Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000538 1 1 Aranda-Guillén M A polygenic risk score to help discriminate primary adrenal insufficiency of different etiologies. J Intern Med 21/05/2023 10.1111/joim.13649 37151110
PGP000375 1 1 Xie J Genetic risk and incident venous thromboembolism in middle-aged and older adults following COVID-19 vaccination. J Thromb Haemost 15/09/2022 10.1111/jth.15879 36111372
PGP000505 0 1 Liu Z Associations of serum uric acid levels with liver disease-related morbidity and mortality: A prospective cohort study of the UK Biobank. Liver Int 29/03/2023 10.1111/liv.15564 36938749
PGP000622 0 1 Åberg F Combined use of the ELF test and CLivD score improves prediction of liver-related outcomes in the general population. Liver Int 23/07/2023 10.1111/liv.15681 37485795
PGP000213 1 1 Arabkhazaeli A The association between a genetic risk score for allergy and the risk of developing allergies in childhood-Results of the WHISTLER cohort. Pediatr Allergy Immunol 22/11/2017 10.1111/pai.12824 29047167
PGP000432 2 2 Toivonen J The value of genetic data from 665,460 individuals in managing iron deficiency anaemia and suitability to donate blood Vox Sanguinis 06/02/2023 10.1111/vox.13564 38018286
PGP000081 6 6 Knevel R Using genetics to prioritize diagnoses for rheumatology outpatients with inflammatory arthritis. Sci Transl Med 01/05/2020 10.1126/scitranslmed.aay1548 32461333
PGP000099 1 1 Reid S High genetic risk score is associated with early disease onset, damage accrual and decreased survival in systemic lupus erythematosus. Ann Rheum Dis 11/12/2019 10.1136/annrheumdis-2019-216227 31826855
PGP000052 4 4 Cánovas R Genomic risk scores for juvenile idiopathic arthritis and its subtypes. Ann Rheum Dis 04/09/2020 10.1136/annrheumdis-2020-217421 32887683
PGP000110 1 1 Bossini-Castillo L Genomic Risk Score impact on susceptibility to systemic sclerosis. Ann Rheum Dis 01/10/2020 10.1136/annrheumdis-2020-218558 33004331
PGP000272 0 1 McCormick N Impact of adiposity on risk of female gout among those genetically predisposed: sex-specific prospective cohort study findings over >32 years. Ann Rheum Dis 02/12/2021 10.1136/annrheumdis-2021-221635 34857519
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
PGP000438 6 6 Briggs SEW Integrating genome-wide polygenic risk scores and non-genetic risk to predict colorectal cancer diagnosis using UK Biobank data: population based cohort study. BMJ 09/11/2022 10.1136/bmj-2022-071707 36351667
PGP000047 1 1 Seibert TM Polygenic hazard score to guide screening for aggressive prostate cancer: development and validation in large scale cohorts. BMJ 10/01/2018 10.1136/bmj.j5757 29321194
PGP000026 1 1 Rutten-Jacobs LC Genetic risk, incident stroke, and the benefits of adhering to a healthy lifestyle: cohort study of 306 473 UK Biobank participants. BMJ 24/10/2018 10.1136/bmj.k4168 30355576
PGP000132 2 2 Richardson TG Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study. BMJ 06/05/2020 10.1136/bmj.m1203 32376654
PGP000627 0 2 Martikainen P Joint association between education and polygenic risk score for incident coronary heart disease events: a longitudinal population-based study of 26 203 men and women. J Epidemiol Community Health 06/01/2021 10.1136/jech-2020-214358 33408166
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
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
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
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
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
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