Neural circuits for evidence accumulation and decision making in larval zebrafish
Open accessAbstract
To make appropriate decisions, animals need to accumulate sensory evidence. Simple integrator models can explain many aspects of such behavior, but how the underlying computations are mechanistically implemented in the brain remains poorly understood. Here we approach this problem by adapting the random-dot motion discrimination paradigm, classically used in primate studies, to larval zebrafish. Using their innate optomotor response as a measure of decision making, we find that larval zebrafish accumulate and remember motion evidence over many seconds and that the behavior is in close agreement with a bounded leaky integrator model. Through the use of brain-wide functional imaging, we identify three neuronal clusters in the anterior hindbrain that are well suited to execute the underlying computations. By relating the dynamics within these structures to individual behavioral choices, we propose a biophysically plausible circuit arrangement in which an evidence integrator competes against a dynamic decision threshold to activate a downstream motor command.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The open-source simZFish faithfully reproduces the zebrafish OMR using experimentally observed neural activity.
“Benefitting from detailed experimental data (25, 29–34) and recent advances in physics simulation technologies (35), our open-source simZFish faithfully reproduces the zebrafish OMR, utilizing experimentally observed neural activity (25).”
From Artificial embodied circuits uncover neural architectures of vertebrate visuomotor behaviors (2025) · cites this paper as [29]
The Results sections on motion integration report experimentally observed neural activity in larval zebrafish, and the Introduction identifies their motion-following behavior as the optomotor response (page numbers unavailable). The paper also compares a network model with measured neural dynamics, but it does not assess simZFish or establish that simZFish faithfully reproduces the OMR. (LLM, conf=0.85)
Experimental — accuracy not yet measuredCurrent models of zebrafish visuomotor transformations rely on correlation-based neural activity, lack realistic retina or motor representations, omit neural connectivity manipulation, and exclude closed-loop observations of neural activation during behavior.
“Current models of zebrafish visuomotor transformations rely on correlation-based neural activity, lack realistic representations of the retina or motor systems (25, 29), omit the ability to manipulate neural connectivity, and exclude closed-loop observations of neural activation during behavior, which limits the integrative investigation of the system within its sensory and physical environment.”
From Artificial embodied circuits uncover neural architectures of vertebrate visuomotor behaviors (2025) · cites this paper as [29]
The Online methods (Algorithmic modeling; Anterior hindbrain network modeling, pages unavailable) describe simplified sensory inputs and swim-bout outputs, consistent with the claim that the model lacks realistic retina and motor-system representations. But the same methods say the authors varied connectivity weights and modeled visual feedback. The Two-photon calcium imaging methods also describe simultaneous neural imaging and behavioral readout with stimulus changes triggered by detected bouts, so the broader claims of omitted connectivity manipulation and excluded closed-loop observations are not supported. (LLM, conf=0.85)
Experimental — accuracy not yet measuredNeural circuits involved in egocentric orientation in teleost fish include mainly several stages of the sensory and perceptual systems, some sensorimotor forebrain circuits, the optic tectum, the cerebellum, and various premotor centers and descending pathways in the brainstem and medulla.
“These neural circuits include mainly several stages of the sensory and perceptual systems, some sensorimotor forebrain circuits, the optic tectum, the cerebellum, and various premotor centers and descending pathways in the brainstem and medulla”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [107]
The Results sections on motion integration and anterior hindbrain imaging identify sensory processing in the pretectum, anterior hindbrain circuits, and projections toward premotor areas (page numbers unavailable). They do not establish the claimed circuit inventory for egocentric orientation in teleost fish, including sensorimotor forebrain circuits, the optic tectum, the cerebellum, or descending pathways in the medulla. (LLM, conf=0.86)
Experimental — accuracy not yet measuredOutput neurons in the intermediate and deep layers of the teleost optic tectum are able to initiate orientation or avoidance responses through their projections to the reticular formation and other pre-motor cell groups in the brainstem, which activate motoneurons in oculomotor nuclei and spinal cord that control orienting eye and body movements.
