Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000595 65 65 Zhang J An ensemble penalized regression method for multi-ancestry polygenic risk prediction. Nat Commun 15/04/2024 10.1038/s41467-024-47357-7 38622117
PGP000545 2 2 Middha P Polygenic risk score for ulcerative colitis predicts immune checkpoint inhibitor-mediated colitis. Nat Commun 26/03/2024 10.1038/s41467-023-44512-4 38531883
PGP000604 158 158 Truong B Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. Cell Genom 12/03/2024 10.1016/j.xgen.2024.100523 38508198
PGP000603 2 2 Loginovic P Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritis. Nat Commun 28/02/2024 10.1038/s41467-024-44917-9 38418465
PGP000602 3 3 Smith JL Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization. Circ Genom Precis Med 21/02/2024 10.1161/circgen.123.004272 38380516
PGP000561 252 252 Jung H Integration of risk factor polygenic risk score with disease polygenic risk score for disease prediction. Commun Biol 13/02/2024 10.1038/s42003-024-05874-7 38351177
PGP000596 8 8 Hu J Using clinical and genetic risk factors for risk prediction of 8 cancers in the UK Biobank. JNCI Cancer Spectr 01/02/2024 10.1093/jncics/pkae008 38366150
PGP000562 3 3 Youssef O High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases. Lab Invest 15/01/2024 10.1016/j.labinv.2024.100325 38220043
PGP000563 4 4 Yang Z Genetic Basis of Altered Platelet Counts and Gestational Thrombocytopenia in Pregnancy. Blood 08/12/2023 10.1182/blood.2023021925 38064665
PGP000610 0 1 Wang JR Association of Polygenic Score With Tumor Molecular Subtypes in Papillary Thyroid Carcinoma. J Clin Endocrinol Metab 01/12/2023 10.1210/clinem/dgad407 37453101
PGP000517 184 184 Monti M R Evaluation of polygenic scoring methods in five biobanks reveals greater variability between biobanks than between methods and highlights benefits of ensemble learning medRxivPre 16/11/2023 10.1101/2023.11.20.23298215 —
PGP000516 0 1 Soh P X.Y. Prostate cancer genetic risk and associated aggressive disease in men of African ancestry Nature Communications 16/11/2023 10.1038/s41467-023-43726-w 38052806
PGP000515 1 1 Tamlander M Genome-wide polygenic risk scores for colorectal cancer have implications for risk-based screening Br J Cancer 13/11/2023 10.1038/s41416-023-02536-z 38172535
PGP000553 0 1 Mao X Prediction of breast cancer risk for sisters of women attending screening. J Natl Cancer Inst 01/11/2023 10.1093/jnci/djad101 37243694
PGP000501 26 26 Shim I Clinical utility of polygenic scores for cardiometabolic disease in Arabs. Nature Communications 18/10/2023 10.1038/s41467-023-41985-1 37852978
PGP000518 2 2 Wei X Development and evaluation of a polygenic risk score for lung cancer in never-smoking women: A large-scale prospective Chinese cohort study. Int J Cancer 17/10/2023 10.1002/ijc.34765 37846649
PGP000513 2 2 Roychowdhury T Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target. Nat Genet 16/10/2023 10.1038/s41588-023-01510-y 37845353
PGP000512 2 2 Shetty NS Sex Differences in the Association of Genome-Wide Systolic Blood Pressure Polygenic Risk Score With Hypertension. Circ Genom Precis Med 09/10/2023 10.1161/circgen.123.004259 37807951
PGP000608 2 2 Zheng SL Genome-wide association analysis reveals insights into the molecular etiology underlying dilated cardiomyopathy medRxivPre 29/09/2023 10.1101/2023.09.28.23295408 —
PGP000489 82 82 Zhang H A new method for multiancestry polygenic prediction improves performance across diverse populations. Nat Genet 25/09/2023 10.1038/s41588-023-01501-z 37749244
PGP000502 60 60 Tanigawa Y Power of inclusion: Enhancing polygenic prediction with admixed individuals AJHG 19/09/2023 10.1016/j.ajhg.2023.09.013 37890495
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 —
PGP000503 6 6 Sofer T A polygenic risk score for Alzheimer's disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. Alzheimers Res Ther 30/08/2023 10.1186/s13195-023-01298-3 37649099
PGP000488 2 2 Wang A W Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants Nature Genetics 21/08/2023 10.1038/s41588-023-01534-4 37945903
PGP000514 5 5 Hassanin E Trans-ancestry polygenic models for the prediction of LDL blood levels: An analysis of the UK Biobank and Taiwan Biobank medRxivPre 06/08/2023 10.1101/2023.08.03.23293320 —
PGP000605 1 1 Deutsch AJ Type 2 Diabetes Polygenic Score Predicts the Risk of Glucocorticoid-Induced Hyperglycemia in Patients Without Diabetes. Diabetes Care 01/08/2023 10.2337/dc23-0353 37353344
