The DOI matches its Crossref record; 59 of the 60 references it cites were found in a registry or an index, and 1 are not checked yet.
A neural heading estimate is compared with an internal goal to guide oriented navigation
Open accessPublished version of a preprint
Abstract
Goal-directed navigation is thought to rely on the activity of head-direction cells, but how this activity guides moment-to-moment actions remains poorly understood. Here we characterize how heading neurons in the Drosophila central complex guide moment-to-moment navigational behavior. We establish an innate, heading-neuron-dependent, tethered navigational behavior where walking flies maintain a straight trajectory along a specific angular bearing for hundreds of body lengths. While flies perform this task, we use chemogenetics to transiently rotate their neural heading estimate and observe that the flies slow down and turn in a direction that aims to return the heading estimate to the angle it occupied before stimulation. These results support a working model in which the fly brain quantitatively compares an internal estimate of current heading with an internal goal heading and uses the sign and magnitude of the difference to determine which way to turn, how hard to turn and how fast to walk forward.
Overview
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
Verification
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 source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“No statistical methods were used to predetermine sample sizes but our sample sizes are similar to those reported in previous publications23,24,33,34,37,38.”
From Multimodal cue integration and learning in a neural representation of head direction (2025) · cites this paper as [33]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Here, behavioral reorientation into the wind is likely mediated by pathways for orientation control that bypass the HD system32,33,44”
From Multimodal cue integration and learning in a neural representation of head direction (2025) · cites this paper as [33]
Experimental — accuracy not yet measuredIn the citing paper
“PEN1 neurons relay information about the fly’s angular velocity to EPG neurons, and so micro-stimulating PEN1 neurons causes the head direction system to register a fictive behavioral turn.”
From Neural circuit mechanisms for steering control in walking Drosophila (2025) · cites this paper as Green et al., 2019
In the citing paper
“PEN1 neurons relay information about the fly’s angular velocity to EPG neurons, and so micro-stimulating PEN1 neurons causes the head direction system to register a fictive behavioral turn.”
From Neural circuit mechanisms for steering control in walking Drosophila (2025) · cites this paper as Green et al., 2019
In the citing paper
“Head direction neurons (EPG neurons) (Seelig and Jayaraman, 2015) can influence steering (Giraldo et al., 2018; Green et al., 2019) via central complex neurons that compare head direction signals with internal goal signals (Beetz et al., 2022; Martin et al., 2015; Mussells Pires et al., 2024; Shiozaki et al., 2020; Westeinde et al., 2024).”
From Neural circuit mechanisms for steering control in walking Drosophila (2025) · cites this paper as Green et al., 2019
In the citing paper
“we find that the fly typically executes a compensatory behavioral turn shortly after the EPG bump jump, as reported previously (Green et al., 2019).”
From Neural circuit mechanisms for steering control in walking Drosophila (2025) · cites this paper as Green et al., 2019
In the citing paper
“we found that briefly micro-stimulating PEN1 neurons causes this bump to ‘jump’ to a new location (Green et al., 2019).”
From Neural circuit mechanisms for steering control in walking Drosophila (2025) · cites this paper as Green et al., 2019
In the citing paper
“the brain region that compares the animal’s current heading to an internal goal direction62,63,76,77.”
