Evolving images for visual neurons using a deep generative network reveals coding principles and neuronal preferences
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Abstract
What specific features should visual neurons encode, given the infinity of real-world images and the limited number of neurons available to represent them? We investigated neuronal selectivity in monkey inferotemporal cortex via the vast hypothesis space of a generative deep neural network, avoiding assumptions about features or semantic categories. A genetic algorithm searched this space for stimuli that maximized neuronal firing. This led to the evolution of rich synthetic images of objects with complex combinations of shapes, colors, and textures, sometimes resembling animals or familiar people, other times revealing novel patterns that did not map to any clear semantic category. These results expand our conception of the dictionary of features encoded in the cortex, and the approach can potentially reveal the internal representations of any system whose input can be captured by a generative model.
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The organization of the cerebral cortex is characterized by extraordinary specialization of neural units at all levels.
“Notably, the organization of the cerebral cortex, widely considered as the likely substrate of human consciousness, is characterized by extraordinary specialization of neural units at all levels [38–40].”
From Integrated information theory (IIT) 4.0: Formulating the properties of phenomenal existence in physical terms (2023) · cites this paper as [39]
The Introduction (page unavailable) describes visual cortical neurons selective for features including motion, color, curvature, and faces. This supports specialization in visual cortex, but the paper does not establish that neural units are specialized throughout the cerebral cortex or at all levels. (LLM, conf=0.85)
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Cites
ImageNet classification with deep convolutional neural networks
Krizhevsky, A., Sutskever, I., & Hinton, G. E. (2017) · Communications of the ACM · doi:10.1145/3065386 · Cited by 112,155 · see citing works
ImageNet: A large-scale hierarchical image database
Deng, J., Dong, W., Socher, R., Li, L.-J., Li, K., & Fei-Fei, L. (2009) · 2009 IEEE Conference on Computer Vision and Pattern Recognition · doi:10.1109/cvpr.2009.5206848 · Cited by 65,333 · see citing works
ImageNet Large Scale Visual Recognition Challenge
Russakovsky, O., Deng, J., Su, H., Krause, J., Satheesh, S., Ma, S., Huang, Z., Karpathy, A., Khosla, A., Bernstein, M., et al. (2015) · International Journal of Computer Vision · doi:10.1007/s11263-015-0816-y · Cited by 39,380 · see citing works
Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex
Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680 · see citing works
Receptive fields and functional architecture of monkey striate cortex
Hubel, D. H., & Wiesel, T. N. (1968) · The Journal of Physiology · doi:10.1113/jphysiol.1968.sp008455 · Cited by 6,571 · see citing works
Caffe: Convolutional Architecture for Fast Feature EmbeddingPreprint
Jia, Y., Shelhamer, E., Donahue, J., Karayev, S., Long, J., Girshick, R., Guadarrama, S., & Darrell, T. (2014) · arXiv (Cornell University) · doi:10.48550/arxiv.1408.5093 · Cited by 4,748 · see citing works
Hierarchical models of object recognition in cortex
Riesenhuber, M., & Poggio, T. (1999) · Nature Neuroscience · doi:10.1038/14819 · Cited by 3,309 · see citing works
Performance-optimized hierarchical models predict neural responses in higher visual cortex
Yamins, D. L. K., Hong, H., Cadieu, C. F., Solomon, E. A., Seibert, D., & DiCarlo, J. J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1403112111 · Cited by 1,924 · see citing works
A Parametric Texture Model Based on Joint Statistics of Complex Wavelet Coefficients
Portilla, J., & Simoncelli, E. P. (2000) · International Journal of Computer Vision · doi:10.1023/a:1026553619983 · Cited by 1,806 · see citing works
Visual properties of neurons in inferotemporal cortex of the Macaque.
