REVIEW 3 major objections 6 minor 1 cited by
Shifting Attention to You: Personalized Brain-Inspired AI Models
T0 review · 3 major / 6 minor · reviewed 2026-08-08 · deepseek-v4-flash
Pith's one-line read Fine-tuning a CLIP model on human behavioral embeddings and millisecond-scale MEG recordings more than doubles its agreement with human similarity judgments (0.78 vs 0.32) and lets per-participant models capture individual neural dynamics.
desk verdict The behavioral fine-tuning result is credible and worth referee time; the personalization claim needs a group-level or permutation baseline before it can be accepted. read the letter →
The pith
A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.
The reading
What carries the argument
The load-bearing mechanism for the behavioral results is the binding of visual features to 66 SPoSE text dimensions via a dot-product projection, trained with mean squared error loss against behavioral SPoSE embeddings using DoRA parameter-efficient fine-tuning on the last text and vision attention layers. For the neural results, the central object is a learned feature-reweighting matrix W in $R^{{T x L}}$ (T MEG timepoints, L = 24 ViT layers), initialized to the last layer and then optimized in two stages; it recombines all ViT layer activations into a time-varying embedding. Temporal scalers alpha_T and beta_T modulate feature magnitude and semantic binding, dimension-wise Gaussian noise mimics neural variability, and a three-term loss combining Pearson correlation, MSE, and time-generalization aligns model RDMs to MEG decoding RDMs. This machinery converts a static CLIP representation into a dynamic one whose similarity geometry can be compared slice-by-slice to the brain's temporal response profile.
What would settle it
Train the group-level or individual CLIP-HBA-MEG pipeline on MEG decoding RDMs whose stimulus labels have been randomly permuted, or on RDMs generated from shuffled classifier outputs, then measure the model's temporal alignment with genuine held-out MEG data. If the permuted-target model still shows the reported peak alignment around 300–400 ms or Spearman correlations near the real model's, the objective was fitting classifier artifacts rather than neural structure; if alignment collapses to chance, the dynamic fine-tuning is genuinely reading representational content.
Extended reading notes
Core claim
On the paper's own terms, the central discovery is that the representational geometry of a pretrained CLIP model is highly malleable: aligning it to human cognitive measurements, rather than only to image-text statistics, is enough to reorganize its embedding space so it tracks both average human similarity judgments and the temporal evolution of individual neural responses. Concretely, the paper reports that CLIP-HBA-Behavior achieves a Spearman correlation of 0.78 (95% CI [0.75, 0.80]) against fully sampled behavioral RDMs, versus 0.32 for baseline CLIP-ViT-L/14, and that CLIP-HBA-MEG, trained on MEG decoding RDMs, outperforms the static baseline in neural alignment across THINGS and three external datasets while peaking at 300–400 ms after stimulus onset. For personalization, 15 models fine-tuned on single participants' MEG data yield a global Spearman correlation of 0.659 (p < 1e-14) between model-embedding distances and participant-neural distances on 18 held-out stimuli. The paper interprets this as evidence that training methodology, not architecture alone, determines how human-like a network's representations become, and that individual cognitive styles can be encoded in model weights.
Load-bearing premise
The neural-alignment claims stand or fall on treating the MEG decoding RDMs, computed by linear-discriminant and support-vector classifiers and averaged over just three participants for group-level training, as faithful, genuinely time-resolved measurements of object representations in the brain; if those RDMs mostly reflect classifier bias or averaging artifacts, the dynamic fine-tuning objective would be fitting noise, and the claim that the model tracks the temporal evolution of individual neural responses would not follow.
Editorial extensions
If this is right
- CLIP-HBA-Behavior's Spearman correlation of 0.78 on held-out similarity judgments (vs 0.32 baseline) means fine-tuning on 66 interpretable behavioral dimensions can make a general vision model approximate human pairwise similarity judgments far better than its original embedding space.
- The NIGHTS benchmark gains (validation/test 0.88 vs 0.81 for 768-d features; 0.85/0.84 vs 0.80/0.79 for SPoSE dimensions) show that the behavioral alignment transfers to a large, independently collected triplet-similarity benchmark.
- CLIP-HBA-MEG's neural alignment, peaking around 300–400 ms and generalizing to external participants and degraded images, implies the model has learned a time-resolved representation that tracks the late semantic phase of visual processing rather than only early image features.
- Personalized models trained on individual MEG data reach a Spearman correlation of 0.659 between model and participant dissimilarity structure on held-out stimuli, implying that stable individual differences in neural dynamics can be encoded in model weights.
- Because only DoRA adapter parameters and the feature-reweighting matrix are updated, the personalization pipeline is cheap enough to run participant-by-participant, supporting sequential or on-device adaptation.