From Fine-grained descending control of steering in walking Drosophila (2023) · cites this paper as [77]
In the citing paper
“When the central complex commands a large and abrupt change in heading, it also commands a sudden decrease in forward velocity62,77”
From Fine-grained descending control of steering in walking Drosophila (2023) · cites this paper as [77]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Fiji: an open-source platform for biological-image analysis
Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B., et al. (2012) · Nature Methods · doi:10.1038/nmeth.2019 · Cited by 66,890
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
Taube, J., Muller, R., & Ranck, J. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00420.1990 · Cited by 1,809
A GAL4-Driver Line Resource for Drosophila Neurobiology
Jenett, A., Rubin, G. M., Ngo, T.-T. B., Shepherd, D., Murphy, C., Dionne, H., Pfeiffer, B. D., Cavallaro, A., Hall, D., Jeter, J., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.09.011 · Cited by 1,449
Zhang, K. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-06-02112.1996 · Cited by 1,001
Homing by path integration in a mammal
Mittelstaedt, M.-L., & Mittelstaedt, H. (1980) · Die Naturwissenschaften · doi:10.1007/bf00450672 · Cited by 728
Neural dynamics for landmark orientation and angular path integration
Seelig, J. D., & Jayaraman, V. (2015) · Nature · doi:10.1038/nature14446 · Cited by 718
Path integration in desert ants, Cataglyphis fortis
Müller, M., & Wehner, R. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.14.5287 · Cited by 677
Visual Navigation in Insects: Coupling of Egocentric and Geocentric Information
Wehner, R., Michel, B., & Antonsen, P. (1996) · Journal of Experimental Biology · doi:10.1242/jeb.199.1.129 · Cited by 634
Nern, A., Pfeiffer, B. D., & Rubin, G. M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1506763112 · Cited by 584
Cited by
Sorted by citations
Hulse, B. K., Haberkern, H., Franconville, R., Turner-Evans, D., Takemura, S.-Y., Wolff, T., Noorman, M., Dreher, M., Dan, C., Parekh, R., et al. (2021) · eLife · doi:10.7554/elife.66039 · Cited by 392
The insect central complex and the neural basis of navigational strategies
Honkanen, A., Adden, A., da Silva Freitas, J., & Heinze, S. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.188854 · Cited by 238
Building an allocentric travelling direction signal via vector computation
Lyu, C., Abbott, L. F., & Maimon, G. (2022) · Nature · doi:10.1038/s41586-021-04067-0 · Cited by 215
Self-citationSensorimotor experience remaps visual input to a heading-direction network
Fisher, Y. E., Lu, J., D’Alessandro, I., & Wilson, R. I. (2019) · Nature · doi:10.1038/s41586-019-1772-4 · Cited by 165
Sun Navigation Requires Compass Neurons in Drosophila
Giraldo, Y. M., Leitch, K. J., Ros, I. G., Warren, T. L., Weir, P. T., & Dickinson, M. H. (2018) · Current Biology · doi:10.1016/j.cub.2018.07.002 · Cited by 161
The Neuroanatomical Ultrastructure and Function of a Biological Ring Attractor
Turner-Evans, D. B., Jensen, K. T., Ali, S., Paterson, T., Sheridan, A., Ray, R. P., Wolff, T., Lauritzen, J. S., Rubin, G. M., Bock, D. D., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.006 · Cited by 168
Generation of stable heading representations in diverse visual scenes
Kim, S. S., Hermundstad, A. M., Romani, S., Abbott, L. F., & Jayaraman, V. (2019) · Nature · doi:10.1038/s41586-019-1767-1 · Cited by 172
The neuroanatomical ultrastructure and function of a biological ring attractor
Turner-Evans, D. B., Jensen, K. T., Ali, S., Paterson, T., Sheridan, A., Ray, R. P., Wolff, T., Lauritzen, S., Rubin, G. M., Bock, D., et al. (2019) · doi:10.1101/847152 · Cited by 166
A Neural Network for Wind-Guided Compass Navigation
Okubo, T. S., Patella, P., D’Alessandro, I., & Wilson, R. I. (2020) · Neuron · doi:10.1016/j.neuron.2020.06.022 · Cited by 114
Mechanisms Underlying the Neural Computation of Head Direction
Hulse, B. K., & Jayaraman, V. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031516 · Cited by 130
