Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
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
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
PGP000621 3 3 Gao G Polygenic risk scores for prediction of breast cancer risk in women of African ancestry: a cross-ancestry approach. Hum Mol Genet 01/09/2022 10.1093/hmg/ddac102 35554533
PGP000671 1 1 Gao P Association between serum urea concentrations and the risk of colorectal cancer, particularly in individuals with type 2 diabetes: A cohort study. Int J Cancer 06/09/2023 10.1002/ijc.34719 37671773
PGP000426 1 1 Gao XR Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma. Nat Commun 30/11/2022 10.1038/s41467-022-35188-3 36450729
PGP000288 0 1 Garcia-Etxebarria K Local genetic variation of inflammatory bowel disease in Basque population and its effect in risk prediction. Sci Rep 01/03/2022 10.1038/s41598-022-07401-2 35232999
PGP000460 1 1 García-González P Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men. Int J Mol Sci 04/01/2023 10.3390/ijms24020898 36674414
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
PGP000594 1 1 Ghouse J Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nat Genet 17/04/2024 10.1038/s41588-024-01720-y 38632349
PGP000398 1 1 Ghouse J Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism. Nat Genet 19/01/2023 10.1038/s41588-022-01286-7 36658437
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
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
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
PGP000582 2 2 Gorman BR Distinctive cross-ancestry genetic architecture for age-related macular degeneration medRxivPre 21/08/2022 10.1101/2022.08.16.22278855 —
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
PGP000050 16 16 Graff RE Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts. Nat Commun 12/02/2021 10.1038/s41467-021-21288-z 33579919
PGP000230 12 12 Graham SE The power of genetic diversity in genome-wide association studies of lipids. Nature 09/12/2021 https://doi.org/10.1038/s41586-021-04064-3 34887591
PGP000330 0 1 Gratton J LDL-C Concentrations and the 12-SNP LDL-C Score for Polygenic Hypercholesterolaemia in Self-Reported South Asian, Black and Caribbean Participants of the UK Biobank. Front Genet 31/03/2022 10.3389/fgene.2022.845498 35432461
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
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
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
PGP000098 1 1 Grove J Identification of common genetic risk variants for autism spectrum disorder. Nat Genet 25/02/2019 10.1038/s41588-019-0344-8 30804558
PGP000599 0 9 Guarischi-Sousa R Contemporary Polygenic Scores of Low-Density Lipoprotein Cholesterol and Coronary Artery Disease Predict Coronary Atherosclerosis in Adolescents and Young Adults. Circ Genom Precis Med 06/07/2023 10.1161/circgen.122.004047 37409455
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
PGP000370 6 6 Gui Y Sex-specific genetic association between psychiatric disorders and cognition, behavior and brain imaging in children and adults. Transl Psychiatry 26/08/2022 10.1038/s41398-022-02041-6 36028495
PGP000319 0 1 Guo F Polygenic Risk Score for Defining Personalized Surveillance Intervals After Adenoma Detection and Removal at Colonoscopy. Clin Gastroenterol Hepatol 21/03/2022 10.1016/j.cgh.2022.03.013 35331942
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
PGP000566 1 2 Gu X Association of air pollution and genetic risks with incidence of elderly-onset atopic dermatitis: A prospective cohort study. Ecotoxicol Environ Saf 27/02/2023 10.1016/j.ecoenv.2023.114683 36857917
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
PGP000044 1 1 Hajek C Coronary Heart Disease Genetic Risk Score Predicts Cardiovascular Disease Risk in Men, Not Women. Circ Genom Precis Med 01/10/2018 10.1161/CIRCGEN.118.002324 30354305
PGP000315 0 1 Hämmerle M A Family and a Genome-Wide Polygenic Risk Score Are Independently Associated With Stroke in a Population-Based Study. Stroke 07/04/2022 10.1161/strokeaha.121.036551 35387493
PGP000190 1 1 Hang D Colorectal cancer susceptibility variants and risk of conventional adenomas and serrated polyps: results from three cohort studies. Int J Epidemiol 01/02/2020 10.1093/ije/dyz096 31038671
PGP000381 0 6 Hao L Development of a clinical polygenic risk score assay and reporting workflow. Nat Med 18/04/2022 10.1038/s41591-022-01767-6 35437332
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
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
PGP000514 5 5 Hassanin E Trans-ancestry polygenic models for the prediction of LDL blood levels: An analysis of the UK Biobank and Taiwan Biobank medRxivPre 06/08/2023 10.1101/2023.08.03.23293320 —
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
PGP000490 1 1 Hatoum AS Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders. Nat Ment Health 22/03/2023 10.1038/s44220-023-00034-y 37250466
PGP000585 2 2 Hawkes G Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood. Diabetologia 06/06/2023 10.1007/s00125-023-05923-6 37280435
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
PGP000600 0 1 Hendi NN The Genetic Architecture of Vitamin D Deficiency among an Elderly Lebanese Middle Eastern Population: An Exome-Wide Association Study. Nutrients 20/07/2023 10.3390/nu15143216 37513634
PGP000673 1 1 Herold JM Genetic Risk Score Analysis Supports a Joint View of Two Classification Systems for Age-Related Macular Degeneration. Invest Ophthalmol Vis Sci 01/09/2023 10.1167/iovs.64.12.31 37721739
PGP000321 1 1 He W Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on Aging. JAMA Ophthalmol 21/04/2022 10.1001/jamaophthalmol.2022.0891 35446358
PGP000218 0 1 He Y Comparisons of Polyexposure, Polygenic, and Clinical Risk Scores in Risk Prediction of Type 2 Diabetes. Diabetes Care 09/02/2021 10.2337/dc20-2049 33563654
PGP000320 1 1 He YQ A polygenic risk score for nasopharyngeal carcinoma shows potential for risk stratification and personalized screening. Nat Commun 12/04/2022 10.1038/s41467-022-29570-4 35414057
PGP000108 0 1 Hindy G Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease. Arterioscler Thromb Vasc Biol 22/09/2020 10.1161/atvbaha.120.314856 32957805
PGP000468 0 1 Hodel F Associations of genetic and infectious risk factors with coronary heart disease. Elife 14/02/2023 10.7554/elife.79742 36785929
PGP000056 2 2 Ho-Le TP Prediction of Bone Mineral Density and Fragility Fracture by Genetic Profiling. J Bone Miner Res 26/10/2016 10.1002/jbmr.2998 27649491
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
PGP000286 1 1 Honda S Polygenic risk scores are associated with radiographic progression in patients with rheumatoid arthritis. Arthritis Rheumatol 20/01/2022 10.1002/art.42051 35048562
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