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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)
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
PGP000314
1
1
Pujol-Gualdo N
Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse.
Nat Commun
23/06/2022
10.1038/s41467-022-31188-5
35739095
PGP000531
4
4
Kurniansyah N
A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood.
Nat Commun
21/06/2022
10.1038/s41467-022-31080-2
35729114
PGP000391
3
3
Agrawal S
Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots.
Nat Commun
30/06/2022
10.1038/s41467-022-30931-2
35773277
PGP000320
1
1
He YQ
A polygenic risk score for nasopharyngeal carcinoma shows potential for risk stratification and personalized screening.
Nat Commun
12/04/2022
10.1038/s41467-022-29570-4
35414057
PGP000164
3
3
Khan Z
Genetic variation associated with thyroid autoimmunity shapes the systemic immune response to PD-1 checkpoint blockade.
Nat Commun
07/06/2021
10.1038/s41467-021-23661-4
34099659
PGP000231
1
1
de Rojas I
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
Nat Commun
07/06/2021
10.1038/s41467-021-22491-8
34099642
PGP000201
3
3
Pazoki R
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes.
Nat Commun
10/05/2021
10.1038/s41467-021-22338-2
33972514
PGP000147
0
11
Thareja G
Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits.
Nat Commun
23/02/2021
10.1038/s41467-021-21381-3
33623009
PGP000050
16
16
Graff RE
Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts.
Nat Commun
12/02/2021
10.1038/s41467-021-21288-z
33579919
PGP000149
1
1
Huynh-Le MP
Polygenic hazard score is associated with prostate cancer in multi-ethnic populations.
Nat Commun
23/02/2021
10.1038/s41467-021-21287-0
33623038
PGP000160
1
1
Wang YF
Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups.
Nat Commun
03/02/2021
10.1038/s41467-021-21049-y
33536424
PGP000138
3
3
Fontanillas P
Disease risk scores for skin cancers.
Nat Commun
08/01/2021
10.1038/s41467-020-20246-5
33420020
PGP000102
1
3
Mars N
The role of polygenic risk and susceptibility genes in breast cancer over the course of life
Nat Commun
14/12/2020
10.1038/s41467-020-19966-5
33318493
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