A Neural Representation of Naturalistic Motion-Guided Behavior in the Zebrafish Brain

Ultrasensitive fluorescent proteins for imaging neuronal activity

Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474 · see citing works

Spatiotemporal energy models for the perception of motion

Adelson, E. H., & Bergen, J. R. (1985) · Journal of the Optical Society of America A · doi:10.1364/josaa.2.000284 · Cited by 3,442 · see citing works

Sensory Communication

(1961) · Information and Control · doi:10.1016/s0019-9958(61)80064-8 · Cited by 2,904 · see citing works

Natural Image Statistics and Neural Representation

Simoncelli, E. P., & Olshausen, B. A. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1193 · Cited by 2,460 · see citing works

Whole-brain functional imaging at cellular resolution using light-sheet microscopy

Ahrens, M. B., Orger, M. B., Robson, D. N., Li, J. M., & Keller, P. J. (2013) · Nature Methods · doi:10.1038/nmeth.2434 · Cited by 1,392 · see citing works

Possible Principles Underlying the Transformations of Sensory Messages

Barlow, H. B. (2012) · The MIT Press eBooks · doi:10.7551/mitpress/9780262518420.003.0013 · Cited by 1,318 · see citing works

Independent component filters of natural images compared with simple cells in primary visual cortex

van Hateren, J. H., & van der Schaaf, A. (1998) · Proceedings of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rspb.1998.0303 · Cited by 1,106 · see citing works

The functional diversity of retinal ganglion cells in the mouse

Baden, T., Berens, P., Franke, K., Román Rosón, M., Bethge, M., & Euler, T. (2016) · Nature · doi:10.1038/nature16468 · Cited by 999 · see citing works

Statistics of natural images: Scaling in the woods

Ruderman, D., & Bialek, W. (1994) · Physical Review Letters · doi:10.1103/physrevlett.73.814 · Cited by 954 · see citing works

Systemtheoretische Analyse der Zeit-, Reihenfolgen- und Vorzeichenauswertung bei der Bewegungsperzeption des Rüsselkäfers Chlorophanus

Hassenstein, B., & Reichardt, W. (1956) · Zeitschrift für Naturforschung B · doi:10.1515/znb-1956-9-1004 · Cited by 893 · see citing works

Biological image motion processing: A review

Nakayama, K. (1985) · Vision Research · doi:10.1016/0042-6989(85)90171-3 · Cited by 887 · see citing works

Eye Smarter than Scientists Believed: Neural Computations in Circuits of the Retina

Gollisch, T., & Meister, M. (2010) · Neuron · doi:10.1016/j.neuron.2009.12.009 · Cited by 795 · see citing works

Brain-wide neuronal dynamics during motor adaptation in zebrafish

Ahrens, M. B., Li, J. M., Orger, M. B., Robson, D. N., Schier, A. F., Engert, F., & Portugues, R. (2012) · Nature · doi:10.1038/nature11057 · Cited by 729 · see citing works

What Does the Retina Know about Natural Scenes?

Atick, J. J., & Redlich, A. (1992) · Neural Computation · doi:10.1162/neco.1992.4.2.196 · Cited by 706 · see citing works

Could information theory provide an ecological theory of sensory processing?

Atick, J. J. (2011) · Network: Computation in Neural Systems · doi:10.3109/0954898x.2011.638888 · Cited by 679 · see citing works

Drift-balanced random stimuli: a general basis for studying non-Fourier motion perception

Chubb, C. F., & Sperling, G. (1988) · Journal of the Optical Society of America A · doi:10.1364/josaa.5.001986 · Cited by 657 · see citing works

Design Principles of Insect and Vertebrate Visual Systems

Sanes, J. R., & Zipursky, S. L. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.018 · Cited by 559 · see citing works

Whole-brain activity mapping onto a zebrafish brain atlas

Randlett, O., Wee, C. L., Naumann, E. A., Nnaemeka, O., Schoppik, D., Fitzgerald, J. E., Portugues, R., Lacoste, A. M. B., Riegler, C., Engert, F., et al. (2015) · Nature Methods · doi:10.1038/nmeth.3581 · Cited by 528 · see citing works

How MT cells analyze the motion of visual patterns

Rust, N. C., Mante, V., Simoncelli, E. P., & Movshon, J. A. (2006) · Nature Neuroscience · doi:10.1038/nn1786 · Cited by 516 · see citing works

