Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000048 2 2 Yang X Evaluation of polygenic risk scores for ovarian cancer risk prediction in a prospective cohort study. J Med Genet 05/05/2018 10.1136/jmedgenet-2018-105313 29730597
PGP000037 1 1 Lakeman IMM Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families. J Med Genet 11/06/2019 10.1136/jmedgenet-2019-106072 31186341
PGP000155 1 1 Bobbili DR Excess of singleton loss-of-function variants in Parkinson's disease contributes to genetic risk. J Med Genet 13/02/2020 10.1136/jmedgenet-2019-106316 32054687
PGP000197 1 1 Potjer TP Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma. J Med Genet 29/09/2020 10.1136/jmedgenet-2020-107251 32994281
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
PGP000148 1 1 Hung RJ Assessing Lung Cancer Absolute Risk Trajectory Based on a Polygenic Risk Model. Cancer Res 20/01/2021 10.1158/0008-5472.can-20-1237 33472890
PGP000413 14 14 Namba S Common germline risk variants impact somatic alterations and clinical features across cancers. Cancer Res 26/10/2022 10.1158/0008-5472.can-22-1492 36286845
PGP000620 3 3 Sun X Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants that Confer Risk for Breast Cancer. Cancer Res 04/06/2024 10.1158/0008-5472.can-23-3854 38832928
PGP000123 1 1 Kim J Genetic and Circulating Biomarker Data Improve Risk Prediction for Pancreatic Cancer in the General Population. Cancer Epidemiol Biomarkers Prev 22/04/2020 10.1158/1055-9965.epi-19-1389 32321713
PGP000616 0 1 Rosner B Simplified Breast Risk Tool Integrating Questionnaire Risk Factors, Mammographic Density, and Polygenic Risk Score: Development and Validation. Cancer Epidemiol Biomarkers Prev 04/12/2020 10.1158/1055-9965.epi-20-0900 33277321
PGP000251 1 1 Song N Polygenic Risk Score Improves Risk Stratification and Prediction of Subsequent Thyroid Cancer after Childhood Cancer. Cancer Epidemiol Biomarkers Prev 31/08/2021 10.1158/1055-9965.epi-21-0448 34465587
PGP000287 1 1 Testori A Genetic analysis in African American children supports ancestry specific neuroblastoma susceptibility. Cancer Epidemiol Biomarkers Prev 07/02/2022 10.1158/1055-9965.epi-21-0782 35131881
PGP000380 0 1 Chou A Association of Prostate-Specific Antigen Levels with Prostate Cancer Risk in a Multiethnic Population: Stability over Time and Comparison with Polygenic Risk Score. Cancer Epidemiol Biomarkers Prev 20/09/2022 10.1158/1055-9965.epi-22-0443 36126957
PGP000441 1 1 Su YR Validation of a genetic-enhanced risk prediction model for colorectal cancer in a large community-based cohort. Cancer Epidemiol Biomarkers Prev 09/01/2023 10.1158/1055-9965.epi-22-0817 36622766
PGP000646 0 1 Trendowski MR Assessing a Polygenic Risk Score for Lung Cancer Susceptibility in Non-Hispanic White and Black Populations. Cancer Epidemiol Biomarkers Prev 01/11/2023 10.1158/1055-9965.epi-23-0174 37578347
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
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
PGP000350 0 1 Niedermaier T Combined Performance of Fecal Immunochemical Tests and a Genetic Risk Score for Advanced Neoplasia Detection. Cancer Prev Res (Phila) 01/08/2022 10.1158/1940-6207.capr-21-0552 35679356
PGP000455 0 2 Spaeth EL Validation of an abridged breast cancer risk prediction model for the general population. Cancer Prev Res (Phila) 02/03/2023 10.1158/1940-6207.capr-22-0460 36862830
PGP000082 1 1 Tikkanen E Genetic risk prediction and a 2-stage risk screening strategy for coronary heart disease. Arterioscler Thromb Vasc Biol 18/04/2013 10.1161/atvbaha.112.301120 23599444
PGP000421 1 1 Wang J Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically. Arterioscler Thromb Vasc Biol 20/10/2016 10.1161/atvbaha.116.308027 27765764
PGP000647 3 3 Trinder M Causal Inference for Genetically Determined Levels of High-Density Lipoprotein Cholesterol and Risk of Infectious Disease. Arterioscler Thromb Vasc Biol 07/11/2019 10.1161/atvbaha.119.313381 31694394