“the output neurons in the intermediate and deep layers of the teleost optic tectum are able to initiate orientation or avoidance responses through their projections to the reticular formation and other pre-motor cell groups in the brainstem, which in turn activate the motoneurons in the oculomotor nuclei and spinal cord that control orienting eye and body movements”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [107]
Split into 2 atoms — 0 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 2 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
In situ click chemistry generation of cyclooxygenase-2 inhibitors
Bhardwaj, A., Kaur, J., Wuest, M., & Wuest, F. (2017) · Nature Communications · doi:10.1038/s41467-016-0009-6 · Cited by 7,448 · see citing works
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
Avants, B., Epstein, C. L., Grossman, M., & Gee, J. C. (2007) · Medical Image Analysis · doi:10.1016/j.media.2007.06.004 · Cited by 5,618 · see citing works
Neural Basis of a Perceptual Decision in the Parietal Cortex (Area LIP) of the Rhesus Monkey
Shadlen, M. N., & Newsome, W. T. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.4.1916 · Cited by 1,755 · see citing works
Diffusion decision model: Current issues and history
Ratcliff, R., Smith, P. L., Brown, S. D., & McKoon, G. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.01.007 · Cited by 1,630 · see citing works
Newsome, W., & Pare, E. (1988) · The Journal of Neuroscience · doi:10.1523/jneurosci.08-06-02201.1988 · Cited by 1,615 · see citing works
Roitman, J. D., & Shadlen, M. N. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09475.2002 · Cited by 1,589 · see citing works
Probabilistic decision making by slow reverberation in cortical circuits
Wang, X.-J. (2002) · Neuron · doi:10.1016/s0896-6273(02)01092-9 · Cited by 1,242 · see citing works
Multiple Dirac cones at the surface of the topological metal LaBi
Nayak, J., Wu, S.-C., Kumar, N., Shekhar, C., Singh, S., Fink, J., Rienks, E. E. D., Fecher, G. H., Parkin, S., Yan, B., et al. (2017) · Nature Communications · doi:10.1038/ncomms13942 · Cited by 1,179 · see citing works
Neuronal correlates of a perceptual decision
Newsome, W. T., Britten, K. H., & Movshon, J. A. (1989) · Nature · doi:10.1038/341052a0 · Cited by 1,177 · see citing works
NoRMCorre: An online algorithm for piecewise rigid motion correction of calcium imaging data
Pnevmatikakis, E. A., & Giovannucci, A. (2017) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2017.07.031 · Cited by 1,038 · see citing works
Simultaneous Denoising, Deconvolution, and Demixing of Calcium Imaging Data
Pnevmatikakis, E. A., Soudry, D., Gao, Y., Machado, T. A., Merel, J., Pfau, D., Reardon, T. R., Mu, Y., Lacefield, C., Yang, W., et al. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.037 · Cited by 1,035 · see citing works
Attentional Routes to Conscious Perception
Chica, A. B., & Bartolomeo, P. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00001 · Cited by 929 · see citing works
Cortical microstimulation influences perceptual judgements of motion direction
Salzman, C. D., Britten, K. H., & Newsome, W. T. (1990) · Nature · doi:10.1038/346174a0 · Cited by 881 · 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
Self-citationDecision Making as a Window on Cognition
Shadlen, M. N., & Kiani, R. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.047 · Cited by 660 · see citing works
The Cost of Accumulating Evidence in Perceptual Decision Making
Drugowitsch, J., Moreno-Bote, R., Churchland, A. K., Shadlen, M. N., & Pouget, A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4010-11.2012 · Cited by 577 · 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
Self-citationDistinct relationships of parietal and prefrontal cortices to evidence accumulation
Hanks, T. D., Kopec, C. D., Brunton, B. W., Duan, C. A., Erlich, J. C., & Brody, C. D. (2015) · Nature · doi:10.1038/nature14066 · Cited by 486 · 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
Performance Evaluation of RANSAC Family
Choi, S., Kim, T., & Yu, W. (2009) · British Machine Vision Conference (BMVC) · doi:10.5244/c.23.81 · Cited by 422 · see citing works
Posterior parietal cortex represents sensory history and mediates its effects on behaviour
Akrami, A., Kopec, C. D., Diamond, M. E., & Brody, C. D. (2018) · Nature · doi:10.1038/nature25510 · Cited by 380 · see citing works
Elapsed Decision Time Affects the Weighting of Prior Probability in a Perceptual Decision Task
Hanks, T. D., Mazurek, M. E., Kiani, R., Hopp, E., & Shadlen, M. N. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5613-10.2011 · Cited by 378 · see citing works
Whole-brain serial-section electron microscopy in larval zebrafish
