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Open access Oct 2026

Decomposing polygenic risk of coronary artery disease into distinct biological processes

Standard polygenic risk scores capture overall genetic liability to coronary artery disease (CAD) but do not reveal the biological processes contributing to risk in an individual. Here, we applied data-driven latent factor decomposition to 526 genome-wide significant CAD-associated variants, using their associations wi...

J. Morze, K. Smith, M. Kierczak et al. · 0 citations
Open access Oct 2026

A national ecosystem for long-read genome sequencing: Integrating population genomics and rare disease diagnostics in Sweden

To evaluate the clinical implementation of long-read genome sequencing (lrGS) and establish the population reference resources needed to support its use in diagnostics, we integrate two complementary initiatives: Genome of Sweden (GoS), Sweden's contribution to Genome of Europe (GoE), and the Genomic Medicine Sweden -...

A. Ameur, F. Taylan, M. Ek et al. · 0 citations

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