Reading between the lines
- Editorial extension: because behavioral fine-tuning saturates with roughly 100 training stimuli, the same recipe could be used to align models to small, hard-to-collect behavioral datasets from special populations such as infants, patients, or non-verbal individuals, where large-scale judgments are impractical.
- Editorial extension: the dynamic saliency maps are claimed to show where a person attends at each millisecond, but the paper does not compare them to eye-tracking or fixation data; such a comparison would be a direct, testable way to validate whether the model's dynamic attention is perceptual attention or merely a correlate of RDM geometry.
- Editorial extension: the loss terms and reweighting mechanism are architecture-agnostic, so a natural next test is to apply the same MEG-targeted fine-tuning to a non-CLIP transformer and check whether the same 300–400 ms semantic peak appears; if it does, the effect is driven by the training objective rather than by CLIP's text-binding component.
- Editorial extension: the paper frames personalized models as cognitive digital twins, but a stronger test of that framing would be to see whether a personalized model trained on one recording session can predict that same participant's neural RDMs from a later session, or distinguish them from other participants' data; the current 18-stimulus held-out validation is a single-session check.
Signed reviews
Editorial analysis
A structured set of objections, weighed in public.
Referee Report
Summary. The manuscript introduces CLIP-HBA, a family of CLIP-ViT-L/14 models fine-tuned with human-derived targets. CLIP-HBA-Behavior is trained with an MSE loss to predict 66 SPoSE behavioral embeddings from THINGS images, and is reported to reach Spearman rho=0.78 (95% CI [0.75,0.80]) against a fully sampled behavioral RDM for 48 held-out objects, versus 0.32 for the CLIP baseline, with improved NIGHTS triplet scores (Table 1). CLIP-HBA-MEG extends the method with a dynamic feature-reweighting matrix and a three-part loss (Eq. 10) aligned to MEG decoding RDMs, and is evaluated on THINGS MEG data and three external datasets (Tables 2-3). Finally, 15 participant-specific models are trained on individual MEG RDMs; a global Spearman correlation of rho=0.659 (p<1e-14) between model-pair distances and participant-pair distances on 18 held-out stimuli is presented as evidence of personalized neural alignment. The paper also reports dynamic saliency maps and discusses applications to personalized medicine and human-AI interaction.
Significance. If the main claims hold, the paper constitutes a useful contribution to human-aligned representation learning: the design excludes held-out stimuli from training, the NIGHTS and external MEG validations are appropriate generalization checks, and the SPoSE-based embedding space offers a degree of interpretability. However, the central novelty, personalized neural fine-tuning, is supported by a single correlational statistic without group-level or permutation controls, and the neural targets themselves are decoding RDMs whose fidelity to true neural geometry is not established. The behavioral gains are large relative to the CLIP baseline but lack comparison to competing human-aligned models and to a noise ceiling. The paper also contains no code or data availability statement. The strengths and weaknesses are unbalanced enough that the conclusions should be revised rather than accepted as stated.
major comments (3)
- [§2.7, §4.4–4.5] The individual-level claim that personalized models capture participant-specific neural dynamics rests on a single global Spearman correlation (rho=0.659, p<1e-14) between pairwise distances among 15 models and pairwise distances among participants' MEG RDMs, computed on 18 held-out stimuli. The analysis lacks a group-level baseline (e.g., one model trained on averaged MEG RDMs), a permutation test with shuffled participant–model assignments, and a cross-participant evaluation (train on A, test on B). Since each model is trained on its own participant's MEG RDMs and evaluated on the same participant's held-out neural RDMs, the correlation could be driven by shared object representational structure or by participant-specific decoding artifacts rather than by genuine individual dynamics. Moreover, the description of this analysis in §4.5 is internally inconsistent: it first describes a per-pair Spearman correlation over time, then a between-pair distance correlation, and the reported value changes from 0.659 to 0.65 without explanation. Please add a group-average model comparison and a shuffled-assignment permutation test, and clarify the exact evaluation protocol.
- [§4.3.4, Tables 2–3] The neural targets are 'MEG decoding RDMs' produced by LDA/SVM classifiers, but the manuscript does not specify how these RDMs are constructed, how many trials support each RDM, or whether the decoding RDMs are cross-validated. Because the model is optimized to match these RDMs (Eqs. 5–10), the reported neural-alignments could reflect the model reproducing classifier decision boundaries rather than the geometry of neural population responses. At least one central claim, such as the group-level temporal alignment in Figure 2B or the individual alignment in §2.7, should be validated against raw sensor- or source-space RDMs, or the authors should provide evidence that the decoding RDMs are stable across trials, are not dominated by classifier bias, and capture stimulus-specific representational structure.
