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Adversarially trained neural representations may already be as robust as corresponding biological neural representations. arXiv. 2022. doi:https://doi.org/10.48550/arXiv.2206.11228.
(1.99 MB)
(1.99 MB) Aligning Model and Macaque Inferior Temporal Cortex Representations Improves Model-to-Human Behavioral Alignment and Adversarial Robustness. bioRxiv. 2022. doi:https://doi.org/10.1101/2022.07.01.498495.
. Animals, Brain, Electrophysiology, Fluorescent Dyes, Macaca mulatta, Microelectrodes, Neurosciences. Biomedical Engineering Society. 1995.
. Anterior Inferotemporal Neurons of Monkeys Engaged in Object Recognition Can be Highly Sensitive to Object Retinal Position. Journal of Neurophysiology. 2003;89(6):3264 - 3278. doi:10.1152/jn.00358.2002. (424.39 KB)
(424.39 KB). Balanced increases in selectivity and invariance produce constant sparseness across the ventral visual pathway. Journal of Vision. 2009;9(8):738 - 738. doi:10.1167/9.8.738.
. Balanced Increases in Selectivity and Tolerance Produce Constant Sparseness along the Ventral Visual Stream. Journal of Neuroscience. 2012;32(30):10170 - 10182. doi:10.1523/JNEUROSCI.6125-11.2012.
. Is the “binding problem” a problem in inferiotemporal cortex?. Society for Neuroscience. 2005.
Brain-Like Object Recognition with High-Performing Shallow Recurrent ANNs. In: Neural Information Processing Systems. Neural Information Processing Systems.; 2019. doi:https://papers.nips.cc/paper/9441-brain-like-object-recognition-with-high-performing-shallow-recurrent-anns.
Brain-Score: Which Artificial Neural Network for Object Recognition is most Brain-Like?. bioRxiv. 2018. doi:https://doi.org/10.1101/407007.
. 'Breaking' position-invariant object recognition. Nature Neuroscience. 2005;8(9):1145 - 1147. doi:10.1038/nn1519. (175.59 KB) (49.96 KB) (87.63 KB)
(175.59 KB) (49.96 KB) (87.63 KB) Catalyzing next-generation Artificial Intelligence through NeuroAI. Nature Communications. 2023;14(1):1597. doi:10.1038/s41467-023-37180-x. (749.44 KB)
(749.44 KB). Chemogenetic suppression of macaque V4 neurons produces retinotopically specific deficits in downstream IT neural activity patterns and core object recognition behavior. Journal of Vision. 2021;21(9):2489-2489. doi:https://doi.org/10.1167/jov.21.9.2489.
. Chronically implantable LED arrays for behavioral optogenetics in primates. bioRxiv. 2020. doi:10.1101/2020.09.10.291583. (2.64 MB)
(2.64 MB). Chronically implantable LED arrays for behavioral optogenetics in primates. Nature Methods. 2021;18(9):1112 - 1116. doi:10.1038/s41592-021-01238-9. (6.95 MB)
(6.95 MB). Combining Different V1 Brain Model Variants to Improve Robustness to Image Corruptions in CNNs. Shared Visual Representations in Human & Machine Intelligence - NeurIPS Workshop. 2021. Available at: https://arxiv.org/abs/2110.10645. (1000.31 KB)
(1000.31 KB). Comparing novel object learning in humans, models, and monkeys. Journal of Vision. 2019;19(10):114b. doi:10.1167/19.10.114b.
. Comparing-State-of-the-Art Visual Features on Invariant Object Recognition Tasks. IEEE Workshop on Applications of Computer Vision (WACV). 2011:463-470. doi:10.1109/WACV.2011.5711540.
. Comparison of Object Recognition Behavior in Human and Monkey. Journal of Neuroscience. 2015;35(35):12127 - 12136. doi:10.1523/JNEUROSCI.0573-15.2015.
. Computational models of category-selective brain regions enable high-throughput tests of selectivity. Nature Communications. 2021;12(1). doi:10.1038/s41467-021-25409-6. (6.47 MB)
(6.47 MB). Concurrent increases in selectivity and tolerance produce constant sparseness across the ventral visual stream. Computation and Systems Neuroscience (COSYNE). 2008. Available at: http://www.cosyne.org/c/images/8/8e/Cosyne_pf_new.pdf.
. CORnet: Modeling the Neural Mechanisms of Core Object Recognition. bioRxiv. 2018. doi:https://doi.org/10.1101/408385.
