaitė, A., Erisken, S., Franzen, F., Katzner, S., & Busse, L. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00138.2013 · Cited by 85

Local and Global Influences of Visual Spatial Selection and Locomotion in Mouse Primary Visual Cortex

McBride, E. G., Lee, S.-Y. J., & Callaway, E. M. (2019) · Current Biology · doi:10.1016/j.cub.2019.03.065 · Cited by 39

Effects of Locomotion on Visual Responses in the Mouse Superior Colliculus

Savier, E. L., Chen, H., & Cang, J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1854-19.2019 · Cited by 54