A synaptic threshold mechanism for computing escape decisions

Evans, D. A., Stempel, A. V., Vale, R., Ruehle, S., Lefler, Y., & Branco, T. (2018) · Nature · doi:10.1038/s41586-018-0244-6 · Cited by 449 · see citing works

Selective Sensitivity to Direction of Movement in Ganglion Cells of the Rabbit Retina

Barlow, H. B., & Hill, R. M. (1963) · Science · doi:10.1126/science.139.3553.412 · Cited by 435 · see citing works

Genetic disorders of vision revealed by a behavioral screen of 400 essential loci in zebrafish

Neuhauss, S. C. F., Biehlmaier, O., Seeliger, M. W., Das, T., Kohler, K., Harris, W. A., & Baier, H. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-19-08603.1999 · Cited by 414 · see citing works

Nonrigid image registration in shared-memory multiprocessor environments with application to brains, breasts, and bees

Torsten Rohlfing, B., & Maurer, C. R. (2003) · IEEE Transactions on Information Technology in Biomedicine · doi:10.1109/titb.2003.808506 · Cited by 373 · see citing works

ON and OFF pathways in Drosophila motion vision

Joesch, M., Schnell, B., Raghu, S. V., Reiff, D. F., & Borst, A. (2010) · Nature · doi:10.1038/nature09545 · Cited by 352 · see citing works

Visual prey capture in larval zebrafish is controlled by identified reticulospinal neurons downstream of the tectum

Gahtan, E., Tanger, P., & Baier, H. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2678-05.2005 · Cited by 350 · see citing works

Neural circuits underlying visually evoked escapes in larval zebrafish

Dunn, T. W., Gebhardt, C., Naumann, E. A., Riegler, C., Ahrens, M. B., Engert, F., & Del Bene, F. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.021 · Cited by 347 · see citing works

Fly Motion Vision

Borst, A., Haag, J., & Reiff, D. F. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153155 · Cited by 336 · see citing works

Prey capture behavior evoked by simple visual stimuli in larval zebrafish

Bianco, I. H., Kampff, A. R., & Engert, F. (2011) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2011.00101 · Cited by 332 · see citing works

Forward genetic analysis of visual behavior in zebrafish

Muto, A., Orger, M. B., Wehman, A. M., Smear, M. C., Kay, J. N., Page-McCaw, P. S., Gahtan, E., Xiao, T., Nevin, L. M., Gosse, N. J., et al. (2005) · PLoS Genetics · doi:10.1371/journal.pgen.0010066 · Cited by 321 · see citing works

From Whole-Brain Data to Functional Circuit Models: The Zebrafish Optomotor Response

Naumann, E. A., Fitzgerald, J. E., Dunn, T. W., Rihel, J., Sompolinsky, H., & Engert, F. (2016) · Cell · doi:10.1016/j.cell.2016.10.019 · Cited by 315 · see citing works

A dedicated circuit links direction-selective retinal ganglion cells to the primary visual cortex

Cruz‐Martín, A., El-Danaf, R. N., Osakada, F., Sriram, B., Dhande, O. S., Nguyen, P. L., Callaway, E. M., Ghosh, A., & Huberman, A. D. (2014) · Nature · doi:10.1038/nature12989 · Cited by 312 · see citing works

Brain-wide mapping of neural activity controlling zebrafish exploratory locomotion

Dunn, T. W., Mu, Y., Narayan, S., Randlett, O., Naumann, E. A., Yang, C.-T., Schier, A. F., Freeman, J., Engert, F., & Ahrens, M. B. (2016) · eLife · doi:10.7554/elife.12741 · Cited by 312 · see citing works

Three-systems theory of human visual motion perception: review and update

Lu, Z., & Sperling, G. (2001) · Journal of the Optical Society of America A · doi:10.1364/josaa.18.002331 · Cited by 306 · see citing works

Whole-brain activity maps reveal stereotyped, distributed networks for visuomotor behavior

Portugues, R., Feierstein, C. E., Engert, F., & Orger, M. B. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.019 · Cited by 305 · see citing works

Visual projection neurons in the Drosophila lobula link feature detection to distinct behavioral programs

Wu, M., Nern, A., Williamson, W. R., Morimoto, M. M., Reiser, M. B., Card, G. M., & Rubin, G. M. (2016) · eLife · doi:10.7554/elife.21022 · Cited by 304 · see citing works