. Correlation-based spatial layout of deep neural network features generates ventral stream topography. Computation and Systems Neuroscience (COSYNE). 2020. Available at: http://cosyne.org/cosyne20/Cosyne2020_program_book.pdf.
. Deep learning reaches the motor system. Nature Methods. 2018;15(10):772 - 773. doi:10.1038/s41592-018-0152-6.
Deep Neural Networks Rival the Representation of Primate IT Cortex for Core Visual Object Recognition. . PLoS Computational Biology. 2014;10(12):e1003963. doi:10.1371/journal.pcbi.1003963.
. Discrimination Training Alters Object Representations in Human Extrastriate Cortex. Journal of Neuroscience. 2006;26(50):13025 - 13036. doi:10.1523/JNEUROSCI.2481-06.2006. (455.73 KB)
(455.73 KB). Do we have a strategy for understanding how the visual system accomplishes object recognition?. In: Object Categorization: Computer and Human Vision Perspectives. Object Categorization: Computer and Human Vision Perspectives. New York, NY, USA: Cambridge University Press; 2010.
. Does Learned Shape Selectivity in Inferior Temporal Cortex Automatically Generalize Across Retinal Position?. Journal of Neuroscience. 2008;28(40):10045 - 10055. doi:10.1523/JNEUROSCI.2142-08.2008. (8.59 MB)
(8.59 MB). Does the visual system use natural experience to construct size invariant object representations?. Computation and Systems Neuroscience (COSYNE). 2010. doi:10.3389/conf.fnins.2010.03.00326.
. The effect of visual experience on the position tolerance of primate object representations. Society for Neuroscience. 2004.
. Eight open questions in the computational modeling of higher sensory cortex. Current Opinion in Neurobiology. 2016;37:114 - 120. doi:10.1016/j.conb.2016.02.001.
. An empirical assay of view-invariant object learning in humans and comparison with baseline image-computable models. bioRxiv. 2023:2022.12.31.522402. doi:https://www.biorxiv.org/content/10.1101/2022.12.31.522402v1.
. Establishing Good Benchmarks and Baselines for Face Recognition. In: European Conference on Computer Vision-Faces in 'Real-Life' Images Workshop. European Conference on Computer Vision-Faces in 'Real-Life' Images Workshop. Marseille, France: EECV; 2008. (1.74 MB)
(1.74 MB). Evidence that recurrent circuits are critical to the ventral stream’s execution of core object recognition behavior. Nature Neuroscience. 2019;22(6):974 - 983. doi:10.1038/s41593-019-0392-5.
. Evidence that recurrent circuits are critical to the ventral stream's execution of core object recognition behavior. bioRxiv. 2018. doi:https://doi.org/10.1101/354753.
. Explicit information for category-orthogonal object properties increases along the ventral stream. Nature Neuroscience. 2016;19(4):613 - 622. doi:10.1038/nn.4247.
. Fast Readout of Object Identity from Macaque Inferior Temporal Cortex. Science. 2005;310:863 - 866. doi:10.1126/science.1117593. (209.48 KB) (1.26 MB)
(209.48 KB) (1.26 MB). Fast recurrent processing via ventral prefrontal cortex is needed by the primate ventral stream for robust core visual object recognition. BioRxiv. 2020. doi:https://doi.org/10.1101/2020.05.10.086959.
. Fast Recurrent Processing Via Ventral Prefrontal Cortex is Needed by the Primate Ventral Stream for Robust Core Visual Object Recognition. Neuron. 2021;109(1):164-167.e5. doi:https://doi.org/10.1016/j.neuron.2020.09.035. (3.92 MB)
(3.92 MB) Fine-Scale Spatial Organization of Face and Object Selectivity in the Temporal Lobe: Do Functional Magnetic Resonance Imaging, Optical Imaging, and Electrophysiology Agree?. Journal of Neuroscience. 2008;28(46):11796 - 11801. doi:10.1523/JNEUROSCI.3799-08.2008.
. Flexible and robust object recognition in inferior temporal cortex supported by neurons with limited position and clutter tolerance. Society for Neuroscience. 2006.
. Form processing and attention effects in somatosensory cortex. In: Somesthesis and the Neurobiology of the Somatosensory Cortex. Somesthesis and the Neurobiology of the Somatosensory Cortex. Switzerland: Birkhauser Basel; 1996.
. Form processing in area 3b. International Symposium on Brain Mechanisms of Tactile Perception. 1999.
