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REVIEW 4 major objections 4 minor 59 references

Multiview Graph Fusion with Covariates

T0 review · 4 major / 4 minor · reviewed 2026-07-13 · grok-4.5

Pith's one-line read A hierarchical Bayesian model jointly learns multiple graphs on shared nodes while linking them to predictors, with proven predictive consistency and better node recovery than separate or tensor methods.

desk verdict Solid multiview graph-response Bayesian model with shared node selection, Hellinger consistency, and a usable fMRI illustration; the shared-ξ prior is a real modeling choice that simulations never stress-test against view-specific alternatives. read the letter →

arxiv 2603.22215 v2 pith:O2FFV7VG submitted 2026-03-23 stat.ME stat.AP

classification stat.MEstat.AP MSC 62F1562H1262J12
keywords multiviewgraphshierarchicalBayesianmodelingposteriorconsistencyfunctionalconnectivityspike-and-slablow-rankgraphcoefficientsgraph-on-predictorsregression
verification ladder T0 review T1 audit T2 compute T3 formal

The pith

A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.

The reading

Researchers often observe several related networks—brain connectivity under different tasks, for example—together with subject-level predictors such as cognitive scores. Treating those networks as independent or flattening them into unstructured tensors discards shared node structure and symmetry, and usually provides no uncertainty. This paper builds a single hierarchical Bayesian model that keeps each graph’s symmetry, allows continuous or binary edges, and shares a low-rank node-effect representation across views through a common spike-and-slab prior. The model therefore estimates which nodes and edges are linked to each predictor, produces predictions for new graphs, and supplies full posterior uncertainty. Theory shows that the posterior predictive density converges to the true data-generating density when the number of nodes grows slower than sample size over log n. Simulations and a functional-connectivity study confirm gains over independent graph regressions and over tensor-on-vector regression.

What carries the argument

A shared spike-and-slab prior on the stacked node-specific latent vectors across all graph views (equation 4), which induces joint selection of nodes associated with a predictor and couples the low-rank graph coefficient matrices through a common covariance.

What would settle it

Generate multiview graphs in which a non-empty set of nodes is truly active in only one view and inactive in the others; if the joint model still forces those nodes to be selected (or unselected) across all views and loses estimation accuracy relative to independent learning, the shared-indicator claim fails.

Watch

Extended reading notes

Core claim

Under mild growth and sparsity conditions, the posterior predictive density of the proposed multiview generalized linear model converges in Hellinger distance to the true data-generating density, while the shared hierarchical prior on node-specific latent vectors yields more accurate coefficient estimates and node selection than independent graph-on-predictors learning or predictor-dependent tensor learning.

Load-bearing premise

A node is either associated with a key predictor in every graph view or in none; view-specific associations break the shared selection mechanism.

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Editorial analysis

A structured set of objections, weighed in public.

Desk editor's note, referee report, and a circularity audit.

Referee Report

4 major / 4 minor

Summary. The paper proposes a hierarchical Bayesian GLM for joint predictor-dependent learning of multiview undirected graphs on a common node set, allowing continuous or binary edge weights. Graph coefficients for key predictors are given a low-rank factorization through node-specific latent vectors, coupled across views by a joint spike-and-slab prior with shared inclusion indicators ξ_{p,k} and an inverse-Wishart covariance (Eq. 4). Auxiliary predictors enter with scalar coefficients. The authors prove Hellinger consistency of the posterior predictive density under growth and sparsity assumptions (Theorem 3.1), give a Gibbs sampler via standard full conditionals, report lower coefficient MSE and good node AUC versus independent learning (IL) and tensor learning (TL) in continuous-edge simulations (n=150, K=40, M=2), and apply the method to task-based fMRI functional connectivity (inhibition/initiation) related to MMSE, selecting 88 ROIs.

