Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000343 1 1 Marques-Vidal P Association between genetic risk of high SBP and hypertension control: the CoLaus|PsyColaus study. J Hypertens 10/06/2022 10.1097/hjh.0000000000003158 35703291
PGP000538 1 1 Aranda-Guillén M A polygenic risk score to help discriminate primary adrenal insufficiency of different etiologies. J Intern Med 21/05/2023 10.1111/joim.13649 37151110
PGP000660 1 1 Kim Y Replacing device-measured sedentary time with physical activity is associated with lower risk of coronary heart disease regardless of genetic risk. J Intern Med 24/08/2023 10.1111/joim.13715 37614046
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
PGP000558 1 1 Vasavda C A Polygenic Risk Score for Predicting Racial and Genetic Susceptibility to Prurigo Nodularis. J Invest Dermatol 26/05/2023 10.1016/j.jid.2023.04.033 37245863
PGP000451 6 6 Al-Janabi A Atopic polygenic risk score is associated with paradoxical eczema developing in psoriasis patients treated with biologics. J Invest Dermatol 15/02/2023 10.1016/j.jid.2023.01.021 36804406
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
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
PGP000197 1 1 Potjer TP Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma. J Med Genet 29/09/2020 10.1136/jmedgenet-2020-107251 32994281
PGP000048 2 2 Yang X Evaluation of polygenic risk scores for ovarian cancer risk prediction in a prospective cohort study. J Med Genet 05/05/2018 10.1136/jmedgenet-2018-105313 29730597
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
PGP000037 1 1 Lakeman IMM Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families. J Med Genet 11/06/2019 10.1136/jmedgenet-2019-106072 31186341
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
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
PGP000033 4 7 Kuchenbaecker KB Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers. J Natl Cancer Inst 01/07/2017 10.1093/jnci/djw302 28376175
PGP000279 1 1 Archambault AN Risk Stratification for Early-Onset Colorectal Cancer Using a Combination of Genetic and Environmental Risk Scores: An International Multi-Center Study. J Natl Cancer Inst 13/01/2022 10.1093/jnci/djac003 35026030
PGP000644 0 1 Arthur RS Genetic Factors, Adherence to Healthy Lifestyle Behavior, and Risk of Invasive Breast Cancer Among Women in the UK Biobank. J Natl Cancer Inst 01/09/2020 10.1093/jnci/djz241 31899501
PGP000001 3 3 Mavaddat N Prediction of breast cancer risk based on profiling with common genetic variants. J Natl Cancer Inst 08/04/2015 10.1093/jnci/djv036 25855707
PGP000245 0 4 Barnes DR Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores. J Natl Cancer Inst 28/07/2021 10.1093/jnci/djab147 34320204
PGP000094 1 1 Shieh Y A Polygenic Risk Score for Breast Cancer in US Latinas and Latin American Women. J Natl Cancer Inst 01/06/2020 10.1093/jnci/djz174 31553449
PGP000040 1 1 Schmit SL Novel Common Genetic Susceptibility Loci for Colorectal Cancer. J Natl Cancer Inst 01/02/2019 10.1093/jnci/djy099 29917119
PGP000400 0 1 Pagadala MS Polygenic risk of any, metastatic, and fatal prostate cancer in the Million Veteran Program. J Natl Cancer Inst 28/10/2022 10.1093/jnci/djac199 36305680
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
PGP000553 0 1 Mao X Prediction of breast cancer risk for sisters of women attending screening. J Natl Cancer Inst 01/11/2023 10.1093/jnci/djad101 37243694
PGP000198 0 2 Borde J Performance of breast cancer polygenic risk scores in 760 female CHEK2 germline mutation carriers. J Natl Cancer Inst 29/12/2020 10.1093/jnci/djaa203 33372680
PGP000596 8 8 Hu J Using clinical and genetic risk factors for risk prediction of 8 cancers in the UK Biobank. JNCI Cancer Spectr 01/02/2024 10.1093/jncics/pkae008 38366150
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
PGP000275 1 1 Kothalawala DM Integration of Genomic Risk Scores to Improve the Prediction of Childhood Asthma Diagnosis J Pers Med 08/01/2022 10.3390/jpm12010075 35055391
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
PGP000661 1 1 Tsepilov YA Development and Replication of a Genome-Wide Polygenic Risk Score for Chronic Back Pain. J Pers Med 10/06/2023 10.3390/jpm13060977 37373966
PGP000111 2 2 Smith MP Evaluation of a Genetic Risk Score for Diagnosis of Psoriatic Arthritis. J Psoriasis Psoriatic Arthritis 04/03/2020 10.1177/2475530320910814 32462110
PGP000358 1 1 Lahey BB Associations of polygenic risk for attention-deficit/hyperactivity disorder with general and specific dimensions of childhood psychological problems and facets of impulsivity. J Psychiatr Res 14/06/2022 10.1016/j.jpsychires.2022.06.019 35752070
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
PGP000522 1 1 Wu Q Sleep patterns, genetic susceptibility, and risk of new-onset gout: The UK Biobank prospective cohort study. J Psychosom Res 18/05/2023 10.1016/j.jpsychores.2023.111381 37244070
PGP000375 1 1 Xie J Genetic risk and incident venous thromboembolism in middle-aged and older adults following COVID-19 vaccination. J Thromb Haemost 15/09/2022 10.1111/jth.15879 36111372
PGP000431 5 5 Ko CL Genome-wide association study reveals ethnicity-specific SNPs associated with ankylosing spondylitis in the Taiwanese population. J Transl Med 12/12/2022 10.1186/s12967-022-03701-3 36510243
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
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
PGP000411 1 1 Steinbrenner I A Polygenic Score for Reduced Kidney Function and Adverse Outcomes in a Chronic Kidney Disease Cohort. Kidney Int 05/12/2022 10.1016/j.kint.2022.11.013 36481179
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
PGP000562 3 3 Youssef O High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases. Lab Invest 15/01/2024 10.1016/j.labinv.2024.100325 38220043
PGP000003 1 1 Mega JL Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials. Lancet 04/03/2015 10.1016/S0140-6736(14)61730-X 25748612
PGP000200 1 1 Talmud PJ Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study. Lancet 22/02/2013 10.1016/s0140-6736(12)62127-8 23433573
PGP000207 1 1 van der Lee SJ The effect of APOE and other common genetic variants on the onset of Alzheimer's disease and dementia: a community-based cohort study. Lancet Neurol 16/03/2018 10.1016/s1474-4422(18)30053-x 29555425
PGP000235 2 2 Nalls MA Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet Neurol 01/12/2019 10.1016/s1474-4422(19)30320-5 31701892
PGP000292 0 3 Saad M Genetic predisposition to cancer across people of different ancestries in Qatar: a population-based, cohort study. Lancet Oncol 09/02/2022 10.1016/s1470-2045(21)00752-x 35150601
PGP000387 1 2 Qin N Association of the interaction between mosaic chromosomal alterations and polygenic risk score with the risk of lung cancer: an array-based case-control association and prospective cohort study. Lancet Oncol 17/10/2022 10.1016/s1470-2045(22)00600-3 36265503
PGP000525 0 18 Yajnik CS Polygenic scores of diabetes-related traits in subgroups of type 2 diabetes in India: a cohort study. Lancet Reg Health Southeast Asia 02/05/2023 10.1016/j.lansea.2023.100182 37492423
PGP000264 2 2 Moll M Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts. Lancet Respir Med 01/07/2020 10.1016/s2213-2600(20)30101-6 32649918
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