Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000177 1 1 de Toro-Martín J The Challenge of Stratifying Obesity: Attempts in the Quebec Family Study. Front Genet 10/10/2019 10.3389/fgene.2019.00994 31649740
PGP000176 1 1 Sordillo JE Pharmacogenetic Polygenic Risk Score for Bronchodilator Response in Children and Adolescents with Asthma: Proof-of-Concept. J Pers Med 20/04/2021 10.3390/jpm11040319 33923870
PGP000175 1 1 Lahrouchi N Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Circulation 20/05/2020 10.1161/circulationaha.120.045956 32429735
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
PGP000173 0 2 Darst BF Combined Effect of a Polygenic Risk Score and Rare Genetic Variants on Prostate Cancer Risk. Eur Urol 01/05/2021 10.1016/j.eururo.2021.04.013 33941403
PGP000172 1 1 Bakshi A Genomic Risk Score for Melanoma in a Prospective Study of Older Individuals. J Natl Cancer Inst 10/04/2021 10.1093/jnci/djab076 33837773
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
PGP000170 1 0 Huyghe JR Discovery of common and rare genetic risk variants for colorectal cancer. Nat Genet 03/12/2018 10.1038/s41588-018-0286-6 30510241
PGP000169 1 1 Cole BS The Role of Genetic Ancestry as a Risk Factor for Primary Open-angle Glaucoma in African Americans. Invest Ophthalmol Vis Sci 01/02/2021 10.1167/iovs.62.2.28 33605984
PGP000168 0 1 Plym A Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer. J Natl Cancer Inst 01/04/2021 10.1093/jnci/djab058 33792693
PGP000167 0 3 Maguire S Common Susceptibility Loci for Male Breast Cancer. J Natl Cancer Inst 01/04/2021 10.1093/jnci/djaa101 32785646
PGP000166 0 1 Marston NA Genetic Risk Score to Identify Risk of Venous Thromboembolism in Patients With Cardiometabolic Disease. Circ Genom Precis Med 12/01/2021 10.1161/circgen.120.003006 33434447
PGP000165 2 2 Cherny SS Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank. Eur J Hum Genet 20/03/2020 10.1038/s41431-020-0603-2 32203203
PGP000164 3 3 Khan Z Genetic variation associated with thyroid autoimmunity shapes the systemic immune response to PD-1 checkpoint blockade. Nat Commun 07/06/2021 10.1038/s41467-021-23661-4 34099659
PGP000163 1 1 Lu T A polygenic risk score to predict future adult short stature amongst children. J Clin Endocrinol Metab 31/03/2021 10.1210/clinem/dgab215 33788949
PGP000162 2 2 Ouyang H Association between genetic risk scores and risk of narcolepsy: a case-control study. Ann Transl Med 01/02/2020 10.21037/atm.2019.12.95 32175396
PGP000161 1 1 Cho SK Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals. Sci Rep 08/06/2020 10.1038/s41598-020-66064-z 32514006
PGP000160 1 1 Wang YF Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups. Nat Commun 03/02/2021 10.1038/s41467-021-21049-y 33536424
PGP000159 1 1 Klarin D Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Circulation 28/09/2020 10.1161/circulationaha.120.047544 32981348
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
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
PGP000155 1 1 Bobbili DR Excess of singleton loss-of-function variants in Parkinson's disease contributes to genetic risk. J Med Genet 13/02/2020 10.1136/jmedgenet-2019-106316 32054687
PGP000154 0 1 Lu T Improved prediction of fracture risk leveraging a genome-wide polygenic risk score. Genome Med 03/02/2021 10.1186/s13073-021-00838-6 33536041
PGP000153 0 1 Manousaki D A Polygenic Risk Score as a Risk Factor for Medication-Associated Fractures. J Bone Miner Res 20/07/2020 10.1002/jbmr.4104 32511779
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
PGP000151 3 3 Cust AE Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies. J Invest Dermatol 08/06/2018 10.1016/j.jid.2018.05.023 29890168
PGP000150 1 2 Karunamuni RA Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer. Prostate Cancer Prostatic Dis 08/01/2021 10.1038/s41391-020-00311-2 33420416
