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Divisive Normalization in Olfactory Population Codes
Open accessAbstract
In many regions of the visual system, the activity of a neuron is normalized by the activity of other neurons in the same region. Here we show that a similar normalization occurs during olfactory processing in the Drosophila antennal lobe. We exploit the orderly anatomy of this circuit to independently manipulate feedforward and lateral input to second-order projection neurons (PNs). Lateral inhibition increases the level of feedforward input needed to drive PNs to saturation, and this normalization scales with the total activity of the olfactory receptor neuron (ORN) population. Increasing total ORN activity also makes PN responses more transient. Strikingly, a model with just two variables (feedforward and total ORN activity) accurately predicts PN odor responses. Finally, we show that discrimination by a linear decoder is facilitated by two complementary transformations: the saturating transformation intrinsic to each processing channel boosts weak signals, while normalization helps equalize responses to different stimuli.
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Citations
Cites
DISCHARGE PATTERNS AND FUNCTIONAL ORGANIZATION OF MAMMALIAN RETINA
Kuffler, S. W. (1953) · Journal of Neurophysiology · doi:10.1152/jn.1953.16.1.37 · Cited by 2,609
Normalization of cell responses in cat striate cortex
Heeger, D. J. (1992) · Visual Neuroscience · doi:10.1017/s0952523800009640 · Cited by 1,835
The Normalization Model of Attention
Reynolds, J. H., & Heeger, D. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.002 · Cited by 1,457
Coding of Odors by a Receptor Repertoire
Hallem, E. A., & Carlson, J. R. (2006) · Cell · doi:10.1016/j.cell.2006.01.050 · Cited by 1,286
Striate cortex of monkey and cat: contrast response function.
Albrecht, D. G., & Hamilton, D. B. (1982) · Journal of Neurophysiology · doi:10.1152/jn.1982.48.1.217 · Cited by 953
Linearity and Normalization in Simple Cells of the Macaque Primary Visual Cortex
Carandini, M., Heeger, D. J., & Movshon, J. A. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08621.1997 · Cited by 926
Summation and inhibition in the frog's retina
Barlow, H. B. (1953) · The Journal of Physiology · doi:10.1113/jphysiol.1953.sp004829 · Cited by 912
Natural signal statistics and sensory gain control
Schwartz, O., & Simoncelli, E. P. (2001) · Nature Neuroscience · doi:10.1038/90526 · Cited by 835
Nature and Interaction of Signals From the Receptive Field Center and Surround in Macaque V1 Neurons
Cavanaugh, J. R., Bair, W., & Movshon, J. A. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00692.2001 · Cited by 784
Olfactory network dynamics and the coding of multidimensional signals
Laurent, G. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn964 · Cited by 738
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Normalization as a canonical neural computation
Carandini, M., & Heeger, D. J. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3136 · Cited by 1,906
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BackgroundOdorant Reception in Insects: Roles of Receptors, Binding Proteins, and Degrading Enzymes
Leal, W. S. (2012) · Annual Review of Entomology · doi:10.1146/annurev-ento-120811-153635 · Cited by 1,708
Central gain control in tinnitus and hyperacusis
Auerbach, B. D., Rodrigues, P. V., & Salvi, R. J. (2014) · Frontiers in Neurology · doi:10.3389/fneur.2014.00206 · Cited by 439
Neural Circuitry of Reward Prediction Error
Watabe-Uchida, M., Eshel, N., & Uchida, N. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031109 · Cited by 437
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
Early Olfactory Processing in Drosophila: Mechanisms and Principles
Wilson, R. I. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150533 · Cited by 394
