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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)
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
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
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
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
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
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
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
PGP000022
1
1
Weng LC
Genetic Predisposition, Clinical Risk Factor Burden, and Lifetime Risk of Atrial Fibrillation.
Circulation
12/11/2017
10.1161/CIRCULATIONAHA.117.031431
29129827
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
PGP000554
1
1
Marston NA
Predicting Benefit From Evolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial.
Circulation
11/11/2019
10.1161/circulationaha.119.043805
31707849
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
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
PGP000125
1
1
Marston NA
Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients with Cardiometabolic Disease.
Circulation
13/11/2020
10.1161/circulationaha.120.051927
33185476
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
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
PGP000240
2
2
Vaura F
Polygenic Risk Scores Predict Hypertension Onset and Cardiovascular Risk.
Hypertension
22/02/2021
10.1161/hypertensionaha.120.16471
33611940
PGP000233
2
2
Kauko A
Sex Differences in Genetic Risk for Hypertension.
Hypertension
15/08/2021
10.1161/hypertensionaha.121.17796
34397277
PGP000317
0
2
Parcha V
Association of Polygenic Risk Score With Blood Pressure and Adverse Cardiovascular Outcomes in Individuals With Type II Diabetes: Insights From the ACCORD Trial.
Hypertension
04/04/2022
10.1161/hypertensionaha.122.18976
35369713
PGP000311
0
1
Olmastroni E
Twelve Variants Polygenic Score for Low-Density Lipoprotein Cholesterol Distribution in a Large Cohort of Patients With Clinically Diagnosed Familial Hypercholesterolemia With or Without Causative Mutations.
J Am Heart Assoc
24/03/2022
10.1161/jaha.121.023668
35322671
PGP000209
0
1
Neumann JT
Predictive Performance of a Polygenic Risk Score for Incident Ischemic Stroke in a Healthy Older Population.
Stroke
27/05/2021
10.1161/strokeaha.120.033670
34039031
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
PGP000423
6
6
Bakker MK
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.
Stroke
19/01/2023
10.1161/strokeaha.122.040715
36655558
PGP000450
1
1
Mayerhofer E
Genetic Risk Score Improves Risk Stratification for Anticoagulation-Related Intracerebral Hemorrhage.
Stroke
09/02/2023
10.1161/strokeaha.122.041764
36756894
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
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
PGP000471
2
2
Tran JH
Genetic Associations Between Smoking- and Glaucoma-Related Traits.
Transl Vis Sci Technol
01/02/2023
10.1167/tvst.12.2.20
36786746
PGP000611
1
1
de Toro-Martín J
Polygenic risk score for predicting weight loss after bariatric surgery.
JCI Insight
06/09/2018
10.1172/jci.insight.122011
30185664
PGP000065
4
4
Zheutlin AB
Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems.
Am J Psychiatry
16/08/2019
10.1176/appi.ajp.2019.18091085
31416338
PGP000103
1
1
Maukonen M
Genetic Associations of Chronotype in the Finnish General Population.
J Biol Rhythms
24/06/2020
10.1177/0748730420935328
32579418
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
PGP000111
2
2
Smith MP
Evaluation of a Genetic Risk Score for Diagnosis of Psoriatic Arthritis.
J Psoriasis Psoriatic Arthritis
04/03/2020
10.1177/2475530320910814
32462110
PGP000220
1
1
Kleinstern G
Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis.
Blood
19/04/2018
10.1182/blood-2017-11-814608
29674426
PGP000563
4
4
Yang Z
Genetic Basis of Altered Platelet Counts and Gestational Thrombocytopenia in Pregnancy.
Blood
08/12/2023
10.1182/blood.2023021925
38064665
PGP000385
0
2
Zhang J
A polygenic risk score and age of diagnosis of COPD.
Eur Respir J
15/09/2022
10.1183/13993003.01954-2021
35115341
PGP000651
0
1
Liang H
Association of genetic risk and lifestyle with incident adult-onset asthma in the UK Biobank cohort.
ERJ Open Res
01/03/2023
10.1183/23120541.00499-2022
37057096
PGP000340
0
1
Vacher M
Assessment of a polygenic hazard score for the onset of pre-clinical Alzheimer's disease.
BMC Genomics
26/05/2022
10.1186/s12864-022-08617-2
35619096
PGP000306
0
1
Thompson PL
Common genetic variants do not predict recurrent events in coronary heart disease patients.
BMC Cardiovasc Disord
09/03/2022
10.1186/s12872-022-02520-0
35264114
PGP000548
1
1
Feng J
Association of laxatives use with incident dementia and modifying effect of genetic susceptibility: a population-based cohort study with propensity score matching.
BMC Geriatr
04/03/2023
10.1186/s12877-023-03854-w
36870957
PGP000114
1
1
Pechlivanis S
Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study.
BMC Med Genet
10/09/2020
10.1186/s12881-020-01113-y
32912153
PGP000396
0
1
Koraishy FM
Polygenic association of glomerular filtration rate decline in world trade center responders.
BMC Nephrol
28/10/2022
10.1186/s12882-022-02967-5
36307804
PGP000059
1
1
Ibanez L
Parkinson disease polygenic risk score is associated with Parkinson disease status and age at onset but not with alpha-synuclein cerebrospinal fluid levels.
BMC Neurol
15/11/2017
10.1186/s12883-017-0978-z
29141588
PGP000578
1
1
Tomassen J
Amyloid-β and APOE genotype predict memory decline in cognitively unimpaired older individuals independently of Alzheimer's disease polygenic risk score.
BMC Neurol
15/12/2022
10.1186/s12883-022-02925-6
36522743
PGP000355
0
2
Borde J
Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers.
BMC Cancer
27/06/2022
10.1186/s12885-022-09780-1
35761208
PGP000430
2
2
Pagadala MS
PRState: Incorporating genetic ancestry in prostate cancer risk scores for men of African ancestry.
BMC Cancer
09/12/2022
10.1186/s12885-022-10258-3
36494783
PGP000119
2
2
Namjou B
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.
BMC Med
17/07/2019
10.1186/s12916-019-1364-z
31311600
PGP000278
1
1
Dashti HS
Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank.
BMC Med
12/01/2022
10.1186/s12916-021-02198-9
35016652
PGP000329
1
1
Zhang Y
Healthy lifestyle counteracts the risk effect of genetic factors on incident gout: a large population-based longitudinal study.
BMC Med
29/04/2022
10.1186/s12916-022-02341-0
35484537
PGP000361
1
1
Chiou JS
Your height affects your health: genetic determinants and health-related outcomes in Taiwan.
BMC Med
13/07/2022
10.1186/s12916-022-02450-w
35831902
PGP000556
0
1
Shannon OM
Mediterranean diet adherence is associated with lower dementia risk, independent of genetic predisposition: findings from the UK Biobank prospective cohort study.
BMC Med
14/03/2023
10.1186/s12916-023-02772-3
36915130
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