Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000212 2 2 Dongiovanni P Causal relationship of hepatic fat with liver damage and insulin resistance in nonalcoholic fatty liver. J Intern Med 27/12/2017 10.1111/joim.12719 29280273
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
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
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
PGP000504 0 1 Duschek E A polygenic and family risk score are both independently associated with risk of type 2 diabetes in a population-based study. Sci Rep 23/03/2023 10.1038/s41598-023-31496-w 36959271
PGP000156 1 1 Du Z A genome-wide association study of prostate cancer in Latinos. Int J Cancer 03/07/2019 10.1002/ijc.32525 31226226
PGP000179 3 6 Du Z Evaluating Polygenic Risk Scores for Breast Cancer in Women of African Ancestry. J Natl Cancer Inst 26/03/2021 10.1093/jnci/djab050 33769540
PGP000255 1 1 Ebenau JL Risk of dementia in <i>APOE</i> ε4 carriers is mitigated by a polygenic risk score. Alzheimers Dement (Amst) 14/09/2021 10.1002/dad2.12229 34541285
PGP000054 2 2 Elliott J Predictive Accuracy of a Polygenic Risk Score-Enhanced Prediction Model vs a Clinical Risk Score for Coronary Artery Disease. JAMA 01/02/2020 10.1001/jama.2019.22241 32068818
PGP000136 1 1 Emdin CA Association of genetic variation with cirrhosis: a multi-trait genome-wide association and gene-environment interaction study. Gastroenterology 10/12/2020 10.1053/j.gastro.2020.12.011 33310085
PGP000283 2 2 Evangelou E Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat Genet 17/09/2018 10.1038/s41588-018-0205-x 30224653
PGP000171 0 2 Fahed AC Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions. Nat Commun 20/08/2020 10.1038/s41467-020-17374-3 32820175
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
PGP000115 1 1 Fan BJ Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis. JAMA Ophthalmol 22/08/2019 10.1001/jamaophthalmol.2019.3109 31436842
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
PGP000541 1 1 Fan L Saturated fatty acid intake, genetic risk and colorectal cancer incidence: A large-scale prospective cohort study. Int J Cancer 23/04/2023 10.1002/ijc.34544 37087737
PGP000467 0 5 Farré X Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Genes (Basel) 05/01/2023 10.3390/genes14010149 36672889
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
PGP000548 1 1 Feng J Association of laxatives use with incident dementia and modifying effect of genetic susceptibility: a population-based cohort study with propensity score matching. BMC Geriatr 04/03/2023 10.1186/s12877-023-03854-w 36870957
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
PGP000549 1 1 Fernández-Rhodes L A Gene-Acculturation Study of Obesity Among US Hispanic/Latinos: The Hispanic Community Health Study/Study of Latinos. Psychosom Med 15/03/2023 10.1097/psy.0000000000001193 36917487
PGP000491 1 0 Fernandez-Rozadilla C Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries. Nat Genet 20/12/2022 10.1038/s41588-022-01222-9 36539618
PGP000091 0 1 Ferrat LA A combined risk score enhances prediction of type 1 diabetes among susceptible children. Nat Med 07/08/2020 10.1038/s41591-020-0930-4 32770166
PGP000195 1 0 Ferreira MA Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nat Genet 30/10/2017 10.1038/ng.3985 29083406
PGP000199 0 1 Ferreira MAR Age-of-onset information helps identify 76 genetic variants associated with allergic disease. PLoS Genet 30/06/2020 10.1371/journal.pgen.1008725 32603359
PGP000097 3 3 Flynn E Sex-specific genetic effects across biomarkers. Eur J Hum Genet 01/09/2020 10.1038/s41431-020-00712-w 32873964
PGP000089 79 79 Folkersen L Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Nat Metab 16/10/2020 10.1038/s42255-020-00287-2 33067605
PGP000449 1 1 Folsom AR Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores. PLoS One 30/01/2023 10.1371/journal.pone.0280657 36716319
PGP000138 3 3 Fontanillas P Disease risk scores for skin cancers. Nat Commun 08/01/2021 10.1038/s41467-020-20246-5 33420020
PGP000120 1 1 Forgetta V Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study. PLoS Med 02/07/2020 10.1371/journal.pmed.1003152 32614825
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
PGP000203 1 1 Forrest IS Genome-wide polygenic risk score for retinopathy of type 2 diabetes. Hum Mol Genet 01/05/2021 10.1093/hmg/ddab067 33704450
PGP000584 1 1 Forthman KL Transdiagnostic behavioral and genetic contributors to repetitive negative thinking: A machine learning approach. J Psychiatr Res 05/05/2023 10.1016/j.jpsychires.2023.05.039 37178517
PGP000055 3 3 Fritsche LG Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb. PLoS Genet 13/06/2019 10.1371/journal.pgen.1008202 31194742
PGP000118 302 302 Fritsche LG Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. Am J Hum Genet 28/09/2020 10.1016/j.ajhg.2020.08.025 32991828
PGP000256 1 1 Gafni A Ability of known colorectal cancer susceptibility SNPs to predict colorectal cancer risk: A cohort study within the UK Biobank. PLoS One 15/09/2021 10.1371/journal.pone.0251469 34525106
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
PGP000612 3 3 Gao C Risk of Breast Cancer Among Carriers of Pathogenic Variants in Breast Cancer Predisposition Genes Varies by Polygenic Risk Score. J Clin Oncol 08/06/2021 10.1200/jco.20.01992 34101481
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
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
PGP000460 1 1 García-González P Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men. Int J Mol Sci 04/01/2023 10.3390/ijms24020898 36674414
PGP000331 1 1 Ge T Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. Genome Med 29/06/2022 10.1186/s13073-022-01074-2 35765100
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
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
PGP000497 1 1 Gibson MJ Identifying the potential causal role of insomnia symptoms on 11,409 health-related outcomes: a phenome-wide Mendelian randomisation analysis in UK Biobank. BMC Med 03/04/2023 10.1186/s12916-023-02832-8 37013595
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
PGP000582 2 2 Gorman BR Distinctive cross-ancestry genetic architecture for age-related macular degeneration medRxivPre 21/08/2022 10.1101/2022.08.16.22278855 —
PGP000124 1 1 Gorski M Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline. Kidney Int 30/10/2020 10.1016/j.kint.2020.09.030 33137338
PGP000050 16 16 Graff RE Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts. Nat Commun 12/02/2021 10.1038/s41467-021-21288-z 33579919
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
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