Significance. If the modeling assumptions hold, the work addresses a real methodological gap: joint multiview graph-on-predictors regression that respects symmetry, accommodates mixed edge types, performs node-level selection with uncertainty quantification, and supplies asymptotic theory for heterogeneous multiview graph responses. The fMRI application is scientifically relevant. Explicit full conditionals, transparent assumptions for the Hellinger result, and comparisons to natural competitors (IL, TL) are genuine strengths. The shared-sparsity prior is the central modeling device that underwrites both the theory and the claimed gains over IL; its empirical and theoretical support is therefore load-bearing for the contribution.

major comments (4)
  1. [§2.3, Eq. (4); §5] Section 2.3, Eq. (4): The shared indicators ξ_{p,k} force a node to be associated with a key predictor in every view or in none. Simulations (§5) generate data under exactly this shared-ξ mechanism (common ξ_k^{(0)}, correlated latents across M=2 views), so JL is correctly specified while IL is not; the reported MSE/AUC advantages are therefore expected under the matching generative model and do not establish robustness. A sensitivity study with view-specific true associations is needed before claiming inferential superiority over independent learning.
  2. [Assumption (A); §6] Assumption (A) requires R_n K_n ≺ n/log(n). The fMRI analysis uses K=200 and n=144, which strains or violates this regime for any nontrivial fitted rank R. The paper should discuss relevance of the asymptotic conditions to the application and supply finite-sample checks (e.g., smaller-K or larger-n experiments) that sit inside the stated growth regime.
  3. [Theorem 3.2; §3] Theorem 3.2 establishes that the posterior probability of over-selecting influential nodes vanishes only under continuous Gaussian edges with known unit variance. The abstract and model emphasize mixed binary/continuous views; the scope of node-selection guarantees should be clarified or the result extended, and the gap between Theorem 3.1 (predictive Hellinger) and node-level inference should be stated explicitly.
  4. [§5] Section 5 restricts all scenarios to continuous edges, M=2, n=150, K=40, and data generated under the same shared-sparsity structure as the prior. Performance under binary edges, larger M, misspecified rank, or view-specific sparsity is not assessed, limiting support for the general claims of the abstract and introduction.
minor comments (4)
  1. [Figure 1] Figure 1 is hard to read in grayscale; a clearer encoding of true activity vs posterior probability would help.
  2. [§2.2–2.3] Notation for stacked latents (β̃_{p,k}) and the distinction between fitted rank R and effective rank induced by λ is introduced densely; a short summary table of parameters would improve readability.
  3. [§6.1] The median-probability threshold 0.5 for ROI selection (§6.1) is standard but should be noted as a free choice; sensitivity to the threshold would strengthen the application.
  4. [§4] Appendix references in the main text (full conditionals, ROI list) are clear, but the main text could briefly state that binary-edge full conditionals follow the same Gibbs structure with logistic likelihood contributions.

Circularity Check

1 steps flagged · score 1.0 of 10

No significant circularity: asymptotic predictive consistency and simulation gains are standard Bayesian results under stated model class and matching DGP, not tautologies of fitted inputs or self-citation chains.

  1. self citation load bearing [§1 Novelty paragraph; also §2.2 low-rank motivation]
    "Our theoretical exposition introduces several novel aspects over existing work in Bayesian predictor-dependent learning of multiple graphs. Firstly, the theoretical framework in this article addresses joint modeling with multiview graph responses, unlike scenarios of a single graph response addressed in prior literature [23, 19, 20]."