- [§2.1–2.2] The headline behavioral improvement (rho=0.78 versus 0.32) is measured on 48 held-out objects from the THINGS benchmark, and the model is fine-tuned on SPoSE embeddings that are themselves fitted to human similarity judgments for the same object set. The external NIGHTS benchmark in Table 1 is a welcome generalization test, but the reported gains are modest (0.88 vs 0.81 for 768-d features; 0.85/0.84 vs 0.80/0.79 for 66-d features) and are reported without error bars or significance tests. The phrase 'over doubles behavioral performance' relies on comparison to a single baseline CLIP-ViT-L/14 and does not establish where the method stands relative to other human-aligned models (e.g., DreamSim, DINOv2) or to a noise ceiling. Please add such comparisons or temper the generalization claims.
minor comments (6)
- [Table 4 and §4.5] The number of held-out stimuli is inconsistent: §2.7 and §4.5 state 18 left-out stimuli, while Table 4 lists a Train/Test Split of 80/20 on 100 stimuli, implying 20 validation stimuli; please reconcile these numbers.
- [General] The manuscript provides no code or data availability statement, which substantially limits reproducibility of the fine-tuning pipeline and the personalized-model analysis.
- [§2.1] The p-value for the behavioral correlation (p<10^-229) is reported without specifying the statistical test or the number of elements in the vectorized RDMs used for the Spearman correlation; please state the test and sample size.
- [Eq. (4)] Equation (4) uses the element-wise product symbol \odot without defining it; please add a definition or explain the notation in the text.
- [§2.7, Figure 6A] The 'lower-bound noise ceiling' is mentioned in the text and shown in Figure 6A but is never defined or estimated in the Methods; please specify how this noise ceiling was computed.
- [References] References [22] and [49] are the same work (Kucyi et al., Network Neuroscience, 2024) and should be merged or cross-referenced.
Circularity Check
No significant circularity: the main behavioral and neural claims are tested on held-out or external benchmarks; the personalization analysis lacks a control baseline but is not circular by construction.
full rationale
The paper's derivation chain is largely self-contained and externally grounded. CLIP-HBA-Behavior is trained to predict SPoSE embeddings via Eq. (2), and its behavioral evaluation uses 48 objects explicitly excluded from training plus the independent NIGHTS triplet benchmark. Although both the training target and the behavioral RDM derive from human similarity judgments within the THINGS paradigm, the held-out object generalization and the external NIGHTS results mean the behavioral improvement is not forced by construction. The same holds for CLIP-HBA-MEG: it is trained against MEG decoding RDMs through Eq. (10), but its neural generalization claims are supported by three external MEG datasets with different participants, stimuli, and image degradations, so the alignment is not merely a refit of training data. The personalized-model analysis is the only place where the evidence is weaker: each model is fine-tuned on a participant's MEG RDMs and then correlated with the same participant's held-out neural RDMs. This is a legitimate held-out-stimulus evaluation, not a circular reduction, but the reported rho = 0.659 lacks a group-level model, cross-participant evaluation, or permutation test, so it cannot by itself establish that participant-specific dynamics rather than shared representational structure drive the correlation. That is a missing experimental control, which belongs in the correctness/validity assessment rather than the circularity score. Self-citations in the paper (e.g., references [43], [57], [58]) support specific design choices such as temporal scalers and multisensory integration; they are not load-bearing for the central claims. Overall, the central predictions are not equivalent to their inputs by definition, and the paper is appropriately benchmarked against external data, so no significant circularity is present.
Assumptions & free parameters
free parameters (4)
- Loss weights w1, w2, w3 =
w1=1, w2=0.1 or 0.15, w3=0.15 or 0.1 depending on dataset
- Temporal scalars alpha_T and beta_T =
not specified
- Feature reweighting matrix W =
learned T x 24 matrix, initialized as a one-hot at the last layer
- DoRA rank, dropout, and learning rates =
r=32 group-level, r=6 individual-level; dropout 0.1; learning rates 3e-4, 3e-5, 3e-3
assumptions (5)
- domain assumption SPoSE 66-dimensional embeddings capture the psychologically relevant structure of human similarity judgments
- domain assumption MEG decoding RDMs are valid proxies for dynamic neural representations of object vision
- domain assumption Off-the-shelf CLIP-ViT-L/14 last-layer features are an appropriate baseline for human alignment
- domain assumption THINGS MEG group data from 3 participants is sufficient to train a generalizable neural alignment model
- standard math Standard CLIP pretrained weights and transformer training dynamics are accepted as background
Cite this review
Pith. "Pith review of Shifting Attention to You: Personalized Brain-Inspired AI Models." pith.science (2026). https://pith.science/paper/ABWC65QS
@misc{pith2026250204658,
author = {Pith},
title = {Pith review of: Shifting Attention to You: Personalized Brain-Inspired AI Models},
year = {2026},
howpublished = {\url{https://pith.science/paper/ABWC65QS}},
note = {Machine review of arXiv:2502.04658}
}
read the original abstract
The integration of human and artificial intelligence offers a powerful avenue for advancing our understanding of information processing, as each system provides unique computational insights. However, despite the promise of human-AI integration, current AI models are largely trained on massive datasets, optimized for population-level performance, lacking mechanisms to align their computations with individual users' perceptual semantics and neural dynamics. Here we show that integrating human behavioral insights and millisecond scale neural data within a fine tuned CLIP based model not only captures generalized and individualized aspects of perception but also over doubles behavioral performance compared to the unmodified CLIP baseline. By embedding human inductive biases and mirroring dynamic neural processes during training, personalized neural fine tuning improves predictions of human similarity judgments and tracks the temporal evolution of individual neural responses. Our work establishes a novel, interpretable framework for designing adaptive AI systems, with broad implications for neuroscience, personalized medicine, and human-computer interaction.
