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Majid Lotfian Delouee

Publications and source records attributed to Majid Lotfian Delouee.

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A Correspondence Score for Validating Learned Patient Representations in Clinical Tabular Data

Identifying patients with similar clinical characteristics is important for cohort discovery, clinical decision support, and personalized medicine. However, it is unclear whether learned patient representations preserve the similarities present in the original clinical data. We propose a correspondence score to directly assess how well these relationships are preserved, independently of labeled outcomes. The score combines complementary relationship-preservation metrics, with dataset-specific weights estimated through Bayesian optimization. We evaluated the approach on four complete blood count datasets using representations generated by five tabular foundation models and six classical transformation methods. Correspondence differed substantially across methods and representation dimensionalities. Patient relationships were generally best preserved at intermediate dimensionalities, while stronger reduction or expansion introduced greater deviations from the original data structure. Foundation models preserved correspondence more consistently than classical methods, with improvements ranging from approximately 5% to over 125%. The proposed score provides a way to evaluate representation quality before downstream use and supports informed selection of representation methods and dimensionalities.

q-bio.QM

A Comparative Framework for Evaluating Foundation Models on Tabular Data: A Case Study in Healthcare

Tabular data is the most common format in clinical practice, encompassing laboratory results, medication records, diagnostic codes, and patient demographics. As foundation models for tabular data have grown in number and variety, a practical question has become harder to answer: which model should a clinician or data scientist actually choose for a given task, and why? Existing surveys catalogue what these models can do, but they stop short of providing a structured way to compare them against the specific demands of a real application. We introduce \system{}, a comparative evaluation framework that scores and ranks tabular foundation models (TFMs) across six clinically meaningful dimensions: how well a model generalizes to new datasets, how effectively it protects patient privacy, how much data it needs to perform well, how it scales with growing datasets and feature spaces, how interpretable its predictions are to clinicians, and how fairly it performs across patient subgroups. Each dimension is broken down into measurable sub-components, and groups of sub-components can optionally be combined into supplementary compound scores, called super-metrics, that provide a diagnostic view of how a model performs across several dimensions simultaneously. To show how the framework works in practice, we apply it to two healthcare use cases, screening for iron deficiency and predicting heart failure, demonstrating how the same set of metrics leads to different model rankings depending on what matters most in each clinical context. We also provide a taxonomy of 45 TFMs organized by their underlying architecture, which serves as a reference for researchers and practitioners looking to navigate this rapidly expanding field.

cs.LG

From Latent Biomarkers to Clinical Rules: Embedding-Guided Rule Mining and Attribution-Based Translation for Interpretable Tabular Learning

Clinical decision support tools are most useful when accurate predictions are accompanied by understandable explanations. Rule-based models provide transparency, but rules derived directly from raw clinical measurements may miss patterns arising from interactions between multiple variables. We present a four-step pipeline that mines decision rules in the latent space of an FT-Transformer and translates them back into measurable clinical features. Embedding dimensions that consistently separate patient groups are treated as latent biomarkers, rules are mined using small decision trees, and selected rules are translated using gradient-input saliency and CLS attention attribution. We evaluate the framework on six public clinical and population health datasets at four embedding dimensions. Translated rules outperformed raw-feature rules in five of six datasets, with mean AUROC gains ranging from 0.04 to 0.23. On the heart disease dataset, embedding-space rules reached 0.98 AUROC, but translation reduced this to 0.72, showing that high-performing latent rules cannot always be represented by simple raw-feature conditions. These results show that latent-space rule discovery can uncover predictive patterns while translating them into clinically measurable features that can be evaluated by clinicians.

cs.LG

Embedding-Based Federated Learning with Runtime Governance for Iron Deficiency Prediction

Recent reviews find that the vast majority of published healthcare federated learning (FL) studies never reach real-world deployment. We developed an embedding-based FL pipeline for iron deficiency prediction from routine full blood count (FBC) data and deployed it across real institutional environments at Amsterdam University Medical Centre (AUMC) and NHS Blood and Transplant (NHSBT), two clinical environments that differ markedly in iron deficiency prevalence, ferritin distribution, and subject populations. A frozen domain-specific haematology foundation model, DeepCBC, performs site-local representation extraction, restricting federated training to a compact downstream classifier and substantially reducing recurrent communication relative to full-encoder federation. The two clinical datasets are structurally not independent and identically distributed (non-IID), with heterogeneity arising from distinct population differences rather than sampling artefacts. Runtime governance is enforced by FLA$^3$, a healthcare-oriented FL platform providing study-scoped execution, policy-based authorisation, and signed audit logging. Standard sample-size-weighted aggregation (FedAvg) reduced the area under the receiver operating characteristic curve (ROC-AUC) at both sites relative to local-only training, as the global update was biased towards the larger AUMC distribution. FedMAP, a personalised aggregation method, raised ROC-AUC from 0.9470 to 0.9594 at AUMC and from 0.8558 to 0.8671 at NHSBT relative to local-only training, achieving the highest macro ROC-AUC of 0.9133 and the best macro balanced accuracy overall. These results support personalised aggregation in clinical federations where client sample size and task relevance diverge substantially.

cs.LG