PGP000108 0 1 Hindy G Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease. Arterioscler Thromb Vasc Biol 22/09/2020 10.1161/atvbaha.120.314856 32957805
PGP000205 0 1 Rimbert A Phenotypic Differences Between Polygenic and Monogenic Hypobetalipoproteinemia. Arterioscler Thromb Vasc Biol 19/11/2020 10.1161/atvbaha.120.315491 33207932
PGP000044 1 1 Hajek C Coronary Heart Disease Genetic Risk Score Predicts Cardiovascular Disease Risk in Men, Not Women. Circ Genom Precis Med 01/10/2018 10.1161/CIRCGEN.118.002324 30354305
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
PGP000092 19 19 Xie T Genetic Risk Scores for Complex Disease Traits in Youth. Circ Genom Precis Med 11/06/2020 10.1161/circgen.119.002775 32527150
PGP000626 0 1 Douville NJ Use of a Polygenic Risk Score Improves Prediction of Myocardial Injury After Non-Cardiac Surgery. Circ Genom Precis Med 09/06/2020 10.1161/circgen.119.002817 32517536
PGP000107 1 1 Trinder M Polygenic Contribution to Low-Density Lipoprotein Cholesterol Levels and Cardiovascular Risk in Monogenic Familial Hypercholesterolemia. Circ Genom Precis Med 13/08/2020 10.1161/circgen.120.002919 33079599
PGP000152 4 6 Gola D Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease. Circ Genom Precis Med 10/11/2020 10.1161/circgen.120.002932 33170024
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
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
PGP000252 3 3 Ye Y Interactions Between Enhanced Polygenic Risk Scores and Lifestyle for Cardiovascular Disease, Diabetes, and Lipid Levels. Circ Genom Precis Med 12/01/2021 10.1161/circgen.120.003128 33433237
PGP000654 1 1 Huang Y Sexual Differences in Genetic Predisposition of Coronary Artery Disease. Circ Genom Precis Med 17/12/2020 10.1161/circgen.120.003147 33332181
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
PGP000157 1 1 Dron JS Genetic Predictor to Identify Individuals With High Lipoprotein(a) Concentrations. Circ Genom Precis Med 01/02/2021 10.1161/circgen.120.003182 33522245
PGP000232 1 1 Feitosa MF Heterogeneity of the Predictive Polygenic Risk Scores for Coronary Heart Disease Age-at-Onset in Three Different Coronary Heart Disease Family-Based Ascertainments. Circ Genom Precis Med 12/04/2021 10.1161/circgen.120.003201 33844929
PGP000257 0 1 Wells QS Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults. Circ Genom Precis Med 31/08/2021 10.1161/circgen.121.003341 34463132
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
PGP000349 0 1 Shi M Association of Genome-Wide Polygenic Risk Score for Body Mass Index With Cardiometabolic Health From Childhood Through Midlife. Circ Genom Precis Med 08/06/2022 10.1161/circgen.121.003375 35675159
PGP000532 1 1 Manikpurage HD Polygenic Risk Score for Coronary Artery Disease Improves the Prediction of Early-Onset Myocardial Infarction and Mortality in Men. Circ Genom Precis Med 21/10/2021 10.1161/circgen.121.003452 34670400
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
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
PGP000481 0 1 Lanfear DE Validation of a Polygenic Score for Beta-Blocker Survival Benefit in Patients With Heart Failure Using the United Kingdom Biobank. Circ Genom Precis Med 03/03/2023 10.1161/circgen.121.003835 36866666
PGP000386 0 4 Saad M Validation of Polygenic Risk Scores for Coronary Heart Disease in a Middle Eastern Cohort Using Whole Genome Sequencing. Circ Genom Precis Med 12/10/2022 10.1161/circgen.122.003712 36252120
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
PGP000384 1 1 Parcha V Association of a Multi-Ancestry Genome-Wide Blood Pressure Polygenic Risk Score with Adverse Cardiovascular Events. Circ Genom Precis Med 05/11/2022 10.1161/circgen.122.003946 36334310
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
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
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
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