Figures
Figures from the paper (8 more)
Forward citations
Cited by 1 Pith paper
-
Beginning with You: Perceptual-Initialization Improves Vision-Language Representation and Alignment
Perceptually initializing a CLIP vision encoder with NIGHTS triplet judgments before YFCC15M contrastive training improves zero-shot accuracy and retrieval over an identical random-start baseline.
Reference graph
Works this paper leans on
-
[1]
Ian Goodfellow, Yoshua Bengio, and Aaron Courville. Deep learning. MIT Press, 2016. URL http://www. deeplearningbook.org/. 17 Personalized Brain-Inspired AI Models
work page 2016
-
[2]
If deep learning is the answer, what is the question? Nature Reviews Neuroscience, 22:55–67, 2021
Andrew Saxe, Sandro Nelli, and Christopher Summerfield. If deep learning is the answer, what is the question? Nature Reviews Neuroscience, 22:55–67, 2021. doi:10.1038/s41583-020-00395-8
-
[3]
Matteo Ferrante, Tommaso Boccato, Grigorii Rashkov, and Nicola Toschi. Towards neural foundation models for vision: Aligning eeg, meg, and fmri representations for decoding, encoding, and modality conversion, 2024. URL https://arxiv.org/abs/2411.09723
arXiv 2024
-
[4]
Achieving more human brain-like vision via human eeg representa- tional alignment
Zitong Lu, Yile Wang, and Julie D Golomb. Achieving more human brain-like vision via human eeg representa- tional alignment. arXiv preprint arXiv:2401.17231, 2024
arXiv 2024
-
[5]
Bruna, Ilia Sucholutsky, Christopher Kello, and Thomas L
Sunayana Rane, Polyphony J. Bruna, Ilia Sucholutsky, Christopher Kello, and Thomas L. Griffiths. Concept alignment, 2024. URL https://arxiv.org/abs/2401.08672
arXiv 2024
-
[6]
Mahner, Lukas Muttenthaler, Umut Güçlü, and Martin N
Florian P. Mahner, Lukas Muttenthaler, Umut Güçlü, and Martin N. Hebart. Dimensions underlying the representa- tional alignment of deep neural networks with humans, June 2024. URL http://arxiv.org/abs/2406.19087. arXiv:2406.19087 [cs, q-bio]
arXiv 2024
- [7]
-
[8]
Distributional measures of semantic abstraction
Sabine Schulte Im Walde and Diego Frassinelli. Distributional measures of semantic abstraction. Frontiers in Artificial Intelligence, 4:796756, 2022. doi:10.3389/frai.2021.796756. URL https://doi.org/10.3389/frai. 2021.796756
Show all 64 references
-
[9]
Lampinen, Klaus-Robert Müller, and Michael C
Frieda Born, Lukas Muttenthaler, Klaus Greff, Thomas Unterthiner, Andrew K. Lampinen, Klaus-Robert Müller, and Michael C. Mozer. Evaluating and supervising vision models with multi-level similarity judgments. Cognitive Computational Neuroscience Conference (CCN), 2024. URL htt...
2024
-
[10]
McDermott
Jenelle Feather, Guillaume Leclerc, Aleksander M ˛ adry, and Josh H. McDermott. Model metamers reveal divergent invariances between biological and artificial neural networks. Nature Neuroscience, 26(11):2017–2034, November
2017
-
[11]
Comparison of deep neural networks to spatio-temporal cortical dynamics of human visual object recognition reveals hierarchical correspondence
Radoslaw Martin Cichy, Aditya Khosla, Dimitrios Pantazis, Antonio Torralba, and Aude Oliva. Comparison of deep neural networks to spatio-temporal cortical dynamics of human visual object recognition reveals hierarchical correspondence. Scientific Reports, 6(1):27755, June 2016...
