Publications
Export 155 results:
Let's move forward: Image-computable models and a common model evaluation scheme are prerequisites for a scientific understanding of human visionAbstract. Behavioral and Brain Sciences. 2023;4634. doi:10.1017/S0140525X23001607. (2.56 MB)
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Marking microelectrode penetrations with fluorescent dyes. Journal of Neuroscience Methods. 1996;64(1):75 - 81. doi:10.1016/0165-0270(95)00113-1. (8.62 MB)
. Minimally invasive multimode optical fiber microendoscope for deep brain fluorescence imaging. Biomedical Optics Express. 2018;9(4):1492-1509. doi:10.1364/BOE.9.001492.
. Multiple Object Response Normalization in Monkey Inferotemporal Cortex. Journal of Neuroscience. 2005;25(36):8150 - 8164. doi:10.1523/JNEUROSCI.2058-05.2005. (643.95 KB)
. Multi-scale hierarchical neural network models that bridge from single neurons in the primate primary visual cortex to object recognition behavior. bioRxiv. 2021. doi:10.1101/2021.03.01.433495. (3.12 MB)
. Neural dynamics at successive stages of the ventral visual stream are consistent with hierarchical error signals. eLife. 2018;7. doi:10.7554/eLife.42870.
. Neural Mechanisms Underlying Visual Object Recognition. Cold Spring Harbor Symposia on Quantitative Biology. 2014;79:99 - 107. doi:10.1101/sqb.2014.79.024729.
. A neural network approach to hippocampal function in classical conditioning. Behavioral Neuroscience. 1991;105(1):82 - 110. doi:10.1037/0735-7044.105.1.82. (3.46 MB)
. Neural population control via deep image synthesis. Science. 2019;364(6439):eaav9436. doi:10.1126/science.aav9436.
. The Neural Representation Benchmark and its Evaluation on Brain and Machine. arXiv. 2013. doi:https://arxiv.org/abs/1301.3530.
. Neuronal Learning of Invariant Object Representation in the Ventral Visual Stream Is Not Dependent on Reward. Journal of Neuroscience. 2012;32(19):6611 - 6620. doi:10.1523/JNEUROSCI.3786-11.2012.
. Neurophysiological Organization of the Middle Face Patch in Macaque Inferior Temporal Cortex. The Journal of Neuroscience. 2016;36(50):12729 - 12745. doi:10.1523/JNEUROSCI.0237-16.2016.
. Object Selectivity of Local Field Potentials and Spikes in the Macaque Inferior Temporal Cortex. Neuron. 2006;49(3):433 - 445. doi:10.1016/j.neuron.2005.12.019. (778.45 KB)
. An Open Resource for Non-human Primate Optogenetics. Neuron. 2020. doi:10.1016/j.neuron.2020.09.027.
Optogenetic and pharmacological suppression of spatial clusters of face neurons reveal their causal role in face gender discrimination. Proceedings of the National Academy of Sciences. 2015:6730 - 6735. doi:10.1073/pnas.1423328112.
. Performance-optimized hierarchical models predict neural responses in higher visual cortex. Proceedings of the National Academy of Sciences. 2014:8619 - 8624. doi:10.1073/pnas.1403112111.
. Precedence of the Eye Region in Neural Processing of Faces. Journal of Neuroscience. 2012;32(47):16666 - 16682. doi:10.1523/JNEUROSCI.2391-12.2012.
. The Quest for an Integrated Set of Neural Mechanisms Underlying Object Recognition in Primates. arXiv. 2023. doi: https://doi.org/10.48550/arXiv.2312.05956. (5.76 MB)
. Receptive field structure in cortical area 3b of the alert monkey. Behavioural Brain Research. 2002;135(1-2):167 - 178. doi:10.1016/S0166-4328(02)00162-6. (382.63 KB)
. Reversible Inactivation of Different Millimeter-Scale Regions of Primate IT Results in Different Patterns of Core Object Recognition Deficits. Neuron. 2019;102(2):493 - 505.e5. doi:10.1016/j.neuron.2019.02.001.
. Reversible inactivation of different millimeter-scale regions of primate IT results in different patterns of core object recognition deficits. bioRxiv. 2018. doi:https://doi.org/10.1101/390245.
. Robustified ANNs Reveal Wormholes Between Human Category Percepts. arXiv. 2023. doi: https://doi.org/10.48550/arXiv.2308.06887 Focus to learn more. (3.53 MB)
. A rodent model for the study of invariant visual object recognition. Proceedings of the National Academy of Sciences. 2009;106(21):8748 - 8753. doi:10.1073/pnas.0811583106. (730.6 KB)
. Selectivity and Tolerance ("Invariance") Both Increase as Visual Information Propagates from Cortical Area V4 to IT. Journal of Neuroscience. 2010;30(39):12978 - 12995. doi:10.1523/JNEUROSCI.0179-10.2010.
. Shape Similarity, Better than Semantic Membership, Accounts for the Structure of Visual Object Representations in a Population of Monkey Inferotemporal Neurons. PLoS Computational Biology. 2013;9(8):e1003167. doi:10.1371/journal.pcbi.1003167.
. Simple Learned Weighted Sums of Inferior Temporal Neuronal Firing Rates Accurately Predict Human Core Object Recognition Performance. Journal of Neuroscience. 2015;35(39):13402 - 13418. doi:10.1523/JNEUROSCI.5181-14.2015.