Gross, C. G., Rocha‐Miranda, C. E., & Bender, D. B. (1972) · Journal of Neurophysiology · doi:10.1152/jn.1972.35.1.96 · Cited by 1,488 · see citing works
The neural mechanism of binocular depth discrimination
Barlow, H. B., Blakemore, C. B., & Pettigrew, J. D. (1967) · The Journal of Physiology · doi:10.1113/jphysiol.1967.sp008360 · Cited by 1,435 · see citing works
Stimulus-selective properties of inferior temporal neurons in the macaque
Desimone, R., Albright, T. D., Gross, C. G., & Bruce, C. J. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-08-02051.1984 · Cited by 1,424 · see citing works
Visual neurones responsive to faces in the monkey temporal cortex
Perrett, D. I., Rolls, E. T., & Caan, W. (1982) · Experimental Brain Research · doi:10.1007/bf00239352 · Cited by 1,386 · see citing works
Zeki, S. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010452 · Cited by 982 · see citing works
Kobatake, E., & Tanaka, K. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.71.3.856 · Cited by 807 · see citing works
Proceedings of the 22nd ACM international conference on Multimedia
(2014) · doi:10.1145/2647868 · Cited by 741 · see citing works
The two-dimensional spectral structure of simple receptive fields in cat striate cortex
Jones, J. P., Stepnoski, A., & Palmer, L. A. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.58.6.1212 · Cited by 735 · see citing works
The two-dimensional spatial structure of simple receptive fields in cat striate cortex
Jones, J. P., & Palmer, L. A. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.58.6.1187 · Cited by 676 · see citing works
The Code for Facial Identity in the Primate Brain
Chang, L., & Tsao, D. Y. (2017) · Cell · doi:10.1016/j.cell.2017.05.011 · Cited by 644 · see citing works
Single unit activity in striate cortex of unrestrained cats
Hubel, D. H. (1959) · The Journal of Physiology · doi:10.1113/jphysiol.1959.sp006238 · Cited by 578 · see citing works
Inceptionism: Going Deeper into Neural Networks
Mordvintsev, A., Olah, C., & Tyka, M. (2015) · Cited by 569 · see citing works
Population coding of shape in area V4
Pasupathy, A., & Connor, C. E. (2002) · Nature Neuroscience · doi:10.1038/972 · Cited by 552 · see citing works
Responses to Contour Features in Macaque Area V4
Pasupathy, A., & Connor, C. E. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.5.2490 · Cited by 548 · see citing works
Conceptual distinctiveness supports detailed visual long-term memory for real-world objects.
Konkle, T., Brady, T. F., Alvarez, G. A., & Oliva, A. (2010) · Journal of Experimental Psychology General · doi:10.1037/a0019165 · Cited by 468 · see citing works
A face feature space in the macaque temporal lobe
Freiwald, W. A., Tsao, D. Y., & Livingstone, M. S. (2009) · Nature Neuroscience · doi:10.1038/nn.2363 · Cited by 441 · see citing works
Self-citationSynthesizing the preferred inputs for neurons in neural networks via deep generator networksPreprint
Nguyen, A., Dosovitskiy, A., Yosinski, J., Brox, T., & Clune, J. (2016) · arXiv (Cornell University) · doi:10.48550/arxiv.1605.09304 · Cited by 435 · see citing works
Size and position invariance of neuronal responses in monkey inferotemporal cortex
Ito, M., Tamura, H., Fujita, I., & Tanaka, K. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.73.1.218 · Cited by 432 · see citing works
Colour coding in rhesus monkey prestriate cortex
Zeki, S. (1973) · Brain Research · doi:10.1016/0006-8993(73)90227-8 · Cited by 431 · see citing works
Neural population control via deep image synthesis
Bashivan, P., Kar, K., & DiCarlo, J. J. (2019) · Science · doi:10.1126/science.aav9436 · Cited by 426 · see citing works
Norm-based face encoding by single neurons in the monkey inferotemporal cortex
Leopold, D. A., Bondar, I. V., & Giese, M. A. (2006) · Nature · doi:10.1038/nature04951 · Cited by 379 · see citing works
Receptive field properties of neurons in area V3 of macaque monkey extrastriate cortex
Felleman, D. J., & Essen, D. C. V. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.57.4.889 · Cited by 375 · see citing works
Seeing faces is necessary for face-domain formation
Arcaro, M. J., Schade, P. F., Vincent, J. L., Ponce, C. R., & Livingstone, M. S. (2017) · Nature Neuroscience · doi:10.1038/nn.4635 · Cited by 311 · see citing works
