Publications

PGS Publication/Study ID (PGP) PGS Developed PGS Evaluated First Author Title Journal Name Publication Date Digital object identifier (doi) PubMed ID (PMID)
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
PGP000155 1 1 Bobbili DR Excess of singleton loss-of-function variants in Parkinson's disease contributes to genetic risk. J Med Genet 13/02/2020 10.1136/jmedgenet-2019-106316 32054687
PGP000156 1 1 Du Z A genome-wide association study of prostate cancer in Latinos. Int J Cancer 03/07/2019 10.1002/ijc.32525 31226226
PGP000157 1 1 Dron JS Genetic Predictor to Identify Individuals With High Lipoprotein(a) Concentrations. Circ Genom Precis Med 01/02/2021 10.1161/circgen.120.003182 33522245
PGP000159 1 1 Klarin D Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Circulation 28/09/2020 10.1161/circulationaha.120.047544 32981348
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
PGP000161 1 1 Cho SK Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals. Sci Rep 08/06/2020 10.1038/s41598-020-66064-z 32514006
PGP000162 2 2 Ouyang H Association between genetic risk scores and risk of narcolepsy: a case-control study. Ann Transl Med 01/02/2020 10.21037/atm.2019.12.95 32175396
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
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
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
PGP000166 0 1 Marston NA Genetic Risk Score to Identify Risk of Venous Thromboembolism in Patients With Cardiometabolic Disease. Circ Genom Precis Med 12/01/2021 10.1161/circgen.120.003006 33434447
PGP000167 0 3 Maguire S Common Susceptibility Loci for Male Breast Cancer. J Natl Cancer Inst 01/04/2021 10.1093/jnci/djaa101 32785646
PGP000168 0 1 Plym A Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer. J Natl Cancer Inst 01/04/2021 10.1093/jnci/djab058 33792693
PGP000169 1 1 Cole BS The Role of Genetic Ancestry as a Risk Factor for Primary Open-angle Glaucoma in African Americans. Invest Ophthalmol Vis Sci 01/02/2021 10.1167/iovs.62.2.28 33605984
PGP000170 1 0 Huyghe JR Discovery of common and rare genetic risk variants for colorectal cancer. Nat Genet 03/12/2018 10.1038/s41588-018-0286-6 30510241
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
PGP000172 1 1 Bakshi A Genomic Risk Score for Melanoma in a Prospective Study of Older Individuals. J Natl Cancer Inst 10/04/2021 10.1093/jnci/djab076 33837773
PGP000173 0 2 Darst BF Combined Effect of a Polygenic Risk Score and Rare Genetic Variants on Prostate Cancer Risk. Eur Urol 01/05/2021 10.1016/j.eururo.2021.04.013 33941403
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
PGP000175 1 1 Lahrouchi N Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Circulation 20/05/2020 10.1161/circulationaha.120.045956 32429735
PGP000176 1 1 Sordillo JE Pharmacogenetic Polygenic Risk Score for Bronchodilator Response in Children and Adolescents with Asthma: Proof-of-Concept. J Pers Med 20/04/2021 10.3390/jpm11040319 33923870
PGP000177 1 1 de Toro-Martín J The Challenge of Stratifying Obesity: Attempts in the Quebec Family Study. Front Genet 10/10/2019 10.3389/fgene.2019.00994 31649740
PGP000178 2 2 Chen L Genome-wide assessment of genetic risk for systemic lupus erythematosus and disease severity. Hum Mol Genet 01/06/2020 10.1093/hmg/ddaa030 32077931
PGP000179 3 6 Du Z Evaluating Polygenic Risk Scores for Breast Cancer in Women of African Ancestry. J Natl Cancer Inst 26/03/2021 10.1093/jnci/djab050 33769540
PGP000180 1 1 Innes H Genome-Wide Association Study for Alcohol-Related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1. Gastroenterology 16/06/2020 10.1053/j.gastro.2020.06.014 32561361
PGP000181 1 1 Liu G Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease. Nat Genet 06/05/2021 10.1038/s41588-021-00847-6 33958783
PGP000182 1 2 Tadros R Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Nat Genet 25/01/2021 10.1038/s41588-020-00762-2 33495596
PGP000183 1 1 Zhou X Genetic and polygenic risk score analysis for Alzheimer's disease in the Chinese population. Alzheimers Dement (Amst) 05/08/2020 10.1002/dad2.12074 32775599
PGP000184 1 1 Clark H Differential associations of allergic disease genetic variants with developmental profiles of eczema, wheeze and rhinitis. Clin Exp Allergy 15/10/2019 10.1111/cea.13485 31441980
PGP000185 1 1 Adel Fahmideh M A Weighted Genetic Risk Score of Adult Glioma Susceptibility Loci Associated with Pediatric Brain Tumor Risk. Sci Rep 02/12/2019 10.1038/s41598-019-54701-1 31792337
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
PGP000187 1 1 Severance LM Using a genetic risk score to calculate the optimal age for an individual to undergo coronary artery calcium screening. J Cardiovasc Comput Tomogr 09/05/2019 10.1016/j.jcct.2019.05.005 31104941
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
PGP000189 2 2 Dijk FN Genetic risk scores do not improve asthma prediction in childhood. J Allergy Clin Immunol 27/05/2019 10.1016/j.jaci.2019.05.017 31145937
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
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
PGP000192 1 1 Kawai VK Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis. Lupus 12/05/2021 10.1177/09612033211014952 33977795
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
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
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
PGP000196 2 2 Najar J Polygenic risk scores for Alzheimer's disease are related to dementia risk in APOE ɛ4 negatives. Alzheimers Dement (Amst) 22/01/2021 10.1002/dad2.12142 33532541
PGP000197 1 1 Potjer TP Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma. J Med Genet 29/09/2020 10.1136/jmedgenet-2020-107251 32994281
PGP000198 0 2 Borde J Performance of breast cancer polygenic risk scores in 760 female CHEK2 germline mutation carriers. J Natl Cancer Inst 29/12/2020 10.1093/jnci/djaa203 33372680
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
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
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
PGP000202 1 2 Bauer A Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study. Genet Epidemiol 03/06/2021 10.1002/gepi.22389 34082474
PGP000203 1 1 Forrest IS Genome-wide polygenic risk score for retinopathy of type 2 diabetes. Hum Mol Genet 01/05/2021 10.1093/hmg/ddab067 33704450
PGP000204 2 2 Luo J Immunotherapy-mediated thyroid dysfunction: genetic risk and impact on outcomes with PD-1 blockade in non-small cell lung cancer. Clin Cancer Res 08/07/2021 10.1158/1078-0432.ccr-21-0921 34244291
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