Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000455 0 2 Spaeth EL Validation of an abridged breast cancer risk prediction model for the general population. Cancer Prev Res (Phila) 02/03/2023 10.1158/1940-6207.capr-22-0460 36862830
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
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 —
PGP000458 0 1 Pavelka L Age at onset as stratifier in idiopathic Parkinson's disease - effect of ageing and polygenic risk score on clinical phenotypes. NPJ Parkinsons Dis 09/08/2022 10.1038/s41531-022-00342-7 35945230
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
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
PGP000461 10 10 Dahl A Phenotype integration improves power and preserves specificity in biobank-based genetic studies of MDD bioRxivPre 15/08/2022 10.1101/2022.08.15.503980 —
PGP000462 3 3 Honigberg MC Polygenic prediction of preeclampsia and gestational hypertension. Nat Med 29/05/2023 10.1038/s41591-023-02374-9 37248299
PGP000463 2 2 Kleeman SO Cystatin C is glucocorticoid responsive, directs recruitment of Trem2+ macrophages, and predicts failure of cancer immunotherapy. Cell Genom 23/06/2023 10.1016/j.xgen.2023.100347 37601967
PGP000464 132 132 Liu N Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Nat Genet 19/06/2023 10.1038/s41588-023-01425-8 37337106
PGP000465 2 2 Hatoum AS Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Biol Psychiatry 14/07/2022 10.1016/j.biopsych.2022.06.034 36150907
PGP000466 3 3 Patel AP A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease. Nat Med 06/07/2023 10.1038/s41591-023-02429-x 37414900
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
PGP000468 0 1 Hodel F Associations of genetic and infectious risk factors with coronary heart disease. Elife 14/02/2023 10.7554/elife.79742 36785929
PGP000469 8 8 Wedekind LE The utility of a type 2 diabetes polygenic score in addition to clinical variables for prediction of type 2 diabetes incidence in birth, youth and adult cohorts in an Indigenous study population. Diabetologia 02/03/2023 10.1007/s00125-023-05870-2 36862161
PGP000470 11 11 Xin J Prognostic evaluation of polygenic risk score underlying pan-cancer analysis: evidence from two large-scale cohorts. EBioMedicine 03/02/2023 10.1016/j.ebiom.2023.104454 36739632
PGP000471 2 2 Tran JH Genetic Associations Between Smoking- and Glaucoma-Related Traits. Transl Vis Sci Technol 01/02/2023 10.1167/tvst.12.2.20 36786746
PGP000472 4 4 Shoaib M Evaluation of polygenic risk scores to differentiate between type 1 and type 2 diabetes. Genet Epidemiol 23/02/2023 10.1002/gepi.22521 36821788
PGP000473 1 1 Sato JR Polygenic risk score for attention-deficit/hyperactivity disorder and brain functional networks segregation in a community-based sample. Genes Brain Behav 21/02/2023 10.1111/gbb.12838 36811275
PGP000474 1 1 Hurwitz LM Association of Frequent Aspirin Use With Ovarian Cancer Risk According to Genetic Susceptibility. JAMA Netw Open 01/02/2023 10.1001/jamanetworkopen.2023.0666 36826816
PGP000475 3 3 Kwon YC Higher Genetic Risk Loads Confer More Diverse Manifestations and Higher Risk of Lupus Nephritis in Systemic Lupus Erythematosus. Arthritis Rheumatol 03/04/2023 10.1002/art.42516 37011055
PGP000476 0 1 Biddinger KJ Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank. JAMA Cardiol 01/07/2022 10.1001/jamacardio.2022.1061 35583889
PGP000477 0 2 Deutsch AJ Polygenic Scores Help Reduce Racial Disparities in Predictive Accuracy of Automated Type 1 Diabetes Classification Algorithms. Diabetes Care 01/04/2023 10.2337/dc22-1833 36745605
PGP000478 2 3 Ohbe H Development and validation of genome-wide polygenic risk scores for predicting breast cancer incidence in Japanese females: a population-based case-cohort study. Breast Cancer Res Treat 20/12/2022 10.1007/s10549-022-06843-6 36538246
PGP000479 0 1 Blauwendraat C Polygenic Parkinson's Disease Genetic Risk Score as Risk Modifier of Parkinsonism in Gaucher Disease. Mov Disord 03/03/2023 10.1002/mds.29342 36869417