Hildebrand, D. G. C., Cicconet, M., Torres, R., Choi, W., Quan, T. M., Moon, J., Wetzel, A. W., Champion, A. S., Graham, B. J., Randlett, O., et al. (2017) · Nature · doi:10.1038/nature22356 · Cited by 378 · see citing works
Self-citationTorsten 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
AlRashidi, M., Kosztolányi, A., Küpper, C., Cuthill, I. C., Javed, S., & Székely, T. (2010) · Frontiers in Zoology · doi:10.1186/1742-9994-7-1 · Cited by 361 · see citing works
Microstimulation of macaque area LIP affects decision-making in a motion discrimination task
Hanks, T. D., Ditterich, J., & Shadlen, M. N. (2006) · Nature Neuroscience · doi:10.1038/nn1683 · Cited by 360 · see citing works
Memory without Feedback in a Neural Network
Goldman, M. S. (2009) · Neuron · doi:10.1016/j.neuron.2008.12.012 · Cited by 342 · 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
Self-citationBrain-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
Self-citationWhole-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
Self-citationControl 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
Self-citationA Cellular-Resolution Atlas of the Larval Zebrafish Brain
Kunst, M., Laurell, E., Mokayes, N., Kramer, A., Kubo, F., Fernandes, A. M., Förster, D., Maschio, M. D., & Baier, H. (2018) · Neuron · doi:10.1016/j.neuron.2019.04.034 · Cited by 272 · see citing works
Theory of correlations in stochastic neural networks
Ginzburg, I., & Sompolinsky, H. (1994) · Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics · doi:10.1103/physreve.50.3171 · Cited by 239 · see citing works
Pan-neuronal calcium imaging with cellular resolution in freely swimming zebrafish
Kim, D. H., Kim, J., Marques, J. C., Grama, A., Hildebrand, D. G. C., Gu, W., Li, J. M., & Robson, D. N. (2017) · Nature Methods · doi:10.1038/nmeth.4429 · Cited by 228 · see citing works
Transgenic tools to characterize neuronal properties of discrete populations of zebrafish neurons
Satou, C., Kimura, Y., Hirata, H., Suster, M. L., Kawakami, K., & Higashijima, S. (2013) · Development · doi:10.1242/dev.099531 · Cited by 224 · 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
Balanced cortical microcircuitry for maintaining information in working memory
Lim, S., & Goldman, M. S. (2013) · Nature Neuroscience · doi:10.1038/nn.3492 · Cited by 208 · see citing works
A novel mechanism for mechanosensory-based rheotaxis in larval zebrafish
Oteiza, P., Odstrcil, I., Lauder, G., Portugues, R., & Engert, F. (2017) · Nature · doi:10.1038/nature23014 · Cited by 199 · see citing works
Self-citationChen, 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
Self-citationKubo, 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
dal Maschio, M., Donovan, J. C., Helmbrecht, T. O., & Baier, H. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.034 · Cited by 169 · see citing works
Thura, D., & Cisek, P. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2230-15.2016 · Cited by 148 · 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
Spinal projection neurons control turning behaviors in zebrafish
Huang, K.-H., Ahrens, M. B., Dunn, T. W., & Engert, F. (2013) · Current Biology · doi:10.1016/j.cub.2013.06.044 · Cited by 133 · see citing works
Self-citationFoxP influences the speed and accuracy of a perceptual decision in Drosophila
Dasgupta, S., Ferreira, C. H., & Miesenböck, G. (2014) · Science · doi:10.1126/science.1252114 · Cited by 102 · see citing works
A Brain Wide Circuit Model of Heat Evoked Swimming Behavior in Larval Zebrafish
Haesemeyer, M., Robson, D. N., Li, J., Schier, A. F., & Engert, F. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.013 · Cited by 99 · see citing works
Self-citationVisual acuity in larval zebrafish: behavior and histology
Haug, M. F., Biehlmaier, O., Mueller, K. P., & Neuhauss, S. C. F. (2010) · Frontiers in Zoology · doi:10.1186/1742-9994-7-8 · Cited by 94 · see citing works
Visual Evidence Accumulation Guides Decision-Making in Unrestrained Mice
Odoemene, O., Pisupati, S., Nguyen, H., & Churchland, A. K. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3478-17.2018 · Cited by 86 · see citing works
Marquart, G. D., Tabor, K. M., Horstick, E. J., Brown, M., Geoca, A. K., Polys, N. F., Nogare, D. D., & Burgess, H. A. (2017) · GigaScience · doi:10.1093/gigascience/gix056 · Cited by 86 · see citing works
Control of Movement Initiation Underlies the Development of Balance
Ehrlich, D., & Schoppik, D. (2017) · Current Biology · doi:10.1016/j.cub.2016.12.003 · Cited by 83 · see citing works
Dendritic Integration of Sensory Evidence in Perceptual Decision-Making
Groschner, L. N., Hak, L. C. W., Bogacz, R., Dasgupta, S., & Miesenböck, G. (2018) · Cell · doi:10.1016/j.cell.2018.03.075 · Cited by 77 · see citing works
