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Erik Weis

Publications and source records attributed to Erik Weis.

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Identifying and Upweighting Power-Niche Users to Mitigate Popularity Bias in Recommendations

Recommender systems have been shown to exhibit popularity bias by over-recommending popular items and under-recommending relevant niche items. We seek to understand niche users in benchmark recommendation datasets as a step toward mitigating popularity bias. We find that, compared to mainstream users, niche-preferring users exhibit a longer-tailed activity-level distribution, indicating the existence of users who both prefer niche items and exhibit high activity levels on platforms. We partition users along two axes: (1) activity level ("power" vs. "light") and (2) item-popularity preference ("mainstream" vs. "niche"), and show that in three benchmark datasets, the number of power-niche users (high activity and niche preference) is statistically significantly larger than expected. We also find that interaction data from power-niche users is especially valuable for improving recommendations for not only niche but also mainstream users. In contrast, many existing popularity bias mitigation methods have focused on upweighting niche users regardless of activity level. Motivated by the value of power-niche user data, we propose PAIR (Popularity-and-Activity-Informed Reweighting), a framework for reweighting the Bayesian Personalized Ranking (BPR) loss that simultaneously reweights based on user activity level and item popularity, upweighting power-niche users the most. We instantiate the framework on both deep and shallow collaborative filtering models, and experiments on benchmark datasets show that PAIR reduces popularity bias and can increase overall performance. Although existing popularity-bias mitigation methods yield a trade-off between performance and bias, our results suggest that considering both user activity level and popularity preference leads to Pareto-dominant performance.

cs.IR

Message passing for epidemiological interventions on networks with loops

Spreading models capture key dynamics on networks, such as cascading failures in economic systems, (mis)information diffusion, and pathogen transmission. Here, we focus on design intervention problems -- for example, designing optimal vaccination rollouts or wastewater surveillance systems -- which can be solved by comparing outcomes under various counterfactuals. A leading approach to computing these outcomes is message passing, which allows for the rapid and direct computation of the marginal probabilities for each node. However, despite its efficiency, classical message passing tends to overestimate outbreak sizes on real-world networks, leading to incorrect predictions and, thus, interventions. Here, we improve these estimates by using the neighborhood message passing (NMP) framework for the epidemiological calculations. We evaluate the quality of the improved algorithm and demonstrate how it can be used to test possible solutions to three intervention design problems: influence maximization, optimal vaccination, and sentinel surveillance.

cs.SI

Characterization Of Diseases In Temporal Comorbidity Networks

Comorbidity networks, which capture disease-disease co-occurrence usually based on electronic health records, reveal structured patterns in how diseases cluster and progress across individuals. However, how these networks evolve across different age groups and how this evolution relates to properties like disease prevalence and mortality remains understudied. To address these issues, we used publicly available comorbidity networks extracted from a comprehensive dataset of 45 million Austrian hospital stays from 1997 to 2014, covering 8.9 million patients. These networks grow and become denser with age. We identified groups of diseases that exhibit similar patterns of structural centrality throughout the lifespan, revealing three dominant age-related components with peaks in early childhood, midlife, and late life. To uncover the drivers of this structural change, we examined the relationship between prevalence and degree. This allowed us to identify conditions that were disproportionately connected to other diseases. Using betweenness centrality in combination with mortality data, we further identified high-mortality bridging diseases. Several diseases show high connectivity relative to their prevalence, such as iron deficiency anemia (D50) in children, nicotine dependence (F17), and lipoprotein metabolism disorders (E78) in adults. We also highlight structurally central diseases with high mortality that emerge at different life stages, including cancers (C group), liver cirrhosis (K74), subarachnoid hemorrhage (I60), and chronic kidney disease (N18). These findings underscore the importance of targeting age-specific, network-central conditions with high mortality for prevention and integrated care.

physics.soc-ph