Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000428 1 1 Nyberg T CanRisk-Prostate: A Comprehensive, Externally Validated Risk Model for the Prediction of Future Prostate Cancer. J Clin Oncol 09/12/2022 10.1200/jco.22.01453 36493335
PGP000427 1 1 Krohn L Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects. Nat Commun 05/12/2022 10.1038/s41467-022-34732-5 36470867
PGP000426 1 1 Gao XR Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma. Nat Commun 30/11/2022 10.1038/s41467-022-35188-3 36450729
PGP000425 0 1 Olsen CM Risk Factors Associated With First and Second Primary Melanomas in a High-Incidence Population. JAMA Dermatol 01/01/2023 10.1001/jamadermatol.2022.4975 36416830
PGP000424 1 1 Olsen CM Does polygenic risk influence associations between sun exposure and melanoma? A prospective cohort analysis. Br J Dermatol 17/12/2019 10.1111/bjd.18703 31747047
PGP000423 6 6 Bakker MK Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity. Stroke 19/01/2023 10.1161/strokeaha.122.040715 36655558
PGP000422 1 4 Vanhoye X A new 165-SNP low-density lipoprotein cholesterol polygenic risk score based on next generation sequencing outperforms previously published scores in routine diagnostics of familial hypercholesterolemia. Transl Res 15/12/2022 10.1016/j.trsl.2022.12.002 36528340
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
PGP000420 1 1 Trinder M Risk of Premature Atherosclerotic Disease in Patients With Monogenic Versus Polygenic Familial Hypercholesterolemia. J Am Coll Cardiol 01/07/2019 10.1016/j.jacc.2019.05.043 31345425
PGP000419 1 1 Lamri A The genetic risk of gestational diabetes in South Asian women. Elife 22/11/2022 10.7554/elife.81498 36412575
PGP000418 1 1 Pieri K Polygenic risk in Type III hyperlipidaemia and risk of cardiovascular disease: An epidemiological study in UK Biobank and Oxford Biobank. Int J Cardiol 19/11/2022 10.1016/j.ijcard.2022.11.024 36410544
PGP000417 0 1 Dite GS A combined clinical and genetic model for predicting risk of ovarian cancer. Eur J Cancer Prev 27/10/2022 10.1097/cej.0000000000000771 36503897
PGP000416 1 2 Robinson JR Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics. Obesity (Silver Spring) 13/11/2022 10.1002/oby.23561 36372681
PGP000415 4 4 Jee YH Polygenic risk scores for prediction of breast cancer in Korean women. Int J Epidemiol 07/11/2022 10.1093/ije/dyac206 36343017
PGP000414 1 1 Xin J Risk assessment for colorectal cancer via polygenic risk score and lifestyle exposure: a large-scale association study of East Asian and European populations. Genome Med 24/01/2023 10.1186/s13073-023-01156-9 36694225
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
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
PGP000411 1 1 Steinbrenner I A Polygenic Score for Reduced Kidney Function and Adverse Outcomes in a Chronic Kidney Disease Cohort. Kidney Int 05/12/2022 10.1016/j.kint.2022.11.013 36481179
PGP000410 20 20 Saunders GRB Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature 07/12/2022 10.1038/s41586-022-05477-4 36477530
PGP000409 2 2 Aragam KG Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Nat Genet 06/12/2022 10.1038/s41588-022-01233-6 36474045
PGP000408 0 1 Borg SÁ Subclinical atherosclerosis determined by coronary artery calcium deposition in patients with clinical familial hypercholesterolemia. Atheroscler Plus 11/11/2022 10.1016/j.athplu.2022.10.002 36643796
PGP000407 1 1 Downie ML Shared genetic risk across different presentations of gene test-negative idiopathic nephrotic syndrome. Pediatr Nephrol 10/11/2022 10.1007/s00467-022-05789-7 36357634
PGP000406 0 1 Gandhi GD Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobank. J Transl Med 03/11/2022 10.1186/s12967-022-03697-w 36329474
PGP000405 18 18 Kim YJ The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. Nat Commun 04/11/2022 10.1038/s41467-022-34163-2 36333282
PGP000404 1 1 Teleka S Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men. Sci Rep 31/10/2022 10.1038/s41598-022-23225-6 36316463
