Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000230 12 12 Graham SE The power of genetic diversity in genome-wide association studies of lipids. Nature 09/12/2021 https://doi.org/10.1038/s41586-021-04064-3 34887591
PGP000274 3 3 Steinberg J Independent evaluation of melanoma polygenic risk scores in UK and Australian prospective cohorts. Br J Dermatol 18/12/2021 10.1111/bjd.20956 34921685
PGP000281 0 1 Koch S Validity and Prognostic Value of a Polygenic Risk Score for Parkinson's Disease. Genes (Basel) 23/11/2021 10.3390/genes12121859 34946808
PGP000273 1 1 Haas ME Machine learning enables new insights into genetic contributions to liver fat accumulation. Cell Genom 01/12/2021 10.1016/j.xgen.2021.100066 34957434
PGP000265 1 1 Bonfiglio F GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome. Cell Genom 08/12/2021 10.1016/j.xgen.2021.100069 34957435
PGP000298 1 1 Song SH Prediction of clinically significant prostate cancer using polygenic risk models in Asians. Investig Clin Urol 01/01/2022 10.4111/icu.20210305 34983122
PGP000263 430 430 Privé F Portability of 245 polygenic scores when derived from the UK Biobank and applied to 9 ancestry groups from the same cohort Am J Hum Genet 06/01/2022 10.1016/j.ajhg.2021.11.008 34995502
PGP000297 0 1 Hurson AN Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries. Int J Epidemiol 01/01/2022 10.1093/ije/dyab036 34999890
PGP000278 1 1 Dashti HS Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank. BMC Med 12/01/2022 10.1186/s12916-021-02198-9 35016652
PGP000279 1 1 Archambault AN Risk Stratification for Early-Onset Colorectal Cancer Using a Combination of Genetic and Environmental Risk Scores: An International Multi-Center Study. J Natl Cancer Inst 13/01/2022 10.1093/jnci/djac003 35026030
PGP000277 2 2 Dareng EO Polygenic risk modeling for prediction of epithelial ovarian cancer risk. Eur J Hum Genet 14/01/2022 10.1038/s41431-021-00987-7 35027648
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
PGP000286 1 1 Honda S Polygenic risk scores are associated with radiographic progression in patients with rheumatoid arthritis. Arthritis Rheumatol 20/01/2022 10.1002/art.42051 35048562
PGP000275 1 1 Kothalawala DM Integration of Genomic Risk Scores to Improve the Prediction of Childhood Asthma Diagnosis J Pers Med 08/01/2022 10.3390/jpm12010075 35055391
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
PGP000293 1 1 Sharma S Predicting Pancreatic Cancer in the UK Biobank Cohort Using Polygenic Risk Scores and Diabetes Mellitus. Gastroenterology 21/01/2022 10.1053/j.gastro.2022.01.016 35065983
PGP000051 26 26 Xu Y Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease Cell Genom 12/01/2022 10.1016/j.xgen.2021.100086 35072137
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
PGP000385 0 2 Zhang J A polygenic risk score and age of diagnosis of COPD. Eur Respir J 15/09/2022 10.1183/13993003.01954-2021 35115341
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
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
PGP000295 1 1 Yu Y Polygenic risk impacts PDGFRA mutation penetrance in nonsyndromic cleft lip and palate. Hum Mol Genet 11/02/2022 10.1093/hmg/ddac037 35147171
PGP000299 1 1 Zekavat SM Photoreceptor Layer Thinning Is an Early Biomarker for Age-Related Macular Degeneration: Epidemiologic and Genetic Evidence from UK Biobank OCT Data. Ophthalmology 08/02/2022 10.1016/j.ophtha.2022.02.001 35149155
PGP000292 0 3 Saad M Genetic predisposition to cancer across people of different ancestries in Qatar: a population-based, cohort study. Lancet Oncol 09/02/2022 10.1016/s1470-2045(21)00752-x 35150601
PGP000397 1 1 Huynh-Le MP Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score. Prostate Cancer Prostatic Dis 12/02/2022 10.1038/s41391-022-00497-7 35152271
PGP000300 1 1 Zhang P Association of smoking and polygenic risk with the incidence of lung cancer: a prospective cohort study. Br J Cancer 22/02/2022 10.1038/s41416-022-01736-3 35194190