Self-citationArithmetic and local circuitry underlying dopamine prediction errors
Eshel, N., Bukwich, M., Rao, V., Hemmelder, V., Tian, J., & Uchida, N. (2015) · Nature · doi:10.1038/nature14855 · Cited by 401
Activity of Defined Mushroom Body Output Neurons Underlies Learned Olfactory Behavior in Drosophila
Owald, D., Felsenberg, J., Talbot, C. B., Das, G., Perisse, E., Huetteroth, W., & Waddell, S. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.025 · Cited by 401
Buzsáki, G. (2019) · doi:10.1093/oso/9780190905385.001.0001 · Cited by 383
A normalization model of multisensory integration
Ohshiro, T., Angelaki, D. E., & DeAngelis, G. C. (2011) · Nature Neuroscience · doi:10.1038/nn.2815 · Cited by 320
Sparse, decorrelated odor coding in the mushroom body enhances learned odor discrimination
Lin, A. C., Bygrave, A. M., de Calignon, A., Lee, T., & Miesenböck, G. (2014) · Nature Neuroscience · doi:10.1038/nn.3660 · Cited by 317
Miyamichi, K., Shlomai, Y., Shu, M., Weissbourd, B., Luo, L., & Mizrahi, A. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.027 · Cited by 309
Dopamine neurons share common response function for reward prediction error
Eshel, N., Tian, J., Bukwich, M., & Uchida, N. (2016) · Nature Neuroscience · doi:10.1038/nn.4239 · Cited by 321
Glutamate is an inhibitory neurotransmitter in the Drosophila olfactory system
Liu, W. W., & Wilson, R. I. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1220560110 · Cited by 297
Self-citationCellular-Resolution Population Imaging Reveals Robust Sparse Coding in the Drosophila Mushroom Body
Honegger, K. S., Campbell, R. A. A., & Turner, G. C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1099-11.2011 · Cited by 250
Noise in Neural Populations Accounts for Errors in Working Memory
Bays, P. M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3204-13.2014 · Cited by 250
Eckstein, N., Bates, A. S., Champion, A., Du, M., Yin, Y., Schlegel, P., Lu, A. K.-Y., Rymer, T., Finley-May, S., Paterson, T., et al. (2024) · Cell · doi:10.1016/j.cell.2024.03.016 · Cited by 277
“GABAergic inhibition has been implicated in “divisive inhi-bition“ (Wilson and Laurent, 2005a; Olsen and Wilson, 2008; Olsen et al., 2010).”
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Martin, J. P., Beyerlein, A., Dacks, A. M., Reisenman, C. E., Riffell, J. A., Lei, H., & Hildebrand, J. G. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.09.007 · Cited by 225
Distributed and Mixed Information in Monosynaptic Inputs to Dopamine Neurons
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Brouwer, G. J., & Heeger, D. J. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00540.2011 · Cited by 226
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Dasgupta, S., Stevens, C. F., & Navlakha, S. (2017) · Science · doi:10.1126/science.aam9868 · Cited by 231
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Jovanic, T., Schneider-Mizell, C. M., Shao, M., Masson, J., Denisov, G., Fetter, R. D., Mensh, B. D., Truman, J. W., Cardona, A., & Zlatic, M. (2016) · Cell · doi:10.1016/j.cell.2016.09.009 · Cited by 216
The wiring diagram of a glomerular olfactory system
Berck, M. E., Khandelwal, A., Claus, L., Hernandez-Nunez, L., Si, G., Tabone, C. J., Li, F., Truman, J. W., Fetter, R. D., Louis, M., et al. (2016) · eLife · doi:10.7554/elife.14859 · Cited by 209
Prefrontal Cortex Regulates Sensory Filtering through a Basal Ganglia-to-Thalamus Pathway
Nakajima, M., Schmitt, L. I., & Halassa, M. M. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.026 · Cited by 218
The Neuroscience of Learning: Beyond the Hebbian Synapse
Gallistel, C. R., & Matzel, L. D. (2012) · Annual Review of Psychology · doi:10.1146/annurev-psych-113011-143807 · Cited by 212
Electrical Coupling between Olfactory Glomeruli
