Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000724 7 7 Smit RAJ Polygenic prediction of body mass index and obesity through the life course and across ancestries. Nat Med 21/07/2025 10.1038/s41591-025-03827-z 40691366
PGP000752 1 1 Sutoh Y Genetic predisposition for immunoglobulin E production explains atopic risk in children: Tohoku Medical Megabank cohort study. Am J Hum Genet 15/07/2025 10.1016/j.ajhg.2025.06.015 40695273
PGP000746 1 1 Sun D Impact of genetic risk and lifestyles on cardiovascular disease-free and total life expectancy: a cohort study. Genome Med 22/07/2025 10.1186/s13073-025-01487-9 40696436
PGP000735 9 9 Foote IF Uncovering the multivariate genetic architecture of frailty with genomic structural equation modeling Nat Genet 04/08/2025 10.1038/s41588-025-02269-0 40759756
PGP000773 25 25 Huerta-Chagoya A Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries medRxivPre 23/07/2025 10.1101/2025.07.21.25331778 40778152
PGP000739 4 4 Arehart CH Modeling the genomic architecture of adiposity and anthropometrics across the lifespan. Nat Commun 13/08/2025 10.1038/s41467-025-62730-w 40796553
PGP000744 1 1 Olowofela AS Association of Genetic Predisposition to Inflammation With Cancer-Related Cognitive Impairment and Fatigue in Women Who Received Chemotherapy for Nonmetastatic Breast Cancer. JCO Precis Oncol 16/09/2025 10.1200/po-25-00303 40956996
PGP000750 3 3 Sarnowski C Association of genetic scores related to insulin resistance with neurological outcomes in ancestrally diverse cohorts from the Trans-Omics for Precision Medicine (TOPMed) program. Commun Biol 24/09/2025 10.1038/s42003-025-08674-9 40993182
PGP000770 7 2 Hrytsenko Y Obstructive sleep apnea mediates genetic risk of Diabetes Mellitus in Hispanic and Latino communities. Commun Med (Lond) 25/09/2025 10.1038/s43856-025-01107-y 40999017
PGP000759 20 20 Jordà P Genetic analyses across cardiovascular traits: leveraging genetic correlations to empower locus discovery and prediction in common cardiovascular diseases. NPJ Genom Med 29/09/2025 10.1038/s41525-025-00515-2 41022758
PGP000742 6 6 Guo B G Polygenic risk score for type 2 diabetes shows context-dependent effects across populations. Nat Commun 25/06/2025 10.1038/s41467-025-63546-4 41034193
PGP000769 1 1 Zhu J Plasma Proteomic Biomarkers Underlying Polygenic Risk of Idiopathic Pulmonary Fibrosis. Am J Respir Crit Care Med 28/10/2025 10.1164/rccm.202505-1202rl 41151026
PGP000757 1 1 Enzan N Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population. Nat Commun 03/11/2025 10.1038/s41467-025-64659-6 41184235
PGP000733 1 1 Rand SA Genome-wide association study and polygenic risk prediction of hypothyroidism. Nat Genet 14/11/2025 10.1038/s41588-025-02410-z 41238958
PGP000680 4 4 Barnes DR Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer. NPJ Genom Med 20/11/2025 10.1038/s41525-025-00529-w 41266372
PGP000760 6 6 Saklatvala JR Genetic liability to psoriasis predicts severe disease outcomes. Genome Med 17/12/2025 10.1186/s13073-025-01561-2 41408349
PGP000747 4 4 Kany S Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk. Nat Genet 19/12/2025 10.1038/s41588-025-02397-7 41419685
PGP000745 1 1 Small AM Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction. Nat Genet 19/12/2025 10.1038/s41588-025-02417-6 41419686
PGP000771 5 5 Tanha HM Performance of different polygenic risk scores for breast cancer risk prediction: in-depth evaluations across large UK and Australian cohorts. Eur J Hum Genet 13/01/2026 10.1038/s41431-025-02003-8 41526671
PGP000774 10 10 Li JL Improved polygenic risk prediction models for breast cancer subtypes in women of African ancestry. Nat Genet 02/02/2026 10.1038/s41588-026-02501-5 41629673
PGP000781 3 3 Qu HQ Sex specific genomic insights into type 1 diabetes through GWAS and single cell transcriptome analysis. Diabetes Res Clin Pract 20/02/2026 10.1016/j.diabres.2026.113181 41724362
PGP000790 8 8 Hu J Leveraging pleiotropy to improve genetic risk prediction across diseases. Genet Med 05/03/2026 10.1016/j.gim.2026.102548 41800596
PGP000693 16 16 Kim MS Metabolic polygenic risk scores for prediction of obesity, type 2 diabetes, and related morbidities. Cell Metab 16/03/2026 10.1016/j.cmet.2026.02.009 41844147
PGP000783 1 1 Chen H Optimizing colorectal cancer screening through polygenic risk score-based risk stratification: evidence from a population-based cohort and screening trial. Genome Med 19/03/2026 10.1186/s13073-026-01623-z 41851747
PGP000785 1 1 Trimarchi MP Multi-trait Analysis of GWAS Expands Eosinophilic Esophagitis Genetic Susceptibility and Polygenic Risk Scores. J Allergy Clin Immunol 20/03/2026 10.1016/j.jaci.2026.03.008 41865802
PGP000685 2 2 Yang X An integrated germline and somatic genomic model for coronary artery disease. Nat Commun 26/03/2026 10.1038/s41467-026-70379-2 41888514
PGP000461 10 10 Dahl A Phenotype integration improves power and preserves specificity in biobank-based genetic studies of MDD bioRxivPre 15/08/2022 10.1101/2022.08.15.503980 —
PGP000748 17 17 White SL Global multi-ancestry genetic study elucidates genes and biological pathways associated with thyroid cancer and benign thyroid diseases medRxivPre 16/05/2025 10.1101/2025.05.15.25327513 —
PGP000656 1 22 Ritchie SC Integrated clinical risk prediction of type 2 diabetes with a multifactorial polygenic risk score medRxivPre 22/08/2024 10.1101/2024.08.22.24312440 —
PGP000606 0 1 Szczerbinski L Algorithms for the identification of prevalent diabetes in the All of Us Research Program validated using polygenic scores - a new resource for diabetes precision medicine medRxivPre 05/09/2023 10.1101/2023.09.05.23295061 —
PGP000457 84 84 Ding Y Polygenic scoring accuracy varies across the genetic ancestry continuum in all human populations bioRxivPre 29/09/2022 10.1101/2022.09.28.509988 —
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