Fisher, D., Olasagasti, I., Tank, D. W., Aksay, E. R. F., & Goldman, M. S. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.041 · Cited by 75 · see citing works
The Role of the Lateral Intraparietal Area in (the Study of) Decision Making
Huk, A. C., Katz, L. N., & Yates, J. L. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031508 · Cited by 72 · see citing works
Visual information processing in the fly's landing system
Borst, A., & Bahde, S. (1988) · Journal of Comparative Physiology A · doi:10.1007/bf00612426 · Cited by 68 · see citing works
An optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits
Förster, D., Maschio, M. D., Laurell, E., & Baier, H. (2017) · Nature Communications · doi:10.1038/s41467-017-00160-z · Cited by 64 · see citing works
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
Direction selectivity in the larval zebrafish tectum is mediated by asymmetric inhibition
Grama, A., & Engert, F. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00059 · Cited by 50 · see citing works
Self-citationThe Effects of Evidence Bounds on Decision-Making: Theoretical and Empirical Developments
Zhang, J. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00263 · Cited by 29 · see citing works
Whole-field visual motion drives swimming in larval zebrafish via a stochastic process
Portugues, R., Haesemeyer, M., Blum, M. L., & Engert, F. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.118299 · Cited by 29 · see citing works
Self-citationNORTHMORE, D. P. M. (2017) · Vision Research · doi:10.1016/j.visres.2016.12.001 · Cited by 27 · see citing works
Marquart, G. D., Tabor, K. M., Horstick, E. J., et al. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/081000 · Cited by 13 · see citing works
Chen, X., Mu, Y., Hu, Y., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/289413 · Cited by 9 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
The connectome of an insect brain
Winding, M., Pedigo, B. D., Barnes, C. L., Patsolic, H. G., Park, Y., Kazimiers, T., Fushiki, A., Andrade, I. V., Khandelwal, A., Valdes-Aleman, J., et al. (2023) · Science · doi:10.1126/science.add9330 · Cited by 435 · see citing works
Signal propagation in complex networks
Ji, P., Ye, J., Mu, Y., Lin, W. J., Tian, Y., Hens, C., Perc, M., Tang, Y. S., Sun, J., & Kurths, J. (2023) · Physics Reports · doi:10.1016/j.physrep.2023.03.005 · Cited by 365 · see citing works
The geometry of decision-making in individuals and collectives
Sridhar, V. H., Li, L., Gorbonos, D., Nagy, M., Schell, B. R., Sorochkin, T., Gov, N. S., & Couzin, I. D. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2102157118 · Cited by 120 · see citing works
Imaging whole-brain activity to understand behaviour
Lin, A., Witvliet, D. K., Hernandez-Nunez, L., Linderman, S. W., Samuel, A. D. T., & Venkatachalam, V. (2022) · Nature Reviews Physics · doi:10.1038/s42254-022-00430-w · Cited by 77 · see citing works
Norepinephrine changes behavioral state through astroglial purinergic signaling
Chen, A., Duque, M., Rymbek, A., Dhanasekar, M., Wang, V. M., Mi, X., Tocquer, L., Narayan, S., Legorreta, E. M., Eddison, M., et al. (2025) · Science · doi:10.1126/science.adq5233 · Cited by 79 · see citing works
Self-citationA 3D adult zebrafish brain atlas (AZBA) for the digital age
Kenney, J. W., Steadman, P. E., Young, O., Shi, M. T., Polanco, M., Dubaishi, S., Covert, K., Mueller, T., & Frankland, P. W. (2021) · eLife · doi:10.7554/elife.69988 · Cited by 72 · see citing works
Precise visuomotor transformations underlying collective behavior in larval zebrafish
Harpaz, R., Nguyen, M. N., Bahl, A., & Engert, F. (2021) · Nature Communications · doi:10.1038/s41467-021-26748-0 · Cited by 63 · see citing works
Self-citationCollective detection based on visual information in animal groups
Davidson, J. D., Sosna, M. M. G., Twomey, C. R., Sridhar, V. H., Leblanc, S. P., & Couzin, I. D. (2021) · Journal of The Royal Society Interface · doi:10.1098/rsif.2021.0142 · Cited by 68 · 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
Fontana, B. D., Müller, T. E., Cleal, M., de Abreu, M. S., Norton, W., Demin, K. A., Amstislavskaya, T. G., Petersen, E. V., Kalueff, A. V., Parker, M. O., et al. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.101993 · Cited by 61 · see citing works
Spatial Cognition in Teleost Fish: Strategies and Mechanisms
Rodríguez, F., Quintero, B., Amores, L., Madrid, D., Salas-Peña, C., & Salas, C. (2021) · Animals · doi:10.3390/ani11082271 · Cited by 59 · see citing works
Im, J., Eom, H.-J., & Choi, J. (2022) · Archives of Environmental Contamination and Toxicology · doi:10.1007/s00244-022-00924-9 · Cited by 58 · 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
