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EFO_0001645
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PGS Catalog
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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)
PGP000511
1
1
Rasooly D
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure.
Nat Commun
10/07/2023
10.1038/s41467-023-39253-3
37429843
PGP000492
1
3
Thomas M
Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations.
Nat Commun
02/10/2023
10.1038/s41467-023-41819-0
37783704
PGP000501
26
26
Shim I
Clinical utility of polygenic scores for cardiometabolic disease in Arabs.
Nature Communications
18/10/2023
10.1038/s41467-023-41985-1
37852978
PGP000516
0
1
Soh P X.Y.
Prostate cancer genetic risk and associated aggressive disease in men of African ancestry
Nature Communications
16/11/2023
10.1038/s41467-023-43726-w
38052806
PGP000545
2
2
Middha P
Polygenic risk score for ulcerative colitis predicts immune checkpoint inhibitor-mediated colitis.
Nat Commun
26/03/2024
10.1038/s41467-023-44512-4
38531883
PGP000603
2
2
Loginovic P
Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritis.
Nat Commun
28/02/2024
10.1038/s41467-024-44917-9
38418465
PGP000564
1
1
Xin J
Integration of pathologic characteristics, genetic risk and lifestyle exposure for colorectal cancer survival assessment.
Nat Commun
08/04/2024
10.1038/s41467-024-47204-9
38589358
PGP000595
65
65
Zhang J
An ensemble penalized regression method for multi-ancestry polygenic risk prediction.
Nat Commun
15/04/2024
10.1038/s41467-024-47357-7
38622117
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
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
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
PGP000458
0
1
Pavelka L
Age at onset as stratifier in idiopathic Parkinson's disease - effect of ageing and polygenic risk score on clinical phenotypes.
NPJ Parkinsons Dis
09/08/2022
10.1038/s41531-022-00342-7
35945230
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
PGP000333
2
3
Mishra A
Stroke genetics informs drug discovery and risk prediction across ancestries
Nature
30/09/2022
10.1038/s41586-022-05165-3
36180795
PGP000382
6
6
Yengo L
A saturated map of common genetic variants associated with human height.
Nature
12/10/2022
10.1038/s41586-022-05275-y
36224396
PGP000410
20
20
Saunders GRB
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
07/12/2022
10.1038/s41586-022-05477-4
36477530
PGP000019
1
1
Schumacher FR
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
Nat Genet
11/06/2018
10.1038/s41588-018-0142-8
29892016
PGP000061
1
1
MacGregor S
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma.
Nat Genet
27/07/2018
10.1038/s41588-018-0176-y
30054594
PGP000006
5
5
Khera AV
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Nat Genet
13/08/2018
10.1038/s41588-018-0183-z
30104762
PGP000283
2
2
Evangelou E
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Nat Genet
17/09/2018
10.1038/s41588-018-0205-x
30224653
PGP000023
1
0
Mahajan A
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
Nat Genet
08/10/2018
10.1038/s41588-018-0241-6
30297969
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
PGP000086
1
1
Shrine N
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Nat Genet
25/02/2019
10.1038/s41588-018-0321-7
30804560
PGP000098
1
1
Grove J
Identification of common genetic risk variants for autism spectrum disorder.
Nat Genet
25/02/2019
10.1038/s41588-019-0344-8
30804558
PGP000390
1
1
Wuttke M
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Nat Genet
31/05/2019
10.1038/s41588-019-0407-x
31152163
PGP000063
1
1
Tin A
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
Nat Genet
02/10/2019
10.1038/s41588-019-0504-x
31578528
PGP000030
1
1
Klarin D
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease.
Nat Genet
01/11/2019
10.1038/s41588-019-0519-3
31676865
PGP000066
1
1
Craig JE
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Nat Genet
20/01/2020
10.1038/s41588-019-0556-y
31959993
PGP000122
1
1
Conti DV
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Nat Genet
04/01/2021
10.1038/s41588-020-00748-0
33398198
PGP000128
46
46
Sinnott-Armstrong N
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Nat Genet
18/01/2021
10.1038/s41588-020-00757-z
33462484
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
PGP000146
1
1
Harper AR
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
Nat Genet
25/01/2021
10.1038/s41588-020-00764-0
33495597
PGP000068
8
8
Cai N
Minimal phenotyping yields genome-wide association signals of low specificity for major depression.
Nat Genet
30/03/2020
10.1038/s41588-020-0594-5
32231276
PGP000088
5
7
Zhang H
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.
Nat Genet
18/05/2020
10.1038/s41588-020-0609-2
32424353
PGP000104
1
1
Koyama S
Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.
Nat Genet
05/10/2020
10.1038/s41588-020-0705-3
33020668
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
PGP000246
3
3
Chen J
The trans-ancestral genomic architecture of glycemic traits.
Nat Genet
31/05/2021
10.1038/s41588-021-00852-9
34059833
PGP000211
33
34
Aly DM
Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
Nat Genet
04/11/2021
10.1038/s41588-021-00948-2
34737425
PGP000296
1
1
Pirruccello JP
Deep learning enables genetic analysis of the human thoracic aorta.
Nat Genet
26/11/2021
10.1038/s41588-021-00962-4
34837083
PGP000302
2
2
Horowitz JE
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease.
Nat Genet
03/03/2022
10.1038/s41588-021-01006-7
35241825
PGP000260
1
1
Barc J
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Nat Genet
24/02/2022
10.1038/s41588-021-01007-6
35210625
PGP000309
1
1
Bellenguez C
New insights into the genetic etiology of Alzheimer's disease and related dementias.
Nat Genet
04/04/2022
10.1038/s41588-022-01024-z
35379992
PGP000332
415
415
Weissbrod O
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores.
Nat Genet
07/04/2022
10.1038/s41588-022-01036-9
35393596
PGP000268
1
1
Tcheandjieu C
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease.
Nat Genet
30/05/2022
10.1038/s41588-022-01070-7
35637384
PGP000341
1
1
Vujkovic M
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.
Nat Genet
02/06/2022
10.1038/s41588-022-01078-z
35654975
PGP000357
1
1
Ishigaki K
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis.
Nat Genet
04/11/2022
10.1038/s41588-022-01213-w
36333501
PGP000491
1
0
Fernandez-Rozadilla C
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries.
Nat Genet
20/12/2022
10.1038/s41588-022-01222-9
36539618
PGP000409
2
2
Aragam KG
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.
Nat Genet
06/12/2022
10.1038/s41588-022-01233-6
36474045
PGP000392
1
1
Miyazawa K
Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction.
Nat Genet
19/01/2023
10.1038/s41588-022-01284-9
36653681
PGP000398
1
1
Ghouse J
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.
Nat Genet
19/01/2023
10.1038/s41588-022-01286-7
36658437
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