Self-citationA neural code for three-dimensional object shape in macaque inferotemporal cortex
Yamane, Y., Carlson, E. T., Bowman, K. C., Wang, Z., & Connor, C. E. (2008) · Nature Neuroscience · doi:10.1038/nn.2202 · Cited by 291 · see citing works
Colour coding in the superior temporal sulcus of rhesus monkey visual cortex
Zeki, S. M. (1977) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1977.0065 · Cited by 208 · see citing works
“Black” Responses Dominate Macaque Primary Visual Cortex V1
Yeh, C.-I., Xing, D., & Shapley, R. M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1991-09.2009 · Cited by 173 · see citing works
Trade-Off between Object Selectivity and Tolerance in Monkey Inferotemporal Cortex
Zoccolan, D., Kouh, M., Poggio, T., & DiCarlo, J. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1897-07.2007 · Cited by 169 · see citing works
Complex–unoriented cells in a subregion of primate area 18
Hubel, D. H., & Livingstone, M. S. (1985) · Nature · doi:10.1038/315325a0 · Cited by 163 · see citing works
Self-citationGenerating Images with Perceptual Similarity Metrics based on Deep NetworksPreprint
Dosovitskiy, A., & Brox, T. (2016) · arXiv (Cornell University) · doi:10.48550/arxiv.1602.02644 · Cited by 159 · see citing works
Precedence of the Eye Region in Neural Processing of Faces
Issa, E. B., & DiCarlo, J. J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2391-12.2012 · Cited by 148 · see citing works
Michael, C. R. (1978) · Journal of Neurophysiology · doi:10.1152/jn.1978.41.5.1233 · Cited by 140 · see citing works
Medial Axis Shape Coding in Macaque Inferotemporal Cortex
Hung, C.-C., Carlson, E. T., & Connor, C. E. (2012) · Neuron · doi:10.1016/j.neuron.2012.04.029 · Cited by 139 · see citing works
A Sparse Object Coding Scheme in Area V4
Carlson, E. T., Rasquinha, R. J., Zhang, K., & Connor, C. E. (2011) · Current Biology · doi:10.1016/j.cub.2011.01.013 · Cited by 118 · see citing works
Gaska, J., Jacobson, L. D., Chen, H., & Pollen, D. A. (1994) · Visual Neuroscience · doi:10.1017/s0952523800003102 · Cited by 54 · see citing works
Gilbert, N. (2011) · Nature · doi:10.1038/476265a · Cited by 54 · see citing works
A Channel for 3D Environmental Shape in Anterior Inferotemporal Cortex
Vaziri, S., Carlson, E. T., Wang, Z., & Connor, C. E. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.043 · Cited by 53 · see citing works
The DeepTune framework for modeling and characterizing neurons in visual cortex area V4Preprint
Abbasi-Asl, R., Chen, Y., Bloniarz, A. E., Oliver, M., Willmore, B. D. B., Gallant, J. L., & Yu, B. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/465534 · Cited by 33 · see citing works
Pigarev, I. N., Nothdurft, H., & Kästner, S. (2002) · Experimental Brain Research · doi:10.1007/s00221-002-1112-y · Cited by 30 · see citing works
Representation of Gravity-Aligned Scene Structure in Ventral Pathway Visual Cortex
Vaziri, S., & Connor, C. E. (2016) · Current Biology · doi:10.1016/j.cub.2016.01.022 · Cited by 29 · see citing works
Shape Selectivity of Middle Superior Temporal Sulcus Body Patch Neurons
Kalfas, I., Kumar, S., & Vogels, R. (2017) · eNeuro · doi:10.1523/eneuro.0113-17.2017 · Cited by 28 · see citing works
Inception in visual cortex: in vivo-silico loops reveal most exciting imagesPreprint
Walker, E. Y., Sinz, F. H., Froudarakis, E., Fahey, P. G., Muhammad, T., Ecker, A. S., Cobos, E., Reimer, J., Pitkow, X., & Tolias, A. S. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/506956 · Cited by 9 · see citing works
Visualization of information encoded by neurons in the higher-level areas of the visual system
Malakhova, K. (2018) · Journal of Optical Technology · doi:10.1364/jot.85.000494 · Cited by 5 · see citing works
Flagged first, then by citations
1 of the 52 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
The neural architecture of language: Integrative modeling converges on predictive processing
Schrimpf, M., Blank, I. A., Tuckute, G., Kauf, C., Hosseini, E. A., Kanwisher, N., Tenenbaum, J. B., & Fedorenko, E. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2105646118 · Cited by 517 · see citing works
If deep learning is the answer, what is the question?