Brain-Wide Mapping of Water Flow Perception in Zebrafish
Vanwalleghem, G. C., Schuster, K., Taylor, M. A., Favre‐Bulle, I. A., & Scott, E. K. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0049-20.2020 · Cited by 55 · see citing works
An Algorithmic Approach to Natural Behavior
Hein, A. M., Altshuler, D. L., Cade, D. E., Liao, J. C., Martin, B. T., & Taylor, G. K. (2020) · Current Biology · doi:10.1016/j.cub.2020.04.018 · Cited by 52 · see citing works
Current Methods to Investigate Nociception and Pain in Zebrafish
Ohnesorge, N., Heinl, C., & Lewejohann, L. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.632634 · Cited by 48 · see citing works
Response competition between neurons and antineurons in the mushroom body
Vrontou, E., Groschner, L. N., Szydlowski, S. N., Brain, R., Krebbers, A., & Miesenböck, G. (2021) · Current Biology · doi:10.1016/j.cub.2021.09.008 · Cited by 50 · see citing works
A rise-to-threshold process for a relative-value decision
Vijayan, V., Wang, F., Wang, K., Chakravorty, A., Adachi, A., Akhlaghpour, H., Dickson, B. J., & Maimon, G. (2023) · Nature · doi:10.1038/s41586-023-06271-6 · Cited by 49 · 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
Collective behavior emerges from genetically controlled simple behavioral motifs in zebrafish
Harpaz, R., Aspiras, A., Chambule, S., Tseng, S., Bind, M.-A. C., Engert, F., Fishman, M., & Bahl, A. (2021) · bioRxiv · doi:10.1126/sciadv.abi7460 · Cited by 48 · see citing works
Self-citationThe Role of Zebrafish and Laboratory Rodents in Schizophrenia Research
Langová, V., Valeš, K., Horka, P., & Horáček, J. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00703 · Cited by 41 · see citing works
Navarro, M. A., Salari, A., Lin, J. L., Cowan, L. M., Penington, N. J., Milescu, M., & Milescu, L. S. (2020) · eLife · doi:10.7554/elife.54940 · Cited by 43 · 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
Neural substrates involved in the cognitive information processing in teleost fish
Calvo, R. A., & Schluessel, V. (2021) · Animal Cognition · doi:10.1007/s10071-021-01514-3 · Cited by 39 · see citing works
A Customizable Low-Cost System for Massively Parallel Zebrafish Behavioral Phenotyping
Joo, W. J., Vivian, M. D., Graham, B. J., Soucy, E. R., & Thyme, S. B. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.606900 · Cited by 34 · 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
A Neural Representation of Naturalistic Motion-Guided Behavior in the Zebrafish Brain
Yildizoglu, T., Riegler, C., Fitzgerald, J. E., & Portugues, R. (2020) · Current Biology · doi:10.1016/j.cub.2020.04.043 · Cited by 34 · see citing works
Functional neuronal circuits emerge in the absence of developmental activity
Barabási, D. L., Schuhknecht, G. F. P., & Engert, F. (2024) · Nature Communications · doi:10.1038/s41467-023-44681-2 · Cited by 31 · see citing works
Self-citationFish Capsules: A System for High‐Throughput Screening of Combinatorial Drugs
Tang, M., Duan, X., Yang, A., He, S., Zhou, Y., Liu, Y., Zhang, L., Luo, X., Shi, P., Li, H., et al. (2022) · Advanced Science · doi:10.1002/advs.202104449 · Cited by 34 · see citing works
From perception to behavior: The neural circuits underlying prey hunting in larval zebrafish
Zhu, S., & Goodhill, G. J. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1087993 · Cited by 31 · 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
Duque, M., Chen, A., Hsu, E. T., Narayan, S., Rymbek, A., Begum, S., Saher, G., Cohen, A. E., Olson, D. E., Li, Y., et al. (2024) · Neuron · doi:10.1016/j.neuron.2024.11.011 · Cited by 31 · see citing works
Self-citationNaturalistic neuroscience and virtual reality
Thurley, K. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.896251 · Cited by 28 · see citing works
Structure and function in artificial, zebrafish and human neural networks
Ji, P., Wang, Y., Peron, T., Li, C., Nagler, J., & Du, J. (2023) · Physics of Life Reviews · doi:10.1016/j.plrev.2023.04.004 · Cited by 27 · see citing works
Hasty sensorimotor decisions rely on an overlap of broad and selective changes in motor activity
Derosière, G., Thura, D., Cisek, P., & Duque, J. (2021) · bioRxiv · doi:10.1371/journal.pbio.3001598 · Cited by 19 · see citing works
Zebrafish and nematodes as whole organism models to measure developmental neurotoxicity
Hughes, S., & Hessel, E. V. S. (2024) · Critical Reviews in Toxicology · doi:10.1080/10408444.2024.2342448 · Cited by 25 · see citing works
The neural network RTNet exhibits the signatures of human perceptual decision-making
Rafiei, F., Shekhar, M., & Rahnev, D. (2024) · Nature Human Behaviour · doi:10.1038/s41562-024-01914-8 · Cited by 35 · see citing works
Complex computation from developmental priors
