Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
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
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
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
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
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
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
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
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
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
PGP000617 1 1 Yun JS Polygenic risk for type 2 diabetes, lifestyle, metabolic health, and cardiovascular disease: a prospective UK Biobank study. Cardiovasc Diabetol 14/07/2022 10.1186/s12933-022-01560-2 35836215
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
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
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
PGP000373 0 3 Kim MS Testing the generalizability of ancestry-specific polygenic risk scores to predict prostate cancer in sub-Saharan Africa. Genome Biol 13/09/2022 10.1186/s13059-022-02766-z 36100952
PGP000366 4 4 Kanoni S Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biol 27/12/2022 10.1186/s13059-022-02837-1 36575460
PGP000029 2 3 Abraham G Genomic prediction of celiac disease targeting HLA-positive individuals. Genome Med 16/07/2015 10.1186/s13073-015-0196-5 26244058
PGP000057 0 3 Homburger JR Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores. Genome Med 26/11/2019 10.1186/s13073-019-0682-2 31771638
PGP000121 4 4 Tam CHT Development of genome-wide polygenic risk scores for lipid traits and clinical applications for dyslipidemia, subclinical atherosclerosis, and diabetes cardiovascular complications among East Asians. Genome Med 19/02/2021 10.1186/s13073-021-00831-z 33608049
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
PGP000331 1 1 Ge T Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. Genome Med 29/06/2022 10.1186/s13073-022-01074-2 35765100
PGP000414 1 1 Xin J Risk assessment for colorectal cancer via polygenic risk score and lifestyle exposure: a large-scale association study of East Asian and European populations. Genome Med 24/01/2023 10.1186/s13073-023-01156-9 36694225
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
PGP000619 3 3 Mandla R Polygenic scores for longitudinal prediction of incident type 2 diabetes in an ancestrally and medically diverse primary care physician network: a patient cohort study. Genome Med 26/04/2024 10.1186/s13073-024-01337-0 38671457
PGP000188 0 1 Tangtanatakul P Meta-analysis of genome-wide association study identifies FBN2 as a novel locus associated with systemic lupus erythematosus in Thai population. Arthritis Res Ther 08/08/2020 10.1186/s13075-020-02276-y 32771030
PGP000282 1 1 Wu Q An early prediction model for gestational diabetes mellitus based on genetic variants and clinical characteristics in China. Diabetol Metab Syndr 24/01/2022 10.1186/s13098-022-00788-y 35073990
PGP000527 3 3 Green RE Investigating associations between blood metabolites, later life brain imaging measures, and genetic risk for Alzheimer's disease. Alzheimers Res Ther 22/02/2023 10.1186/s13195-023-01184-y 36814324
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
PGP000612 3 3 Gao C Risk of Breast Cancer Among Carriers of Pathogenic Variants in Breast Cancer Predisposition Genes Varies by Polygenic Risk Score. J Clin Oncol 08/06/2021 10.1200/jco.20.01992 34101481
PGP000034 1 4 Lecarpentier J Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores. J Clin Oncol 27/04/2017 10.1200/JCO.2016.69.4935 28448241
PGP000428 1 1 Nyberg T CanRisk-Prostate: A Comprehensive, Externally Validated Risk Model for the Prediction of Future Prostate Cancer. J Clin Oncol 09/12/2022 10.1200/jco.22.01453 36493335
PGP000572 0 1 Lopes Cardozo JMN Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival. J Clin Oncol 23/01/2023 10.1200/jco.22.01978 36689693
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
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
PGP000610 0 1 Wang JR Association of Polygenic Score With Tumor Molecular Subtypes in Papillary Thyroid Carcinoma. J Clin Endocrinol Metab 01/12/2023 10.1210/clinem/dgad407 37453101
PGP000214 4 5 Aksit MA Genetic Modifiers of Cystic Fibrosis-Related Diabetes Have Extensive Overlap With Type 2 Diabetes and Related Traits. J Clin Endocrinol Metab 01/05/2020 10.1210/clinem/dgz102 31697830
PGP000024 0 1 Udler MS Genetic Risk Scores for Diabetes Diagnosis and Precision Medicine. Endocr Rev 01/12/2019 10.1210/er.2019-00088 31322649
PGP000039 2 2 Tosto G Polygenic risk scores in familial Alzheimer disease. Neurology 17/02/2017 10.1212/WNL.0000000000003734 28213371
PGP000285 1 1 Lu X Development and Validation of a Polygenic Risk Score for Stroke in the Chinese Population. Neurology 24/05/2021 10.1212/wnl.0000000000012263 34031205
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
PGP000369 0 1 Jaworek T Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke. Neurology 31/08/2022 10.1212/wnl.0000000000201006 36240095
PGP000529 2 2 Acosta JN Polygenic Susceptibility to Hypertension and Blood Pressure Control in Stroke Survivors. Neurology 23/01/2023 10.1212/wnl.0000000000206763 36690452
PGP000280 2 2 Kujala UM Polygenic Risk Scores and Physical Activity. Med Sci Sports Exerc 01/07/2020 10.1249/mss.0000000000002290 32049886
PGP000560 1 1 Zhang J Association of Combined Exposure to Ambient Air Pollutants, Genetic Risk, and Incident Rheumatoid Arthritis: A Prospective Cohort Study in the UK Biobank. Environ Health Perspect 13/03/2023 10.1289/ehp10710 36913237
PGP000028 1 1 Abraham G Accurate and robust genomic prediction of celiac disease using statistical learning. PLoS Genet 13/02/2014 10.1371/journal.pgen.1004137 24550740
PGP000055 3 3 Fritsche LG Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb. PLoS Genet 13/06/2019 10.1371/journal.pgen.1008202 31194742
PGP000199 0 1 Ferreira MAR Age-of-onset information helps identify 76 genetic variants associated with allergic disease. PLoS Genet 30/06/2020 10.1371/journal.pgen.1008725 32603359
PGP000630 2 2 Wu Y Exclusive breastfeeding can attenuate body-mass-index increase among genetically susceptible children: A longitudinal study from the ALSPAC cohort. PLoS Genet 11/06/2020 10.1371/journal.pgen.1008790 32525877
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