    Authors cite their own single-graph papers for contrast and for the low-rank/transitivity construction. This is ordinary background, not load-bearing: the multiview shared-ξ prior (eq. 4), the joint posterior, and Theorems 3.1–3.2 are derived and proved in the present paper under new assumptions; no uniqueness theorem from the self-citations is invoked to force the multiview result.

full rationale

The central claims (Theorem 3.1 Hellinger consistency of the posterior predictive under Assumptions (A)–(G); finite-sample MSE/AUC superiority of JL vs IL/TL) do not reduce by construction to their inputs. The model (eqs. 1–4) is a hierarchical GLM with low-rank graph coefficients and a shared spike-and-slab on node latents; the theorems prove posterior concentration for that class under external growth/sparsity conditions on Kn, Rn, sn and the true low-rank coefficients (Assumptions A–G), using standard techniques (Hellinger balls, prior mass, testing) whose proofs appear self-contained in Appendix A and cite external results (Ghosal–van der Vaart, Jiang). Simulations generate data from the same shared-ξ / correlated-latent mechanism that defines the prior, so JL is correctly specified while IL is not; the reported gains are therefore expected under correct specification, not a fitted parameter renamed as a prediction. Mild self-citations of the authors’ prior single-graph work ([19,21,23,20]) supply background motivation and contrast, but the multiview joint prior, the shared-ξ construction, and the multiview consistency theorems are new and do not rest on an unverified uniqueness claim imported from those papers. The shared-ξ assumption is a modeling choice whose misspecification risk is real (as the skeptic notes) but is a correctness/robustness issue, not circularity of the derivation. Score 1 reflects only the ordinary background self-citation; the derivation chain itself is independent.

Assumptions & free parameters 5 free parameters · 5 assumptions · 2 invented entities

The central claims rest on a low-rank graph-coefficient factorization, a shared-across-views spike-and-slab, GLM link families, and asymptotic growth/sparsity conditions. Free hyperparameters (rank R, Dirichlet ω, beta b_η, IW ν, IG error priors) and the modeling choice that node activity is common to all views are load-bearing. No new physical entities; invented structure is the joint prior and multiview low-rank coefficient construction.

free parameters (5)
  • Fitted latent rank R (R_n)
    User-chosen dimension of node latents; theory requires R_n ≥ true ranks and R_n K_n ≺ n/log(n). Simulations use R > R^(0); application rank not tightly constrained by asymptotics.
  • Spike-and-slab hyperparameter b_η
    Beta(1,b_η) multiplicity correction; Assumption (F) requires b_η s_n / K_n ≻ n, so the hyperparameter is tied to the consistency claim.
  • Dirichlet weight ω for λ^(r)_{p,m}
    Controls shrinkage of higher latent dimensions via E[|λ^(r)|]=2/(2+rω); chosen ω>1 to limit effective rank.
  • Inverse-Wishart ν and IG(a_σ,b_σ) for J_p and σ_m²
    Prior scale for cross-view latent covariance and continuous-edge noise; standard but free choices affecting finite-sample UQ.
  • Node-inclusion threshold 0.5 (median probability rule)
    Used in §6 to declare 88 ROIs associated with MMSE; affects scientific conclusions though not the asymptotic theorems.
assumptions (5)
  • domain assumption True and fitted graph coefficients admit low-rank factorizations with R_n ≥ R^*_{n,m} (Assumptions B–C, eq. 3).
    Parsimony and transitivity of edge coefficients; if true associations are full-rank unstructured, the model is misspecified.
  • ad hoc to paper Node activity indicators ξ_{p,k} are shared across all M views (eq. 4).
    Enables joint selection and coupling; not implied by multiview data alone and is the main joint-modeling restriction.
  • domain assumption R_n K_n ≺ n/log(n) and related sparsity growth b_η s_n/K_n ≻ n (Assumptions A, F).
    Required for Theorems 3.1–3.2; may fail in high-K neuroimaging samples.
  • standard math Edges follow GLM densities with link derivatives satisfying Assumption (E); continuous case uses i.i.d. Gaussian errors for Thm 3.2.
    Standard exponential-family regression setup for predictive Hellinger consistency.
  • domain assumption Covariates are bounded |x|≤a_0 (Assumption G); no self-loops; undirected symmetry of each view.
    Technical and structural conditions used throughout model and proofs.
invented entities (2)
  • Joint multiview node-latent vector β̃_{p,k} with shared spike-and-slab and IW covariance J_p across views
    purpose: Couples graph views and selects nodes jointly for each key predictor.
    Core modeling device of the paper; independent evidence is only indirect via simulation recovery and fMRI interpretability, not external validation of the shared-activity mechanism.
  • Discrete λ^{(r)}_{p,m} ∈ {-1,0,1} with Dirichlet(rω,1,1) for effective rank control
    purpose: Prevent overfitting of the user-chosen rank R while keeping low-rank Γ_{p,m}.
    Ad hoc shrinkage device; not a physical entity, but a paper-specific prior construction without external falsifiable prediction.