Saxe, A., Nelli, S., & Summerfield, C. (2021) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-00395-8 · Cited by 397 · see citing works
A map of object space in primate inferotemporal cortex
Bao, P., She, L., McGill, M., & Tsao, D. Y. (2020) · Nature · doi:10.1038/s41586-020-2350-5 · Cited by 396 · see citing works
Artificial Neural Networks for Neuroscientists: A Primer
Yang, G. R., & Wang, X. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.005 · Cited by 386 · see citing works
Direct Fit to Nature: An Evolutionary Perspective on Biological and Artificial Neural Networks
Hasson, U., Nastase, S. A., & Goldstein, A. (2020) · Neuron · doi:10.1016/j.neuron.2019.12.002 · Cited by 387 · see citing works
Albantakis, L., Barbosa, L., Findlay, G., Grasso, M., Haun, A. M., Marshall, W., Mayner, W. G. P., Zaeemzadeh, A., Boly, M., Juel, B. E., et al. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011465 · Cited by 292 · see citing works
Deep Learning: The Good, the Bad, and the Ugly
Serre, T. (2019) · Annual Review of Vision Science · doi:10.1146/annurev-vision-091718-014951 · Cited by 261 · see citing works
Integrative benchmarking to advance neurally mechanistic models of human intelligence
Schrimpf, M., Kubilius, J., Lee, M. J., Ratan Murty, N. A., Ajemian, R., & DiCarlo, J. J. (2020) · Neuron · doi:10.1016/j.neuron.2020.07.040 · Cited by 233 · see citing works
A Review on Generative Adversarial Networks: Algorithms, Theory, and ApplicationsPreprint
Gui, J., Sun, Z., Wen, Y., Tao, D., & Ye, J. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2001.06937 · Cited by 252 · see citing works
The neuroconnectionist research programme
Doerig, A., Sommers, R. P., Seeliger, K., Richards, B., Ismael, J., Lindsay, G. W., Kording, K. P., Konkle, T., van Gerven, M. A. J., Kriegeskorte, N., et al. (2023) · Nature Reviews Neuroscience · doi:10.1038/s41583-023-00705-w · Cited by 233 · see citing works
Bayesian Computation through Cortical Latent Dynamics
Sohn, H., Narain, D., Meirhaeghe, N., & Jazayeri, M. (2019) · Neuron · doi:10.1016/j.neuron.2019.06.012 · Cited by 226 · see citing works
Inception loops discover what excites neurons most using deep predictive models
Walker, E. Y., Sinz, F. H., Cobos, E., Muhammad, T., Froudarakis, E., Fahey, P. G., Ecker, A. S., Reimer, J., Pitkow, X., & Tolias, A. S. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0517-x · Cited by 221 · see citing works
Hyperalignment: Modeling shared information encoded in idiosyncratic cortical topographies
Haxby, J. V., Guntupalli, J. S., Nastase, S. A., & Feilong, M. (2020) · eLife · doi:10.7554/elife.56601 · Cited by 185 · see citing works
Engineering a Less Artificial Intelligence
Sinz, F. H., Pitkow, X., Reimer, J., Bethge, M., & Tolias, A. S. (2019) · Neuron · doi:10.1016/j.neuron.2019.08.034 · Cited by 164 · see citing works
Performance vs. competence in human–machine comparisons
Firestone, C. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1905334117 · Cited by 150 · see citing works
Understanding Neural Networks via Feature Visualization: A Survey
Nguyen, A., Yosinski, J., & Clune, J. (2019) · Lecture notes in computer science · doi:10.1007/978-3-030-28954-6_4 · Cited by 157 · see citing works
The Origins and Prevalence of Texture Bias in Convolutional Neural NetworksPreprint
Hermann, K. L., Chen, T., & Kornblith, S. (2019) · arXiv (Cornell University) · doi:10.48550/arxiv.1911.09071 · Cited by 177 · see citing works
Data augmentation for motor imagery signal classification based on a hybrid neural network.
Zhang, K., Xu, G., Han, Z., Ma, K., Zheng, X., Chen, L., Duan, N., & Zhang, S. (2020) · Sensors · doi:10.3390/s20164485 · Cited by 130 · see citing works
The macaque face patch system: a turtle’s underbelly for the brain
Hesse, J. K., & Tsao, D. Y. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-00393-w · Cited by 139 · see citing works
Anterior Cingulate Cortex and the Control of Dynamic Behavior in Primates
Monosov, I. E., Haber, S. N., Leuthardt, E. C., & Jezzini, A. (2020) · Current Biology · doi:10.1016/j.cub.2020.10.009 · Cited by 118 · see citing works
Computational models of category-selective brain regions enable high-throughput tests of selectivity
Murty, N. A. R., Bashivan, P., Abate, A., DiCarlo, J. J., & Kanwisher, N. (2021) · Nature Communications · doi:10.1038/s41467-021-25409-6 · Cited by 113 · see citing works
Brain hierarchy score: Which deep neural networks are hierarchically brain-like?
Nonaka, S., Majima, K., Aoki, S., & Kamitani, Y. (2021) · iScience · doi:10.1016/j.isci.2021.103013 · Cited by 84 · see citing works
Does the brain's ventral visual pathway compute object shape?