Building a functional connectome of the Drosophila central complex
Franconville, R., Beron, C. C., & Jayaraman, V. (2018) · eLife · doi:10.7554/elife.37017 · Cited by 129
Converting an allocentric goal into an egocentric steering signal
Mussells Pires, P., Zhang, L., Parache, V., Abbott, L. F., & Maimon, G. (2024) · Nature · doi:10.1038/s41586-023-07006-3 · Cited by 110
Self-citationTwo brain pathways initiate distinct forward walking programs in Drosophila
Bidaye, S. S., Laturney, M., Chang, A. K., Liu, Y., Bockemühl, T., Büschges, A., & Scott, K. (2020) · Neuron · doi:10.1016/j.neuron.2020.07.032 · Cited by 109
Whole-brain annotation and multi-connectome cell typing quantifies circuit stereotypy in Drosophila
Schlegel, P., Yin, Y., Bates, A. S., Dorkenwald, S., Eichler, K., Brooks, P., Han, D. S., Gkantia, M., dos Santos, M., Munnelly, E. J., et al. (2023) · doi:10.1101/2023.06.27.546055 · Cited by 102
Transforming a head direction signal into a goal-oriented steering command
Westeinde, E. A., Kellogg, E., Dawson, P. M., Lu, J., Hamburg, L., Midler, B., Druckmann, S., & Wilson, R. I. (2024) · Nature · doi:10.1038/s41586-024-07039-2 · Cited by 85
Building a heading signal from anatomically defined neuron types in the Drosophila central complex
Green, J., & Maimon, G. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.06.010 · Cited by 81
Self-citationDopamine promotes head direction plasticity during orienting movements
Fisher, Y. E., Marquis, M., D’Alessandro, I., & Wilson, R. I. (2022) · Nature · doi:10.1038/s41586-022-05485-4 · Cited by 67
Flexible navigational computations in the Drosophila central complex
Fisher, Y. E. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.12.001 · Cited by 74
Haberkern, H., Basnak, M. A., Ahanonu, B., Schauder, D., Cohen, J. D., Bolstad, M., Bruns, C. M., & Jayaraman, V. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.033 · Cited by 71
Neural circuit mechanisms for steering control in walking Drosophila
Rayshubskiy, A., Holtz, S. L., Bates, A. S., Vanderbeck, Q. X., Capdevila, L. S., Rockwell, V., & Wilson, R. I. (2020) · doi:10.1101/2020.04.04.024703 · Cited by 64
A neuronal ensemble encoding adaptive choice during sensory conflict in Drosophila
Sareen, P., McCurdy, L. Y., & Nitabach, M. N. (2021) · Nature Communications · doi:10.1038/s41467-021-24423-y · Cited by 66
Differential mechanisms underlie trace and delay conditioning in Drosophila
Grover, D., Chen, J., Xie, J. L., Li, J., Changeux, J., & Greenspan, R. J. (2022) · Nature · doi:10.1038/s41586-022-04433-6 · Cited by 63
Visual processing in the fly, from photoreceptors to behavior
Currier, T. A., Pang, M. M., & Clandinin, T. R. (2023) · GENETICS · doi:10.1093/genetics/iyad064 · Cited by 63
Causal evidence of a line attractor encoding an affective state
Vinograd, A., Nair, A., Kim, J. H., Linderman, S. W., & Anderson, D. J. (2024) · Nature · doi:10.1038/s41586-024-07915-x · Cited by 79
Encoding and control of orientation to airflow by a set of Drosophila fan-shaped body neurons
Currier, T. A., Matheson, A. M. M., & Nagel, K. I. (2020) · eLife · doi:10.7554/elife.61510 · Cited by 60
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 63
Fine-grained descending control of steering in walking Drosophila
Yang, H. H., Brezovec, B. E., Serratosa Capdevila, L., Vanderbeck, Q. X., Adachi, A., Mann, R. S., & Wilson, R. I. (2024) · Cell · doi:10.1016/j.cell.2024.08.033 · Cited by 55
Self-citationNeural representation of goal direction in the monarch butterfly brain
Beetz, M. J., Kraus, C., & el Jundi, B. (2023) · Nature Communications · doi:10.1038/s41467-023-41526-w · Cited by 60
Hulse, B. K., Haberkern, H., Franconville, R., Turner-Evans, D. B., Takemura, S., Wolff, T., Noorman, M., Dreher, M., Dan, C., Parekh, R., et al. (2020) · doi:10.1101/2020.12.08.413955 · Cited by 392
“This activity, which localizes to a contiguous ‘bump’ spanning the processes of EPG neurons in neighboring sectors, is required for flies to stably maintain arbitrary headings as they walk or fly (Giraldo et al., 2018; Green et al., 2019).”
