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Publications
Publications
PGS Publication/Study ID
(PGP)
PGS Developed
PGS Evaluated
First Author
Title
Journal Name
Publication Date
Digital object identifier
(doi)
PubMed ID
(PMID)
PGP000042
1
1
Natarajan P
Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention Setting.
Circulation
21/02/2017
10.1161/CIRCULATIONAHA.116.024436
28223407
PGP000707
0
1
Claessen G
Reduced Ejection Fraction in Elite Endurance Athletes: Clinical and Genetic Overlap With Dilated Cardiomyopathy.
Circulation
18/12/2023
10.1161/circulationaha.122.063777
38109351
PGP000568
0
1
Khan SS
Predictive Utility of a Validated Polygenic Risk Score for Long-Term Risk of Coronary Heart Disease in Young and Middle-Aged Adults.
Circulation
26/07/2022
10.1161/circulationaha.121.058426
35880530
PGP000304
1
1
Nauffal V
Monogenic and Polygenic Contributions to QTc Prolongation in the Population.
Circulation
07/04/2022
10.1161/circulationaha.121.057261
35389749
PGP000060
0
1
Khera AV
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction.
Circulation
01/03/2019
10.1161/circulationaha.118.035658
30586733
PGP000134
1
1
Lanfear DE
Polygenic Score for β-Blocker Survival Benefit in European Ancestry Patients With Reduced Ejection Fraction Heart Failure.
Circ Heart Fail
04/10/2020
10.1161/circheartfailure.119.007012
33012170
PGP000107
1
1
Trinder M
Polygenic Contribution to Low-Density Lipoprotein Cholesterol Levels and Cardiovascular Risk in Monogenic Familial Hypercholesterolemia.
Circ Genom Precis Med
13/08/2020
10.1161/circgen.120.002919
33079599
PGP000257
0
1
Wells QS
Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults.
Circ Genom Precis Med
31/08/2021
10.1161/circgen.121.003341
34463132
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
PGP000349
0
1
Shi M
Association of Genome-Wide Polygenic Risk Score for Body Mass Index With Cardiometabolic Health From Childhood Through Midlife.
Circ Genom Precis Med
08/06/2022
10.1161/circgen.121.003375
35675159
PGP000252
3
3
Ye Y
Interactions Between Enhanced Polygenic Risk Scores and Lifestyle for Cardiovascular Disease, Diabetes, and Lipid Levels.
Circ Genom Precis Med
12/01/2021
10.1161/circgen.120.003128
33433237
PGP000626
0
1
Douville NJ
Use of a Polygenic Risk Score Improves Prediction of Myocardial Injury After Non-Cardiac Surgery.
Circ Genom Precis Med
09/06/2020
10.1161/circgen.119.002817
32517536
PGP000386
0
4
Saad M
Validation of Polygenic Risk Scores for Coronary Heart Disease in a Middle Eastern Cohort Using Whole Genome Sequencing.
Circ Genom Precis Med
12/10/2022
10.1161/circgen.122.003712
36252120
PGP000591
2
2
Wang X
Genetic Susceptibility to Atrial Fibrillation Identified via Deep Learning of 12-Lead Electrocardiograms.
Circ Genom Precis Med
06/06/2023
10.1161/circgen.122.003808
37278238
PGP000092
19
19
Xie T
Genetic Risk Scores for Complex Disease Traits in Youth.
Circ Genom Precis Med
11/06/2020
10.1161/circgen.119.002775
32527150
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
PGP000008
0
2
Wünnemann F
Validation of Genome-Wide Polygenic Risk Scores for Coronary Artery Disease in French Canadians.
Circ Genom Precis Med
11/06/2019
10.1161/CIRCGEN.119.002481
31184202
PGP000602
3
3
Smith JL
Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization.
Circ Genom Precis Med
21/02/2024
10.1161/circgen.123.004272
38380516
PGP000384
1
1
Parcha V
Association of a Multi-Ancestry Genome-Wide Blood Pressure Polygenic Risk Score with Adverse Cardiovascular Events.
Circ Genom Precis Med
05/11/2022
10.1161/circgen.122.003946
36334310
PGP000586
0
1
Khurshid S
Predictive Accuracy of a Clinical and Genetic Risk Model for Atrial Fibrillation.
