Evidence map›Paper›PMID 41902401›Full record

ArticleHGG advances2026

Investigations on transferability of polygenic risk scores depending on demography and dominance coefficients.

Leonie Fohler, Edita Latifi, Andreas Mayr, Carlo Maj, Christian Staerk, Hannah Klinkhammer, Peter M Krawitz

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Article in HGG advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Leonie FohlerInstitute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, 53127 Bonn, Germany.
Edita LatifiInstitute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, 53127 Bonn, Germany.
Andreas MayrInstitute for Medical Biometry and Statistics, Marburg University, 35043 Marburg, Germany.
Carlo MajCenter for Human Genetics, Marburg University, 35043 Marburg, Germany.
Christian StaerkIUF - Leibniz Research Institute for Environmental Medicine, 40225 Düsseldorf, Germany; Department of Statistics, TU Dortmund University, 44227 Dortmund, Germany.
Hannah KlinkhammerInstitute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, 53127 Bonn, Germany; Institute for Medical Biometry and Statistics, Marburg University, 35043 Marburg, Germany.
Peter M KrawitzInstitute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, 53127 Bonn, Germany. Electronic address: pkrawitz@uni-bonn.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genetic liability to a complex phenotype can be assessed using polygenic risk scores (PRSs) and is calculated as the sum of genotypes weighted by effect-size estimates derived from summary statistics of genome-wide association study (GWAS) data. Due to different allele frequencies (AFs) and linkage disequilibrium (LD) patterns across populations, PRSs developed in one population drop drastically in predictive performance when transferred to another. One of the major factors contributing to AF and LD heterogeneity is genetic drift, which acts strongly during population bottlenecks and is influenced by the dominance of certain alleles. In particular, because causal variants on empirical data are typically not known, the presence of population-specific LD patterns will strongly affect the transferability of PRS models. In this work, we therefore conducted demographic simulations to investigate the influence of the dominance coefficient on the transferability of PRSs among European, African, and Asian populations. By modifying the length and size of the bottleneck leading to the split of Eurasian and African populations, we gain a deeper understanding of the underlying dynamics. Finally, we illustrate that in our simulations, PRS models that are adapted to the underlying dominance coefficient can substantially increase the prediction performance in out-of-target populations.

Indexed as

Multifactorial InheritanceComputer SimulationDemographyGene FrequencyGenetic Predisposition to DiseaseGenetic Risk ScoreGenetics, PopulationGenome-Wide Association StudyHumansLinkage DisequilibriumModels, GeneticPolymorphism, Single Nucleotidedominance coefficientinfluence of demographic bottleneckspolygenic risk scorespopulation genetic simulationsPRStransferability of PRS

Identifiers

PMID41902401
PMCPMC13125173

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.