PGP000480 1 1 Wang H Identification of specific susceptibility loci for the early-onset colorectal cancer. Genome Med 03/03/2023 10.1186/s13073-023-01163-w 36869385
PGP000481 0 1 Lanfear DE Validation of a Polygenic Score for Beta-Blocker Survival Benefit in Patients With Heart Failure Using the United Kingdom Biobank. Circ Genom Precis Med 03/03/2023 10.1161/circgen.121.003835 36866666
PGP000482 0 1 Hassanin E Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence. BMC Med Genomics 05/03/2023 10.1186/s12920-023-01469-z 36872334
PGP000483 0 1 Cui Q Integrating polygenic and clinical risks to improve stroke risk stratification in prospective Chinese cohorts. Sci China Life Sci 03/03/2023 10.1007/s11427-022-2280-3 36881318
PGP000484 1 1 Zhang J Associations of risk factor burden and genetic predisposition with the 10-year risk of atrial fibrillation: observations from a large prospective study of 348,904 participants. BMC Med 08/03/2023 10.1186/s12916-023-02798-7 36882748
PGP000485 1 1 Mourtzi N Genetic propensity for cerebral amyloidosis and risk of mild cognitive impairment and Alzheimer's disease within a cognitive reserve framework. Alzheimers Dement 09/03/2023 10.1002/alz.12980 36895094
PGP000486 1 1 Zheng Z Physical Frailty, Genetic Predisposition, and Incident Parkinson Disease. JAMA Neurol 01/05/2023 10.1001/jamaneurol.2023.0183 36912851
PGP000487 1 1 Scammell BH Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration. Hum Mol Genet 29/06/2023 10.1093/hmg/ddad101 37384397
PGP000488 2 2 Wang A W Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants Nature Genetics 21/08/2023 10.1038/s41588-023-01534-4 37945903
PGP000489 82 82 Zhang H A new method for multiancestry polygenic prediction improves performance across diverse populations. Nat Genet 25/09/2023 10.1038/s41588-023-01501-z 37749244
PGP000490 1 1 Hatoum AS Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders. Nat Ment Health 22/03/2023 10.1038/s44220-023-00034-y 37250466
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
PGP000492 1 3 Thomas M T Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity. medRxivPre 19/01/2023 10.1101/2023.01.19.23284737 —
PGP000493 4 4 Li J Age and Genetic Risk Score and Rates of Blood Lipid Changes in China. JAMA Netw Open 01/03/2023 10.1001/jamanetworkopen.2023.5565 36988954
PGP000494 0 6 Ho PJ Polygenic risk scores for the prediction of common cancers in East Asians: A population-based prospective cohort study. Elife 27/03/2023 10.7554/elife.82608 36971353
PGP000495 0 2 Bakshi A Association of polygenic scores with chronic kidney disease phenotypes in a longitudinal study of older adults. Kidney Int 29/03/2023 10.1016/j.kint.2023.03.017 37001602
PGP000496 2 2 Sofer T Genome-wide association study of obstructive sleep apnoea in the Million Veteran Program uncovers genetic heterogeneity by sex. EBioMedicine 28/03/2023 10.1016/j.ebiom.2023.104536 36989840
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
PGP000498 1 1 Clark R A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration. EBioMedicine 11/04/2023 10.1016/j.ebiom.2023.104551 37055258
PGP000499 1 1 Zhang Z Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population. BMC Med 19/04/2023 10.1186/s12916-023-02844-4 37076872
PGP000500 4 4 Shrine N Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Nat Genet 13/03/2023 10.1038/s41588-023-01314-0 36914875
PGP000501 26 26 Shim I Clinical utility of polygenic scores for cardiometabolic disease in Arabs. Nature Communications 18/10/2023 10.1038/s41467-023-41985-1 37852978
PGP000502 60 60 Tanigawa Y Power of inclusion: Enhancing polygenic prediction with admixed individuals AJHG 19/09/2023 10.1016/j.ajhg.2023.09.013 37890495
PGP000503 6 6 Sofer T A polygenic risk score for Alzheimer's disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. Alzheimers Res Ther 30/08/2023 10.1186/s13195-023-01298-3 37649099
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
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