arXiv subjects

Theodore J. LaGrow

Publications and source records attributed to Theodore J. LaGrow.

3 recordsLinked to original sources

arXiv2026

Label Agreement Does Not Measure Authorization

Many groups now delegate label ontology and metadata harmonization to agentic LLM pipelines. We built one and audited it. Our aggregate scores looked healthy, but the pipeline kept failing in ways they did not show, so we set out to find what they hid. Label agreement asks whether a proposed label matches a reference. It does not ask whether the agent was entitled to propose it, whether the output was complete enough to act on, or whether the label moved when the evidence moved. We measured those three separately on COBRE and FBIRN, two schizophrenia and control neuroimaging cohorts from different consortia, and they come apart, from label agreement and from each other. Showing the agent an upstream proposal barely moves label agreement, 0.857 to 0.870, while agreement on the chosen action doubles, 0.409 to 0.830. Output that parses as JSON still drops a required field on 10% of one model's cases and 33% of the other's. And an agent that replays its first answer scores perfectly on original cases and zero once we change the evidence that decides them. Downstream, a row-order error that none of these metrics reports erases most of the diagnostic signal. So we measure these properties apart, pair each with a control, and gate commitment on the result, which makes failures visible and easy to route to a person. None of this prevents failure. Our reference labels are rule-derived, so agreement with them means consistency, not correctness. Code is available at https://github.com/amir-sbg/Label-Agreement-Does-Not-Measure-Authorization.

cs.AI↗

arXiv2026

Architecture-Induced Recoverability Bias in Differentiable Symbolic Regression

Symbolic regression aims to recover closed-form expressions from numerical data, but in differentiable symbolic regression the recovered expression depends not only on the grammar but also on the fixed architecture through which variables are routed during training. This is relevant to signal-processing settings in which closed-form models and interpretable nonlinear structure are useful. This architecture-specific effect has rarely been isolated directly, because existing comparisons often vary architecture together with operator family, grammar, or search procedure. Three depth-3 architectures are compared across twenty-four operator--shape--leaf combinations, holding operator family, grammar, and training protocol fixed as far as possible while varying the variable-routing architecture. Recovery changes from $0/64$ to $64/64$ trials on the same target under an architecture-plus-native-training-protocol comparison. The best architecture on one target is the worst on another, and trees with two equal-depth subtrees fail in every configuration tested ($0/3{,}776$). As a proof-of-concept mitigation, a small architecture set is trained and the hardened expression with the lowest held-out RMSE is selected. On the jointly-run subset, this improves recovery from $34.4\%$ for the only architecture present in all three configurations to $50.1\%$. On a Shockley diode target, the validation selector recovers cases missed by that baseline architecture, which by itself recovers $0/32$ seeds. Since the jointly-run subset contains only three configurations, the selector result is evidence that validation-based architecture selection is promising, not a complete benchmark. These results support treating architecture as a measurable design variable that should be reported, stress-tested, and selected using held-out validation rather than fixed a priori.

cs.NE↗

arXiv2022

Functional Connectivity of the Brain Across Rodents and Humans

Resting-state functional magnetic resonance imaging (rs-fMRI), which measures the spontaneous fluctuations in the blood oxygen level-dependent (BOLD) signal, is increasingly utilized for the investigation of the brain's physiological and pathological functional activity. Rodents, as a typical animal model in neuroscience, play an important role in the studies that examine the neuronal processes that underpin the spontaneous fluctuations in the BOLD signal and the functional connectivity that results. Translating this knowledge from rodents to humans requires a basic knowledge of the similarities and differences across species in terms of both the BOLD signal fluctuations and the resulting functional connectivity. This review begins by examining similarities and differences in anatomical features, acquisition parameters, and preprocessing techniques, as factors that contribute to functional connectivity. Homologous functional networks are compared across species, and aspects of the BOLD fluctuations such as the topography of the global signal and the relationship between structural and functional connectivity are examined. Time-varying features of functional connectivity, obtained by sliding windowed approaches, quasi-periodic patterns, and coactivation patterns, are compared across species. Applications demonstrating the use of rs-fMRI as a translational tool for cross-species analysis are discussed, with an emphasis on neurological and psychiatric disorders. Finally, open questions are presented to encapsulate the future direction of the field.

q-bio.NC↗