Barabási, D. L., Beynon, T., Katona, Á., & Perez-Nieves, N. (2023) · Nature Communications · doi:10.1038/s41467-023-37980-1 · Cited by 25 · see citing works
Algorithms underlying flexible phototaxis in larval zebrafish
Chen, A., Deb, D., Bahl, A., & Engert, F. (2021) · Journal of Experimental Biology · doi:10.1242/jeb.238386 · Cited by 24 · see citing works
Self-citationZebrafish as a Model for In-Depth Mechanistic Study for Stroke
Chen, W., Xie, L., Yu, F., Li, Y., Chen, C., Xie, W., Huang, T., Zhang, Y., Zhang, S., & Li, P. (2021) · Translational Stroke Research · doi:10.1007/s12975-021-00907-3 · Cited by 23 · see citing works
Ramp-to-threshold dynamics in a hindbrain population controls the timing of spontaneous saccades
Ramirez, A. D., & Aksay, E. R. F. (2021) · Nature Communications · doi:10.1038/s41467-021-24336-w · Cited by 24 · see citing works
Martorell, N., & Medan, V. (2022) · Scientific Reports · doi:10.1038/s41598-022-04998-2 · Cited by 22 · see citing works
Goodwin, R. A., Lai, Y. G., Taflin, D. E., Smith, D. L., McQuirk, J., Trang, R., & Reeves, R. L. (2023) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2023.703946 · Cited by 24 · see citing works
Characterizing ontogeny of quantity discrimination in zebrafish
Sheardown, E., Torres-Pérez, J. V., Anagianni, S., Fraser, S. E., Vallortígara, G., Butterworth, B. L., Petrazzini, M. E. M., & Brennan, C. H. (2022) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2021.2544 · Cited by 21 · see citing works
Narayanan, S., Varma, A., & Thirumalai, V. (2024) · Science Advances · doi:10.1126/sciadv.adi6470 · Cited by 21 · see citing works
Collins, E. S., Hessel, E. V. S., & Hughes, S. (2024) · NeuroToxicology · doi:10.1016/j.neuro.2024.03.005 · Cited by 20 · see citing works
The neuroscience of mental illness: Building toward the future
Gordon, J. A., Dzirasa, K., & Petzschner, F. H. (2024) · Cell · doi:10.1016/j.cell.2024.09.028 · Cited by 20 · see citing works
Stimulus Contrast Information Modulates Sensorimotor Decision Making in Goldfish
Otero-Coronel, S., Martorell, N., de Astrada, M. B., & Medan, V. (2020) · Frontiers in Neural Circuits · doi:10.3389/fncir.2020.00023 · Cited by 18 · see citing works
A 3D Adult Zebrafish Brain Atlas (AZBA) for the Digital Age
Kenney, J. W., Steadman, P. E., Young, O., Shi, M. T., Polanco, M., Dubaishi, S., Covert, K., Mueller, T., & Frankland, P. W. (2021) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5061/dryad.dfn2z351g · Cited by 18 · see citing works
Brain-wide, scale-wide physiology underlying behavioral flexibility in zebrafish
Mu, Y., Narayan, S., Mensh, B. D., & Ahrens, M. B. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.08.013 · Cited by 17 · see citing works
Neural circuits underlying divergent visuomotor strategies of zebrafish and Danionella cerebrum
Fouke, K. E., He, Z., Loring, M. D., & Naumann, E. A. (2025) · Current Biology · doi:10.1016/j.cub.2025.04.027 · Cited by 16 · see citing works
Sy, S. K. H., Chan, D. C. W., Chan, R. C. H., Lyu, J., Li, Z., Wong, K. K. Y., Choi, C. H. J., Mok, V., Lai, H. M., Randlett, O., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-35836-2 · Cited by 16 · 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
Ferrario, A., Palyanov, A. Y., Koutsikou, S., Li, W., Soffe, S. R., Roberts, A., & Borisyuk, R. M. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009654 · Cited by 15 · see citing works
Structural and genetic determinants of zebrafish functional brain networks
Légaré, A., Lemieux, M., Boily, V., Poulin, S., Légaré, A., Desrosiers, P., & Koninck, P. D. (2025) · Science Advances · doi:10.1126/sciadv.adv7576 · Cited by 15 · see citing works
Bukwich, M., Campbell, M. G., Zoltowski, D. M., Kingsbury, L., Tomov, M. S., Stern, J., Kim, H. R., Drugowitsch, J., Linderman, S. W., & Uchida, N. (2025) · Neuron · doi:10.1016/j.neuron.2025.07.008 · Cited by 17 · see citing works
A push for examining subjective experience in value-based decision-making
Schreiner, D. C., Yalcinbas, E. A., & Gremel, C. M. (2021) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2021.03.020 · Cited by 15 · see citing works
A connectomic resource for neural cataloguing and circuit dissection of the larval zebrafish brainPreprint
Petkova, M. D., Januszewski, M., Blakely, T. M., Herrera, K. J., Schuhknecht, G. F. P., Tiller, R., Choi, J., Schalek, R. L., Boulanger-Weill, J., Peleg, A., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.10.658982 · Cited by 14 · see citing works
Self-citationNature versus laboratory: how to optimize housing conditions for zebrafish neuroscience research
Tsang, B., & Gerlai, R. T. (2024) · Trends in Neurosciences · doi:10.1016/j.tins.2024.08.013 · Cited by 12 · see citing works