A visual pathway for looming-evoked escape in larval zebrafish

Temizer, I., Donovan, J. C., Baier, H., & Semmelhack, J. L. (2015) · Current Biology · doi:10.1016/j.cub.2015.06.002 · Cited by 292 · see citing works

Control of visually guided behavior by distinct populations of spinal projection neurons

Orger, M. B., Kampff, A. R., Severi, K. E., Bollmann, J. H., & Engert, F. (2008) · Nature Neuroscience · doi:10.1038/nn2048 · Cited by 274 · see citing works

Elementary Computation of Object Approach by a Wide-Field Visual Neuron

Hatsopoulos, N., Gabbiani, F., & Laurent, G. (1995) · Science · doi:10.1126/science.270.5238.1000 · Cited by 263 · see citing works

A spike-timing mechanism for action selection

von Reyn, C. R., Breads, P., Peek, M. Y., Zheng, G. Z., Williamson, W. R., Yee, A. L., Leonardo, A., & Card, G. M. (2014) · Nature Neuroscience · doi:10.1038/nn.3741 · Cited by 254 · see citing works

Development of the retinofugal projections in the embryonic and larval zebrafish ( <i>Brachydanio rerio</i> )

Burrill, J. D., & Easter, S. S. (1994) · Journal of Comparative Neurology · doi:10.1002/cne.903460410 · Cited by 248 · see citing works

Structure of the Zebrafish Locomotor Repertoire Revealed with Unsupervised Behavioral Clustering

Marques, J. C., Lackner, S., Félix, R., & Orger, M. B. (2018) · Current Biology · doi:10.1016/j.cub.2017.12.002 · Cited by 245 · see citing works

Zebrafish Differentially Process Color across Visual Space to Match Natural Scenes

Zimmermann, M. J. Y., Nevala, N. E., Yoshimatsu, T., Osorio, D., Nilsson, D.-E., Berens, P., & Baden, T. (2018) · Current Biology · doi:10.1016/j.cub.2018.04.075 · Cited by 227 · see citing works

Visuomotor behaviors in larval zebrafish after GFP-guided laser ablation of the optic tectum

Roeser, T., & Baier, H. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-09-03726.2003 · Cited by 222 · see citing works

Common circuit design in fly and mammalian motion vision

Borst, A., & Helmstaedter, M. N. (2015) · Nature Neuroscience · doi:10.1038/nn.4050 · Cited by 218 · see citing works

Visuomotor Transformations Underlying Hunting Behavior in Zebrafish

Bianco, I. H., & Engert, F. (2015) · Current Biology · doi:10.1016/j.cub.2015.01.042 · Cited by 217 · see citing works

Considerations on models of movement detection

Poggio, T., & Reichardt, W. (1973) · Kybernetik · doi:10.1007/bf00274887 · Cited by 212 · see citing works

Vision Drives Accurate Approach Behavior during Prey Capture in Laboratory Mice

Hoy, J. L., Yavorska, I., Wehr, M., & Niell, C. M. (2016) · Current Biology · doi:10.1016/j.cub.2016.09.009 · Cited by 212 · see citing works

Perception of Fourier and non-Fourier motion by larval zebrafish

Orger, M. B., Smear, M. C., Anstis, S., & Baier, H. (2000) · Nature Neuroscience · doi:10.1038/80649 · Cited by 211 · see citing works

Circuit Neuroscience in Zebrafish

Friedrich, R. W., Jacobson, G. A., & Zhu, P. (2010) · Current Biology · doi:10.1016/j.cub.2010.02.039 · Cited by 207 · see citing works

A dedicated visual pathway for prey detection in larval zebrafish

Semmelhack, J. L., Donovan, J. C., Thiele, T. R., Kuehn, E., Laurell, E., & Baier, H. (2014) · eLife · doi:10.7554/elife.04878 · Cited by 204 · see citing works

Fundamental mechanisms of visual motion detection: models, cells and functions

Clifford, C. W. G., & Ibbotson, M. R. (2002) · Progress in Neurobiology · doi:10.1016/s0301-0082(02)00154-5 · Cited by 202 · see citing works

The Retinal Projectome Reveals Brain-Area-Specific Visual Representations Generated by Ganglion Cell Diversity

Robles, E., Laurell, E., & Baier, H. (2014) · Current Biology · doi:10.1016/j.cub.2014.07.080 · Cited by 201 · see citing works

Brain-wide Organization of Neuronal Activity and Convergent Sensorimotor Transformations in Larval Zebrafish

