Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
PGP000346 1 1 Lai D Gene-based polygenic risk scores analysis of alcohol use disorder in African Americans. Transl Psychiatry 05/07/2022 10.1038/s41398-022-02029-2 35790736
PGP000084 6 6 Barr PB Using polygenic scores for identifying individuals at increased risk of substance use disorders in clinical and population samples. Transl Psychiatry 18/06/2020 10.1038/s41398-020-00865-8 32555147
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
PGP000397 1 1 Huynh-Le MP Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score. Prostate Cancer Prostatic Dis 12/02/2022 10.1038/s41391-022-00497-7 35152271
PGP000219 0 1 Huynh-Le MP Common genetic and clinical risk factors: association with fatal prostate cancer in the Cohort of Swedish Men. Prostate Cancer Prostatic Dis 15/03/2021 10.1038/s41391-021-00341-4 33723363
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
PGP000521 1 1 Merino J Genetic predisposition to macronutrient preference and workplace food choices. Mol Psychiatry 23/05/2023 10.1038/s41380-023-02107-x 37217678
PGP000569 1 1 Lake J Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease. Mol Psychiatry 18/05/2023 10.1038/s41380-023-02089-w 37198259
PGP000080 1 1 Coleman JRI Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Mol Psychiatry 23/01/2020 10.1038/s41380-019-0546-6 31969693
PGP000448 8 8 Berndt SI Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes. Leukemia 22/10/2022 10.1038/s41375-022-01711-0 36273105
PGP000234 0 1 Kleinstern G Polygenic risk score and risk of monoclonal B-cell lymphocytosis in caucasians and risk of chronic lymphocytic leukemia (CLL) in African Americans. Leukemia 20/07/2021 10.1038/s41375-021-01344-9 34285341
PGP000677 0 4 Renier TJ Elucidating pathways to pediatric obesity: a study evaluating obesity polygenic risk scores related to appetitive traits in children. Int J Obes (Lond) 22/09/2023 10.1038/s41366-023-01385-3 37736781
PGP000195 1 0 Ferreira MA Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nat Genet 30/10/2017 10.1038/ng.3985 29083406
PGP000223 1 1 Lotta LA Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance. Nat Genet 14/11/2016 10.1038/ng.3714 27841877
PGP000010 1 1 Läll K Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores. Genet Med 11/08/2016 10.1038/gim.2016.103 27513194
PGP000032 0 1 Pashayan N Implications of polygenic risk-stratified screening for prostate cancer on overdiagnosis. Genet Med 08/01/2015 10.1038/gim.2014.192 25569441
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
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
PGP000049 1 1 Dai J Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations. Lancet Respir Med 17/07/2019 10.1016/S2213-2600(19)30144-4 31326317
PGP000025 1 1 Belsky DW Polygenic risk and the development and course of asthma: an analysis of data from a four-decade longitudinal study. Lancet Respir Med 28/06/2013 10.1016/S2213-2600(13)70101-2 24429243
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
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
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
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
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
PGP000191 1 1 He CY Performance of common genetic variants in risk prediction for colorectal cancer in Chinese: A two-stage and multicenter study. Genomics 02/02/2021 10.1016/j.ygeno.2021.01.025 33545268
PGP000679 130 130 Gunn S Comparison of Methods for Building Polygenic Scores for Diverse Populations. HGG Adv 25/09/2024 10.1016/j.xhgg.2024.100355 39323095
PGP000193 5 5 Polfus LM Genetic discovery and risk characterization in type 2 diabetes across diverse populations. HGG Adv 09/03/2021 10.1016/j.xhgg.2021.100029 34604815
PGP000604 158 158 Truong B Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. Cell Genom 12/03/2024 10.1016/j.xgen.2024.100523 38508198
PGP000463 2 2 Kleeman SO Cystatin C is glucocorticoid responsive, directs recruitment of Trem2+ macrophages, and predicts failure of cancer immunotherapy. Cell Genom 23/06/2023 10.1016/j.xgen.2023.100347 37601967
PGP000592 1 1 Wu Y 150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility. Cell Genom 05/06/2023 10.1016/j.xgen.2023.100326 37492107
PGP000262 18 18 Wang Y Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts. Cell Genom 04/01/2023 10.1016/j.xgen.2022.100241 36777179
PGP000703 20 20 Tsuo K Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity. Cell Genom 08/11/2022 10.1016/j.xgen.2022.100212 36778051
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
PGP000051 26 26 Xu Y Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease Cell Genom 12/01/2022 10.1016/j.xgen.2021.100086 35072137
PGP000265 1 1 Bonfiglio F GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome. Cell Genom 08/12/2021 10.1016/j.xgen.2021.100069 34957435
PGP000273 1 1 Haas ME Machine learning enables new insights into genetic contributions to liver fat accumulation. Cell Genom 01/12/2021 10.1016/j.xgen.2021.100066 34957434
PGP000422 1 4 Vanhoye X A new 165-SNP low-density lipoprotein cholesterol polygenic risk score based on next generation sequencing outperforms previously published scores in routine diagnostics of familial hypercholesterolemia. Transl Res 15/12/2022 10.1016/j.trsl.2022.12.002 36528340
PGP000597 0 1 Shi Z Cancer-associated thrombosis by cancer sites and inherited factors in a prospective population-based cohort. Thromb Res 26/06/2023 10.1016/j.thromres.2023.06.023 37419004
PGP000523 1 1 Lin J Association of time spent in outdoor light and genetic susceptibility with the risk of type 2 diabetes. Sci Total Environ 16/05/2023 10.1016/j.scitotenv.2023.164253 37201819
PGP000657 1 1 Cao Z Polygenic risk score for Parkinson's disease and olfaction among middle-aged to older women. Parkinsonism Relat Disord 17/08/2023 10.1016/j.parkreldis.2023.105815 37611509
PGP000352 1 1 Waksmunski AR Glaucoma genetic risk scores in the Million Veteran Program. Ophthalmology 16/06/2022 10.1016/j.ophtha.2022.06.012 35718050
PGP000299 1 1 Zekavat SM Photoreceptor Layer Thinning Is an Early Biomarker for Age-Related Macular Degeneration: Epidemiologic and Genetic Evidence from UK Biobank OCT Data. Ophthalmology 08/02/2022 10.1016/j.ophtha.2022.02.001 35149155
PGP000225 1 1 Qassim A An Intraocular Pressure Polygenic Risk Score Stratifies Multiple Primary Open-Angle Glaucoma Parameters Including Treatment Intensity. Ophthalmology 07/01/2020 10.1016/j.ophtha.2019.12.025 32081492
PGP000588 0 1 Marshall HN High Polygenic Risk Is Associated with Earlier Trabeculectomy in Patients with Primary Open-Angle Glaucoma. Ophthalmol Glaucoma 13/07/2022 10.1016/j.ogla.2022.06.009 35842105
PGP000374 0 1 Zaccardi F Self-reported walking pace, polygenic risk scores and risk of coronary artery disease in UK biobank. Nutr Metab Cardiovasc Dis 02/09/2022 10.1016/j.numecd.2022.08.021 36163213
PGP000649 1 1 Lawingco T Genetic variants in glutamate-, Aβ-, and tau-related pathways determine polygenic risk for Alzheimer's disease. Neurobiol Aging 12/11/2020 10.1016/j.neurobiolaging.2020.11.009 33303219
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
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
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