BackgroundA neural circuit architecture for rapid learning in goal-directed navigation
Dan, C., Hulse, B. K., Kappagantula, R., Jayaraman, V., & Hermundstad, A. M. (2024) · Neuron · doi:10.1016/j.neuron.2024.04.036 · Cited by 51
“By combining these physiological and behavioral results with RL algorithms and circuit modeling that were informed by previous CX studies, 24,36–38, 44, 48, 52,”
MethodA unified mechanism for innate and learned visual landmark guidance in the insect central complex
Goulard, R., Buehlmann, C., Niven, J. E., Graham, P., & Webb, B. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009383 · Cited by 51
Zittrell, F., Pfeiffer, K., & Homberg, U. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005192117 · Cited by 52
The brain of Cataglyphis ants: Neuronal organization and visual projections
Habenstein, J., Amini, E., Grübel, K., el Jundi, B., & Rößler, W. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24934 · Cited by 47
Kottler, B., Faville, R., Bridi, J. C., & Hirth, F. (2019) · Current Biology · doi:10.1016/j.cub.2019.01.017 · Cited by 48
Sullivan, L. F., Warren, T. L., & Doe, C. Q. (2019) · eLife · doi:10.7554/elife.43482 · Cited by 46
Wystrach, A., Moël, F. L., Clément, L., & Schwarz, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.13.249193 · Cited by 43
The neuronal building blocks of the navigational toolkit in the central complex of insects
Pfeiffer, K. (2022) · Current Opinion in Insect Science · doi:10.1016/j.cois.2022.100972 · Cited by 52
Angelaki, D. E., & Laurens, J. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.12.002 · Cited by 51
Behavioral signatures of structured feature detection during courtship in Drosophila
Ning, J., Li, Z., Zhang, X., Wang, J., Chen, D., Liu, Q., & Sun, Y. (2022) · Current Biology · doi:10.1016/j.cub.2022.01.024 · Cited by 41
Neural networks for navigation: From connections to computations
Wilson, R. I. (2023) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-110920-032645 · Cited by 38
Fast tuning of posture control by visual feedback underlies gaze stabilization in walking Drosophila
Cruz, T. L., Pérez, S. M., & Chiappe, M. E. (2021) · Current Biology · doi:10.1016/j.cub.2021.08.041 · Cited by 35
Integration of Spatial and Temporal Patterning in the Invertebrate and Vertebrate Nervous System
Chen, Y., & Konstantinides, N. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.854422 · Cited by 35
Neural mechanisms to exploit positional geometry for collision avoidance
Tanaka, R., & Clark, D. A. (2022) · Current Biology · doi:10.1016/j.cub.2022.04.023 · Cited by 35
Neuroarchitecture of the central complex in the brain of the honeybee: Neuronal cell types
Hensgen, R., England, L., Homberg, U., & Pfeiffer, K. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24941 · Cited by 36
How the insect central complex could coordinate multimodal navigation
Sun, X., Yue, S., & Mangan, M. (2021) · eLife · doi:10.7554/elife.73077 · Cited by 35
Multisensory control of navigation in the fruit fly
Currier, T. A., & Nagel, K. I. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.11.017 · Cited by 36
The sky compass network in the brain of the desert locust
Homberg, U., Hensgen, R., Jahn, S., Pegel, U., Takahashi, N., Zittrell, F., & Pfeiffer, K. (2022) · Journal of Comparative Physiology A · doi:10.1007/s00359-022-01601-x · Cited by 38
Multi-regional circuits underlying visually guided decision-making in Drosophila