Yaksi, E., & Wilson, R. I. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.041 · Cited by 190
Self-citationBanerjee, A., Marbach, F., Anselmi, F., Koh, M., Davis, M. B., da Silva, P. G., Delevich, K. M., Oyibo, H. K., Gupta, P., Li, B., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.06.019 · Cited by 183
Parvalbumin-Expressing Interneurons Linearly Control Olfactory Bulb Output
Kato, H., Gillet, S. N., Peters, A. J., Isaacson, J. S., & Komiyama, T. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.036 · Cited by 186
Murthy, V. N. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113738 · Cited by 175
The Impact of Adult Neurogenesis on Olfactory Bulb Circuits and Computations
Lepousez, G., Valley, M. T., & Lledo, P. (2012) · Annual Review of Physiology · doi:10.1146/annurev-physiol-030212-183731 · Cited by 178
Coding and Transformations in the Olfactory System
Uchida, N., Poo, C., & Haddad, R. (2014) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-013941 · Cited by 161
Plasticity-driven individualization of olfactory coding in mushroom body output neurons
Hige, T., Aso, Y., Rubin, G. M., & Turner, G. C. (2015) · Nature · doi:10.1038/nature15396 · Cited by 160
A computational perspective on autism
Rosenberg, A., Patterson, J. S., & Angelaki, D. E. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510583112 · Cited by 156
Chirimuuta, M. (2013) · Synthese · doi:10.1007/s11229-013-0369-y · Cited by 157
Integration of the olfactory code across dendritic claws of single mushroom body neurons
Gruntman, E., & Turner, G. C. (2013) · Nature Neuroscience · doi:10.1038/nn.3547 · Cited by 151
Olfactory coding in the insect brain: data and conjectures
Galizia, C. G. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12558 · Cited by 163
Asymmetric neurotransmitter release enables rapid odour lateralization in Drosophila
Gaudry, Q., Hong, E. J., Kain, J., de Bivort, B. L., & Wilson, R. I. (2013) · Nature · doi:10.1038/nature11747 · Cited by 146
Self-citationValue normalization in decision making: theory and evidence
Rangel, A., & Clithero, J. A. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.07.011 · Cited by 165
Dense EM-based reconstruction of the interglomerular projectome in the zebrafish olfactory bulb
Wanner, A. A., Genoud, C., Masudi, T., Siksou, L., & Friedrich, R. W. (2016) · Nature Neuroscience · doi:10.1038/nn.4290 · Cited by 144
Rapid Sensory Adaptation Redux: A Circuit Perspective
Whitmire, C. J., & Stanley, G. B. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.046 · Cited by 145
Generating sparse and selective third-order responses in the olfactory system of the fly
Luo, S. X., Axel, R., & Abbott, L. F. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005635107 · Cited by 139
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Larsch, J., Flavell, S. W., Liu, Q., Gordus, A. G., Albrecht, D. R., & Bargmann, C. I. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.08.032 · Cited by 143
Elementary sensory-motor transformations underlying olfactory navigation in walking fruit-flies
Álvarez-Salvado, E., Licata, A., Connor, E. G., McHugh, M. K., King, B. M., Stavropoulos, N., Victor, J. D., Crimaldi, J. P., & Nagel, K. I. (2018) · eLife · doi:10.7554/elife.37815 · Cited by 139
Eckstein, N., Bates, A. S., Champion, A., Du, M., Yin, Y., Schlegel, P., Lu, A. K.-Y., Rymer, T., Finley-May, S., Paterson, T., et al. (2020) · doi:10.1101/2020.06.12.148775 · Cited by 115
Marginalization in Neural Circuits with Divisive Normalization
Beck, J. M., Latham, P. E., & Pouget, A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1706-11.2011 · Cited by 135
Odor Discrimination in Drosophila: From Neural Population Codes to Behavior
Parnas, M., Lin, A. C., Huetteroth, W., & Miesenböck, G. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.006 · Cited by 129