. Form representation in monkey inferotemporal cortex is virtually unaltered by free viewing. Nature Neuroscience. 2000;3(8):814 - 821. doi:10.1038/77722. (225.75 KB)
(225.75 KB) fROI-level computational models enable broad-scale experimental testing and expose key divergences between models and brains. Journal of Vision. 2023;23(9):5788 - 5788. Available at: https://doi.org/10.1167/jov.23.9.5788.
. From luminance to semantics: how natural objects are represented in monkey inferotemporal cortex. Computational and Systems Neuroscience (COSYNE). 2011. Available at: http://www.cosyne.org/c/index.php?title=Cosyne_11_posters/I-89.
Funcitional Properties of Circuits, Cellular Populations, and Areas. In: The Neocortex.Vol 27. The Neocortex. Cambridge, MA: The MIT Press; 2019:223-265. doi:10.7551/mitpress/12593.001.0001. (1.06 MB)
(1.06 MB). Hierarchical Modular Optimization of Convolutional Networks Achieves Representations Similar to Macaque IT and Human Ventral Stream. In: Advances in Neural Information Processing Systems. Advances in Neural Information Processing Systems. Lake Tahoe, Nevada, United States.; 2013. doi:https://papers.nips.cc/paper/4991-hierarchical-modular-optimization-of-convolutional-networks-achieves-representations-similar-to-macaque-it-and-human-ventral-stream.
. High-Resolution Three-Dimensional Microelectrode Brain Mapping Using Stereo Microfocal X-ray Imaging. Journal of Neurophysiology. 2008;100(5):2966 - 2976. doi:10.1152/jn.90672.2008. (1.25 MB)
(1.25 MB). A High-Throughput Screening Approach to Biologically-Inspired Object Recognition. Learning Workshop-Computation and Systems Neuroscience (COSYNE). 2010.
. A High-Throughput Screening Approach to Discovering Good Forms of Biologically Inspired Visual Representation. . PLoS Computational Biology. 2009;5(11):e1000579. doi:10.1371/journal.pcbi.1000579. (538.96 KB) (141.46 KB)
(538.96 KB) (141.46 KB). A high-throughput screening approach to discovering good forms of visual representation. Computation and Systems Neuroscience (COSYNE). 2008.
. A hippocampal theory of schizophrenia. Behavioral and Brain Sciences. 1991;14:47-49. doi:10.1017/S0140525X00065353.
. How Does the Brain Solve Visual Object Recognition?. Neuron. 2012;73(3):415 - 434. doi:10.1016/j.neuron.2012.01.010.
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)
(7.22 MB). How far can you get with a modern face recognition test set using only simple features?. In: IEEE Computer Society Conference on Computer Vision and Pattern Recognition Workshops (CVPR Workshops). IEEE Computer Society Conference on Computer Vision and Pattern Recognition Workshops (CVPR Workshops). Miami, FL: IEEE; 2009. doi:10.1109/CVPR.2009.5206605. (375.73 KB)
(375.73 KB). How well do rudimentary plasticity rules predict adult visual object learning?. . PLOS Computational Biology. 2023;19(12):e1011713. doi:10.1371/journal.pcbi.1011713. (11.69 MB)
(11.69 MB). How well do rudimentary plasticity rules predict adult visual object learning?. . PLOS Computational Biology. 2023;19(12):e1011713. doi:10.1371/journal.pcbi.1011713. (11.69 MB)
(11.69 MB). Human versus machine: comparing visual object recognition systems on a level playing field. Computation and Systems Neuroscience (COSYNE). 2010. doi:10.3389/conf.fnins.2010.03.00283.
. Increases in selectivity are offset by increases in tolerance ("invariance") to maintain sparseness across the ventral visual pathway. Society for Neuroscience. 2008:514.8. Available at: https://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=fc0d0a2d-b563-4b41-8311-0805f08bde8a&cKey=8a2c998e-bc76-4d92-96ac-ad5199da59bf&mKey=%7bAFEA068D-D012-4520-8E42-10E4D1AF7944%7d.
. The inferior temporal cortex is a potential cortical precursor of orthographic processing in untrained monkeys. Nature Communications. 2020;11(1). doi:10.1038/s41467-020-17714-3.
. Inferior temporal cortex robustly signals encounters with new objects, but is not an online representation of the visual world. Society for Neuroscience. 2008:316.6. Available at: https://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=ee83e7f7-5aea-4ec8-a948-436658d20e37&cKey=fc64f0af-c81e-4b0e-b809-796349279531&mKey=%7bAFEA068D-D012-4520-8E42-10E4D1AF7944%7d.