Large-scale F0 CRISPR screens in vivo using MIC-Drop
Parvez, S., Brandt, Z. J., & Peterson, R. T. (2023) · Nature Protocols · doi:10.1038/s41596-023-00821-y · Cited by 11 · see citing works
Zaupa, M., Nagaraj, N., Sylenko, A., Baier, H., Sawamiphak, S., & Filosa, A. (2024) · Neuron · doi:10.1016/j.neuron.2024.01.001 · Cited by 11 · see citing works
Three systems of circuit formation: assembly, updating and tuning
Barabási, D. L., Castro, A. F., & Engert, F. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-00910-9 · Cited by 11 · see citing works
Self-citationSwimming into the future: Machine learning in zebrafish behavioral research
Fontana, B. D., Canzian, J., & Rosemberg, D. B. (2025) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2025.111398 · Cited by 11 · see citing works
Attentional switching in larval zebrafish
Krishnan, K., Muthukumar, A. V., Sterrett, S. C., Pflitsch, P., Fairhall, A. L., Fishman, M. C., Bahl, A., Zwaka, H., & Engert, F. (2025) · Science Advances · doi:10.1126/sciadv.ads4994 · Cited by 14 · see citing works
Self-citationInformation integration for decision-making in desert locusts
Günzel, Y., Oberhauser, F. B., & Couzin-Fuchs, E. (2023) · iScience · doi:10.1016/j.isci.2023.106388 · Cited by 10 · see citing works
Norepinephrine changes behavioral state via astroglial purinergic signalingPreprint
Chen, A., Duque, M., Wang, V. M., Dhanasekar, M., Mi, X., Rymbek, A., Tocquer, L., Narayan, S., Prober, D. A., Yu, G., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.23.595576 · Cited by 10 · see citing works
Self-citationBoulanger-Weill, J., Kämpf, F., Schuhknecht, G. F. P., Schalek, R. L., Garza, R., Petkova, M. D., Vohra, S. K., Wu, Y., Savaliya, J. H., Tiller, R., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.14.643363 · Cited by 8 · see citing works
Self-citationAbout Welfare and Stress in the Early Stages of Fish
Ramos, J., Balasch, J. C., & Tort, L. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.634434 · Cited by 9 · see citing works
Curpăn, A.-Ș., Balmuș, I.-M., Dobrin, R., Ciobica, A. S., Chele, G. E., Gorgan, L., & Boloș, A. (2022) · Brain Sciences · doi:10.3390/brainsci12091147 · Cited by 9 · see citing works
Visuomotor decision-making through multifeature convergence in the larval zebrafish hindbrain
Slangewal, K., Aimon, S., Capelle, M. Q., Kämpf, F., Naumann, H., Slanchev, K., Baier, H., & Bahl, A. (2026) · Nature Communications · doi:10.1038/s41467-026-69633-4 · Cited by 9 · see citing works
Self-citationScalable Electrophysiology of Millimeter-Scale Animals with Electrode Devices
Dong, K., Liu, W.-C., Su, Y., Lyu, Y., Huang, H., Zheng, N., Rogers, J. A., & Nan, K. (2023) · BME Frontiers · doi:10.34133/bmef.0034 · Cited by 10 · 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
Zebrafish brain atlases: a collective effort for a tiny vertebrate brain
Légaré, A., Lemieux, M., Desrosiers, P., & Koninck, P. D. (2023) · Neurophotonics · doi:10.1117/1.nph.10.4.044409 · 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
Anatomical and functional organization of the interpeduncular nucleus in larval zebrafishPreprint
Wu, Y. K., Petrucco, L., & Portugues, R. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.09.617353 · Cited by 7 · see citing works
Jacobs, E. A. K., & Ryu, S. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1143391 · Cited by 6 · see citing works
Hentig, J., Cloghessy, K., & Hyde, D. R. (2021) · Journal of Visualized Experiments · doi:10.3791/62745 · Cited by 6 · see citing works
A Visual Interface for Exploring Hypotheses About Neural Circuits
Vohra, S. K., Harth, P., Isoe, Y., Bahl, A., Fotowat, H., Engert, F., Hege, H., & Baum, D. (2023) · IEEE Transactions on Visualization and Computer Graphics · doi:10.1109/tvcg.2023.3243668 · Cited by 6 · see citing works
Self-citationExperience-dependent modulation of collective behavior in larval zebrafish
Harpaz, R., Phillips-Batra, M., Goel, R., Bind, M.-A. C., Fishman, M., & Engert, F. (2026) · Nature Communications · doi:10.1038/s41467-026-74872-6
Self-citationA cerebellar internal model calibrates a feedback controller involved in sensorimotor controlPreprint
Markov, D. A., Petrucco, L., Kist, A. M., & Portugues, R. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.12.945956 · Cited by 6 · see citing works
Nature over Nurture: Functional neuronal circuits emerge in the absence of developmental activityPreprint
Barabási, D. L., Schuhknecht, G. F. P., & Engert, F. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.24.513526 · Cited by 6 · see citing works
Self-citationBehavioral algorithms of ontogenetic switching in larval and juvenile zebrafish phototaxis
Capelle, M. Q., Slangewal, K., Eleftheriadis, P. E., & Bahl, A. (2026) · iScience · doi:10.1016/j.isci.2026.116190 · Cited by 4 · see citing works