Chen, X., Mu, Y., Hu, Y., Kuan, A. T., Nikitchenko, M., Randlett, O., Chen, A. B., Gavornik, J. P., Sompolinsky, H., Engert, F., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.042 · Cited by 199 · see citing works

Transient and steady-state response properties of movement detectors

Egelhaaf, M., & Borst, A. (1989) · Journal of the Optical Society of America A · doi:10.1364/josaa.6.000116 · Cited by 188 · see citing works

Identification of Mauthner-initiated response patterns in goldfish: Evidence from simultaneous cinematography and electrophysiology

Eaton, R. C., Lavender, W. A., & Wieland, C. M. (1981) · Journal of Comparative Physiology A · doi:10.1007/bf01326837 · Cited by 186 · see citing works

Functional Architecture of an Optic Flow-Responsive Area that Drives Horizontal Eye Movements in Zebrafish

Kubo, F., Hablitzel, B., Dal Maschio, M., Driever, W., Baier, H., & Arrenberg, A. B. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.043 · Cited by 182 · see citing works

The neural processing of 3‐D visual information: evidence from eye movements

Miles, F. A. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00112.x · Cited by 178 · see citing works

Neural circuits for evidence accumulation and decision making in larval zebrafish

Bahl, A., & Engert, F. (2020) · Nature Neuroscience · doi:10.1038/s41593-019-0534-9 · Cited by 166 · see citing works

Parametric Functional Maps of Visual Inputs to the Tectum

Nikolaou, N., Lowe, A., Walker, A., Abbas, F. H., Hunter, P. R., Thompson, I. D., & Meyer, M. P. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.040 · Cited by 162 · see citing works

Understanding Retinal Color Coding from First Principles

Atick, J. J., Zhaoping, L., & Redlich, A. (1992) · Neural Computation · doi:10.1162/neco.1992.4.4.559 · Cited by 160 · see citing works

Central neural mechanisms for detecting second-order motion

Baker, C. L. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)80069-5 · Cited by 150 · see citing works

Accuracy of velocity estimation by Reichardt correlators

Dror, R. O., O’Carroll, D. C., & Laughlin, S. B. (2001) · Journal of the Optical Society of America A · doi:10.1364/josaa.18.000241 · Cited by 144 · see citing works

Fly motion vision is based on Reichardt detectors regardless of the signal-to-noise ratio

Haag, J., Denk, W. T., & Borst, A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407368101 · Cited by 140 · see citing works

Synaptic Activity and Activity-Dependent Competition Regulates Axon Arbor Maturation, Growth Arrest, and Territory in the Retinotectal Projection

Fredj, N. B., Hammond, S. E., Otsuna, H., Chien, C.-B., Burrone, J., & Meyer, M. P. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1556-10.2010 · Cited by 135 · see citing works

Sensorimotor computation underlying phototaxis in zebrafish

Wolf, S., Dubreuil, A. M., Bertoni, T., Böhm, U. L., Bormuth, V., Candelier, R., Karpenko, S., Hildebrand, D. G. C., Bianco, I. H., Monasson, R., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00310-3 · Cited by 134 · see citing works

Theoretical understanding of the early visual processes by data compression and data selection

Li Zhaoping, A. (2006) · Network Computation in Neural Systems · doi:10.1080/09548980600931995 · Cited by 131 · see citing works

Flies see second-order motion

Theobald, J. C., Duistermars, B. J., Ringach, D. L., & Frye, M. A. (2008) · Current Biology · doi:10.1016/j.cub.2008.03.050 · Cited by 118 · see citing works

Power spectra and distribution of contrasts of natural images from different habitats

Balboa, R. M., & Grzywacz, N. M. (2003) · Vision Research · doi:10.1016/s0042-6989(03)00471-1 · Cited by 104 · see citing works

Flies and humans share a motion estimation strategy that exploits natural scene statistics

Clark, D. A., Fitzgerald, J. E., Ales, J. M., Gohl, D. M., Silies, M., Norcia, A. M., & Clandinin, T. R. (2014) · Nature Neuroscience · doi:10.1038/nn.3600 · Cited by 94 · see citing works

Neural modulation of visuomotor functions underlying prey-catching behaviour in anurans: perception, attention, motor performance, learning

Ewert, J. ‐., Buxbaum-Conradi, H., Dreisvogt, F., Glagow, M., Merkel-Harff, C., Röttgen, A., Schürg-Pfeiffer, E., & Schwippert, W. W. (2001) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/s1095-6433(00)00333-0 · Cited by 90 · see citing works