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Cite this review

Pith. "Pith review of Multiview Graph Fusion with Covariates." pith.science (2026). https://pith.science/paper/O2FFV7VG

@misc{pith2026260322215,
  author       = {Pith},
  title        = {Pith review of: Multiview Graph Fusion with Covariates},
  year         = {2026},
  howpublished = {\url{https://pith.science/paper/O2FFV7VG}},
  note         = {Machine review of arXiv:2603.22215}
}
read the original abstract

Joint modeling of multiview graphs with a common set of nodes between views and auxiliary predictors is an essential, yet less explored, area in statistical methodology. Traditional approaches often treat graphs in different views as independent or fail to adequately incorporate predictors, potentially missing complex dependencies within and across graph views and leading to reduced inferential accuracy. Motivated by such methodological shortcomings, we introduce an integrative Bayesian approach for joint learning of a multiview graph with vector-valued predictors. Our modeling framework assumes a common set of nodes for each graph view while allowing for diverse interconnections or edge weights between nodes across graph views, accommodating both binary and continuous valued edge weights. By adopting a hierarchical Bayesian modeling approach, our framework seamlessly integrates information from diverse graphs through carefully designed prior distributions on model parameters. This approach enables the estimation of crucial model parameters defining the relationship between these graph views and predictors, as well as offers predictive inference of the graph views. Crucially, the approach provides uncertainty quantification in all such inferences. Theoretical analysis establishes that the posterior predictive density for our model asymptotically converges to the true data-generating density, under mild assumptions on the true data-generating density and the growth of the number of graph nodes relative to the sample size. Simulation studies validate the inferential advantages of our approach over predictor-dependent tensor learning and independent learning of different graph views with predictors. We further illustrate model utility by analyzing functional connectivity graphs in neuroscience under cognitive control tasks, relating task-related brain connectivity with phenotypic measures.

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Reference graph

Works this paper leans on

59 extracted references · 1 linked inside Pith

  1. [1]

    R., Snyder, A

    Andrews-Hanna, J. R., Snyder, A. Z., Vincent, J. L., Lustig, C., Head, D., Raichle, M., and Buckner, R. L. (2007). Disruption of large-scale brain systems in advanced aging. Neuron,56(5), 924–935

  2. [2]

    W., Murray, J

    Anticevic, A., Cole, M. W., Murray, J. D., Corlett, P. R., Wang, X.-J., and Krystal, J. H. (2012). The role of default network deactivation in cognition and disease.Trends in Cognitive Sciences,16(12), 584–592

  3. [3]

    Barbieri, M. M. and Berger, J. O. (2004). Optimal predictive model selection.The Annals of Statistics,32(3), 870–897

  4. [4]

    and Sporns, O

    Bullmore, E. and Sporns, O. (2009). Complex brain networks: graph theoretical analysis of structural and functional systems.Nature Reviews. Neuroscience,10(3), 186–198

  5. [5]

    Cabeza, R., Albert, M., Belleville, S., Craik, F. I. M., Duarte, A., Grady, C. L., Linden- berger, U., Nyberg, L., Park, D. C., Reuter-Lorenz, P. A., Rugg, M. D., Steffener, J., and Rajah, M. N. (2018). Maintenance, reserve and compensation: the cognitive neuroscience of healthy ageing.Nature Reviews Neuroscience,19(11), 701–710

  6. [6]

