Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000341 1 1 Vujkovic M A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Nat Genet 02/06/2022 10.1038/s41588-022-01078-z 35654975
PGP000268 1 1 Tcheandjieu C High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease. Nat Genet 30/05/2022 10.1038/s41588-022-01070-7 35637384
PGP000336 2 2 Sedaghati-Khayat B Risk assessment for hip and knee osteoarthritis using polygenic risk scores. Arthritis Rheumatol 29/05/2022 10.1002/art.42246 35644035
PGP000340 0 1 Vacher M Assessment of a polygenic hazard score for the onset of pre-clinical Alzheimer's disease. BMC Genomics 26/05/2022 10.1186/s12864-022-08617-2 35619096
PGP000339 1 1 Xicota L Association of APOE-Independent Alzheimer Disease Polygenic Risk Score With Brain Amyloid Deposition in Asymptomatic Older Adults. Neurology 23/05/2022 10.1212/wnl.0000000000200544 35606148
PGP000337 1 1 Mayerhofer E Genetically predicted on-statin LDL response is associated with higher intracerebral haemorrhage risk. Brain 22/05/2022 10.1093/brain/awac186 35598204
PGP000335 1 1 Namjou B Multiancestral polygenic risk score for pediatric asthma. J Allergy Clin Immunol 18/05/2022 10.1016/j.jaci.2022.03.035 35595084
PGP000270 2 2 Breeyear JH Blood Pressure Polygenic Scores Are Associated With Apparent Treatment-Resistant Hypertension. Circ Genom Precis Med 06/05/2022 10.1161/circgen.121.003554 35522175
PGP000338 0 2 Oram RA Utility of Diabetes Type-Specific Genetic Risk Scores for the Classification of Diabetes Type Among Multiethnic Youth. Diabetes Care 01/05/2022 10.2337/dc20-2872 35312757
PGP000329 1 1 Zhang Y Healthy lifestyle counteracts the risk effect of genetic factors on incident gout: a large population-based longitudinal study. BMC Med 29/04/2022 10.1186/s12916-022-02341-0 35484537
PGP000342 1 1 Pezzilli S Contribution of rare variants in monogenic diabetes-genes to early-onset type 2 diabetes. Diabetes Metab 26/04/2022 10.1016/j.diabet.2022.101353 35487478
PGP000321 1 1 He W Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on Aging. JAMA Ophthalmol 21/04/2022 10.1001/jamaophthalmol.2022.0891 35446358
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
PGP000271 5 5 Mars N Genome-wide risk prediction of common diseases across ancestries in one million people. Cell Genom 13/04/2022 10.1016/j.xgen.2022.100118 35591975
PGP000323 1 1 Shen M Associations of combined lifestyle and genetic risks with incident psoriasis: A prospective cohort study among UK Biobank participants of European ancestry. J Am Acad Dermatol 12/04/2022 10.1016/j.jaad.2022.04.006 35427684
PGP000320 1 1 He YQ A polygenic risk score for nasopharyngeal carcinoma shows potential for risk stratification and personalized screening. Nat Commun 12/04/2022 10.1038/s41467-022-29570-4 35414057
PGP000322 0 1 Klein RJ Prostate cancer polygenic risk score and prediction of lethal prostate cancer. NPJ Precis Oncol 08/04/2022 10.1038/s41698-022-00266-8 35396534
PGP000332 415 415 Weissbrod O Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores. Nat Genet 07/04/2022 10.1038/s41588-022-01036-9 35393596
PGP000315 0 1 Hämmerle M A Family and a Genome-Wide Polygenic Risk Score Are Independently Associated With Stroke in a Population-Based Study. Stroke 07/04/2022 10.1161/strokeaha.121.036551 35387493
PGP000304 1 1 Nauffal V Monogenic and Polygenic Contributions to QTc Prolongation in the Population. Circulation 07/04/2022 10.1161/circulationaha.121.057261 35389749
PGP000347 1 1 Yuan C The age-dependent association of risk factors with pancreatic cancer. Ann Oncol 06/04/2022 10.1016/j.annonc.2022.03.276 35398288
PGP000348 0 1 Hu X Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program. Am J Hum Genet 05/04/2022 10.1016/j.ajhg.2022.03.007 35385699
PGP000309 1 1 Bellenguez C New insights into the genetic etiology of Alzheimer's disease and related dementias. Nat Genet 04/04/2022 10.1038/s41588-022-01024-z 35379992
PGP000317 0 2 Parcha V Association of Polygenic Risk Score With Blood Pressure and Adverse Cardiovascular Outcomes in Individuals With Type II Diabetes: Insights From the ACCORD Trial. Hypertension 04/04/2022 10.1161/hypertensionaha.122.18976 35369713