2016 doi
-
[12]
Vandermeulen, and Simon Kornblith
Lukas Muttenthaler, Jonas Dippel, Lorenz Linhardt, Robert A. Vandermeulen, and Simon Kornblith. Hu- man alignment of neural network representations, April 2023. URL http://arxiv.org/abs/2211.01201. arXiv:2211.01201 [cs, q-bio]
2023 arXiv
-
[13]
Dickerson, Krishna P
Vedant Nanda, Ayan Majumdar, Camila Kolling, John P. Dickerson, Krishna P. Gummadi, Bradley C. Love, and Adrian Weller. Do Invariances in Deep Neural Networks Align with Human Perception? Proceedings of the AAAI Conference on Artificial Intelligence, 37(8):9277–9285, June 2023...
2023 doi
-
[14]
Sinz, Xaq Pitkow, Jacob Reimer, Matthias Bethge, and Andreas S
Fabian H. Sinz, Xaq Pitkow, Jacob Reimer, Matthias Bethge, and Andreas S. Tolias. Engineering a less artificial intelligence. Neuron, 103(6):967–979, 2019. doi:10.1016/j.neuron.2019.08.034. URL https://www.cell. com/neuron/fulltext/S0896-6273(19)30740-8
2019 doi
-
[15]
Peterson, and Thomas L
Raja Marjieh, Nori Jacoby, Joshua C. Peterson, and Thomas L. Griffiths. The Universal Law of Generalization Holds for Naturalistic Stimuli, June 2023. URL http://arxiv.org/abs/2306.08564. arXiv:2306.08564 [cs, q-bio, stat]
2023 arXiv
-
[16]
Griffiths
Raja Marjieh, Sreejan Kumar, Declan Campbell, Liyi Zhang, Gianluca Bencomo, Jake Snell, and Thomas L. Griffiths. Using Contrastive Learning with Generative Similarity to Learn Spaces that Capture Human Inductive Biases, May 2024. URL http://arxiv.org/abs/2405.19420. arXiv:2405...
2024 arXiv
-
[17]
Learning Transferable Visual Models From Natural Language Supervision, February 2021
Alec Radford, Jong Wook Kim, Chris Hallacy, Aditya Ramesh, Gabriel Goh, Sandhini Agarwal, Girish Sastry, Amanda Askell, Pamela Mishkin, Jack Clark, Gretchen Krueger, and Ilya Sutskever. Learning Transferable Visual Models From Natural Language Supervision, February 2021. URL h...
2021 arXiv
-
[18]
Hebart, Adam H
Martin N. Hebart, Adam H. Dickter, Alexis Kidder, Wan Y . Kwok, Anna Corriveau, Caitlin Van Wicklin, and Chris I. Baker. THINGS: A database of 1,854 object concepts and more than 26,000 naturalistic object images. PLOS ONE, 14(10):e0223792, October 2019. ISSN 1932-6203. doi:10...
2019 doi
-
[19]
THINGS-data, a multimodal collection of large-scale datasets for investigating object representations in human brain and behavior
Martin N Hebart, Oliver Contier, Lina Teichmann, Adam H Rockter, Charles Y Zheng, Alexis Kidder, Anna Corriveau, Maryam Vaziri-Pashkam, and Chris I Baker. THINGS-data, a multimodal collection of large-scale datasets for investigating object representations in human brain and b...
2023 doi
-
[20]
Dreamsim: Learning new dimensions of human visual similarity using synthetic data, 2023
Stephanie Fu, Netanel Tamir, Shobhita Sundaram, Lucy Chai, Richard Zhang, Tali Dekel, and Phillip Isola. Dreamsim: Learning new dimensions of human visual similarity using synthetic data, 2023. URL https: //arxiv.org/abs/2306.09344
2023 arXiv
-
[21]
Ruffle, Robert J Gray, Samia Mohinta, Guilherme Pombo, Chaitanya Kaul, Harpreet Hyare, Geraint Rees, and Parashkev Nachev
James K. Ruffle, Robert J Gray, Samia Mohinta, Guilherme Pombo, Chaitanya Kaul, Harpreet Hyare, Geraint Rees, and Parashkev Nachev. Computational limits to the legibility of the imaged human brain. NeuroImage, 291: 120600, May 2024. ISSN 1053-8119. doi:10.1016/j.neuroimage.202...
2024
-
[22]
Braga, Po-Jang Hsieh, and Shao-Min Hung
Aaron Kucyi, Nathan Anderson, Tiara Bounyarith, David Braun, Lotus Shareef-Trudeau, Isaac Treves, Rodrigo M. Braga, Po-Jang Hsieh, and Shao-Min Hung. Individual variability in neural representations of mind-wandering. Network Neuroscience, 8(3):808–836, 10 2024. ISSN 2472-1751...