Intensity Invariant Dynamics and Odor-Specific Latencies in Olfactory Receptor Neuron Response
Martelli, C., Carlson, J. R., & Emonet, T. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0426-12.2013 · Cited by 123
Synaptic organization of the Drosophila antennal lobe and its regulation by the Teneurins
Mosca, T. J., & Luo, L. (2014) · eLife · doi:10.7554/elife.03726 · Cited by 117
Organization of descending neurons in Drosophila melanogaster
Hsu, C. T., & Bhandawat, V. (2016) · Scientific Reports · doi:10.1038/srep20259 · Cited by 117
Self-citationStructured Odorant Response Patterns across a Complete Olfactory Receptor Neuron Population
Si, G., Kanwal, J. K., Hu, Y., Tabone, C. J., Baron, J., Berck, M., Vignoud, G., & Samuel, A. D. T. (2019) · Neuron · doi:10.1016/j.neuron.2018.12.030 · Cited by 113
Tuned Normalization Explains the Size of Attention Modulations
Ni, A. M., Ray, S., & Maunsell, J. H. R. (2012) · Neuron · doi:10.1016/j.neuron.2012.01.006 · Cited by 109
GABAergic Projection Neurons Route Selective Olfactory Inputs to Specific Higher-Order Neurons
Liang, L., Li, Y., Potter, C. J., Yizhar, O., Deisseroth, K. A., Tsien, R. W., & Luo, L. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.014 · Cited by 116
Stereotyped connectivity and computations in higher-order olfactory neurons
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Yoo, S. B. M., & Hayden, B. Y. (2018) · Neuron · doi:10.1016/j.neuron.2018.06.038 · Cited by 110
Presynaptic gain control drives sweet and bitter taste integration in Drosophila
Chu, B., Chui, V., Mann, K., & Gordon, M. D. (2014) · Current Biology · doi:10.1016/j.cub.2014.07.020 · Cited by 100
Decoding of Context-Dependent Olfactory Behavior in Drosophila
Badel, L., Ohta, K., Tsuchimoto, Y., & Kazama, H. (2016) · Neuron · doi:10.1016/j.neuron.2016.05.022 · Cited by 98
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Schulze, A., Gómez-Marín, À., Rajendran, V. G., Lott, G. K., Musy, M., Ahammad, P., Deogade, A., Sharpe, J. A., Riedl, J., Jarriault, D., et al. (2015) · eLife · doi:10.7554/elife.06694 · Cited by 98
Understanding smell—The olfactory stimulus problem
Auffarth, B. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.06.009 · Cited by 105
Decision by sampling implements efficient coding of psychoeconomic functions.
Bhui, R., & Gershman, S. J. (2018) · Psychological Review · doi:10.1037/rev0000123 · Cited by 105
Gorur-Shandilya, S., Demir, M., Long, J., Clark, D. A., & Emonet, T. (2017) · eLife · doi:10.7554/elife.27670 · Cited by 94
Antagonism in olfactory receptor neurons and its implications for the perception of odor mixtures
Reddy, G., Zak, J. D., Vergassola, M., & Murthy, V. N. (2018) · eLife · doi:10.7554/elife.34958 · Cited by 94
Simultaneous Encoding of Odors by Channels with Diverse Sensitivity to Inhibition
Hong, E. J., & Wilson, R. I. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.040 · Cited by 93
Self-citationInternal state configures olfactory behavior and early sensory processing in Drosophila larvae
Vogt, K., Zimmerman, D. M., Schlichting, M., Hernandez-Nunez, L., Qin, S., Malacon, K. E., Rosbash, M., Pehlevan, C., Cardona, A., & Samuel, A. D. T. (2021) · Science Advances · doi:10.1126/sciadv.abd6900 · Cited by 96
An excitatory basis for divisive normalization in visual cortex
Sato, T. K., Haider, B., Häusser, M., & Carandini, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4249 · Cited by 91
Temporal coding of odor mixtures in an olfactory receptor neuron
Su, C., Martelli, C., Emonet, T., & Carlson, J. R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100369108 · Cited by 89
The Organization of Projections from Olfactory Glomeruli onto Higher-Order Neurons
Jeanne, J. M., Fişek, M., & Wilson, R. I. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.011 · Cited by 89
Self-citationWhat the fly’s nose tells the fly’s brain
