Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000742 6 6 Guo B G Polygenic risk score for type 2 diabetes shows context-dependent effects across populations. Nat Commun 25/06/2025 10.1038/s41467-025-63546-4 41034193
PGP000679 130 130 Gunn S Comparison of Methods for Building Polygenic Scores for Diverse Populations. HGG Adv 25/09/2024 10.1016/j.xhgg.2024.100355 39323095
PGP000370 6 6 Gui Y Sex-specific genetic association between psychiatric disorders and cognition, behavior and brain imaging in children and adults. Transl Psychiatry 26/08/2022 10.1038/s41398-022-02041-6 36028495
PGP000174 1 1 Guffanti G Depression genetic risk score is associated with anhedonia-related markers across units of analysis. Transl Psychiatry 19/09/2019 10.1038/s41398-019-0566-7 31537779
PGP000599 0 9 Guarischi-Sousa R Contemporary Polygenic Scores of Low-Density Lipoprotein Cholesterol and Coronary Artery Disease Predict Coronary Atherosclerosis in Adolescents and Young Adults. Circ Genom Precis Med 06/07/2023 10.1161/circgen.122.004047 37409455
PGP000098 1 1 Grove J Identification of common genetic risk variants for autism spectrum disorder. Nat Genet 25/02/2019 10.1038/s41588-019-0344-8 30804558
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
PGP000527 3 3 Green RE Investigating associations between blood metabolites, later life brain imaging measures, and genetic risk for Alzheimer's disease. Alzheimers Res Ther 22/02/2023 10.1186/s13195-023-01184-y 36814324
PGP000367 0 1 Green HD Applying a genetic risk score for prostate cancer to men with lower urinary tract symptoms in primary care to predict prostate cancer diagnosis: a cohort study in the UK Biobank. Br J Cancer 18/08/2022 10.1038/s41416-022-01918-z 35978138
PGP000330 0 1 Gratton J LDL-C Concentrations and the 12-SNP LDL-C Score for Polygenic Hypercholesterolaemia in Self-Reported South Asian, Black and Caribbean Participants of the UK Biobank. Front Genet 31/03/2022 10.3389/fgene.2022.845498 35432461
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
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
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
PGP000582 2 2 Gorman BR Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries. Nat Genet 02/12/2024 10.1038/s41588-024-01764-0 39623103
PGP000698 0 1 Gorijala P Alzheimer's polygenic risk scores are associated with cognitive phenotypes in Down syndrome. Alzheimers Dement 19/10/2023 10.1002/alz.13506 37855447
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
PGP000729 4 5 Gibson TM Polygenic risk scores, radiation treatment exposures and subsequent cancer risk in childhood cancer survivors. Nat Med 07/03/2024 10.1038/s41591-024-02837-7 38454124
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
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
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
PGP000594 1 1 Ghouse J Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nat Genet 17/04/2024 10.1038/s41588-024-01720-y 38632349
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
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
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
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
PGP000671 1 1 Gao P Association between serum urea concentrations and the risk of colorectal cancer, particularly in individuals with type 2 diabetes: A cohort study. Int J Cancer 06/09/2023 10.1002/ijc.34719 37671773
PGP000621 3 3 Gao G Polygenic risk scores for prediction of breast cancer risk in women of African ancestry: a cross-ancestry approach. Hum Mol Genet 01/09/2022 10.1093/hmg/ddac102 35554533
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
PGP000765 0 1 Gandhi SE Motor Complications in Parkinson's Disease: Results from 3343 Patients Followed for up to 12 Years. Mov Disord Clin Pract 08/04/2024 10.1002/mdc3.14044 38587023
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
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
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
PGP000709 1 1 Frederiksen TC Interaction of genetic risk and lifestyle on the incidence of atrial fibrillation. Heart 15/04/2024 10.1136/heartjnl-2023-323333 38016806
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
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
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
PGP000735 9 9 Foote IF Uncovering the multivariate genetic architecture of frailty with genomic structural equation modeling Nat Genet 04/08/2025 10.1038/s41588-025-02269-0 40759756
PGP000138 3 3 Fontanillas P Disease risk scores for skin cancers. Nat Commun 08/01/2021 10.1038/s41467-020-20246-5 33420020
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
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
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
PGP000732 1 1 Flores AM Polygenic Prediction of Peripheral Artery Disease and Major Adverse Limb Events. JAMA Cardiol 21/05/2025 10.1001/jamacardio.2025.1182 40397457
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
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
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
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
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
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
Showing 551 to 600 of 750 rows