2024 doi
-
[23]
Inductive biases for deep learning of higher-level cognition
Anirudh Goyal and Yoshua Bengio. Inductive biases for deep learning of higher-level cognition. Proceedings of the Royal Society A, 478(20210068), 2022. doi:10.1098/rspa.2021.0068. URL http://doi.org/10.1098/ rspa.2021.0068
2022
-
[24]
Zheng, Francisco Pereira, Chris I
Charles Y . Zheng, Francisco Pereira, Chris I. Baker, and Martin N. Hebart. Revealing interpretable object representations from human behavior, 2019. URL https://arxiv.org/abs/1901.02915
2019 arXiv
-
[25]
Hebart, Charles Y
Martin N. Hebart, Charles Y . Zheng, Francisco Pereira, and Chris I. Baker. Revealing the multidimensional mental representations of natural objects underlying human similarity judgements. Nature Human Behaviour, 4(11): 1173–1185, October 2020. ISSN 2397-3374. doi:10.1038/s415...
2020 doi
-
[26]
Representational similarity analysis – connecting the branches of systems neuroscience
Nikolaus Kriegeskorte. Representational similarity analysis – connecting the branches of systems neuroscience. Frontiers in Systems Neuroscience, 2008. ISSN 16625137. doi:10.3389/neuro.06.004.2008. URL http:// journal.frontiersin.org/article/10.3389/neuro.06.004.2008/abstract
2008 doi
-
[27]
Hyperalignment of dynamic responses using meg
Tijl Grootswagers, Emma Contini, and Thomas Carlson. Hyperalignment of dynamic responses using meg. In Proceedings of the Organization for Human Brain Mapping Annual Meeting, page 3548, Vancouver, Canada,
-
[28]
Wardle, and Thomas A
Tijl Grootswagers, Susan G. Wardle, and Thomas A. Carlson. Decoding dynamic brain patterns from evoked responses: A tutorial on multivariate pattern analysis applied to time series neuroimaging data. Journal of Cognitive Neuroscience, 29(4):677–697, 04 2017. ISSN 0898-929X. do...
2017 doi
-
[29]
Representation learning for neural population activity with neural data transform- ers
Joel Ye and Chethan Pandarinath. Representation learning for neural population activity with neural data transform- ers. Neurons, Behavior, Data analysis, and Theory, 5(3), August 2021. ISSN 2690-2664. doi:10.51628/001c.27358. URL http://dx.doi.org/10.51628/001c.27358
2021 doi
-
[30]
Tang, Mikio C
Marino Pagan, Vincent D. Tang, Mikio C. Aoi, Jonathan W. Pillow, Valerio Mante, David Sussillo, and Carlos D. Brody. Individual variability of neural computations underlying flexible decisions. Nature, 2024. doi:10.1038/s41586-024-08433-6. URL https://doi.org/10.1038/s41586-02...
2024 doi
-
[31]
RISE: randomized input sampling for explanation of black-box models
Vitali Petsiuk, Abir Das, and Kate Saenko. RISE: randomized input sampling for explanation of black-box models. CoRR, abs/1806.07421, 2018. URL http://arxiv.org/abs/1806.07421
2018 arXiv
-
[32]
Mahner, Jonas Perkuhn, and Martin N
Philipp Kaniuth, Florian P. Mahner, Jonas Perkuhn, and Martin N. Hebart. A high-throughput approach for the efficient prediction of perceived similarity of natural objects, July 2024. URL http://biorxiv.org/lookup/ doi/10.1101/2024.06.28.601184
2024 doi
-
[33]
A high-throughput approach for the efficient prediction of perceived similarity of natural objects
Philipp Kaniuth, Florian P Mahner, Jonas Perkuhn, and Martin N Hebart. A high-throughput approach for the efficient prediction of perceived similarity of natural objects. bioRxiv, pages 2024–06, 2024
2024
-
[34]
Improving neural network representations using human similarity judgments
Lukas Muttenthaler, Lorenz Linhardt, Jonas Dippel, Robert A Vandermeulen, Katherine Hermann, Andrew K Lampinen, and Simon Kornblith. Improving neural network representations using human similarity judgments. arXiv preprint arXiv:2306.04507, 2023
2023 arXiv
-
[35]
Variability in neural activity and behavior
Alfonso Renart and Christian K Machens. Variability in neural activity and behavior. Current Opinion in Neurobiology, 25:211–220, 2014. ISSN 0959-4388. doi:https://doi.org/10.1016/j.conb.2014.02.013. URL https: //www.sciencedirect.com/science/article/pii/S0959438814000488. The...
2014 doi
-
[36]
Garcia, Nina Lauharatanahirun, Sarah F
Kanika Bansal, Javier O. Garcia, Nina Lauharatanahirun, Sarah F. Muldoon, Paul Sajda, and Jean M. Vettel. Scale-specific dynamics of high-amplitude bursts in eeg capture behaviorally meaningful variability. NeuroImage, 241:118425, November 2021. ISSN 1053-8119. doi:10.1016/j.n...