Stevens, C. F. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510103112 · Cited by 87
Storace, D. A., & Cohen, L. B. (2017) · Nature Communications · doi:10.1038/s41467-017-00036-2 · Cited by 86
A Biological Vision Inspired Framework for Image Enhancement in Poor Visibility Conditions
Yang, K.-F., Zhang, X.-S., & Li, Y. (2019) · IEEE Transactions on Image Processing · doi:10.1109/tip.2019.2938310 · Cited by 86
Dynamic Divisive Normalization Predicts Time-Varying Value Coding in Decision-Related Circuits
Louie, K., LoFaro, T., Webb, R., & Glimcher, P. W. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2851-14.2014 · Cited by 85
Olfactory circuits and behaviors of nematodes
Rengarajan, S., & Hallem, E. A. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.09.002 · Cited by 84
Signaling of the Strongest Stimulus in the Owl Optic Tectum
Mysore, S. P., Asadollahi, A., & Knudsen, E. I. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4592-10.2011 · Cited by 83
Odor mixtures of opposing valence unveil inter-glomerular crosstalk in the Drosophila antennal lobe
Mohamed, A. A. M., Retzke, T., Chakraborty, S. D., Fabian, B., Hansson, B. S., Knaden, M., & Sachse, S. (2019) · Nature Communications · doi:10.1038/s41467-019-09069-1 · Cited by 87
Neural pathways for the detection and discrimination of conspecific song in D. melanogaster
Vaughan, A. G., Zhou, C., Manoli, D. S., & Baker, B. S. (2014) · Current Biology · doi:10.1016/j.cub.2014.03.048 · Cited by 81
Idiosyncratic neural coding and neuromodulation of olfactory individuality in Drosophila
Honegger, K. S., Smith, M. A.-Y., Churgin, M. A., Turner, G. C., & de Bivort, B. L. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1901623116 · Cited by 84
Organization of the Drosophila larval visual circuit
Larderet, I., Fritsch, P. M. J., Gendre, N., Neagu-Maier, G. L., Fetter, R. D., Schneider-Mizell, C. M., Truman, J. W., Zlatic, M., Cardona, A., & Sprecher, S. G. (2017) · eLife · doi:10.7554/elife.28387 · Cited by 79
Adaptation in auditory processing
Willmore, B. D. B., & King, A. J. (2022) · Physiological Reviews · doi:10.1152/physrev.00011.2022 · Cited by 82
Ohshiro, T., Angelaki, D. E., & DeAngelis, G. C. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.043 · Cited by 81
Olfactory modulation of flight in Drosophila is sensitive, selective and rapid
Bhandawat, V., Maimon, G., Dickinson, M. H., & Wilson, R. I. (2010) · Journal of Experimental Biology · doi:10.1242/jeb.040402 · Cited by 75
Self-citationExperience-Dependent Plasticity of Odor Representations in the Telencephalon of Zebrafish
Jacobson, G. A., Rupprecht, P., & Friedrich, R. W. (2018) · Current Biology · doi:10.1016/j.cub.2017.11.007 · Cited by 74
Behavior Reveals Selective Summation and Max Pooling among Olfactory Processing Channels
Bell, J. S., & Wilson, R. I. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.011 · Cited by 74
Self-citationEqualization of odor representations by a network of electrically coupled inhibitory interneurons
Zhu, P., Frank, T., & Friedrich, R. W. (2013) · Nature Neuroscience · doi:10.1038/nn.3528 · Cited by 74
New advances in understanding decisions among multiple alternatives
Churchland, A. K., & Ditterich, J. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.04.009 · Cited by 72
Suppressive mechanisms in visual motion processing: From perception to intelligence
Tadin, D. (2015) · Vision Research · doi:10.1016/j.visres.2015.08.005 · Cited by 71
Mysore, S. P., & Knudsen, E. I. (2012) · Neuron · doi:10.1016/j.neuron.2011.10.037 · Cited by 71
A recurrent circuit implements normalization, simulating the dynamics of V1 activity
Heeger, D. J., & Zemlianova, K. O. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005417117 · Cited by 72
DSL-Notch Signaling in the Drosophila Brain in Response to Olfactory Stimulation