    Y., Park, D

    Chan, M. Y., Park, D. C., Savalia, N. K., Petersen, S. E., and Wig, G. S. (2014). Decreased segregation of brain systems across the healthy adult lifespan.Proceedings of the National Academy of Sciences,111(46), E4997–E5006

  7. [7]

    and Huang, J

    Chen, L. and Huang, J. Z. (2012). Sparse reduced-rank regression for simultaneous di- mension reduction and variable selection.Journal of the American Statistical Association, 107(500), 1533–1545. 26

  8. [8]

    Cheng, J., Levina, E., Wang, P., and Zhu, J. (2014). A sparse ising model with covariates. Biometrics,70(4), 943–953

Show all 59 references
  1. [9]

    W., Raamana, P., Spring, R., and Strother, S

    Churchill, N. W., Raamana, P., Spring, R., and Strother, S. C. (2017). Optimizing fmri preprocessing pipelines for block-design tasks as a function of age.NeuroImage,154, 240–254

  2. [10]

    Coombes, B., Basu, S., Guha, S., and Schork, N. (2015). Weighted score tests imple- menting model-averaging schemes in detection of rare variants in case-control studies.Plos one,10(10), e0139355

  3. [11]

    and Shulman, G

    Corbetta, M. and Shulman, G. L. (2002). Control of goal-directed and stimulus-driven attention in the brain.Nature Reviews Neuroscience,3(3), 201–215

  4. [12]

    Danaher, P., Wang, P., and Witten, D. M. (2014). The joint graphical lasso for inverse covariance estimation across multiple classes.Journal of the Royal Statistical Society Series B: Statistical Methodology,76(2), 373–397

  5. [13]

    Dolcos, F., Denkova, E., and Dolcos, S. (2012). Neural correlates of emotional memories: A review of evidence from brain imaging studies.Psychologia,55(2), 80–111

  6. [14]

    Mini-mental state

    Folstein, M. F., Folstein, S. E., and McHugh, P. R. (1975). “Mini-mental state”: A practical method for grading the cognitive state of patients for the clinician.Journal of Psychiatric Research,12(3), 189–198

  7. [15]

    Fosdick, B. K. and Hoff, P. D. (2015). Testing and modeling dependencies between a network and nodal attributes.Journal of the American Statistical Association,110(511), 1047–1056

  8. [16]

    K., and Chen, K

    Goh, G., Dey, D. K., and Chen, K. (2017). Bayesian sparse reduced rank multivariate regression.Journal of multivariate analysis,157, 14–28. 27

  9. [17]

    and Murphy, T

    Gollini, I. and Murphy, T. B. (2016). Joint modeling of multiple network views.Journal of Computational and Graphical Statistics,25(1), 246–265

  10. [18]

    L., Protzner, A

    Grady, C. L., Protzner, A. B., Kovacevic, N., Strother, S. C., Afshin-Pour, B., Wojtow- icz, M., Anderson, J. A. E., Churchill, N., and McIntosh, A. R. (2010). A multivariate analysis of age-related differences in default mode and task-positive networks across mul- tiple cogni...

  11. [19]

    and Guhaniyogi, R

    Guha, S. and Guhaniyogi, R. (2021). Bayesian generalized sparse symmetric tensor-on- vector regression.Technometrics,63(2), 160–170

  12. [20]

    and Guhaniyogi, R

    Guha, S. and Guhaniyogi, R. (2023). Covariate-dependent clustering of undirected networks with brain-imaging data. Technical report

  13. [21]

    and Guhaniyogi, R

    Guha, S. and Guhaniyogi, R. (2024). Covariate-dependent clustering of undirected networks with brain-imaging data.Technometrics, pages 1–23

  14. [22]

    and Rodriguez, A

    Guha, S. and Rodriguez, A. (2021). Bayesian regression with undirected network pre- dictors with an application to brain connectome data.Journal of the American Statistical Association,116(534), 581–593