Direction Selectivity in Drosophila Emerges from Preferred-Direction Enhancement and Null-Direction Suppression

Leong, J. C. S., Esch, J. J., Poole, B., Ganguli, S., & Clandinin, T. R. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1272-16.2016 · Cited by 90 · see citing works

Evidence accumulation during a sensorimotor decision task revealed by whole-brain imaging

Dragomir, E. I., Štih, V., & Portugues, R. (2020) · Nature Neuroscience · doi:10.1038/s41593-019-0535-8 · Cited by 89 · see citing works

Parallel Computations in Insect and Mammalian Visual Motion Processing

Clark, D. A., & Demb, J. B. (2016) · Current Biology · doi:10.1016/j.cub.2016.08.003 · Cited by 84 · see citing works

Comparison of optomotor and optokinetic reflexes in mice

Kretschmer, F., Tariq, M., Chatila, W. K., Wu, B. P., & Badea, T. C. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00055.2017 · Cited by 80 · see citing works

Spatial organization of nonlinear interactions in form perception

Victor, J. D., & Conte, M. M. (1991) · Vision Research · doi:10.1016/0042-6989(91)90125-o · Cited by 79 · see citing works

Asymmetry of Drosophila ON and OFF motion detectors enhances real-world velocity estimation

Leonhardt, A., Ammer, G., Meier, M., Serbe-Kamp, E., Bahl, A., & Borst, A. (2016) · Nature Neuroscience · doi:10.1038/nn.4262 · Cited by 78 · see citing works

Neuronal Architecture of a Visual Center that Processes Optic Flow

Kramer, A., Wu, Y., Baier, H., & Kubo, F. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.018 · Cited by 78 · see citing works

From the optic tectum to the primary visual cortex: migration through evolution of the saliency map for exogenous attentional guidance

Li Zhaoping, A. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.06.017 · Cited by 71 · see citing works

Elementary Motion Detection inDrosophila: Algorithms and Mechanisms

Yang, H. H., & Clandinin, T. R. (2018) · Annual Review of Vision Science · doi:10.1146/annurev-vision-091517-034153 · Cited by 71 · see citing works

Visual Control of Walking Speed in Drosophila

Creamer, M. S., Mano, O., & Clark, D. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.028 · Cited by 67 · see citing works

Direct Measurement of Correlation Responses in Drosophila Elementary Motion Detectors Reveals Fast Timescale Tuning

Salazar-Gatzimas, E., Chen, J., Creamer, M. S., Mano, O., Mandel, H. B., Matulis, C. A., Pottackal, J., & Clark, D. A. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.017 · Cited by 63 · see citing works

A minimal synaptic model for direction selective neurons in Drosophila

Zavatone-Veth, J. A., Badwan, B. A., & Clark, D. A. (2020) · Journal of Vision · doi:10.1167/jov.20.2.2 · Cited by 62 · see citing works

Motion Perception: From Detection to Interpretation

Nishida, S., Kawabe, T., Sawayama, M., & Fukiage, T. (2018) · Annual Review of Vision Science · doi:10.1146/annurev-vision-091517-034328 · Cited by 60 · see citing works

Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum

Wang, K., Hinz, J., Haikala, V., Reiff, D. F., & Arrenberg, A. B. (2019) · BMC Biology · doi:10.1186/s12915-019-0648-2 · Cited by 60 · see citing works

Optomotor Swimming in Larval Zebrafish Is Driven by Global Whole-Field Visual Motion and Local Light-Dark Transitions

Kist, A. M., & Portugues, R. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.024 · Cited by 55 · see citing works

Molecular Fingerprinting of On–Off Direction-Selective Retinal Ganglion Cells Across Species and Relevance to Primate Visual Circuits

Dhande, O. S., Stafford, B. K., Franke, K., El-Danaf, R. N., Percival, K. A., Phan, A. H., Li, P., Hansen, B. J., Nguyen, P. L., Berens, P., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1784-18.2018 · Cited by 54 · see citing works

Nonlinear circuits for naturalistic visual motion estimation

Fitzgerald, J. E., & Clark, D. A. (2015) · eLife · doi:10.7554/elife.09123 · Cited by 52 · see citing works

The statistics of local motion signals in naturalistic movies

Nitzany, E. I., & Victor, J. D. (2014) · Journal of Vision · doi:10.1167/14.4.10 · Cited by 48 · see citing works