PGP000149 1 1 Huynh-Le MP Polygenic hazard score is associated with prostate cancer in multi-ethnic populations. Nat Commun 23/02/2021 10.1038/s41467-021-21287-0 33623038
PGP000148 1 1 Hung RJ Assessing Lung Cancer Absolute Risk Trajectory Based on a Polygenic Risk Model. Cancer Res 20/01/2021 10.1158/0008-5472.can-20-1237 33472890
PGP000147 0 11 Thareja G Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Nat Commun 23/02/2021 10.1038/s41467-021-21381-3 33623009
PGP000146 1 1 Harper AR Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity. Nat Genet 25/01/2021 10.1038/s41588-020-00764-0 33495597
PGP000145 1 1 Roberts GHL Family Clustering of Autoimmune Vitiligo Results Principally from Polygenic Inheritance of Common Risk Alleles. Am J Hum Genet 18/07/2019 10.1016/j.ajhg.2019.06.013 31327509
PGP000144 3 3 Tadros R Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores. Eur Heart J 01/10/2019 10.1093/eurheartj/ehz435 31504448
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
PGP000142 1 1 Archambault AN Cumulative Burden of Colorectal Cancer-Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer. Gastroenterology 19/12/2019 10.1053/j.gastro.2019.12.012 31866242
PGP000141 0 1 Brandkvist M Genetic associations with temporal shifts in obesity and severe obesity during the obesity epidemic in Norway: A longitudinal population-based cohort (the HUNT Study). PLoS Med 14/12/2020 10.1371/journal.pmed.1003452 33315864
PGP000140 0 2 Brandkvist M Separating the genetics of childhood and adult obesity: a validation study of genetic scores for body mass index in adolescence and adulthood in the HUNT Study. Hum Mol Genet 04/12/2020 10.1093/hmg/ddaa256 33276378
PGP000139 1 2 Karunamuni RA African-specific improvement of a polygenic hazard score for age at diagnosis of prostate cancer. Int J Cancer 24/09/2020 10.1002/ijc.33282 32930425
PGP000138 3 3 Fontanillas P Disease risk scores for skin cancers. Nat Commun 08/01/2021 10.1038/s41467-020-20246-5 33420020
PGP000137 3 4 Ritchie SC Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases Nat Metab 08/11/2021 10.1038/s42255-021-00478-5 34750571
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
PGP000135 7 8 Jia G Evaluating the Utility of Polygenic Risk Scores in Identifying High-Risk Individuals for Eight Common Cancers. JNCI Cancer Spectr 12/03/2020 10.1093/jncics/pkaa021 32596635
PGP000134 1 1 Lanfear DE Polygenic Score for β-Blocker Survival Benefit in European Ancestry Patients With Reduced Ejection Fraction Heart Failure. Circ Heart Fail 04/10/2020 10.1161/circheartfailure.119.007012 33012170
PGP000133 0 1 Naito T Prevalence and Effect of Genetic Risk of Thromboembolic Disease in Inflammatory Bowel Disease. Gastroenterology 21/10/2020 10.1053/j.gastro.2020.10.019 33098885
PGP000132 2 2 Richardson TG Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study. BMJ 06/05/2020 10.1136/bmj.m1203 32376654
PGP000130 1 1 Sipeky C Prostate cancer risk prediction using a polygenic risk score. Sci Rep 13/10/2020 10.1038/s41598-020-74172-z 33051487
PGP000129 0 1 Mosley JD Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease. JAMA 01/02/2020 10.1001/jama.2019.21782 32068817
PGP000128 46 46 Sinnott-Armstrong N Genetics of 35 blood and urine biomarkers in the UK Biobank. Nat Genet 18/01/2021 10.1038/s41588-020-00757-z 33462484
PGP000127 1 1 Trinder M Clinical Utility of Lipoprotein(a) and LPA Genetic Risk Score in Risk Prediction of Incident Atherosclerotic Cardiovascular Disease. JAMA Cardiol 06/10/2020 10.1001/jamacardio.2020.5398 33021622
PGP000126 1 1 Pirruccello JP Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Nat Commun 07/05/2020 10.1038/s41467-020-15823-7 32382064
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