. Inferotemporal representations underlying object recognition in the free viewing monkey. Society for Neuroscience. 2000.
. Integrative Benchmarking to Advance Neurally Mechanistic Models of Human Intelligence. Neuron. 2020. doi:10.1016/j.neuron.2020.07.040. (1.04 MB)
(1.04 MB). Laminar differences in spatiotemporal receptive field structure of neurons in area 3b of the awake macaque. Society for Neuroscience. 1996.
. Large-Scale, High-Resolution Comparison of the Core Visual Object Recognition Behavior of Humans, Monkeys, and State-of-the-Art Deep Artificial Neural Networks. The Journal of Neuroscience. 2018;38(33):7255 - 7269. doi:10.1523/JNEUROSCI.0388-18.2018.
. Large-scale, high-resolution comparison of the core visual object recognition behavior of humans, monkeys, and state-of-the-art deep artificial neural networks. bioRxiv. 2018. doi:https://doi.org/10.1101/240614.
. Large-Scale, High-Resolution Neurophysiological Maps Underlying fMRI of Macaque Temporal Lobe. Journal of Neuroscience. 2013;33(38):15207 - 15219. doi:10.1523/JNEUROSCI.1248-13.2013.
. A large-scale shape map in monkey inferior temporal cortex. Society for Neuroscience. 2006.
. Learning and neural plasticity in visual object recognition. Current Opinion in Neurobiology. 2006;16(2):152 - 158. doi:10.1016/j.conb.2006.03.012. (181.23 KB)
(181.23 KB). Learning only a handful of latent variables produces neural-aligned CNN models of the ventral stream. In: Computational and Systems Neuroscience (COSYNE) . Computational and Systems Neuroscience (COSYNE) . Lisbon, Portugal; 2024. Available at: https://hdl.handle.net/1721.1/153744. (2.57 MB)
(2.57 MB) 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)
(2.56 MB). Linear and non-linear processing of tactile spatial form in area 3b of the awake macaque. Society for Neuroscience. 1996.
. Mapping functional neuronal processing chains underlying sensory-motor tasks in the primate. Gordon Conference: Sensory coding and the natural environment. 2004.
. 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)
(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)
(643.95 KB). Multiple object response normalization in monkey inferotemporal cortex. Society for Neuroscience. 2005.
. 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)
(3.12 MB). Natural experience drives online learning of tolerant object representations in visual cortex. Computation and Systems Neuroscience (COSYNE). 2008. Available at: http://www.cosyne.org/c/images/8/8e/Cosyne_pf_new.pdf.
. 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 dynamics of hippocampal modulation of classical conditioning. In: Neural Network Models of Conditioning and Action. Neural Network Models of Conditioning and Action. Hillsdale, NJ: Lawrence Erlbaum Association; 1991.
. Neural dynamics of hippocampal modulation of classical conditioning. 12th Symposium on Models of Behavior: Neural Network Models of Conditioning and Action. 1989.
. 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)
(3.46 MB). Neural population control via deep image synthesis. Science. 2019;364(6439):eaav9436. doi:10.1126/science.aav9436.
Neural Population Geometry Reveals the Role of Stochasticity in Robust Perception. In: Neural Information Processing Systems (NeurIPS). Neural Information Processing Systems (NeurIPS). Lisbon, Portugal; 2021. Available at: https://proceedings.neurips.cc/paper/2021/file/8383f931b0cefcc631f070480ef340e1-Paper.pdf. (4.04 MB)
(4.04 MB). 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 recognition by selective spike and LFP data in macaque inferior temporal cortex. Society for Neuroscience. 2004.
. 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)
(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.
. Primate Inferotemporal Cortex Neurons Generalize Better to Novel Image Distributions Than Analogous Deep Neural Networks Units. In: SVHRM Workshop at Neural Information Processing Systems (NeurIPS). SVHRM Workshop at Neural Information Processing Systems (NeurIPS). Lisbon, Portugal; 2022. Available at: https://openreview.net/pdf?id=iPF7mhoWkOl. (3.86 MB)
(3.86 MB) Probing Biological and Artificial Neural Networks with Task-dependent Neural Manifolds. In: Conference on Parsimony and Learning (Proceedings Track). Conference on Parsimony and Learning (Proceedings Track). Hong Kong, China; 2023. Available at: https://openreview.net/forum?id=MxBS6aw5Gd. (2.75 MB)
(2.75 MB). 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)
(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)
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