PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000008 0 2 Wünnemann F Validation of Genome-Wide Polygenic Risk Scores for Coronary Artery Disease in French Canadians. Circ Genom Precis Med 11/06/2019 10.1161/CIRCGEN.119.002481 31184202
PGP000586 0 1 Khurshid S Predictive Accuracy of a Clinical and Genetic Risk Model for Atrial Fibrillation. Circ Genom Precis Med 31/08/2021 10.1161/circgen.121.003355 34463125
PGP000166 0 1 Marston NA Genetic Risk Score to Identify Risk of Venous Thromboembolism in Patients With Cardiometabolic Disease. Circ Genom Precis Med 12/01/2021 10.1161/circgen.120.003006 33434447
PGP000239 1 1 O'Sullivan JW Combining Clinical and Polygenic Risk Improves Stroke Prediction Among Individuals With Atrial Fibrillation. Circ Genom Precis Med 15/06/2021 10.1161/circgen.120.003168 34029116
PGP000270 2 2 Breeyear JH Blood Pressure Polygenic Scores Are Associated With Apparent Treatment-Resistant Hypertension. Circ Genom Precis Med 06/05/2022 10.1161/circgen.121.003554 35522175
PGP000327 1 1 Coassin S Genome-Wide Characterization of a Highly Penetrant Form of Hyperlipoprotein(a)emia Associated With Genetically Elevated Cardiovascular Risk. Circ Genom Precis Med 08/02/2022 10.1161/circgen.121.003489 35133173
PGP000143 0 1 Fahed AC Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease. Circ Genom Precis Med 07/12/2020 10.1161/circgen.120.003092 33284643
PGP000134 1 1 Lanfear DE Polygenic Score for β-Blocker Survival Benefit in European Ancestry Patients With Reduced Ejection Fraction Heart Failure. Circ Heart Fail 04/10/2020 10.1161/circheartfailure.119.007012 33012170
PGP000125 1 1 Marston NA Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients with Cardiometabolic Disease. Circulation 13/11/2020 10.1161/circulationaha.120.051927 33185476
PGP000060 0 1 Khera AV Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction. Circulation 01/03/2019 10.1161/circulationaha.118.035658 30586733
PGP000554 1 1 Marston NA Predicting Benefit From Evolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial. Circulation 11/11/2019 10.1161/circulationaha.119.043805 31707849
PGP000568 0 1 Khan SS Predictive Utility of a Validated Polygenic Risk Score for Long-Term Risk of Coronary Heart Disease in Young and Middle-Aged Adults. Circulation 26/07/2022 10.1161/circulationaha.121.058426 35880530
PGP000042 1 1 Natarajan P Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention Setting. Circulation 21/02/2017 10.1161/CIRCULATIONAHA.116.024436 28223407
PGP000159 1 1 Klarin D Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Circulation 28/09/2020 10.1161/circulationaha.120.047544 32981348
PGP000304 1 1 Nauffal V Monogenic and Polygenic Contributions to QTc Prolongation in the Population. Circulation 07/04/2022 10.1161/circulationaha.121.057261 35389749
PGP000175 1 1 Lahrouchi N Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Circulation 20/05/2020 10.1161/circulationaha.120.045956 32429735
PGP000022 1 1 Weng LC Genetic Predisposition, Clinical Risk Factor Burden, and Lifetime Risk of Atrial Fibrillation. Circulation 12/11/2017 10.1161/CIRCULATIONAHA.117.031431 29129827
PGP000377 0 1 Plym A Family history of prostate and breast cancer integrated with a polygenic risk score identifies men at highest risk of dying from prostate cancer before age 75 years. Clin Cancer Res 14/09/2022 10.1158/1078-0432.ccr-22-1723 36103261
PGP000204 2 2 Luo J Immunotherapy-mediated thyroid dysfunction: genetic risk and impact on outcomes with PD-1 blockade in non-small cell lung cancer. Clin Cancer Res 08/07/2021 10.1158/1078-0432.ccr-21-0921 34244291
PGP000184 1 1 Clark H Differential associations of allergic disease genetic variants with developmental profiles of eczema, wheeze and rhinitis. Clin Exp Allergy 15/10/2019 10.1111/cea.13485 31441980
PGP000217 0 1 De Vincentis A A Polygenic Risk Score to Refine Risk Stratification and Prediction for Severe Liver Disease by Clinical Fibrosis Scores. Clin Gastroenterol Hepatol 04/06/2021 10.1016/j.cgh.2021.05.056 34091049
PGP000319 0 1 Guo F Polygenic Risk Score for Defining Personalized Surveillance Intervals After Adenoma Detection and Removal at Colonoscopy. Clin Gastroenterol Hepatol 21/03/2022 10.1016/j.cgh.2022.03.013 35331942
PGP000579 1 1 Wu Y Systematic evaluation of narrow-sense validity of polygenic risk score for prostate cancer in a Chinese prostate biopsy cohort. Clin Genet 06/03/2023 10.1111/cge.14315 36840471