  15. [23]

    and Rodriguez, A

    Guha, S. and Rodriguez, A. (2023). High-dimensional bayesian network classification with network global-local shrinkage priors.Bayesian Analysis,1(1), 1–30

  16. [24]

    Guha, S., Rodriguez-Acosta, J., and Dinov, I. D. (2024). A bayesian multiplex graph classifier of functional brain connectivity across diverse tasks of cognitive control.Neu- roinformatics,22(4), 457–472

  17. [25]

    and Rodriguez, A

    Guhaniyogi, R. and Rodriguez, A. (2020). Joint modeling of longitudinal relational data and exogenous variables.Bayesian Analysis,15(2), 477–503

  18. [26]

    and Spencer, D

    Guhaniyogi, R. and Spencer, D. (2021). Bayesian tensor response regression with an application to brain activation studies.Bayesian Analysis,16(4), 1221–1249. 28

  19. [27]

    Guhaniyogi, R., Qamar, S., and Dunson, D. B. (2017). Bayesian tensor regression. Journal of Machine Learning Research,18(79), 1–31

  20. [28]

    Guo, J., Levina, E., Michailidis, G., and Zhu, J. (2011). Joint estimation of multiple graphical models.Biometrika,98(1), 1–15

  21. [29]

    Lee, I., Sinha, D., Mai, Q., Zhang, X., and Bandyopadhyay, D. (2023). Bayesian regres- sion analysis of skewed tensor responses.Biometrics,79(3), 1814–1825

  22. [30]

    Liu, H., Chen, X., Wasserman, L., and Lafferty, J. (2010). Graph-valued regression. Advances in Neural Information Processing Systems,23

  23. [31]

    Lukemire, J., Kundu, S., Pagnoni, G., and Guo, Y. (2021). Bayesian joint modeling of multiple brain functional networks.Journal of the American Statistical Association, 116(534), 518–530

  24. [32]

    S., Cummings, J

    Mega, M. S., Cummings, J. L., Fiorello, T., and Gornbein, J. (1996). The spectrum of behavioral changes in alzheimer’s disease.Neurology,46(1), 130–135

  25. [33]

    Niu, Y., Ni, Y., Pati, D., and Mallick, B. K. (2023). Covariate-assisted bayesian graph learning for heterogeneous data.Journal of the American Statistical Association, pages 1–15

  26. [34]

    C., Polk, T

    Park, D. C., Polk, T. A., Park, R., Minear, M., Savage, A., and Smith, M. R. (2004). Aging reduces neural specialization in ventral visual cortex.Proceedings of the National Academy of Sciences,101(35), 13091–13095

  27. [35]

    Pessoa, L. (2008). On the relationship between emotion and cognition.Nature Reviews Neuroscience,9(2), 148–158

  28. [36]

    C., and Vannucci, M

    Peterson, C., Stingo, F. C., and Vannucci, M. (2015). Bayesian inference of multiple gaussian graphical models.Journal of the American Statistical Association,110(509), 159–174. 29

  29. [37]

    and Kadri, H

    Rabusseau, G. and Kadri, H. (2016). Low-rank regression with tensor responses.Ad- vances in Neural Information Processing Systems,29

  30. [38]

    R., Baracchini, G., Nichol, D., Abdi, H., and Grady, C

    Rieck, J. R., Baracchini, G., Nichol, D., Abdi, H., and Grady, C. L. (2021). Recon- figuration and dedifferentiation of functional networks during cognitive control across the adult lifespan.Neurobiology of Aging,106, 80–94

  31. [39]

    Rodriguez-Acosta, J., Guha, S., Gailliot, S., and Williams, A. (2025). Supervised learn- ing with inter- and intra-dependence in multilayer networks with applications in security systems analysis.Technometrics,0(0), 1–14

  32. [40]

    J., Levina, E., and Zhu, J

    Rothman, A. J., Levina, E., and Zhu, J. (2010). Sparse multivariate regression with covariance estimation.Journal of Computational and Graphical Statistics,19(4), 947–962

  33. [41]

    J., Bullmore, E

    Rubia, K., Russell, T., Overmeyer, S., Brammer, M. J., Bullmore, E. T., Sharma, T., Simmons, A., Williams, S. C., Giampietro, V., Andrew, C. M., and Taylor, E. (2001). Map- ping motor inhibition: Conjunctive brain activations across different versions of go/no-go and stop task...

