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Vitaveska Lanfranchi

Publications and source records attributed to Vitaveska Lanfranchi.

2 recordsLinked to original sources

On the Limits of Maximal Coding Rate Reduction for Out-of-Distribution Generalisation

Substantial efforts have been devoted to making deep learning objectives, representations, and architectures interpretable, with the goal of improving the safety, robustness, and generalisation of learning systems in diverse real-world applications. The recently proposed maximal coding rate reduction ($\mathrm{MCR}^{2}$) offers a promising information-theoretic framework for learning structured, discriminative representations of class-wise submanifolds and has inspired interpretable white-box architectures. However, we observe that $\mathrm{MCR}^{2}$ can completely fail under distribution shift, motivating our study of its out-of-distribution (OOD) generalisation limits. We establish two limitations of $\mathrm{MCR}^{2}$ for OOD generalisation. First, the $\mathrm{MCR}^{2}$ objective alone can admit complete prediction failure: a representation based entirely on unstable environmental features can achieve the global coding optimum yet fail completely after correlation reversal, despite an available perfectly stable feature. This exact-optimum example includes test inputs that cannot occur during training. Even when every possible test input can also occur during training, coding quality can be arbitrarily close to optimal while prediction error is arbitrarily close to 100%. Second, directly incorporating the invariance principle underlying widely successful invariant risk minimisation (IRM) and risk extrapolation (REx) does not eliminate this failure. The failing representation admits the same optimal coding operator across training environments, showing that shared coding optimality does not ensure stable prediction. Reliable OOD guarantees for $\mathrm{MCR}^{2}$ therefore require additional new assumptions or learning principles that establish stable predictive relationships across environments.

cs.LG

DeMMO: Longitudinal and Cross-Disease Modelling of Digital Mobility Outcomes via Multi-Task Learning

Digital mobility outcomes (DMOs) derived from wearable sensors characterise mobility in daily life and offer a promising means of monitoring disease progression. However, existing DMO studies have typically focused on either a single disease or a single visit. To the best of our knowledge, we are the first to define and study the practical problem of cross-disease longitudinal DMO modelling. We argue that this problem should satisfy at least two requirements. First, the temporal progression of DMOs should be modelled within each disease, as mobility-limiting diseases evolve over time. Second, multiple mobility-limiting diseases should be modelled jointly, as different diseases affect different aspects of human mobility. To address this problem, we propose DeMMO, an interpretable framework for longitudinal, multi-disease, and multi-outcome learning. Its central technical contribution is an interpretable cross-disease and cross-outcome relation-learning mechanism that infers signed relations directly from learned longitudinal DMO-outcome mappings, thereby enabling selective information sharing across cohorts without requiring paired participants. We evaluate DeMMO on the recently released, large-scale, multicentre Mobilise-D dataset, which presents a challenging modelling setting involving longitudinal observations, multiple clinical outcomes, and four participant-disjoint cohorts representing distinct mobility-limiting diseases. Compared with eight strong structural longitudinal and deep-regression baselines, DeMMO achieves the best overall predictive performance and outperforms the baselines for most individual outcomes. Stability selection further identifies reliable longitudinal DMO patterns that can inform subsequent clinical validation and disease monitoring. The implementation code is available at https://github.com/menghui-zhou/DeMMO.

cs.LG