2021
-
[37]
Towards a rigorous science of interpretable machine learning
Finale Doshi-Velez and Been Kim. Towards a rigorous science of interpretable machine learning. arXiv preprint arXiv:1702.08608, 2017
2017 arXiv
-
[38]
Stop explaining black box machine learning models for high stakes decisions and use interpretable models instead
Cynthia Rudin. Stop explaining black box machine learning models for high stakes decisions and use interpretable models instead. nat mach intell 1 (5): 206–215, 2019
2019
-
[39]
Tolias, and Doris Tsao
Anthony Zador, Sean Escola, Blake Richards, Bence Ölveczky, Yoshua Bengio, Kwabena Boahen, Matthew Botvinick, Dmitri Chklovskii, Anne Churchland, Claudia Clopath, James DiCarlo, Surya Ganguli, Jeff Hawkins, Konrad Kording, Alexei Koulakov, Yann LeCun, Timothy Lillicrap, Adam M...
2023
-
[40]
Philipp Kaniuth and Martin N. Hebart. Feature-reweighted representational similarity analysis: A method for improving the fit between computational models, brains, and behavior. NeuroImage, 257:119294, August
-
[41]
Multimodal machine learning: A survey and taxonomy
Tadas Baltrušaitis, Chaitanya Ahuja, and Louis-Philippe Morency. Multimodal machine learning: A survey and taxonomy. IEEE Transactions on Pattern Analysis and Machine Intelligence, 41(2):423–443, 2018
2018
-
[42]
The neural bases of multisensory processes
Micah M Murray and Mark T Wallace. The neural bases of multisensory processes. CRC Press, 2011
2011
-
[43]
Selective enhancement of object representations through multisensory integration
David A Tovar, Micah M Murray, and Mark T Wallace. Selective enhancement of object representations through multisensory integration. Journal of Neuroscience, 40(29):5604–5615, 2020
2020
-
[44]
The neuroconnectionist research programme
Adrien Doerig, Rowan P Sommers, Katja Seeliger, Blake Richards, Jenann Ismael, Grace W Lindsay, Konrad P Kording, Talia Konkle, Marcel AJ Van Gerven, Nikolaus Kriegeskorte, et al. The neuroconnectionist research programme. Nature Reviews Neuroscience, 24(7):431–450, 2023
2023
-
[45]
Industrial applications of digital twins.Philosophi- cal Transactions of the Royal Society A, 379(2207):20200360, 2021
Yuchen Jiang, Shen Yin, Kuan Li, Hao Luo, and Okyay Kaynak. Industrial applications of digital twins.Philosophi- cal Transactions of the Royal Society A, 379(2207):20200360, 2021. URL https://royalsocietypublishing. org/doi/10.1098/rsta.2020.0360
2021
-
[46]
Enhancing personalized learning: Ai-driven identification of learning styles and content modification strategies
Md Kabin Hasan Kanchon, Mahir Sadman, Kaniz Fatema Nabila, Ramisa Tarannum, and Riasat Khan. Enhancing personalized learning: Ai-driven identification of learning styles and content modification strategies. International Journal of Cognitive Computing in Engineering, 5:269–278, 2024
2024
-
[47]
Dynamic functional connectivity analysis reveals transient states of dysconnectivity in schizophrenia
Eswar Damaraju, Elena A Allen, Aysenil Belger, Judith M Ford, S McEwen, DH Mathalon, BA Mueller, GD Pearlson, SG Potkin, A Preda, et al. Dynamic functional connectivity analysis reveals transient states of dysconnectivity in schizophrenia. NeuroImage: Clinical, 5:298–308, 2014
2014
-
[48]
The dynamic functional connectome: State-of- the-art and perspectives
Maria Giulia Preti, Thomas AW Bolton, and Dimitri Van De Ville. The dynamic functional connectome: State-of- the-art and perspectives. Neuroimage, 160:41–54, 2017
2017
-
[49]
Individual variability in neural representations of mind-wandering
Aaron Kucyi, Nathan Anderson, Tiara Bounyarith, David Braun, Lotus Shareef-Trudeau, Isaac Treves, Rodrigo M Braga, Po-Jang Hsieh, and Shao-Min Hung. Individual variability in neural representations of mind-wandering. Network Neuroscience, pages 1–66, 2024
2024
-
[50]
An image is worth 16x16 words: Transformers for image recognition at scale
Alexey Dosovitskiy, Lucas Beyer, Alexander Kolesnikov, Dirk Weissenborn, Xiaohua Zhai, Thomas Unterthiner, Mostafa Dehghani, Matthias Minderer, Georg Heigold, Sylvain Gelly, Jakob Uszkoreit, and Neil Houlsby. An image is worth 16x16 words: Transformers for image recognition at...