PGP000600 0 1 Hendi NN The Genetic Architecture of Vitamin D Deficiency among an Elderly Lebanese Middle Eastern Population: An Exome-Wide Association Study. Nutrients 20/07/2023 10.3390/nu15143216 37513634
PGP000520 55 50 Raben TG Biobank-scale methods and projections for sparse polygenic prediction from machine learning. Sci Rep 19/07/2023 10.1038/s41598-023-37580-5 37468507
PGP000609 1 1 Sleiman PM Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study. Alzheimers Dement 14/07/2023 10.1002/alz.13378 37450379
PGP000509 1 1 Barnado A Phenotype Risk Score but Not Genetic Risk Score Aids in Identifying Individuals With Systemic Lupus Erythematosus in the Electronic Health Record. Arthritis Rheumatol 12/07/2023 10.1002/art.42544 37096581
PGP000511 1 1 Rasooly D Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure. Nat Commun 10/07/2023 10.1038/s41467-023-39253-3 37429843
PGP000599 0 9 Guarischi-Sousa R Contemporary Polygenic Scores of Low-Density Lipoprotein Cholesterol and Coronary Artery Disease Predict Coronary Atherosclerosis in Adolescents and Young Adults. Circ Genom Precis Med 06/07/2023 10.1161/circgen.122.004047 37409455
PGP000466 3 3 Patel AP A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease. Nat Med 06/07/2023 10.1038/s41591-023-02429-x 37414900
PGP000598 1 1 Wang X Low-level ambient sulfur dioxide exposure and genetic susceptibility associated with incidence of idiopathic pulmonary fibrosis: A national prospective cohort study. Chemosphere 04/07/2023 10.1016/j.chemosphere.2023.139362 37414299
PGP000487 1 1 Scammell BH Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration. Hum Mol Genet 29/06/2023 10.1093/hmg/ddad101 37384397
PGP000597 0 1 Shi Z Cancer-associated thrombosis by cancer sites and inherited factors in a prospective population-based cohort. Thromb Res 26/06/2023 10.1016/j.thromres.2023.06.023 37419004
PGP000464 132 132 Liu N Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Nat Genet 19/06/2023 10.1038/s41588-023-01425-8 37337106
PGP000583 0 1 Dueñas N Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome. J Med Genet 15/06/2023 10.1136/jmg-2023-109344 37321833
PGP000591 2 2 Wang X Genetic Susceptibility to Atrial Fibrillation Identified via Deep Learning of 12-Lead Electrocardiograms. Circ Genom Precis Med 06/06/2023 10.1161/circgen.122.003808 37278238
PGP000585 2 2 Hawkes G Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood. Diabetologia 06/06/2023 10.1007/s00125-023-05923-6 37280435
PGP000592 1 1 Wu Y 150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility. Cell Genom 05/06/2023 10.1016/j.xgen.2023.100326 37492107
PGP000587 0 1 Luo M Accelerometer-measured intensity-specific physical activity, genetic risk and incident type 2 diabetes: a prospective cohort study. Br J Sports Med 05/06/2023 10.1136/bjsports-2022-106653 37277158
PGP000573 0 1 Niedermaier T A single measurement of fecal hemoglobin concentration outperforms polygenic risk score in colorectal cancer risk assessment. Cancer Commun (Lond) 04/06/2023 10.1002/cac2.12448 37272255
PGP000510 8 2 Kurniansyah N Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups. Nat Commun 02/06/2023 10.1038/s41467-023-38990-9 37268629
PGP000412 2 2 Kachuri L Genetically adjusted PSA levels for prostate cancer screening. Nat Med 01/06/2023 10.1038/s41591-023-02277-9 37264206
PGP000557 1 1 Tan Q Gene-environment interaction in long-term effects of polychlorinated biphenyls exposure on glucose homeostasis and type 2 diabetes: The modifying effects of genetic risk and lifestyle. J Hazard Mater 01/06/2023 10.1016/j.jhazmat.2023.131757 37276697
PGP000536 0 2 Vassy JL Cardiovascular Disease Risk Assessment Using Traditional Risk Factors and Polygenic Risk Scores in the Million Veteran Program. JAMA Cardiol 01/06/2023 10.1001/jamacardio.2023.0857 37133828
PGP000519 0 1 Thomas NJ Age of Diagnosis Does Not Alter the Presentation or Progression of Robustly Defined Adult-Onset Type 1 Diabetes. Diabetes Care 01/06/2023 10.2337/dc22-2159 36802355
PGP000547 3 3 Bui A A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort. Front Genet 31/05/2023 10.3389/fgene.2023.1141010 37323656
PGP000462 3 3 Honigberg MC Polygenic prediction of preeclampsia and gestational hypertension. Nat Med 29/05/2023 10.1038/s41591-023-02374-9 37248299
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