PGP000403 0 1 Siggs OM Association of High Polygenic Risk With Visual Field Worsening Despite Treatment in Early Primary Open-Angle Glaucoma. JAMA Ophthalmol 10/11/2022 10.1001/jamaophthalmol.2022.4688 36355370
PGP000402 1 1 Chen Y Cardiometabolic diseases, polygenic risk score, APOE genotype, and risk of incident dementia: A population-based prospective cohort study. Arch Gerontol Geriatr 31/10/2022 10.1016/j.archger.2022.104853 36347157
PGP000401 0 1 Cho BPH Association of Vascular Risk Factors and Genetic Factors With Penetrance of Variants Causing Monogenic Stroke. JAMA Neurol 27/10/2022 10.1001/jamaneurol.2022.3832 36300346
PGP000400 0 1 Pagadala MS Polygenic risk of any, metastatic, and fatal prostate cancer in the Million Veteran Program. J Natl Cancer Inst 28/10/2022 10.1093/jnci/djac199 36305680
PGP000399 1 1 Fang Y Polygenic Liability to Depression Is Associated With Multiple Medical Conditions in the Electronic Health Record: Phenome-wide Association Study of 46,782 Individuals. Biol Psychiatry 11/06/2022 10.1016/j.biopsych.2022.06.004 35965108
PGP000398 1 1 Ghouse J Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism. Nat Genet 19/01/2023 10.1038/s41588-022-01286-7 36658437
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
PGP000396 0 1 Koraishy FM Polygenic association of glomerular filtration rate decline in world trade center responders. BMC Nephrol 28/10/2022 10.1186/s12882-022-02967-5 36307804
PGP000395 1 1 Valenti L Clinical and genetic determinants of the fatty liver-coagulation balance interplay in individuals with metabolic dysfunction. JHEP Rep 25/09/2022 10.1016/j.jhepr.2022.100598 36313186
PGP000394 1 1 Sumpter NA Association of Gout Polygenic Risk Score with Age at Disease Onset and Tophaceous Disease in European and Polynesian Men with Gout. Arthritis Rheumatol 25/10/2022 10.1002/art.42393 36281732
PGP000393 514 514 Ma Y ExPRSweb: An online repository with polygenic risk scores for common health-related exposures. Am J Hum Genet 23/09/2022 10.1016/j.ajhg.2022.09.001 36152628
PGP000392 1 1 Miyazawa K Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction. Nat Genet 19/01/2023 10.1038/s41588-022-01284-9 36653681
PGP000391 3 3 Agrawal S Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Nat Commun 30/06/2022 10.1038/s41467-022-30931-2 35773277
PGP000390 1 1 Wuttke M A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nat Genet 31/05/2019 10.1038/s41588-019-0407-x 31152163
PGP000389 0 1 Giardiello D PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients. Breast Cancer Res 21/10/2022 10.1186/s13058-022-01567-3 36271417
PGP000388 1 1 Ahmed R Reclassification of coronary artery disease risk using genetic risk score among subjects with borderline or intermediate clinical risk. Int J Cardiol Heart Vasc 13/10/2022 10.1016/j.ijcha.2022.101136 36275420
PGP000387 1 2 Qin N Association of the interaction between mosaic chromosomal alterations and polygenic risk score with the risk of lung cancer: an array-based case-control association and prospective cohort study. Lancet Oncol 17/10/2022 10.1016/s1470-2045(22)00600-3 36265503
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
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
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
PGP000383 1 1 Solé-Navais P Genetic effects on the timing of parturition and links to fetal birth weight. Nat Genet 03/04/2023 10.1038/s41588-023-01343-9 37012456
PGP000382 6 6 Yengo L A saturated map of common genetic variants associated with human height. Nature 12/10/2022 10.1038/s41586-022-05275-y 36224396
PGP000381 0 6 Hao L Development of a clinical polygenic risk score assay and reporting workflow. Nat Med 18/04/2022 10.1038/s41591-022-01767-6 35437332
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
PGP000379 4 4 Shi Z Reliability of Ancestry-specific Prostate Cancer Genetic Risk Score in Four Racial and Ethnic Populations. Eur Urol Open Sci 17/09/2022 10.1016/j.euros.2022.09.001 36353656