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EFO_0001645
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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)
PGP000581
3
3
Keaton JM
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits.
Nat Genet
30/04/2024
10.1038/s41588-024-01714-w
38689001
PGP000645
1
1
Schwantes-An TH
A polygenic risk score for alcohol-associated cirrhosis among heavy drinkers with European ancestry.
Hepatol Commun
10/05/2024
10.1097/hc9.0000000000000431
38727677
PGP000546
60
60
Ohta R
A polygenic score method boosted by non-additive models.
Nat Commun
29/05/2024
10.1038/s41467-024-48654-x
38811555
PGP000631
1
1
Chikowore T
Variability of polygenic prediction for body mass index in Africa.
Genome Med
30/05/2024
10.1186/s13073-024-01348-x
38816834
PGP000620
3
3
Sun X
Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants that Confer Risk for Breast Cancer.
Cancer Res
04/06/2024
10.1158/0008-5472.can-23-3854
38832928
PGP000593
6
6
Ojima T
Body mass index stratification optimizes polygenic prediction of type 2 diabetes in cross-biobank analyses.
Nat Genet
11/06/2024
10.1038/s41588-024-01782-y
38862855
PGP000618
18
18
Jermy B
A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk.
Nat Commun
12/06/2024
10.1038/s41467-024-48938-2
38866767
PGP000643
1
1
Tian J
Developing an optimal stratification model for colorectal cancer screening and reducing racial disparities in multi-center population-based studies.
Genome Med
13/06/2024
10.1186/s13073-024-01355-y
38872215
PGP000517
184
184
Monti R
Evaluation of polygenic scoring methods in five biobanks shows larger variation between biobanks than methods and finds benefits of ensemble learning.
Am J Hum Genet
20/06/2024
10.1016/j.ajhg.2024.06.003
38908374
PGP000669
0
1
Saadatagah S
Polygenic Risk, Rare Variants, and Family History: Independent and Additive Effects on Coronary Heart Disease.
JACC Adv
26/08/2023
10.1016/j.jacadv.2023.100567
38939477
PGP000607
1
1
Boumtje V
Polygenic inheritance and its interplay with smoking history in predicting lung cancer diagnosis: a French-Canadian case-control cohort.
EBioMedicine
05/07/2024
10.1016/j.ebiom.2024.105234
38970920
PGP000668
3
3
China Kadoorie Biobank Collaborative Group.
Joint impact of polygenic risk score and lifestyles on early- and late-onset cardiovascular diseases.
Nat Hum Behav
10/07/2024
10.1038/s41562-024-01923-7
38987358
PGP000663
1
1
Pirruccello JP
The AORTA Gene score for detection and risk stratification of ascending aortic dilation.
Eur Heart J
12/08/2024
10.1093/eurheartj/ehae474
39132911
PGP000665
9
14
Moreno-Grau S
Polygenic risk score portability for common diseases across genetically diverse populations.
Human Genomics
02/09/2024
10.1186/s40246-024-00664-y
39218908
PGP000436
1
1
Kelemen M
Evaluating the cost-effectiveness of polygenic risk score-stratified screening for abdominal aortic aneurysm.
Nat Commun
14/09/2024
10.1038/s41467-024-52452-w
39277617
PGP000679
130
130
Gunn S
Comparison of Methods for Building Polygenic Scores for Diverse Populations.
HGG Adv
25/09/2024
10.1016/j.xhgg.2024.100355
39323095
PGP000666
1
1
Kovalenko E
GWAS and polygenic risk score of severe COVID-19 in Eastern Europe.
Front Med (Lausanne)
19/09/2024
10.3389/fmed.2024.1409714
39364016
PGP000457
84
84
Ding Y
Polygenic scoring accuracy varies across the genetic ancestry continuum in all human populations
bioRxiv
Pre
29/09/2022
10.1101/2022.09.28.509988
—
PGP000608
2
2
Zheng SL
Genome-wide association analysis reveals insights into the molecular etiology underlying dilated cardiomyopathy
medRxiv
Pre
29/09/2023
10.1101/2023.09.28.23295408
—
PGP000606
0
1
Szczerbinski L
Algorithms for the identification of prevalent diabetes in the All of Us Research Program validated using polygenic scores - a new resource for diabetes precision medicine
medRxiv
Pre
05/09/2023
10.1101/2023.09.05.23295061
—
PGP000582
2
2
Gorman BR
Distinctive cross-ancestry genetic architecture for age-related macular degeneration
medRxiv
Pre
21/08/2022
10.1101/2022.08.16.22278855
—
PGP000656
1
22
Ritchie SC
Integrated clinical risk prediction of type 2 diabetes with a multifactorial polygenic risk score
medRxiv
Pre
22/08/2024
10.1101/2024.08.22.24312440
—
PGP000461
10
10
Dahl A
Phenotype integration improves power and preserves specificity in biobank-based genetic studies of MDD
bioRxiv
Pre
15/08/2022
10.1101/2022.08.15.503980
—
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