PGP000316 1 1 Zimmerman SC Association of Genetic Variants Linked to Late-Onset Alzheimer Disease With Cognitive Test Performance by Midlife. JAMA Netw Open 01/04/2022 10.1001/jamanetworkopen.2022.5491 35377426
PGP000318 1 1 Gurung RL Genetic risk score for plasma uric acid levels is associated with early rapid kidney function decline in type 2 diabetes. J Clin Endocrinol Metab 01/04/2022 10.1210/clinem/dgac192 35363857
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
PGP000244 779 814 Tanigawa Y Significant sparse polygenic risk scores across 813 traits in UK Biobank. PLoS Genet 24/03/2022 10.1371/journal.pgen.1010105 35324888
PGP000311 0 1 Olmastroni E Twelve Variants Polygenic Score for Low-Density Lipoprotein Cholesterol Distribution in a Large Cohort of Patients With Clinically Diagnosed Familial Hypercholesterolemia With or Without Causative Mutations. J Am Heart Assoc 24/03/2022 10.1161/jaha.121.023668 35322671
PGP000308 0 1 Schaid DJ Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk. Am J Hum Genet 23/03/2022 10.1016/j.ajhg.2022.03.008 35353984
PGP000319 0 1 Guo F Polygenic Risk Score for Defining Personalized Surveillance Intervals After Adenoma Detection and Removal at Colonoscopy. Clin Gastroenterol Hepatol 21/03/2022 10.1016/j.cgh.2022.03.013 35331942
PGP000312 2 2 Schnurr TM Interactions of physical activity, muscular fitness, adiposity, and genetic risk for NAFLD. Hepatol Commun 15/03/2022 10.1002/hep4.1932 35293152
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
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
PGP000345 1 1 Lai D Evaluating risk for alcohol use disorder: Polygenic risk scores and family history. Alcohol Clin Exp Res 10/03/2022 10.1111/acer.14772 35267208
PGP000306 0 1 Thompson PL Common genetic variants do not predict recurrent events in coronary heart disease patients. BMC Cardiovasc Disord 09/03/2022 10.1186/s12872-022-02520-0 35264114
PGP000334 1 1 Shams H Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans. Brain 07/03/2022 10.1093/brain/awac092 35253861
PGP000305 1 1 Siddiqui MK Young-onset diabetes in Asian Indians is associated with lower measured and genetically determined beta cell function. Diabetologia 05/03/2022 10.1007/s00125-022-05671-z 35247066
PGP000301 1 1 Roselli C Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse. Eur Heart J 04/03/2022 10.1093/eurheartj/ehac049 35245370
PGP000302 2 2 Horowitz JE Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. Nat Genet 03/03/2022 10.1038/s41588-021-01006-7 35241825
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
PGP000324 1 1 Yang Y Incorporating Polygenic Risk Scores and Nongenetic Risk Factors for Breast Cancer Risk Prediction Among Asian Women. JAMA Netw Open 01/03/2022 10.1001/jamanetworkopen.2021.49030 35311964
PGP000290 0 1 Mordi IR Prediction of Major Adverse Cardiovascular Events From Retinal, Clinical, and Genomic Data in Individuals With Type 2 Diabetes: A Population Cohort Study. Diabetes Care 01/03/2022 10.2337/dc21-1124 35043139
PGP000291 1 1 Piekos JA Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid. Hum Genet 28/02/2022 10.1007/s00439-022-02442-z 35226188
PGP000260 1 1 Barc J Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nat Genet 24/02/2022 10.1038/s41588-021-01007-6 35210625
PGP000289 1 1 Lu X A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study. Eur Heart J 23/02/2022 10.1093/eurheartj/ehac093 35195259
PGP000261 2 2 Tamlander M Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes. Commun Biol 23/02/2022 10.1038/s42003-021-02996-0 35197564
PGP000300 1 1 Zhang P Association of smoking and polygenic risk with the incidence of lung cancer: a prospective cohort study. Br J Cancer 22/02/2022 10.1038/s41416-022-01736-3 35194190
PGP000326 1 1 Maj C Dissecting the Polygenic Basis of Primary Hypertension: Identification of Key Pathway-Specific Components. Front Cardiovasc Med 16/02/2022 10.3389/fcvm.2022.814502 35252394
PGP000325 1 1 Tsai CW Prognostic significance of circulating insulin growth-like factor 1 and insulin growth-like factor binding protein 3 in renal cell carcinoma patients. American Journal of Cancer Research 15/02/2022 — 35261807
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