Ayzenberg, V., & Behrmann, M. (2022) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2022.09.019 · Cited by 88 · see citing works
Clune, J. (2019) · arXiv · doi:10.48550/arxiv.1905.10985 · Cited by 82 · see citing works
Foundation model of neural activity predicts response to new stimulus types
Wang, E. Y., Fahey, P. G., Ding, Z., Papadopoulos, S., Ponder, K., Weis, M. A., Chang, A., Muhammad, T., Patel, S. S., Ding, Z., et al. (2025) · Nature · doi:10.1038/s41586-025-08829-y · Cited by 106 · see citing works
Decoding the brain: From neural representations to mechanistic models
Mathis, M. W., Rotondo, A. P., Chang, E. F., Tolias, A. S., & Mathis, A. (2024) · Cell · doi:10.1016/j.cell.2024.08.051 · Cited by 82 · see citing works
Face Recognition by Humans and Machines: Three Fundamental Advances from Deep Learning
O’Toole, A. J., & Castillo, C. D. (2021) · Annual Review of Vision Science · doi:10.1146/annurev-vision-093019-111701 · Cited by 70 · see citing works
Face detection in untrained deep neural networks
Baek, S., Song, M. J., Jang, J., Kim, G., & Paik, S. (2021) · Nature Communications · doi:10.1038/s41467-021-27606-9 · Cited by 74 · see citing works
Driving and suppressing the human language network using large language models
Tuckute, G., Sathe, A., Srikant, S., Taliaferro, M., Wang, M., Schrimpf, M., Kay, K., & Fedorenko, E. G. (2024) · Nature Human Behaviour · doi:10.1038/s41562-023-01783-7 · Cited by 85 · see citing works
Single-neuronal elements of speech production in humans
Khanna, A. R., Muñoz, W., Kim, Y. J., Kfir, Y., Paulk, A. C., Jamali, M., Cai, J., Mustroph, M. L., Caprara, I., Hardstone, R., et al. (2024) · Nature · doi:10.1038/s41586-023-06982-w · Cited by 66 · see citing works
Language in Brains, Minds, and Machines
Tuckute, G., Kanwisher, N., & Fedorenko, E. G. (2024) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-120623-101142 · Cited by 69 · see citing works
The neural mechanisms of face processing: cells, areas, networks, and models
Freiwald, W. A. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.12.007 · Cited by 62 · see citing works
Bakhtiari, S., Mineault, P., Lillicrap, T., Pack, C. C., & Richards, B. A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.18.448989 · Cited by 60 · see citing works
Unveiling functions of the visual cortex using task-specific deep neural networks
Dwivedi, K., Bonner, M. F., Cichy, R. M., & Roig, G. (2021) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1009267 · Cited by 52 · see citing works
Increasing stimulus similarity drives nonmonotonic representational change in hippocampus
Wammes, J. D., Norman, K. A., & Turk-Browne, N. B. (2022) · eLife · doi:10.7554/elife.68344 · Cited by 49 · see citing works
Black Boxes or Unflattering Mirrors? Comparative Bias in the Science of Machine Behaviour
Buckner, C. J. (2021) · The British Journal for the Philosophy of Science · doi:10.1086/714960 · Cited by 53 · see citing works
Jang, H., & Tong, F. (2024) · Nature Communications · doi:10.1038/s41467-024-45679-0 · Cited by 51 · see citing works
Your head is there to move you around: Goal-driven models of the primate dorsal pathwayPreprint
Mineault, P., Bakhtiari, S., Richards, B. A., & Pack, C. C. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.09.451701 · Cited by 54 · see citing works
Studying the visual brain in its natural rhythm
Leopold, D. A., & Park, S. H. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116790 · Cited by 46 · see citing works
Mapping model units to visual neurons reveals population code for social behaviour
Cowley, B. R., Calhoun, A. J., Rangarajan, N., Ireland, E., Turner, M. H., Pillow, J. W., & Murthy, M. (2024) · Nature · doi:10.1038/s41586-024-07451-8 · Cited by 45 · see citing works
The neural code for “face cells” is not face-specific
Vinken, K., Prince, J. S., Konkle, T., & Livingstone, M. S. (2023) · Science Advances · doi:10.1126/sciadv.adg1736 · Cited by 45 · see citing works
Self-citationStable representation of a naturalistic movie emerges from episodic activity with gain variability
Xià, J., Marks, T. D., Goard, M. J., & Weßel, R. (2021) · Nature Communications · doi:10.1038/s41467-021-25437-2 · Cited by 45 · see citing works
Object manifold geometry across the mouse cortical visual hierarchyPreprint
Froudarakis, E., Cohen, U., Diamantaki, M., Patel, S. S., Tan, Z., Muhammad, T., Walker, E. Y., Reimer, J., Berens, P., Sompolinsky, H., et al. (2020) · eLife · doi:10.1101/2020.08.20.258798 · Cited by 44 · see citing works
Jang, H., McCormack, D. R., & Tong, F. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001418 · Cited by 47 · see citing works
