Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
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
PGP000394 1 1 Sumpter NA Association of Gout Polygenic Risk Score with Age at Disease Onset and Tophaceous Disease in European and Polynesian Men with Gout. Arthritis Rheumatol 25/10/2022 10.1002/art.42393 36281732
PGP000362 2 2 Lacaze P Genomic Risk Score for Advanced Osteoarthritis in Older Adults. Arthritis Rheumatol 23/07/2022 10.1002/art.42156 35506208
PGP000632 0 1 Aday AW Polygenic risk score in comparison with C-reactive protein for predicting incident coronary heart disease. Atherosclerosis 26/07/2023 10.1016/j.atherosclerosis.2023.117194 37536150
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
PGP000408 0 1 Borg SÁ Subclinical atherosclerosis determined by coronary artery calcium deposition in patients with clinical familial hypercholesterolemia. Atheroscler Plus 11/11/2022 10.1016/j.athplu.2022.10.002 36643796
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
PGP000399 1 1 Fang Y Polygenic Liability to Depression Is Associated With Multiple Medical Conditions in the Electronic Health Record: Phenome-wide Association Study of 46,782 Individuals. Biol Psychiatry 11/06/2022 10.1016/j.biopsych.2022.06.004 35965108
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 —
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 —
PGP000563 4 4 Yang Z Genetic Basis of Altered Platelet Counts and Gestational Thrombocytopenia in Pregnancy. Blood 08/12/2023 10.1182/blood.2023021925 38064665
PGP000220 1 1 Kleinstern G Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis. Blood 19/04/2018 10.1182/blood-2017-11-814608 29674426
PGP000355 0 2 Borde J Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers. BMC Cancer 27/06/2022 10.1186/s12885-022-09780-1 35761208
PGP000430 2 2 Pagadala MS PRState: Incorporating genetic ancestry in prostate cancer risk scores for men of African ancestry. BMC Cancer 09/12/2022 10.1186/s12885-022-10258-3 36494783
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
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
PGP000548 1 1 Feng J Association of laxatives use with incident dementia and modifying effect of genetic susceptibility: a population-based cohort study with propensity score matching. BMC Geriatr 04/03/2023 10.1186/s12877-023-03854-w 36870957
PGP000119 2 2 Namjou B GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. BMC Med 17/07/2019 10.1186/s12916-019-1364-z 31311600
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
PGP000556 0 1 Shannon OM Mediterranean diet adherence is associated with lower dementia risk, independent of genetic predisposition: findings from the UK Biobank prospective cohort study. BMC Med 14/03/2023 10.1186/s12916-023-02772-3 36915130
PGP000570 1 1 Li D Genetic susceptibility and lifestyle modify the association of long-term air pollution exposure on major depressive disorder: a prospective study in UK Biobank. BMC Med 21/02/2023 10.1186/s12916-023-02783-0 36810050
PGP000278 1 1 Dashti HS Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank. BMC Med 12/01/2022 10.1186/s12916-021-02198-9 35016652
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
PGP000361 1 1 Chiou JS Your height affects your health: genetic determinants and health-related outcomes in Taiwan. BMC Med 13/07/2022 10.1186/s12916-022-02450-w 35831902
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
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
PGP000114 1 1 Pechlivanis S Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study. BMC Med Genet 10/09/2020 10.1186/s12881-020-01113-y 32912153
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
PGP000396 0 1 Koraishy FM Polygenic association of glomerular filtration rate decline in world trade center responders. BMC Nephrol 28/10/2022 10.1186/s12882-022-02967-5 36307804
PGP000059 1 1 Ibanez L Parkinson disease polygenic risk score is associated with Parkinson disease status and age at onset but not with alpha-synuclein cerebrospinal fluid levels. BMC Neurol 15/11/2017 10.1186/s12883-017-0978-z 29141588
PGP000578 1 1 Tomassen J Amyloid-β and APOE genotype predict memory decline in cognitively unimpaired older individuals independently of Alzheimer's disease polygenic risk score. BMC Neurol 15/12/2022 10.1186/s12883-022-02925-6 36522743
PGP000047 1 1 Seibert TM Polygenic hazard score to guide screening for aggressive prostate cancer: development and validation in large scale cohorts. BMJ 10/01/2018 10.1136/bmj.j5757 29321194
PGP000438 6 6 Briggs SEW Integrating genome-wide polygenic risk scores and non-genetic risk to predict colorectal cancer diagnosis using UK Biobank data: population based cohort study. BMJ 09/11/2022 10.1136/bmj-2022-071707 36351667
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
PGP000026 1 1 Rutten-Jacobs LC Genetic risk, incident stroke, and the benefits of adhering to a healthy lifestyle: cohort study of 306 473 UK Biobank participants. BMJ 24/10/2018 10.1136/bmj.k4168 30355576
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
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
PGP000035 1 1 Wen W Prediction of breast cancer risk based on common genetic variants in women of East Asian ancestry. Breast Cancer Res 08/12/2016 10.1186/s13058-016-0786-1 27931260
PGP000248 0 2 Liou L Genomic risk prediction of coronary artery disease in women with breast cancer: a prospective cohort study. Breast Cancer Res 30/09/2021 10.1186/s13058-021-01465-0 34593009
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
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
PGP000018 2 2 Shieh Y Breast cancer risk prediction using a clinical risk model and polygenic risk score. Breast Cancer Res Treat 26/08/2016 10.1007/s10549-016-3953-2 27565998
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
PGP000072 1 1 Smith T The added value of genetic information in colorectal cancer risk prediction models: development and evaluation in the UK Biobank prospective cohort study. Br J Cancer 16/10/2018 10.1038/s41416-018-0282-8 30323197
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
PGP000031 1 1 Pashayan N Reducing overdiagnosis by polygenic risk-stratified screening: findings from the Finnish section of the ERSPC. Br J Cancer 20/08/2015 10.1038/bjc.2015.289 26291059
PGP000515 1 1 Tamlander M Genome-wide polygenic risk scores for colorectal cancer have implications for risk-based screening Br J Cancer 13/11/2023 10.1038/s41416-023-02536-z 38172535
PGP000424 1 1 Olsen CM Does polygenic risk influence associations between sun exposure and melanoma? A prospective cohort analysis. Br J Dermatol 17/12/2019 10.1111/bjd.18703 31747047
PGP000274 3 3 Steinberg J Independent evaluation of melanoma polygenic risk scores in UK and Australian prospective cohorts. Br J Dermatol 18/12/2021 10.1111/bjd.20956 34921685
PGP000613 0 1 Rashkin SR Generalization of a genetic risk score for time to first albuminuria in children with sickle cell anaemia: SCCRIP cohort study results. Br J Haematol 16/06/2021 10.1111/bjh.17647 34137022
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