Motion clouds: model-based stimulus synthesis of natural-like random textures for the study of motion perception

Sanz‐Leon, P., Vanzetta, I., Masson, G. S., & Perrinet, L. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00737.2011 · Cited by 46 · see citing works

Neural connections of the pretectum in zebrafish ( Danio rerio )

Yáñez, J., Suárez, T., Quelle‐Regaldie, A., Folgueira, M., & Anadón, R. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24388 · Cited by 45 · see citing works

A set of high-order spatiotemporal stimuli that elicit motion and reverse-phi percepts

Hu, Q., & Victor, J. D. (2010) · Journal of Vision · doi:10.1167/10.3.9 · Cited by 43 · see citing works

Optimal Prediction in the Retina and Natural Motion Statistics

Salisbury, J. M., & Palmer, S. E. (2016) · Journal of Statistical Physics · doi:10.1007/s10955-015-1439-y · Cited by 43 · see citing works

The Neuronal Basis of an Illusory Motion Percept Is Explained by Decorrelation of Parallel Motion Pathways

Salazar-Gatzimas, E., Agrochão, M., Fitzgerald, J. E., & Clark, D. A. (2018) · Current Biology · doi:10.1016/j.cub.2018.10.007 · Cited by 43 · see citing works

Symmetries in stimulus statistics shape the form of visual motion estimators

Fitzgerald, J. E., Katsov, A. Y., Clandinin, T. R., & Schnitzer, M. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1015680108 · Cited by 42 · see citing works

Statistical mechanics and visual signal processing

Potters, M., & Bialek, W. (1994) · Journal de Physique I · doi:10.1051/jp1:1994219 · Cited by 41 · see citing works

Gal80 intersectional regulation of cell‐type specific expression in vertebrates

Fujimoto, E., Gaynes, B. F., Brimley, C., Chien, C.-B., & Bonkowsky, J. L. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22734 · Cited by 38 · see citing works

Looming responses of telencephalic neurons in the pigeon are modulated by optic flow

Xiao, Q., & Frost, B. J. (2009) · Brain Research · doi:10.1016/j.brainres.2009.10.008 · Cited by 34 · see citing works

A Theory of the Visual Motion Coding in the Primary Visual Cortex

Zhaoping, L. (1996) · Neural Computation · doi:10.1162/neco.1996.8.4.705 · Cited by 32 · see citing works

Reversed Depth in Anticorrelated Random-Dot Stereograms and the Central-Peripheral Difference in Visual Inference

Zhaoping, L., & Ackermann, J. (2018) · Perception · doi:10.1177/0301006618758571 · Cited by 29 · see citing works

Asymmetric ON-OFF processing of visual motion cancels variability induced by the structure of natural scenes

Chen, J., Mandel, H. B., Fitzgerald, J. E., & Clark, D. A. (2019) · eLife · doi:10.7554/elife.47579 · Cited by 26 · see citing works

Neural computations combine low- and high-order motion cues similarly, in dragonfly and monkeyPreprint

Nitzany, E. I., Menda, G., Shamble, P. S., Golden, J. R., Hu, Q., Hoy, R., & Victor, J. D. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/240101 · Cited by 7 · see citing works

Predictive encoding of motion begins in the primate retina

Liu, B., Hong, A. S., Rieke, F. M., & Manookin, M. B. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00899-1 · Cited by 72 · see citing works

A cerebellar internal model calibrates a feedback controller involved in sensorimotor control

Markov, D., Petrucco, L., Kist, A., & Portugues, R. (2020) · Nature Communications · doi:10.1038/s41467-021-26988-0 · Cited by 70 · see citing works

A minimal synaptic model for direction selective neurons in Drosophila

Zavatone-Veth, J. A., Badwan, B. A., & Clark, D. A. (2020) · Journal of Vision · doi:10.1167/jov.20.2.2 · Cited by 62 · see citing works

A brainstem integrator for self-location memory and positional homeostasis in zebrafish

Yang, E., Zwart, M., James, B., Rubinov, M., Wei, Z., Narayan, S., Vladimirov, N., Mensh, B. D., Fitzgerald, J. E., & Ahrens, M. B. (2022) · Cell · doi:10.1016/j.cell.2022.11.022 · Cited by 61 · see citing works

The Visual Systems of Zebrafish

Baier, H., & Scott, E. K. (2024) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-111020-104854 · Cited by 49 · see citing works

