Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
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
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
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
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
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
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
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
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
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
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
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
PGP000097 3 3 Flynn E Sex-specific genetic effects across biomarkers. Eur J Hum Genet 01/09/2020 10.1038/s41431-020-00712-w 32873964
PGP000165 2 2 Cherny SS Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank. Eur J Hum Genet 20/03/2020 10.1038/s41431-020-0603-2 32203203
PGP000194 1 1 Barnes CLK Contribution of common risk variants to multiple sclerosis in Orkney and Shetland. Eur J Hum Genet 04/06/2021 10.1038/s41431-021-00914-w 34088990
PGP000310 1 1 Canzian F A polygenic risk score for multiple myeloma risk prediction. Eur J Hum Genet 30/11/2021 10.1038/s41431-021-00986-8 34845334
PGP000277 2 2 Dareng EO Polygenic risk modeling for prediction of epithelial ovarian cancer risk. Eur J Hum Genet 14/01/2022 10.1038/s41431-021-00987-7 35027648
PGP000117 2 5 Barnes DR Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants. Genet Med 15/07/2020 10.1038/s41436-020-0862-x 32665703
PGP000625 0 1 Lakeman IMM Validation of the BOADICEA model and a 313-variant polygenic risk score for breast cancer risk prediction in a Dutch prospective cohort. Genet Med 06/07/2020 10.1038/s41436-020-0884-4 32624571
PGP000206 1 1 Teumer A Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Nat Commun 11/09/2019 10.1038/s41467-019-11576-0 31511532
PGP000046 3 3 Kuchenbaecker K The transferability of lipid loci across African, Asian and European cohorts. Nat Commun 24/09/2019 10.1038/s41467-019-12026-7 31551420
PGP000027 1 2 Abraham G Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke. Nat Commun 20/12/2019 10.1038/s41467-019-13848-1 31862893
PGP000228 1 1 Revez JA Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Nat Commun 02/04/2020 10.1038/s41467-020-15421-7 32242144
PGP000236 2 2 Ntalla I Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nat Commun 21/05/2020 10.1038/s41467-020-15706-x 32439900
PGP000126 1 1 Pirruccello JP Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Nat Commun 07/05/2020 10.1038/s41467-020-15823-7 32382064
PGP000171 0 2 Fahed AC Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions. Nat Commun 20/08/2020 10.1038/s41467-020-17374-3 32820175
PGP000629 1 1 Saw J Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction. Nat Commun 04/09/2020 10.1038/s41467-020-17558-x 32887874
PGP000112 4 4 Ho WK European polygenic risk score for prediction of breast cancer shows similar performance in Asian women. Nat Commun 31/07/2020 10.1038/s41467-020-17680-w 32737321
PGP000101 1 1 Zhang Q Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture. Nat Commun 23/09/2020 10.1038/s41467-020-18534-1 32968074
PGP000186 16 32 Kachuri L Pan-cancer analysis demonstrates that integrating polygenic risk scores with modifiable risk factors improves risk prediction. Nat Commun 27/11/2020 10.1038/s41467-020-19600-4 33247094
PGP000102 1 3 Mars N The role of polygenic risk and susceptibility genes in breast cancer over the course of life Nat Commun 14/12/2020 10.1038/s41467-020-19966-5 33318493
PGP000138 3 3 Fontanillas P Disease risk scores for skin cancers. Nat Commun 08/01/2021 10.1038/s41467-020-20246-5 33420020
PGP000160 1 1 Wang YF Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups. Nat Commun 03/02/2021 10.1038/s41467-021-21049-y 33536424
PGP000149 1 1 Huynh-Le MP Polygenic hazard score is associated with prostate cancer in multi-ethnic populations. Nat Commun 23/02/2021 10.1038/s41467-021-21287-0 33623038
PGP000058 0 1 Huynh-Le MP Polygenic hazard score is associated with prostate cancer in multi-ethnic populations. Nat Commun 23/02/2021 10.1038/s41467-021-21287-0 33623038
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
PGP000147 0 11 Thareja G Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Nat Commun 23/02/2021 10.1038/s41467-021-21381-3 33623009
PGP000201 3 3 Pazoki R Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes. Nat Commun 10/05/2021 10.1038/s41467-021-22338-2 33972514
PGP000231 1 1 de Rojas I Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Nat Commun 07/06/2021 10.1038/s41467-021-22491-8 34099642
PGP000164 3 3 Khan Z Genetic variation associated with thyroid autoimmunity shapes the systemic immune response to PD-1 checkpoint blockade. Nat Commun 07/06/2021 10.1038/s41467-021-23661-4 34099659
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
PGP000391 3 3 Agrawal S Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Nat Commun 30/06/2022 10.1038/s41467-022-30931-2 35773277
PGP000531 4 4 Kurniansyah N A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood. Nat Commun 21/06/2022 10.1038/s41467-022-31080-2 35729114
PGP000314 1 1 Pujol-Gualdo N Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse. Nat Commun 23/06/2022 10.1038/s41467-022-31188-5 35739095
PGP000405 18 18 Kim YJ The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. Nat Commun 04/11/2022 10.1038/s41467-022-34163-2 36333282
PGP000427 1 1 Krohn L Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects. Nat Commun 05/12/2022 10.1038/s41467-022-34732-5 36470867
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
PGP000429 2 2 Seviiri M A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma. Nat Commun 10/12/2022 10.1038/s41467-022-35345-8 36496446
PGP000434 1 1 Khurshid S Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass. Nat Commun 21/03/2023 10.1038/s41467-023-37173-w 36944631
PGP000510 8 2 Kurniansyah N Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups. Nat Commun 02/06/2023 10.1038/s41467-023-38990-9 37268629
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