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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)
PGP000405
18
18
Kim YJ
The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians.
Nat Commun
04/11/2022
10.1038/s41467-022-34163-2
36333282
PGP000427
1
1
Krohn L
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects.
Nat Commun
05/12/2022
10.1038/s41467-022-34732-5
36470867
PGP000426
1
1
Gao XR
Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma.
Nat Commun
30/11/2022
10.1038/s41467-022-35188-3
36450729
PGP000429
2
2
Seviiri M
A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma.
Nat Commun
10/12/2022
10.1038/s41467-022-35345-8
36496446
PGP000434
1
1
Khurshid S
Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.
Nat Commun
21/03/2023
10.1038/s41467-023-37173-w
36944631
PGP000510
8
2
Kurniansyah N
Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.
Nat Commun
02/06/2023
10.1038/s41467-023-38990-9
37268629
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
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