Dynamic Suppression of Average Facial Structure Shapes Neural Tuning in Three Macaque Face Patches
Koyano, K. W., Jones, A. P., McMahon, D. B. T., Waidmann, E. N., Russ, B. E., & Leopold, D. A. (2020) · Current Biology · doi:10.1016/j.cub.2020.09.070 · Cited by 42 · see citing works
Brain-inspired models for visual object recognition: an overview
Yang, X. N., Yan, J., Wang, W., Li, S., Hu, B., & Lin, J. L. (2022) · Artificial Intelligence Review · doi:10.1007/s10462-021-10130-z · Cited by 43 · see citing works
Single-Unit Recordings Reveal the Selectivity of a Human Face Area
Decramer, T., Premereur, E., Zhu, Q., Paesschen, W. V., van Loon, J., Vanduffel, W., Taubert, J., Janssen, P., & Theys, T. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0349-21.2021 · Cited by 40 · see citing works
Curvature-processing domains in primate V4
Tang, R., Song, Q., Li, Y., Zhang, R., Cai, X., & Lu, H. D. (2020) · eLife · doi:10.7554/elife.57502 · Cited by 36 · see citing works
End-to-end neural system identification with neural information flow
Seeliger, K., Ambrogioni, L., Güçlütürk, Y., van den Bulk, L. M., Güçlü, U., & van Gerven, M. A. J. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008558 · Cited by 38 · see citing works
Generalization in data-driven models of primary visual cortexPreprint
Lurz, K.-K., Bashiri, M., Willeke, K. F., Jagadish, A. K., Wang, E. Y., Walker, E. Y., Cadena, S. A., Muhammad, T., Cobos, E., Tolias, A. S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.05.326256 · Cited by 39 · see citing works
Generating realistic neurophysiological time series with denoising diffusion probabilistic models
Vetter, J., Macke, J. H., & Gao, R. (2024) · Patterns · doi:10.1016/j.patter.2024.101047 · Cited by 40 · see citing works
Interpretability of artificial neural network models in artificial intelligence versus neuroscience
Kar, K., Kornblith, S., & Fedorenko, E. G. (2022) · Nature Machine Intelligence · doi:10.1038/s42256-022-00592-3 · Cited by 36 · see citing works
Deep Gamblers: Learning to Abstain with Portfolio TheoryPreprint
Ziyin, L., Wang, Z., Liang, P. P., Salakhutdinov, R., Morency, L., & Ueda, M. (2019) · arXiv (Cornell University) · doi:10.48550/arxiv.1907.00208 · Cited by 40 · see citing works
Diverse deep neural networks all predict human IT well, after training and fittingPreprint
Storrs, K. R., Kietzmann, T. C., Walther, A., Mehrer, J., & Kriegeskorte, N. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.07.082743 · Cited by 37 · see citing works
Context-dependent selectivity to natural images in the retina
Goldin, M. A., Lefebvre, B., Virgili, S., Cang, M. P. V., Ecker, A. S., Mora, T., Ferrari, U., & Marre, O. (2022) · Nature Communications · doi:10.1038/s41467-022-33242-8 · Cited by 34 · see citing works
Learning to control the brain through adaptive closed-loop patterned stimulation
Tafazoli, S., MacDowell, C. J., Che, Z., Letai, K. C., Steinhardt, C. R., & Buschman, T. J. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/abb860 · Cited by 34 · see citing works
(2021) · doi:10.1162/jocn_a_01755 · Cited by 85 · see citing works
Celeghin, A., Borriero, A., Orsenigo, D., Diano, M., Guerrero, C. A. M., Perotti, A., Petri, G., & Tamietto, M. (2023) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2023.1153572 · Cited by 33 · see citing works
Daube, C., Tian, X., Zhan, J., Webb, A., Ince, R. A. A., Garrod, O., & Schyns, P. G. (2021) · Patterns · doi:10.1016/j.patter.2021.100348 · Cited by 33 · see citing works
Emergence of Visual Center-Periphery Spatial Organization in Deep Convolutional Neural Networks
Mohsenzadeh, Y., Mullin, C., Lahner, B., & Oliva, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-61409-0 · Cited by 31 · see citing works
The neurons that mistook a hat for a face
Arcaro, M. J., Ponce, C. R., & Livingstone, M. S. (2020) · eLife · doi:10.7554/elife.53798 · Cited by 31 · see citing works
Self-citationReal-Time Functional MRI in the Treatment of Mental Health Disorders
Taschereau‐Dumouchel, V., Cushing, C. A., & Lau, H. C. (2022) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-072220-014550 · Cited by 33 · see citing works
Putting representations to use
Cao, R. (2022) · Synthese · doi:10.1007/s11229-022-03522-3 · Cited by 28 · see citing works
A neuronal social trait space for first impressions in the human amygdala and hippocampus
Cao, R., Lin, C., Hodge, J., Li, X., Todorov, A. T., Brandmeir, N. J., & Wang, S. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01583-x · Cited by 26 · see citing works
