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Elena Raffetti

Publications and source records attributed to Elena Raffetti.

2 recordsLinked to original sources

Distributed Lag Neural Additive Models

We introduce Distributed Lag Neural Additive Models (DLNAMs), neural-additive analogues of Distributed Lag Non-linear Models (DLNMs) for learning nonlinear effects distributed over lags. DLNAMs replace a prespecified spline cross-basis with neural components that learn exposure--lag response surfaces, avoiding choices of basis family, dimension, and knot placement while preserving additive interpretability and familiar distributed-lag summaries. Exp-centered input layers, smooth activations, and learned subnetwork mixtures produce smooth, locally adaptive representations; pointwise uncertainty combines a conditional last-layer Laplace approximation with between-member ensemble variation. In simulations, DLNAMs generally outperformed DLNM comparators, including penalized and treed variants, in recovering known response functions, with lower bias, stronger boundary recovery, and better-calibrated cumulative intervals; gains were largest for more demanding functions. The architecture performed consistently across sample sizes, outcome families, lag horizons, and jointly fitted multi-exposure settings, retaining recovery performance as exposures were added; fit-specific changes were largely confined to optimization, and applications recovered established empirical patterns.

stat.ML

Mendelian randomization in a multi-ancestry world: reflections and practical advice

Many Mendelian randomization (MR) papers have been conducted only in people of European ancestry, limiting transportability of results to the global population. Expanding MR to diverse ancestry groups is essential to ensure equitable biomedical insights, yet presents analytical and conceptual challenges. This review examines the practical challenges of MR analyses beyond the European only context, including use of data from multi-ancestry, mismatched ancestry, and admixed populations. We explain how apparent heterogeneity in MR estimates between populations can arise from differences in genetic variant frequencies and correlation patterns, as well as from differences in the distribution of phenotypic variables, complicating the detection of true differences in the causal pathway. We summarize published strategies for selecting genetic instruments and performing analyses when working with limited ancestry-specific data, discussing the assumptions needed in each case for incorporating external data from different ancestry populations. We conclude that differences in MR estimates by ancestry group should be interpreted cautiously, with consideration of how the identified differences may arise due to social and cultural factors. Corroborating evidence of a biological mechanism altering the causal pathway is needed to support a conclusion of differing causal pathways between ancestry groups.

q-bio.PE