Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000578 1 1 Tomassen J Amyloid-β and APOE genotype predict memory decline in cognitively unimpaired older individuals independently of Alzheimer's disease polygenic risk score. BMC Neurol 15/12/2022 10.1186/s12883-022-02925-6 36522743
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
PGP000431 5 5 Ko CL Genome-wide association study reveals ethnicity-specific SNPs associated with ankylosing spondylitis in the Taiwanese population. J Transl Med 12/12/2022 10.1186/s12967-022-03701-3 36510243
PGP000429 2 2 Seviiri M A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma. Nat Commun 10/12/2022 10.1038/s41467-022-35345-8 36496446
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
PGP000430 2 2 Pagadala MS PRState: Incorporating genetic ancestry in prostate cancer risk scores for men of African ancestry. BMC Cancer 09/12/2022 10.1186/s12885-022-10258-3 36494783
PGP000459 1 1 Mukadam N Genetic risk scores and dementia risk across different ethnic groups in UK Biobank. PLoS One 07/12/2022 10.1371/journal.pone.0277378 36477264
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
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
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
PGP000365 8 8 Wong CK Polygenic risk scores for cardiovascular diseases and type 2 diabetes. PLoS One 02/12/2022 10.1371/journal.pone.0278764 36459520
PGP000567 2 2 Jung SH Transferability of Alzheimer Disease Polygenic Risk Score Across Populations and Its Association With Alzheimer Disease-Related Phenotypes. JAMA Netw Open 01/12/2022 10.1001/jamanetworkopen.2022.47162 36520433
PGP000439 1 2 Feng X Association Between Genetic Risk, Adherence to Healthy Lifestyle Behavior, and Thyroid Cancer Risk. JAMA Netw Open 01/12/2022 10.1001/jamanetworkopen.2022.46311 36508215
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
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
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
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
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
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
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
PGP000364 21 21 Mars N Systematic comparison of family history and polygenic risk across 24 common diseases. Am J Hum Genet 07/11/2022 10.1016/j.ajhg.2022.10.009 36347255
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
PGP000357 1 1 Ishigaki K Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis. Nat Genet 04/11/2022 10.1038/s41588-022-01213-w 36333501
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
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
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
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
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
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
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
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
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
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
PGP000448 8 8 Berndt SI Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes. Leukemia 22/10/2022 10.1038/s41375-022-01711-0 36273105
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
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
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
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
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
PGP000530 0 1 Lacaze P Aspirin for Primary Prevention of Cardiovascular Events in Relation to Lipoprotein(a) Genotypes. J Am Coll Cardiol 01/10/2022 10.1016/j.jacc.2022.07.027 36175048
PGP000333 2 3 Mishra A Stroke genetics informs drug discovery and risk prediction across ancestries Nature 30/09/2022 10.1038/s41586-022-05165-3 36180795
PGP000457 84 84 Ding Y Polygenic scoring accuracy varies across the genetic ancestry continuum in all human populations bioRxivPre 29/09/2022 10.1101/2022.09.28.509988 —
PGP000456 24 24 Zhang Y Genetic determinants of cardiometabolic and pulmonary phenotypes and obstructive sleep apnoea in HCHS/SOL. EBioMedicine 26/09/2022 10.1016/j.ebiom.2022.104288 36174398
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
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
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
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