  34. [42]

    Samanez-Larkin, G. R. and Knutson, B. (2015). Decision making in the ageing brain: changes in affective and motivational circuits.Nature Reviews Neuroscience,16(5), 278– 289

  35. [43]

    M., Laumann, T

    Schaefer, A., Kong, R., Gordon, E. M., Laumann, T. O., Zuo, X.-N., Holmes, A. J., Eickhoff, S. B., and Yeo, B. T. (2018). Local-global parcellation of the human cerebral cortex from intrinsic functional connectivity mri.Cerebral cortex,28(9), 3095–3114

  36. [44]

    Shen, X., Zhang, H., Li, L., Yang, W., and Liu, L. (2022). Semi-supervised cross-modal hashing with multi-view graph representation.Information Sciences,604, 45–60

  37. [45]

    Spencer, D., Guhaniyogi, R., and Prado, R. (2020). Joint bayesian estimation of voxel 30 activation and inter-regional connectivity in fmri experiments.psychometrika,85, 845– 869

  38. [46]

    N., Stevens, W

    Spreng, R. N., Stevens, W. D., Viviano, J. D., and Schacter, D. L. (2016). Attenuated anticorrelation between the default and dorsal attention networks with aging: evidence from task and rest.Neurobiology of Aging,45, 149–160

  39. [47]

    Sun, D., Li, D., Ding, Z., Zhang, X., and Tang, J. (2022). A2ae: Towards adaptive multi-view graph representation learning via all-to-all graph autoencoder architecture. Applied Soft Computing,125, 109193

  40. [48]

    and Logan, G

    Verbruggen, F. and Logan, G. D. (2008). Response inhibition in the stop-signal paradigm.Trends in Cognitive Sciences,12(11), 418–424

  41. [49]

    J., and Fink, G

    Vossel, S., Geng, J. J., and Fink, G. R. (2014). Dorsal and ventral attention systems: Distinct neural circuits but collaborative roles.The Neuroscientist,20(2), 150–159. PMID: 23835449

  42. [50]

    Wang, P., Robins, G., Pattison, P., and Lazega, E. (2013). Exponential random graph models for multilevel networks.Social networks,35(1), 96–115

  43. [51]

    Wei, Y., Lei, F., Zhang, Y., Zhao, J., and Liu, K. (2023). Multi-view graph rep- resentation learning for answering hybrid numerical reasoning question.arXiv preprint arXiv:2305.03458

  44. [52]

    Xiao, S., Li, J., Lu, J., Huang, S., Zeng, B., and Wang, S. (2024). Graph neural networks for multi-view learning: a taxonomic review.Artificial Intelligence Review,57(12), 341. 31 Supplementary File: Multiview Graph Fusion with Covariates Abstract This supplementary material ...

  45. [54]

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  46. [55]

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  47. [56]

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  48. [57]

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  49. [58]

    and Van Der Vaart, A

    Ghosal, S. and Van Der Vaart, A. (2007). Convergence rates of posterior distributions for noniid observations.������ �� ����������,��(1), 192–223

  50. [59]

    Guhaniyogi, R., Qamar, S., and Dunson, D. B. (2017). Bayesian tensor regression. ������� �� ������� �������� ��������,��(79), 1–31

  51. [60]

    Jiang, W. (2007). Bayesian variable selection for high dimensional generalized linear models: Convergence rates of the fitted densities.������ �� ����������,��(4), 1487 – 1511. 15

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Reviewed July 13, 2026 · model on record in the stance chip above.