Whole-brain interactions underlying zebrafish behavior

Loring, M. D., Thomson, E. E., & Naumann, E. A. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.09.011 · Cited by 43 · see citing works

Dense Circuit Reconstruction to Understand Neuronal Computation: Focus on Zebrafish

Friedrich, R. W., & Wanner, A. A. (2021) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-110220-013050 · Cited by 33 · see citing works

Optic flow in the natural habitats of zebrafish supports spatial biases in visual self-motion estimation

Alexander, E., Cai, L. T., Fuchs, S., Hladnik, T. C., Zhang, Y., Subramanian, V., Guilbeault, N. C., Vijayakumar, C., Arunachalam, M., Juntti, S. A., et al. (2022) · Current Biology · doi:10.1016/j.cub.2022.10.009 · Cited by 32 · see citing works

A robust receptive field code for optic flow detection and decomposition during self-motion

Zhang, Y., Huang, R., Nörenberg, W., & Arrenberg, A. B. (2022) · Current Biology · doi:10.1016/j.cub.2022.04.048 · Cited by 29 · see citing works

Circuit Organization Underlying Optic Flow Processing in Zebrafish

Matsuda, K., & Kubo, F. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.709048 · Cited by 30 · see citing works

Mechanism for analogous illusory motion perception in flies and humans

Agrochão, M., Tanaka, R., Salazar-Gatzimas, E., & Clark, D. A. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2002937117 · Cited by 30 · see citing works

Predicting individual neuron responses with anatomically constrained task optimization

Mano, O., Creamer, M. S., Badwan, B. A., & Clark, D. A. (2021) · Current Biology · doi:10.1016/j.cub.2021.06.090 · Cited by 24 · see citing works

Structural and functional organization of visual responses in the inferior olive of larval zebrafish

Félix, R., Markov, D. A., Renninger, S. L., Tomás, A. R., Laborde, A., Carey, M. R., Orger, M. B., & Portugues, R. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.2352-21.2023 · Cited by 15 · see citing works

Optimization in Visual Motion Estimation

Clark, D. A., & Fitzgerald, J. E. (2024) · Annual Review of Vision Science · doi:10.1146/annurev-vision-101623-025432 · Cited by 9 · see citing works

Artificial embodied circuits uncover neural architectures of vertebrate visuomotor behaviors

Liu, X., Loring, M. D., Zunino, L., Fouke, K. E., Longchamp, F. A., Bernardino, A., Ijspeert, A. J., & Naumann, E. A. (2025) · Science Robotics · doi:10.1126/scirobotics.adv4408 · Cited by 8 · see citing works

The optomotor response of aging zebrafish reveals a complex relationship between visual motion characteristics and cholinergic system

Karaduman, A., Karoglu-Eravsar, E. T., Kaya, U., Aydin, A., Adams, M. M., & Kafalıgönül, H. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.10.018 · Cited by 8 · see citing works

Spatiotemporal visual statistics of aquatic environments in the natural habitats of zebrafish

Cai, L. T., Krishna, V. S., Hladnik, T. C., Guilbeault, N. C., Vijayakumar, C., Arunachalam, M., Juntti, S. A., Arrenberg, A. B., Thiele, T. R., & Cooper, E. A. (2023) · Scientific Reports · doi:10.1038/s41598-023-36099-z · Cited by 8 · see citing works

Behavioral effects of visual stimuli in adult zebrafish using a novel eight-tank imaging system

Gore, S. V., Hernández, T. D. R., & Créton, R. (2024) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2024.1320126 · Cited by 6 · see citing works

A brainstem integrator for self-localization and positional homeostasisPreprint

Yang, E., Zwart, M., Rubinov, M., James, B., Wei, Z., Narayan, S., Vladimirov, N., Mensh, B. D., Fitzgerald, J. E., & Ahrens, M. B. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.26.468907 · Cited by 5 · see citing works

Theoretical principles for illuminating sensorimotor processing with brain-wide neuronal recordings

Tirthabir Biswas, A., Bishop, W. E., & Fitzgerald, J. E. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.10.021 · Cited by 4 · see citing works

Direct comparison reveals algorithmic similarities in fly and mouse visual motion detection

Chen, J., Gish, C. M., Fransen, J. W., Salazar-Gatzimas, E., Clark, D. A., & Borghuis, B. G. (2023) · iScience · doi:10.1016/j.isci.2023.107928 · Cited by 3 · see citing works