. Simulating a Primary Visual Cortex at the Front of CNNs Improves Robustness to Image Perturbations. Neural Information Processing Systems (NeurIPS; spotlight). 2020. doi:10.1101/2020.06.16.154542. (2.48 MB)
. Spatial and Temporal Structure of Receptive Fields in Primate Somatosensory Area 3b: Effects of Stimulus Scanning Direction and Orientation. The Journal of Neuroscience. 2000;20(1):495 - 510. doi:10.1523/JNEUROSCI.20-01-00495.2000. (692.91 KB)
. A Stable Topography of Selectivity for Unfamiliar Shape Classes in Monkey Inferior Temporal Cortex. Cerebral Cortex. 2007;18(7):1676 - 1694. doi:10.1093/cercor/bhm196. (1.58 MB)
. Stimulus configuration, classical conditioning, and hippocampal function. Psychological Review. 1992;99(2):268 - 305. doi:10.1037/0033-295X.99.2.268. (4.3 MB)
. Structure of Receptive Fields in Area 3b of Primary Somatosensory Cortex in the Alert Monkey. The Journal of Neuroscience. 1998;18(7):2626 - 2645. doi:10.1523/JNEUROSCI.18-07-02626.1998. (1.33 MB)
. Task-Driven Convolutional Recurrent Models of the Visual System. arXiv. 2018. doi:https://arxiv.org/abs/1807.00053.
Teacher Guided Architecture Search. arXiv. 2018. doi:https://arxiv.org/abs/1808.01405.
. ThreeDWorld: A Platform for Interactive Multi-Modal Physical Simulation. arXiv. 2020. Available at: https://arxiv.org/abs/2007.04954. (7.06 MB)
The ThreeDWorld Transport Challenge: A Visually Guided Task-and-Motion Planning Benchmark for Physically Realistic Embodied AI. arXiv. 2021. doi:arXiv:2103.14025. (6.79 MB)
To find better neural network models of human vision, find better neural network models of primate vision. BioRxiv. 2019. doi:https://doi.org/10.1101/688390.
. Topographic deep artificial neural networks reproduce the hallmarks of the primate inferior temporal cortex face processing network. bioRxiv. 2020. doi:https://doi.org/10.1101/2020.07.09.185116.
Trade-Off between Object Selectivity and Tolerance in Monkey Inferotemporal Cortex. Journal of Neuroscience. 2007;27(45):12292 - 12307. doi:10.1523/JNEUROSCI.1897-07.2007. (758.94 KB)
. A Unifying Principle for the Functional Organization of Visual Cortex. bioRxiv. 2023. doi: https://doi.org/10.1101/2023.05.18.541361. (6.57 MB)
. Unsupervised changes in core object recognition behavior are predicted by neural plasticity in inferior temporal cortex. eLife. 2021;10. doi:10.7554/eLife.60830.
. Unsupervised changes in core object recognition behavioral performance are accurately predicted by unsupervised neural plasticity in inferior temporal cortex. BioRxiv. 2020. doi:https://doi.org/10.1101/2020.01.13.900837.
. Unsupervised Natural Experience Rapidly Alters Invariant Object Representation in Visual Cortex. Science. 2008;321:1502 - 1507. doi:10.1126/science.1160028.
. Unsupervised Natural Visual Experience Rapidly Reshapes Size-Invariant Object Representation in Inferior Temporal Cortex. Neuron. 2010;67(6):1062 - 1075. doi:10.1016/j.neuron.2010.08.029.
. Unsupervised neural network models of the ventral visual stream. Proceedings of the National Academy of Sciences. 2021;118(3):e2014196118. doi:10.1073/pnas.2014196118. (2.71 MB)
Unsupervised Neural Network Models of the Ventral Visual Stream. bioRxiv. 2020. doi:10.1101/2020.06.16.155556. (2.7 MB)
Untangling invariant object recognition. Trends in Cognitive Sciences. 2007;11(8):333 - 341. doi:10.1016/j.tics.2007.06.010. (1.48 MB)
. Using goal-driven deep learning models to understand sensory cortex. Nature Neuroscience. 2016;19(3):356 - 365. doi:10.1038/nn.4244.
. Using Neuronal Latency to Determine Sensory–Motor Processing Pathways in Reaction Time Tasks. Journal of Neurophysiology. 2004;93(5):2974 - 2986. doi:10.1152/jn.00508.2004. (949.25 KB) (2.3 MB)
. Velocity Invariance of Receptive Field Structure in Somatosensory Cortical Area 3b of the Alert Monkey. The Journal of Neuroscience. 1999;19(1):401 - 419. doi:10.1523/JNEUROSCI.19-01-00401.1999. (847.96 KB)
. What Response Properties Do Individual Neurons Need to Underlie Position and Clutter “Invariant” Object Recognition?. Journal of Neurophysiology. 2009;102(1):360 - 376. doi:10.1152/jn.90745.2008. (773.41 KB)
. Why is Real-World Visual Object Recognition Hard?. . PLoS Computational Biology. 2008;4:e27. doi:10.1371/journal.pcbi.0040027. (1.93 MB)
. How does the primate brain combine generative and discriminative computations in vision?. 2024. doi: https://doi.org/10.48550/arXiv.2401.06005. (7.22 MB)
Selectivity of local field potentials in macaque inferior temporal cortex. Cambridge, M: MIT; 2004. Available at: https://dspace.mit.edu/handle/1721.1/30417.
. Ultra-fast object recognition from few spikes. Cambridge, MA: MIT; 2005:1-31. Available at: https://dspace.mit.edu/handle/1721.1/30556.
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