Self-citationEvans, C. G., Barry, M. A., Perkins, M. H., Jing, J., Weiss, K. R., & Cropper, E. C. (2023) · Journal of Neurophysiology · doi:10.1152/jn.00190.2023 · Cited by 5 · see citing works
Navigational strategies underlying temporal phototaxis in Drosophila larvae
Zhu, M. L., Herrera, K. J., Vogt, K., & Bahl, A. (2021) · Journal of Experimental Biology · doi:10.1242/jeb.242428 · Cited by 5 · see citing works
Self-citationA 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
RTNet neural network exhibits the signatures of human perceptual decision makingPreprint
Rafiei, F., Shekhar, M., & Rahnev, D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.23.505015 · Cited by 6 · see citing works
Algorithmic dissection of optic flow memory in larval zebrafish
Tanaka, R., & Portugues, R. (2025) · Current Biology · doi:10.1016/j.cub.2025.08.047 · Cited by 5 · see citing works
Compression-based inference of network motif sets
Bénichou, A., Masson, J., & Vestergaard, C. L. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012460 · Cited by 4 · see citing works
Migault, G., Beiza-Canelo, N., Chatterjee, S., Debrégeas, G., & Bormuth, V. (2026) · Communications Biology · doi:10.1038/s42003-026-10141-y · Cited by 4 · 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
Attentional Switching in Larval Zebrafish: The Attentive Leaky IntegratorPreprint
Krishnan, K., Muthukumar, A. V., Sterrett, S. C., Pflitsch, P., Fairhall, A. L., Fishman, M. C., Bahl, A., Zwaka, H., & Engert, F. (2023) · Research Square · doi:10.21203/rs.3.rs-3486824/v1 · Cited by 4 · see citing works
Self-citationMonnens, S. Q., Peters, C., Hesselink, L. W., Smeets, K., & Englitz, B. (2024) · eLife · doi:10.7554/elife.98489 · Cited by 5 · see citing works
Reynolds, P., Marchi, D., Ling, Y. T., Slangewal, K., Capelle, M. Q., Chalakova, Z., Bahl, A., & Hindges, R. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.29.651180 · Cited by 4 · see citing works
Self-citationIntegrated Ising model with global inhibition for decision-making
Tapinova, O., Finkelman, T., Reitich-Stolero, T., Paz, R., Tal, A., & Gov, N. (2025) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.2423557122 · Cited by 2 · see citing works
Synchronization of behavioral and cardiac dynamics in larval zebrafish
Herrera, K. J., Zarghani-Shiraz, A., Ahrens, M. B., Engert, F., & Fishman, M. C. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.116947 · Cited by 3 · see citing works
Self-citationDistinct distributed neural dynamics predict pallium-dependent social approach
Lifshitz, I., Prag, A., Livneh, N., Moshkovitz, M., Karmi, A., & Avitan, L. (2026) · Nature Communications · doi:10.1038/s41467-026-71666-8 · Cited by 3 · see citing works
A thalamus–brainstem attractor network drives history-biased decisions
Zhao, S., Shan, H., Liu, X., Qian, Y., Huang, J., Liu, Y., Jiao, Z., Ye, L., Cong, L., Wang, X., et al. (2026) · Nature · doi:10.1038/s41586-026-10623-3 · Cited by 3 · see citing works
Wilde, M., Poulsen, R. E., Qin, W., Arnold, J., Favre‐Bulle, I. A., Mattingley, J. B., Scott, E. K., & Stednitz, S. J. (2025) · The Journal of Comparative Neurology · doi:10.1002/cne.70046 · Cited by 3 · see citing works
Buerkle, N. P., & Jeanne, J. M. (2021) · Current Biology · doi:10.1016/j.cub.2021.09.039 · Cited by 3 · see citing works
Sleep Disruption Improves Performance in Simple Olfactory and Visual Decision-Making TasksPreprint
Pflitsch, P., Oury, N. H., Krishnan, K., Joo, W. J., Lyons, D. G., Capelle, M. Q., Herrera, K. J., Bahl, A., Rihel, J., Engert, F., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.02.621641 · Cited by 3 · see citing works
Self-citation
- Authors
- Bahl, A., & Engert, F.
- Affiliations
- Harvard University (US)
- Corresponding author
- Bahl, Armin
- Venue
- Nature Neuroscience
- Published
- 2019-12-02
- Volume
- 23
- Issue
- 1
- Pages
- 94-102
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC7295007
- OpenAlex
- W2991987583
- Cited by
- 166
- References
- 61
- Citations by year
- 2026: 28 · 2025: 31 · 2024: 28 · 2023: 22 · 2022: 15 · 2021: 30 · 2020: 11 · 2018: 1
- FWCI
- 8.29
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- KOPS (University of Konstanz) (submittedVersion)
- Funders
- Human Frontier Science Program (LT000626/2016)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Zebrafish Biomedical Research Applications
- Keywords
- evidence accumulation, decision-making, zebrafish larvae, optomotor response, decision threshold, motor command, neural circuits
- MeSH terms
- Animals, Brain, Decision Making, Larva, Models, Neurological, Neural Pathways, Neurons, Zebrafish
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review