Cheong, H. S., Siwanowicz, I., & Card, G. M. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.10.010 · Cited by 33
On the role of the head ganglia in posture and walking in insects
Emanuel, S., Kaiser, M., Pflueger, H.-J., & Libersat, F. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00135 · Cited by 31
Oscillations in the central brain of Drosophila are phase locked to attended visual features
Grabowska, M. J., Jeans, R., Steeves, J., & van Swinderen, B. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2010749117 · Cited by 29
Neural circuit mechanisms for steering control in walking Drosophila
Rayshubskiy, A., Holtz, S. L., Bates, A. S., Vanderbeck, Q. X., Serratosa Capdevila, L., Rockwell, V., & Wilson, R. (2025) · eLife · doi:10.7554/elife.102230 · Cited by 27
Muratore, I. B., Fandozzi, E. M., & Traniello, J. F. A. (2022) · Journal of Comparative Physiology A · doi:10.1007/s00359-021-01539-6 · Cited by 28
Learning accurate path integration in ring attractor models of the head direction system
Vafidis, P., Owald, D., D’Albis, T., & Kempter, R. (2022) · eLife · doi:10.7554/elife.69841 · Cited by 29
Hamid, A., Gattuso, H., Caglar, A. N., Pillai, M., Steele, T., Gonzalez, A., Nagel, K., & Syed, M. H. (2024) · Current Biology · doi:10.1016/j.cub.2023.12.020 · Cited by 24
Emergent spatial goals in an integrative model of the insect central complex
Goulard, R., Heinze, S., & Webb, B. H. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011480 · Cited by 25
Characterizing approach behavior of Drosophila melanogaster in Buridan’s paradigm
Han, R., Wei, T.-M., Tseng, S.-C., & Lo, C. (2021) · PLoS ONE · doi:10.1371/journal.pone.0245990 · Cited by 23
Towards a common terminology for arthropod spatial orientation
Grob, R., el Jundi, B., & Fleischmann, P. N. (2021) · Ethology Ecology & Evolution · doi:10.1080/03949370.2021.1905075 · Cited by 22
A neural circuit basis for context-modulation of individual locomotor behaviorPreprint
Skutt-Kakaria, K., Reimers, P., Currier, T. A., Werkhoven, Z., & de Bivort, B. L. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/797126 · Cited by 23
Hulse, B. K., Stanoev, A., Turner‐Evans, D. B., Seelig, J. D., & Jayaraman, V. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.25.559373 · Cited by 20
Maintaining a stable head direction representation in naturalistic visual environments
Haberkern, H., Chitnis, S. S., Hubbard, P. M., Goulet, T., Hermundstad, A. M., & Jayaraman, V. (2022) · doi:10.1101/2022.05.17.492284 · Cited by 21
Stimulus-dependent orientation strategies in monarch butterflies
Franzke, M., Kraus, C. M., Gayler, M., Dreyer, D., Pfeiffer, K., & el Jundi, B. (2022) · Journal of Experimental Biology · doi:10.1242/jeb.243687 · Cited by 20
Multilevel visuomotor control of locomotion in Drosophila
Cruz, T. L., & Chiappe, M. E. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102774 · Cited by 17
Learning a Spatial Task by Trial and Error in Drosophila
Stern, U., Srivastava, H. K., Chen, H.-L., Mohammad, F., Claridge‐Chang, A., & Yang, C.-H. (2019) · Current Biology · doi:10.1016/j.cub.2019.06.045 · Cited by 22
A neural circuit architecture for rapid behavioral flexibility in goal-directed navigation
Dan, C., Hulse, B. K., Kappagantula, R., Jayaraman, V., & Hermundstad, A. M. (2021) · doi:10.1101/2021.08.18.456004 · Cited by 51
“This was captured by the fraction of time that the bump maintained different angular relationships to the visual scene, a parameter that we and others refer to as the ‘visual offset’ [16, 31, 34, 35, 71] (Fig 2e).”