Zebrafish optomotor response to second-order motion illustrates that age-related changes in motion detection depend on the activated motion system

Karaduman, A., Karoglu-Eravsar, E. T., Kaya, U., Aydin, A., Adams, M. M., & Kafalıgönül, H. (2023) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2023.06.005 · Cited by 3 · see citing works

Fly navigational responses to odor motion and gradient cues are tuned to plume statisticsPreprint

Brudner, S. N., Zhou, B., Jayaram, V., Santana, G. M. T., Clark, D. A., & Emonet, T. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.31.646361 · Cited by 3 · see citing works

Humans can use positive and negative spectrotemporal correlations to detect rising and falling pitch

Vaziri, P. A., McDougle, S. D., & Clark, D. A. (2026) · Nature Human Behaviour · doi:10.1038/s41562-025-02371-7 · Cited by 2 · see citing works

Behavioral alignment as an organizing principle in sensory codingPreprint

Huang, S., Portugues, R., & Fitzgerald, J. E. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.04.703828 · Cited by 2 · see citing works

Molecular and functional dissection using CaMPARI-seq reveals the neuronal organization for dissociating optic flow-dependent behaviors

Matsuda, K., Wang, C., Kakinuma, H., Toyoda, A., Shiraki, T., Kawakami, K., & Kubo, F. (2026) · Nature Communications · doi:10.1038/s41467-026-71371-6 · Cited by 1 · see citing works

The FlEye camera: Sampling the joint distribution of natural scenes and motion

Edelson, C. J., Smith, P., Setayeshgar, S., Bialek, W., & van Steveninck, R. R. D. R. (2026) · Physical review. E · doi:10.1103/31k4-nq97 · Cited by 1 · see citing works

Fly navigational responses exploit plume-specific odor motion and gradient cues

Brudner, S. N., Zhou, B., Jayaram, V., Santana, G. M., Crimaldi, J. P., Clark, D. A., & Emonet, T. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2608896123 · Cited by 4 · see citing works

Complex pectoral-fin-driven locomotion underlies refined visuomotor behavior in the cichlid Astatotilapia burtoni

Guilbeault, N. C., Westbrook, M. E., Krishna, V. S., Ansari, R., Keth, A., Arrenberg, A. B., Juntti, S. A., & Thiele, T. R. (2026) · iScience · doi:10.1016/j.isci.2026.117136 · Cited by 1 · see citing works

A neural basis for learning sequential memory in brain loop structures

Sihn, D., & Kim, S.-P. (2024) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2024.1421458 · Cited by 1 · see citing works

Species difference in visual motion integration in pigeons, primates and other vertebrates

Hataji, Y. (2023) · Hikaku seiri seikagaku(Comparative Physiology and Biochemistry) · doi:10.3330/hikakuseiriseika.40.46

Passive exposure to visual motion leads to short-term changes in the optomotor response of aging zebrafish

Karaduman, A., Karoglu-Eravsar, E. T., Adams, M. M., & Kafalıgönül, H. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114812

Neural circuits dynamics underlying Fourier motion detection and the alternation in perceptive visual states in the zebrafish larva

Duchemin, A. (2022) · doi:10.70675/a84530e7zd91ez4221za7c4z7cc3224a59ce

Innate sensorimotor policies constrain cerebellar adaptive correctionPreprint

Shenoy, A. K., & Portugues, R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.01.754451

Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum

Wang, K., Hinz, J., Haikala, V., Reiff, D. F., & Arrenberg, A. B. (2019) · BMC Biology · doi:10.1186/s12915-019-0648-2 · Cited by 60 · see citing works

Parallel Channels for Motion Feature Extraction in the Pretectum and Tectum of Larval Zebrafish

Wang, K., Hinz, J., Zhang, Y., Thiele, T. R., & Arrenberg, A. B. (2020) · Cell Reports · doi:10.1016/j.celrep.2019.12.031 · Cited by 66 · see citing works

Neuronal Architecture of a Visual Center that Processes Optic Flow

Kramer, A., Wu, Y., Baier, H., & Kubo, F. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.018 · Cited by 78 · see citing works

Motion Processing in the Larval Zebrafish Tectum

Grama, A. (2015) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)

The Zebrafish Visual System: From Circuits to Behavior

Bollmann, J. H. (2019) · Annual Review of Vision Science · doi:10.1146/annurev-vision-091718-014723 · Cited by 123 · see citing works