Improving scalability in systems neuroscience
Chen, Z. S., & Pesaran, B. (2021) · Neuron · doi:10.1016/j.neuron.2021.03.025 · Cited by 25 · see citing works
NeuroGen: Activation optimized image synthesis for discovery neuroscience
Gu, Z., Jamison, K. W., Khosla, M., Allen, E., Wu, Y., St-Yves, G., Naselaris, T., Kay, K., Sabuncu, M. R., & Kuceyeski, A. F. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118812 · Cited by 27 · see citing works
Generative adversarial networks unlock new methods for cognitive science
Goetschalckx, L., Andonian, A., & Wagemans, J. P. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2021.06.006 · Cited by 26 · see citing works
Fine-grained neural decoding with distributed word representations
Wang, S., Zhang, J., Wang, H., Lin, N., & Zong, C. (2019) · Information Sciences · doi:10.1016/j.ins.2019.08.043 · Cited by 27 · see citing works
Yao, D., Zhang, Y., Liu, T., Xu, P., Gong, D., Lu, J., Xia, Y., Luo, C., Guo, D., Dong, L., et al. (2020) · Cognitive Neurodynamics · doi:10.1007/s11571-020-09577-7 · Cited by 25 · see citing works
Efficient coding of natural scenes improves neural system identification
Qiu, Y., Klindt, D. A., Szatko, K. P., Gonschorek, D., Höfling, L., Schubert, T., Busse, L., Bethge, M., & Euler, T. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011037 · Cited by 29 · see citing works
Xiao, W., & Kreiman, G. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007973 · Cited by 22 · see citing works
Self-citationThe Quest for an Integrated Set of Neural Mechanisms Underlying Object Recognition in Primates
Kar, K., & DiCarlo, J. J. (2024) · Annual Review of Vision Science · doi:10.1146/annurev-vision-112823-030616 · Cited by 24 · see citing works
Rapid concerted switching of the neural code in the inferotemporal cortex
Shi, Y., Bi, D., Hesse, J. K., Lanfranchi, F. F., Chen, S., & Tsao, D. Y. (2026) · Nature · doi:10.1038/s41586-026-10267-3 · Cited by 23 · see citing works
Neurorobots as a Means Toward Neuroethology and Explainable AI
Chen, K., Hwu, T. J., Kashyap, H. J., Krichmar, J. L., Stewart, K. M., Xing, J., & Zou, X. (2020) · Frontiers in Neurorobotics · doi:10.3389/fnbot.2020.570308 · Cited by 22 · see citing works
DNNBrain: A Unifying Toolbox for Mapping Deep Neural Networks and Brains
Chen, X. S., Zhou, M. Q., Gong, Z., Xu, W., Liu, X., Huang, T., Zhen, Z., & Jia Liu, B. (2020) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2020.580632 · Cited by 23 · see citing works
Face identity coding in the deep neural network and primate brain
Wang, J., Cao, R., Brandmeir, N. J., Li, X., & Wang, S. (2022) · Communications Biology · doi:10.1038/s42003-022-03557-9 · Cited by 24 · see citing works
Embracing deepfakes and AI‐generated images in neuroscience research
Becker, C., & Laycock, R. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.16052 · Cited by 23 · see citing works
Crossing the Cleft: Communication Challenges Between Neuroscience and Artificial Intelligence
Chance, F. S., Aimone, J. B., Musuvathy, S., Smith, M. R., Vineyard, C. M., & Wang, F. (2020) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2020.00039 · Cited by 22 · see citing works
Data-Driven Approaches to Understanding Visual Neuron Activity
Butts, D. A. (2019) · Annual Review of Vision Science · doi:10.1146/annurev-vision-091718-014731 · Cited by 21 · see citing works
Feature-based encoding of face identity by single neurons in the human amygdala and hippocampusPreprint
Cao, R., Wang, J., Lin, C., Falco, E. D., Peter, A., Rey, H. G., DiCarlo, J. J., Todorov, A. T., Rutishauser, U., Li, X., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.01.278283 · Cited by 21 · see citing works
Foundation model of neural activity predicts response to new stimulus types and anatomyPreprint
Wang, E. Y., Fahey, P. G., Ding, Z., Papadopoulos, S., Ponder, K., Weis, M. A., Chang, A., Muhammad, T., Patel, S. S., Ding, Z., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.21.533548 · Cited by 21 · see citing works
Maier, M., Blume, F., Bideau, P., Hellwich, O., & Rahman, R. A. (2022) · Consciousness and Cognition · doi:10.1016/j.concog.2022.103301 · Cited by 19 · see citing works
Tuning landscapes of the ventral stream
Wang, B., & Ponce, C. R. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111595 · Cited by 18 · see citing works
Self-citationHuman peripheral blur is optimal for object recognition
Pramod, R. T., Katti, H., & Arun, S. P. (2022) · Vision Research · doi:10.1016/j.visres.2022.108083 · Cited by 19 · see citing works
Bipartite invariance in mouse primary visual cortexPreprint