2010 arXiv
-
[51]
Dora: Weight-decomposed low-rank adaptation, 2024
Shih-Yang Liu, Chien-Yi Wang, Hongxu Yin, Pavlo Molchanov, Yu-Chiang Frank Wang, Kwang-Ting Cheng, and Min-Hung Chen. Dora: Weight-decomposed low-rank adaptation, 2024. URL https://arxiv.org/abs/ 2402.09353
2024 arXiv
-
[52]
Hu, Yelong Shen, Phillip Wallis, Zeyuan Allen-Zhu, Yuanzhi Li, Shean Wang, Lu Wang, and Weizhu Chen
Edward J. Hu, Yelong Shen, Phillip Wallis, Zeyuan Allen-Zhu, Yuanzhi Li, Shean Wang, Lu Wang, and Weizhu Chen. LoRA: Low-Rank Adaptation of Large Language Models, October 2021. URL http://arxiv.org/abs/ 2106.09685. arXiv:2106.09685 [cs]
2021 arXiv
-
[53]
Fine-tuning clip’s last visual projector: A few-shot cornucopia, 2024
Mohammad Fahes, Tuan-Hung Vu, Andrei Bursuc, Patrick Pérez, and Raoul de Charette. Fine-tuning clip’s last visual projector: A few-shot cornucopia, 2024. URL https://arxiv.org/abs/2410.05270. 20 Personalized Brain-Inspired AI Models
2024
-
[54]
Jerrold H. Zar. Significance testing of the spearman rank correlation coefficient.Journal of the American Statistical Association, 67(339):578–580, 1972. doi:10.2307/2284441
1972 doi
-
[55]
Decoupled weight decay regularization, 2019
Ilya Loshchilov and Frank Hutter. Decoupled weight decay regularization, 2019. URL https://arxiv.org/ abs/1711.05101
2019 arXiv
-
[56]
High temporal resolution decoding of object position and category
Thomas A Carlson, Hinze Hogendoorn, Ryota Kanai, Juraj Mesik, and Jeremy Turret. High temporal resolution decoding of object position and category. Journal of Vision , 11(10):9, 2011. doi:10.1167/11.10.9. URL https://pubmed.ncbi.nlm.nih.gov/21920851/
2011
-
[57]
Representational dynamics of object vision: the first 1000 ms
Thomas Carlson, David A Tovar, Arjen Alink, and Nikolaus Kriegeskorte. Representational dynamics of object vision: the first 1000 ms. Journal of Vision, 13(10):1, 2013. doi:10.1167/13.10.1. URL https://pubmed.ncbi. nlm.nih.gov/23908380/
2013
-
[58]
Stimulus feature-specific information flow along the columnar cortical microcir- cuit revealed by multivariate laminar spiking analysis
David A Tovar, Jacob A Westerberg, Michele A Cox, Kacie Dougherty, Thomas A Carlson, Mark T Wal- lace, and Alexander Maier. Stimulus feature-specific information flow along the columnar cortical microcir- cuit revealed by multivariate laminar spiking analysis. Frontiers in Sys...
2020
-
[59]
King and S
J-R. King and S. Dehaene. Characterizing the dynamics of mental representations: the tempo- ral generalization method. Trends in Cognitive Sciences , 18(4):203–210, 2014. ISSN 1364-6613. doi:https://doi.org/10.1016/j.tics.2014.01.002. URL https://www.sciencedirect.com/science/...
2014 doi
-
[60]
Pearson’s Correlation Coefficient , pages 1090–1091
Wilhelm Kirch. Pearson’s Correlation Coefficient , pages 1090–1091. Springer Netherlands, Dordrecht,
-
[2008]
doi:10.1007/978-1-4020-5614-7_2569
ISBN 978-1-4020-5614-7. doi:10.1007/978-1-4020-5614-7_2569. URL https://doi.org/10.1007/ 978-1-4020-5614-7_2569 . 21 Personalized Brain-Inspired AI Models 5 Supplemental Figures Figure 8: Example SPoSE Embeddings of Image Stimuli:Behaviorally Fine-tuned CLIP-HBA-Behavior v.s. ...
-
[2017]
Poster Session presented on June 28
Organization for Human Brain Mapping. Poster Session presented on June 28
-
[2022]
doi:10.1016/j.neuroimage.2022.119294
ISSN 10538119. doi:10.1016/j.neuroimage.2022.119294. URL https://linkinghub.elsevier.com/ retrieve/pii/S105381192200413X
2022
-
[2023]
doi:10.1038/s41593-023-01442-0
ISSN 1097-6256, 1546-1726. doi:10.1038/s41593-023-01442-0. URL https://www.nature.com/ articles/s41593-023-01442-0
Reviewed August 8, 2026 · model on record in the stance chip above.
Discussion (0). Continue with ORCID to comment.