PGP000289 1 1 Lu X A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study. Eur Heart J 23/02/2022 10.1093/eurheartj/ehac093 35195259
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
PGP000260 1 1 Barc J Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nat Genet 24/02/2022 10.1038/s41588-021-01007-6 35210625
PGP000291 1 1 Piekos JA Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid. Hum Genet 28/02/2022 10.1007/s00439-022-02442-z 35226188
PGP000288 0 1 Garcia-Etxebarria K Local genetic variation of inflammatory bowel disease in Basque population and its effect in risk prediction. Sci Rep 01/03/2022 10.1038/s41598-022-07401-2 35232999
PGP000302 2 2 Horowitz JE Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. Nat Genet 03/03/2022 10.1038/s41588-021-01006-7 35241825
PGP000301 1 1 Roselli C Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse. Eur Heart J 04/03/2022 10.1093/eurheartj/ehac049 35245370
PGP000305 1 1 Siddiqui MK Young-onset diabetes in Asian Indians is associated with lower measured and genetically determined beta cell function. Diabetologia 05/03/2022 10.1007/s00125-022-05671-z 35247066
PGP000326 1 1 Maj C Dissecting the Polygenic Basis of Primary Hypertension: Identification of Key Pathway-Specific Components. Front Cardiovasc Med 16/02/2022 10.3389/fcvm.2022.814502 35252394
PGP000334 1 1 Shams H Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans. Brain 07/03/2022 10.1093/brain/awac092 35253861
PGP000325 1 1 Tsai CW Prognostic significance of circulating insulin growth-like factor 1 and insulin growth-like factor binding protein 3 in renal cell carcinoma patients. American Journal of Cancer Research 15/02/2022 — 35261807
PGP000306 0 1 Thompson PL Common genetic variants do not predict recurrent events in coronary heart disease patients. BMC Cardiovasc Disord 09/03/2022 10.1186/s12872-022-02520-0 35264114
PGP000345 1 1 Lai D Evaluating risk for alcohol use disorder: Polygenic risk scores and family history. Alcohol Clin Exp Res 10/03/2022 10.1111/acer.14772 35267208
PGP000307 2 2 Forrest IS Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failure. Eur J Heart Fail 12/03/2022 10.1002/ejhf.2482 35278270
PGP000312 2 2 Schnurr TM Interactions of physical activity, muscular fitness, adiposity, and genetic risk for NAFLD. Hepatol Commun 15/03/2022 10.1002/hep4.1932 35293152
PGP000324 1 1 Yang Y Incorporating Polygenic Risk Scores and Nongenetic Risk Factors for Breast Cancer Risk Prediction Among Asian Women. JAMA Netw Open 01/03/2022 10.1001/jamanetworkopen.2021.49030 35311964
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
PGP000303 2 2 Groenland EH Genetic variants associated with low-density lipoprotein cholesterol and systolic blood pressure and the risk of recurrent cardiovascular disease in patients with established vascular disease. Atherosclerosis 11/03/2022 10.1016/j.atherosclerosis.2022.03.006 35317921
PGP000311 0 1 Olmastroni E Twelve Variants Polygenic Score for Low-Density Lipoprotein Cholesterol Distribution in a Large Cohort of Patients With Clinically Diagnosed Familial Hypercholesterolemia With or Without Causative Mutations. J Am Heart Assoc 24/03/2022 10.1161/jaha.121.023668 35322671
PGP000244 779 814 Tanigawa Y Significant sparse polygenic risk scores across 813 traits in UK Biobank. PLoS Genet 24/03/2022 10.1371/journal.pgen.1010105 35324888
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
PGP000308 0 1 Schaid DJ Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk. Am J Hum Genet 23/03/2022 10.1016/j.ajhg.2022.03.008 35353984
PGP000318 1 1 Gurung RL Genetic risk score for plasma uric acid levels is associated with early rapid kidney function decline in type 2 diabetes. J Clin Endocrinol Metab 01/04/2022 10.1210/clinem/dgac192 35363857
PGP000317 0 2 Parcha V Association of Polygenic Risk Score With Blood Pressure and Adverse Cardiovascular Outcomes in Individuals With Type II Diabetes: Insights From the ACCORD Trial. Hypertension 04/04/2022 10.1161/hypertensionaha.122.18976 35369713
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