Ding, Z., Tran, D. T., Ponder, K., Cobos, E., Ding, Z., Fahey, P. G., Wang, E. Y., Muhammad, T., Fu, J., Cadena, S. A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.15.532836 · Cited by 19 · see citing works
Driving and suppressing the human language network using large language modelsPreprint
Tuckute, G., Sathe, A., Srikant, S., Taliaferro, M., Wang, M., Schrimpf, M., Kay, K., & Fedorenko, E. G. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.16.537080 · Cited by 20 · see citing works
Perceptography unveils the causal contribution of inferior temporal cortex to visual perception
Shahbazi, A., Ma, T., Pernuš, M., Scheirer, W. J., & Afraz, A. (2024) · Nature Communications · doi:10.1038/s41467-024-47356-8 · Cited by 18 · see citing works
Beyond linear regression: mapping models in cognitive neuroscience should align with research goals
Ivanova, A. A., Schrimpf, M., Anzellotti, S., Zaslavsky, N., Fedorenko, E. G., & Işık, L. (2022) · Neurons Behavior Data analysis and Theory · doi:10.51628/001c.37507 · Cited by 19 · see citing works
Compact deep neural network models of the visual cortex
Cowley, B. R., Stan, P. L., Pillow, J. W., & Smith, M. A. (2026) · Nature · doi:10.1038/s41586-026-10150-1 · Cited by 21 · see citing works
Sedigh-Sarvestani, M., & Fitzpatrick, D. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.834876 · Cited by 16 · see citing works
A neuronal code for object representation and memory in the human amygdala and hippocampus
Cao, R., Brunner, P., Chakravarthula, P. N., Wahlstrom, K. L., Inman, C. S., Smith, E. H., Li, X., Mamelak, A. N., Brandmeir, N. J., Rutishauser, U., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-56793-y · Cited by 16 · see citing works
Parde, C. J., Colón, Y., Hill, M. Q., Castillo, C. D., Dhar, P., & O’Toole, A. J. (2021) · Journal of Vision · doi:10.1167/jov.21.8.15 · Cited by 16 · see citing works
Face neurons encode nonsemantic features
Bardon, A. G., Xiao, W., Ponce, C. R., Livingstone, M. S., & Kreiman, G. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2118705119 · Cited by 15 · see citing works
Self-citationPersonalized visual encoding model construction with small data
Gu, Z., Jamison, K. W., Sabuncu, M. R., & Kuceyeski, A. F. (2022) · Communications Biology · doi:10.1038/s42003-022-04347-z · Cited by 15 · see citing works
A shared code for perceiving and imagining objects in human ventral temporal cortex
Wadia, V., Reed, C. M., Chung, J. M., Bateman, L. M., Mamelak, A. N., Rutishauser, U., & Tsao, D. Y. (2026) · Science · doi:10.1126/science.adt8343 · Cited by 19 · see citing works
Visual prototypes in the ventral stream are attuned to complexity and gaze behavior
Rose, O., Johnson, J. K., Wang, B., & Ponce, C. R. (2021) · Nature Communications · doi:10.1038/s41467-021-27027-8 · Cited by 13 · see citing works
Self-citationCurrent Advances in Neural Decoding
van Gerven, M. A. J., Seeliger, K., Güçlü, U., & Güçlütürk, Y. (2019) · Lecture notes in computer science · doi:10.1007/978-3-030-28954-6_21 · Cited by 13 · see citing works
Li, Y., Yang, H., & Gu, S. (2024) · 中国科学通报:英文版 · doi:10.1016/j.scib.2024.02.035 · Cited by 13 · see citing works
Generation of Viewed Image Captions From Human Brain Activity Via Unsupervised Text Latent Space
Takada, S., Togo, R., Ogawa, T., & Haseyama, M. (2020) · Proceedings - International Conference on Image Processing · doi:10.1109/icip40778.2020.9191262 · Cited by 13 · see citing works
- Authors
- Ponce, C. R., Xiao, W., Schade, P. F., Hartmann, T. S., Kreiman, G., & Livingstone, M. S.
- Affiliations
- Harvard University (US)
- Boston Children's Hospital (US)
- Corresponding author
- Ponce, Carlos R.
- Livingstone, Margaret S.
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2019-05
- Volume
- 177
- Issue
- 4
- Pages
- 999-1009.e10
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC6718199
- OpenAlex
- W2943083682
- Cited by
- 245
- References
- 52
- Citations by year
- 2026: 40 · 2025: 21 · 2024: 35 · 2023: 27 · 2022: 28 · 2021: 35 · 2020: 37 · 2019: 22
- FWCI
- 17.73
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Science Foundation
- National Institutes of Health
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Keywords
- inferotemporal cortex, visual neurons, neuronal selectivity, coding principles, genetic algorithm, feature dictionary, object recognition, monkey visual cortex, internal representations
- MeSH terms
- Algorithms, Animals, Cerebral Cortex, Macaca mulatta, Male, Nerve Net, Neurons, Temporal Lobe, Visual Perception
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