BackgroundInfluentialTyrosine hydroxylase immunostaining in the central complex of dicondylian insects
Timm, J., Scherner, M., Matschke, J., Kern, M., & Homberg, U. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25151 · Cited by 21
Fine-grained descending control of steering in walking Drosophila
Yang, H. H., Brezovec, L. E., Serratosa Capdevila, L., Vanderbeck, Q. X., Adachi, A., Mann, R. S., & Wilson, R. I. (2023) · doi:10.1101/2023.10.15.562426 · Cited by 55
Self-citationFeng (2024) · doi:10.1101/2024.06.27.601106 · Cited by 18
Hensgen, R., Zittrell, F., Pfeiffer, K., & Homberg, U. (2022) · Journal of Comparative Physiology A · doi:10.1007/s00359-022-01545-2 · Cited by 15
Converting an allocentric goal into an egocentric steering signal
Pires, P. M., Abbott, L. F., & Maimon, G. (2022) · doi:10.1101/2022.11.10.516026 · Cited by 110
Self-citationImpact of central complex lesions on innate and learnt visual navigation in ants
Buehlmann, C., Dell-Cronin, S., Pathirannahelage, A. D., Goulard, R., Webb, B. H., Niven, J. E., & Graham, P. (2023) · Journal of Comparative Physiology A · doi:10.1007/s00359-023-01613-1 · Cited by 17
The influence of stimulus history on directional coding in the monarch butterfly brain
Beetz, M. J., & el Jundi, B. (2023) · Journal of Comparative Physiology A · doi:10.1007/s00359-023-01633-x · Cited by 14
Organization and neural connections of the lateral complex in the brain of the desert locust
Hensgen, R., Göthe, J., Jahn, S., Hümmert, S., Schneider, K. L., Takahashi, N., Pegel, U., Gotthardt, S., & Homberg, U. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25209 · Cited by 15
Neuronal calcium spikes enable vector inversion in the Drosophila brain
Ishida, I. G., Sethi, S., Mohren, T. L., Haraguchi, M., Abbott, L. F., & Maimon, G. (2025) · Cell · doi:10.1016/j.cell.2025.11.040 · Cited by 11
Self-citationGoulard, R., Buehlmann, C., Niven, J. E., Graham, P., & Webb, B. H. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.228601 · Cited by 13
Multimodal cue integration and learning in a neural representation of head direction
Basnak, M. A., Kutschireiter, A., Okubo, T. S., Chen, A., Gorelik, P., Drugowitsch, J., & Wilson, R. I. (2025) · Nature Neuroscience · doi:10.1038/s41593-024-01823-z · Cited by 13
“All the HD cells in this network can be imaged simultaneously as a head-fixed fly navigates in a virtual reality environment 33,34 .”
Han, R., Huang, H.-P., Chuang, C.-L., Yen, H.-H., Kao, W.-T., Chang, H.-Y., & Lo, C. (2021) · eNeuro · doi:10.1523/eneuro.0537-20.2021 · Cited by 12
Dopamine Modulation of Drosophila Ellipsoid Body Neurons, a Nod to the Mammalian Basal Ganglia
Frighetto, G., Zordan, M. A., Castiello, U., Megighian, A., & Martin, J. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.849142 · Cited by 12
3D atlas of cerebral neuropils with previously unknown demarcations in the honey bee brain
Habenstein, J., Grübel, K., Pfeiffer, K., & Rößler, W. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25486 · Cited by 14
Transforming a head direction signal into a goal-oriented steering command
Westeinde, E. A., Kellogg, E., Dawson, P. M., Lu, J., Hamburg, L., Midler, B., Druckmann, S., & Wilson, R. I. (2022) · doi:10.1101/2022.11.10.516039 · Cited by 85
Circuits for self-motion estimation and walking control in Drosophila
Chiappe, M. E. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102748 · Cited by 11
Dillon, N. R., Manning, L., Hirono, K., & Doe, C. Q. (2024) · Development · doi:10.1242/dev.202504 · Cited by 11
A vector-based strategy for olfactory navigation in Drosophila
Siliciano, A. F., Minni, S., Morton, C., Dowell, C. K., Eghbali, N. B., Busch, S. E., Rhee, J. Y., Abbott, L. F., & Ruta, V. (2026) · Nature · doi:10.1038/s41586-026-10827-7 · Cited by 13
Takahashi, N., Zittrell, F., Hensgen, R., & Homberg, U. (2022) · Journal of Experimental Biology · doi:10.1242/jeb.243858 · Cited by 11
Primate neocortex performs balanced sensory amplification
Pattadkal, J. J., Zemelman, B. V., Fiete, I., & Priebe, N. J. (2023) · Neuron · doi:10.1016/j.neuron.2023.11.005 · Cited by 12