Lieber, T., Kidd, S., & Struhl, G. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.015 · Cited by 69
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Ren, M., Liao, R., Urtasun, R., Sinz, F. H., & Zemel, R. S. (2016) · arXiv (Cornell University) · doi:10.48550/arxiv.1611.04520 · Cited by 73
Localized inhibition in the Drosophila mushroom body
Amin, H., Apostolopoulou, A. A., Suárez-Grimalt, R., Vrontou, E., & Lin, A. C. (2020) · eLife · doi:10.7554/elife.56954 · Cited by 66
Smelling on the fly: sensory cues and strategies for olfactory navigation in Drosophila
Gaudry, Q., Nagel, K. I., & Wilson, R. I. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.12.010 · Cited by 65
Self-citationSpectrotemporal Contrast Kernels for Neurons in Primary Auditory Cortex
Rabinowitz, N. C., Willmore, B. D. B., Schnupp, J. W. H., & King, A. J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1715-12.2012 · Cited by 67
Dynamic Signal Compression for Robust Motion Vision in Flies
Drews, M. S., Leonhardt, A., Pirogova, N., Richter, F. G., Schützenberger, A., Braun, L., Serbe-Kamp, E., & Borst, A. (2020) · Current Biology · doi:10.1016/j.cub.2019.10.035 · Cited by 66
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
Attention-related changes in correlated neuronal activity arise from normalization mechanisms
Verhoef, B.-E., & Maunsell, J. H. R. (2017) · Nature Neuroscience · doi:10.1038/nn.4572 · Cited by 63
Olfactory coding from the periphery to higher brain centers in the Drosophila brain
Seki, Y., Dweck, H. K. M., Rybak, J., Wicher, D., Sachse, S., & Hansson, B. S. (2017) · BMC Biology · doi:10.1186/s12915-017-0389-z · Cited by 62
FlpStop, a tool for conditional gene control in Drosophila
Fisher, Y. E., Yang, H. H., Isaacman-Beck, J., Xie, M., Gohl, D. M., & Clandinin, T. R. (2017) · eLife · doi:10.7554/elife.22279 · Cited by 64
Intrinsic and Extrinsic Neuromodulation of Olfactory Processing
Lizbinski, K. M., & Dacks, A. M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00424 · Cited by 60
Pairwise normalization: A neuroeconomic theory of multi-attribute choice
Landry, P., & Webb, R. (2021) · Journal of Economic Theory · doi:10.1016/j.jet.2021.105221 · Cited by 64
The Vestibular System Implements a Linear–Nonlinear Transformation In Order to Encode Self-Motion
Massot, C., Schneider, A. D., Chacron, M. J., & Cullen, K. E. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001365 · Cited by 61
Reisenman, C. E., Lei, H., & Guerenstein, P. G. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00271 · Cited by 66
Metadata
- Authors
- Olsen, S. R., Bhandawat, V., & Wilson, R. I.
- Affiliations
- Harvard University (US)
- Corresponding author
- Wilson, Rachel I.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2010-04
- Volume
- 66
- Issue
- 2
- Pages
- 287-299
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC2866644
- OpenAlex
- W2138260451
- Cited by
- 500
- References
- 56
- Citations by year
- 2026: 20 · 2025: 38 · 2024: 26 · 2023: 29 · 2022: 30 · 2021: 46 · 2020: 31 · 2019: 53 · 2018: 29 · 2017: 29 · 2016: 35 · 2015: 21 · 2014: 27 · 2013: 31 · 2012: 26
- FWCI
- 11.01
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1203 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- McKnight Foundation
- Charles A. King Trust
- National Institutes of Health (R01DC008174)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- divisive normalization, antennal lobe, projection neurons, lateral inhibition, olfactory sensory neurons, signal saturation, transient response, odor discrimination, linear decoder, Drosophila olfaction
- MeSH terms
- Animals, Drosophila, Electrophysiology, Models, Neurological, Nerve Net, Neural Inhibition, Synaptic Transmission, Odorants, Olfactory Pathways, Signal Processing, Computer-Assisted, Smell, Olfactory Receptor Neurons
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