PGP000378 1 2 Schoepf IC Coronary Artery Disease-Associated and Longevity-Associated Polygenic Risk Scores for Prediction of Coronary Artery Disease Events in Persons Living With Human Immunodeficiency Virus: The Swiss HIV Cohort Study. Clin Infect Dis 01/11/2021 10.1093/cid/ciab521 34091660
PGP000507 1 1 Liu X The sulfur microbial diet and increased risk of obesity: Findings from a population-based prospective cohort study. Clin Nutr 17/03/2023 10.1016/j.clnu.2023.03.011 37003050
PGP000575 1 1 Oni-Orisan A Polygenic Risk Score and Statin Relative Risk Reduction for Primary Prevention of Myocardial Infarction in a Real-World Population. Clin Pharmacol Ther 24/08/2022 10.1002/cpt.2715 35862449
PGP000601 0 1 Niedermaier T Variation of Positive Predictive Values of Fecal Immunochemical Tests by Polygenic Risk Score in a Large Screening Cohort. Clin Transl Gastroenterol 19/01/2022 10.14309/ctg.0000000000000458 35060941
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
PGP000261 2 2 Tamlander M Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes. Commun Biol 23/02/2022 10.1038/s42003-021-02996-0 35197564
PGP000372 0 1 Clarke SL Broad clinical manifestations of polygenic risk for coronary artery disease in the Women's Health Initiative. Commun Med (Lond) 25/08/2022 10.1038/s43856-022-00171-y 36034645
PGP000238 4 4 Campos AI Understanding genetic risk factors for common side effects of antidepressant medications Commun Med (Lond) 09/11/2021 10.1038/s43856-021-00046-8 35602235
PGP000062 1 1 Qi Q Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). Diabetes 02/03/2017 10.2337/db16-1150 28254843
PGP000038 0 1 Patel KA Type 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 Diabetes. Diabetes 05/04/2016 10.2337/db15-1690 27207547
PGP000021 1 1 Song M Longitudinal Analysis of Genetic Susceptibility and BMI Throughout Adult Life. Diabetes 06/12/2017 10.2337/db17-1156 29212779
PGP000020 3 3 Vassy JL Polygenic type 2 diabetes prediction at the limit of common variant detection. Diabetes 11/02/2014 10.2337/db13-1663 24520119
PGP000290 0 1 Mordi IR Prediction of Major Adverse Cardiovascular Events From Retinal, Clinical, and Genomic Data in Individuals With Type 2 Diabetes: A Population Cohort Study. Diabetes Care 01/03/2022 10.2337/dc21-1124 35043139
PGP000580 1 1 Zhuang P Effect of Diet Quality and Genetic Predisposition on Hemoglobin A1C and Type 2 Diabetes Risk: Gene-Diet Interaction Analysis of 357,419 Individuals. Diabetes Care 25/08/2021 10.2337/dc21-1051 34433621
PGP000477 0 2 Deutsch AJ Polygenic Scores Help Reduce Racial Disparities in Predictive Accuracy of Automated Type 1 Diabetes Classification Algorithms. Diabetes Care 01/04/2023 10.2337/dc22-1833 36745605
PGP000014 1 2 Sharp SA Development and Standardization of an Improved Type 1 Diabetes Genetic Risk Score for Use in Newborn Screening and Incident Diagnosis. Diabetes Care 01/02/2019 10.2337/dc18-1785 30655379
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
PGP000013 1 2 Onengut-Gumuscu S Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score. Diabetes Care 18/01/2019 10.2337/dc18-1727 30659077
PGP000043 1 1 Morieri ML Genetic Tools for Coronary Risk Assessment in Type 2 Diabetes: A Cohort Study From the ACCORD Clinical Trial. Diabetes Care 27/09/2018 10.2337/dc18-0709 30262460
PGP000218 0 1 He Y Comparisons of Polyexposure, Polygenic, and Clinical Risk Scores in Risk Prediction of Type 2 Diabetes. Diabetes Care 09/02/2021 10.2337/dc20-2049 33563654
PGP000338 0 2 Oram RA Utility of Diabetes Type-Specific Genetic Risk Scores for the Classification of Diabetes Type Among Multiethnic Youth. Diabetes Care 01/05/2022 10.2337/dc20-2872 35312757
PGP000011 1 1 Oram RA A Type 1 Diabetes Genetic Risk Score Can Aid Discrimination Between Type 1 and Type 2 Diabetes in Young Adults. Diabetes Care 17/11/2015 10.2337/dc15-1111 26577414
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
PGP000342 1 1 Pezzilli S Contribution of rare variants in monogenic diabetes-genes to early-onset type 2 diabetes. Diabetes Metab 26/04/2022 10.1016/j.diabet.2022.101353 35487478
PGP000614 0 1 Qu HQ Combined application of genetic and polygenic risk scores for type 1 diabetes risk prediction. Diabetes Obes Metab 03/06/2021 10.1111/dom.14419 33950547
PGP000282 1 1 Wu Q An early prediction model for gestational diabetes mellitus based on genetic variants and clinical characteristics in China. Diabetol Metab Syndr 24/01/2022 10.1186/s13098-022-00788-y 35073990
PGP000445 3 3 Huerta-Chagoya A The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes. Diabetologia 06/05/2023 10.1007/s00125-023-05912-9 37148359