Circ Genom Precis Med
31/08/2021
10.1161/circgen.121.003355
34463125
PGP000143
0
1
Fahed AC
Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease.
Circ Genom Precis Med
07/12/2020
10.1161/circgen.120.003092
33284643
PGP000239
1
1
O'Sullivan JW
Combining Clinical and Polygenic Risk Improves Stroke Prediction Among Individuals With Atrial Fibrillation.
Circ Genom Precis Med
15/06/2021
10.1161/circgen.120.003168
34029116
PGP000654
1
1
Huang Y
Sexual Differences in Genetic Predisposition of Coronary Artery Disease.
Circ Genom Precis Med
17/12/2020
10.1161/circgen.120.003147
33332181
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
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
PGP000232
1
1
Feitosa MF
Heterogeneity of the Predictive Polygenic Risk Scores for Coronary Heart Disease Age-at-Onset in Three Different Coronary Heart Disease Family-Based Ascertainments.
Circ Genom Precis Med
12/04/2021
10.1161/circgen.120.003201
33844929
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
PGP000481
0
1
Lanfear DE
Validation of a Polygenic Score for Beta-Blocker Survival Benefit in Patients With Heart Failure Using the United Kingdom Biobank.
Circ Genom Precis Med
03/03/2023
10.1161/circgen.121.003835
36866666
PGP000512
2
2
Shetty NS
Sex Differences in the Association of Genome-Wide Systolic Blood Pressure Polygenic Risk Score With Hypertension.
Circ Genom Precis Med
09/10/2023
10.1161/circgen.123.004259
37807951
PGP000532
1
1
Manikpurage HD
Polygenic Risk Score for Coronary Artery Disease Improves the Prediction of Early-Onset Myocardial Infarction and Mortality in Men.
Circ Genom Precis Med
21/10/2021
10.1161/circgen.121.003452
34670400
PGP000270
2
2
Breeyear JH
Blood Pressure Polygenic Scores Are Associated With Apparent Treatment-Resistant Hypertension.
Circ Genom Precis Med
06/05/2022
10.1161/circgen.121.003554
35522175
PGP000327
1
1
Coassin S
Genome-Wide Characterization of a Highly Penetrant Form of Hyperlipoprotein(a)emia Associated With Genetically Elevated Cardiovascular Risk.
Circ Genom Precis Med
08/02/2022
10.1161/circgen.121.003489
35133173
PGP000598
1
1
Wang X
Low-level ambient sulfur dioxide exposure and genetic susceptibility associated with incidence of idiopathic pulmonary fibrosis: A national prospective cohort study.
Chemosphere
04/07/2023
10.1016/j.chemosphere.2023.139362
37414299
PGP000693
16
16
Kim MS
Metabolic polygenic risk scores for prediction of obesity, type 2 diabetes, and related morbidities.
Cell Metab
16/03/2026
10.1016/j.cmet.2026.02.009
41844147
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
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
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
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
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
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
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
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
PGP000078
29
27
Vuckovic D
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
Cell
01/09/2020
10.1016/j.cell.2020.08.008
32888494
PGP000017
1
1
Khera AV
Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood.
Cell
01/04/2019
10.1016/j.cell.2019.03.028
31002795
PGP000637
0
2
Kany S
Association of genetic risk and outcomes in patients with atrial fibrillation: interactions with early rhythm control in the EAST-AFNET4 trial.
Cardiovasc Res
01/08/2023
10.1093/cvr/cvad027
37264683
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
PGP000767
0
2
Beck JJ
Breast Cancer Polygenic Risk Score Validation and Effects of Variable Imputation.
Cancers (Basel)
20/04/2024
10.3390/cancers16081578
38672660
PGP000351
0
3
Li S
Genetic Aspects of Mammographic Density Measures Associated with Breast Cancer Risk.
Cancers (Basel)
02/06/2022
10.3390/cancers14112767
35681745
PGP000259
1
1
Yiangou K
Combination of a 15-SNP Polygenic Risk Score and Classical Risk Factors for the Prediction of Breast Cancer Risk in Cypriot Women.
Cancers (Basel)
11/09/2021
10.3390/cancers13184568
34572793
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