Wosnitza, A., Martin, J. P., Pollack, A. J., Svenson, G. J., & Ritzmann, R. E. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.893004 · Cited by 10
Neural Control of Naturalistic Behavior Choices
Asinof, S. K., & Card, G. M. (2024) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-111020-094019 · Cited by 10
Neural circuit mechanisms for steering control in walking Drosophila
Rayshubskiy, A., Holtz, S. L., Bates, A. S., Vanderbeck, Q. X., Capdevila, L. S., Rockwell, V., & Wilson, R. I. (2025) · eLife · doi:10.7554/elife.102230.3 · Cited by 9
Insect Orientation: Stay on Course with the Sun
Beetz, M. J., & el Jundi, B. (2018) · Current Biology · doi:10.1016/j.cub.2018.07.032 · Cited by 8
Lavian, H., Prat, O., Petrucco, L., Štih, V., & Portugues, R. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.25.614953 · Cited by 8
Castor is a temporal transcription factor that specifies early born central complex neuron identity
Dillon, N. R., & Doe, C. Q. (2024) · Development · doi:10.1242/dev.204318 · Cited by 7
Neural mechanisms to incorporate visual counterevidence in self-movement estimation
Tanaka, R., Zhou, B., Agrochão, M., Badwan, B. A., Au, B., Matos, N. C. B., & Clark, D. A. (2023) · Current Biology · doi:10.1016/j.cub.2023.10.011 · Cited by 11
Neural representation of goal direction in the monarch butterfly brainPreprint
Beetz, M. J., Kraus, C. M., & el Jundi, B. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.15.512348 · Cited by 7
Neuronal circuit mechanisms of competitive interaction between action-based and coincidence learning
Rozenfeld, E., & Parnas, M. (2024) · Science Advances · doi:10.1126/sciadv.adq3016 · Cited by 10
Lavian, H., Prat, O., Petrucco, L., Štih, V., & Portugues, R. (2025) · Nature Communications · doi:10.1038/s41467-025-66084-1 · Cited by 12
Neural circuit mechanisms for steering control in walking Drosophila
Rayshubskiy, A., Holtz, S. L., Bates, A., Vanderbeck, Q. X., Capdevila, L. S., & Wilson, R. I. (2024) · doi:10.7554/elife.102230.1 · Cited by 5
Sensory fusion in the hoverfly righting reflex
Verbe, A., Martinez, D., & Viollet, S. (2023) · Scientific Reports · doi:10.1038/s41598-023-33302-z · Cited by 5
Pae, H., Liao, J., Yuen, N., & Giraldo, Y. M. (2024) · Journal of Experimental Biology · doi:10.1242/jeb.246817 · Cited by 5
The routes of one-eyed ants suggest a revised model of normal route following
Woodgate, J., Perl, C. D., & Collett, T. S. (2021) · Journal of Experimental Biology · doi:10.1242/jeb.242167 · Cited by 6
A dynamical model exploring sensory integration in the insect central complex substructures
Pickard, S. C., Quinn, R. D., & Szczecinski, N. S. (2019) · Bioinspiration & Biomimetics · doi:10.1088/1748-3190/ab57b6 · Cited by 5
Woller, A., Bandow, P., Aimon, S., & Kadow, I. C. G. (2021) · Journal of Visualized Experiments · doi:10.3791/61876 · Cited by 5
Metadata
- Authors
- Green, J., Vijayan, V., Mussells Pires, P., Adachi, A., & Maimon, G.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Maimon, Gaby
- Venue
- Nature Neuroscience
- Published
- 2019-07-22
- Volume
- 22
- Issue
- 9
- Pages
- 1460-1468
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC7688015
- OpenAlex
- W2963869135
- Cited by
- 137
- References
- 60
- Citations by year
- 2026: 15 · 2025: 15 · 2024: 21 · 2023: 16 · 2022: 19 · 2021: 19 · 2020: 14 · 2019: 13
- FWCI
- 7.76
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- Locations
- Nature Neuroscience (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- McKnight Foundation
- Leon Levy Foundation
- Nature
- National Institutes of Health (NIH P40OD018537, P40OD018537)
- National Institute on Drug Abuse (DP2DA035148)
- National Institute of Neurological Disorders and Stroke (R01NS104934)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
- Keywords
- heading estimation, head direction cells, goal-directed navigation, Drosophila, central complex, turning behavior
- MeSH terms
- Orientation, Spatial, Animals, Brain, Cues, Drosophila, Female, Neurons, Spatial Navigation
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