ArticleJournal of the Royal Statistical Society. Series A, (Statistics in Society)2026
Incorporating external risk information with the Cox model under population heterogeneity: applications to trans-ancestry polygenic hazard scores.
Article in Journal of the Royal Statistical Society. Series A, (Statistics in Society), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- survkl: an R package for transfer-learning-based integrated Cox models.Bioinformatics advances · 2026Article
- Statistical construction of calibrated prediction intervals for polygenic score-based phenotype prediction.Nature genetics · 2025Article
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Authors and funding
8 authors.
Funding
Abstract
Polygenic hazard scores (PHS) designed for European ancestry (EUR) individuals provide ample information regarding risk discrimination. Incorporating such information can improve the performance of risk discrimination in the target small-sized non-EUR cohort. However, given that external EUR-based PHS and internal individual-level data come from different populations, ignoring population heterogeneity can introduce substantial bias. In this article, we develop a Kullback-Leibler-based Cox model (CoxKL) to integrate internal individual-level time-to-event data with external risk scores derived from published prediction models. Partial-likelihood-based KL information is utilized to measure the discrepancy between the external risk information and the internal data. We establish the asymptotic properties of the CoxKL estimator. Simulation studies show that the integration model by the proposed CoxKL method achieves improved estimation efficiency and prediction accuracy. We apply the proposed method to develop transancestry PHS models for prostate cancer and breast cancer and find that integrating EUR-based PHS with internal genotype data of African ancestry individuals yields considerable improvement on the cancer risk discrimination.
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