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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)
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
PGP000101
1
1
Zhang Q
Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture.
Nat Commun
23/09/2020
10.1038/s41467-020-18534-1
32968074
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
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
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
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
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
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
PGP000236
2
2
Ntalla I
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
Nat Commun
21/05/2020
10.1038/s41467-020-15706-x
32439900
PGP000046
3
3
Kuchenbaecker K
The transferability of lipid loci across African, Asian and European cohorts.
Nat Commun
24/09/2019
10.1038/s41467-019-12026-7
31551420
PGP000171
0
2
Fahed AC
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.
Nat Commun
20/08/2020
10.1038/s41467-020-17374-3
32820175
PGP000206
1
1
Teumer A
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.
Nat Commun
11/09/2019
10.1038/s41467-019-11576-0
31511532
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
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
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
PGP000186
16
32
Kachuri L
Pan-cancer analysis demonstrates that integrating polygenic risk scores with modifiable risk factors improves risk prediction.
Nat Commun
27/11/2020
10.1038/s41467-020-19600-4
33247094
PGP000027
1
2
Abraham G
Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke.
Nat Commun
20/12/2019
10.1038/s41467-019-13848-1
31862893
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
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
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
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
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
PGP000138
3
3
Fontanillas P
Disease risk scores for skin cancers.
Nat Commun
08/01/2021
10.1038/s41467-020-20246-5
33420020
PGP000112
4
4
Ho WK
European polygenic risk score for prediction of breast cancer shows similar performance in Asian women.
Nat Commun
31/07/2020
10.1038/s41467-020-17680-w
32737321
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
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
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
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
PGP000479
0
1
Blauwendraat C
Polygenic Parkinson's Disease Genetic Risk Score as Risk Modifier of Parkinsonism in Gaucher Disease.
Mov Disord
03/03/2023
10.1002/mds.29342
36869417
PGP000087
1
1
Pihlstrøm L
A cumulative genetic risk score predicts progression in Parkinson's disease.
Mov Disord
08/02/2016
10.1002/mds.26505
26853697
PGP000250
1
1
Sia MW
Polygenic Risk Scores in a Prospective Parkinson's Disease Cohort.
Mov Disord
17/08/2021
10.1002/mds.28761
34402545
PGP000569
1
1
Lake J
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease.
Mol Psychiatry
18/05/2023
10.1038/s41380-023-02089-w
37198259
PGP000521
1
1
Merino J
Genetic predisposition to macronutrient preference and workplace food choices.
Mol Psychiatry
23/05/2023
10.1038/s41380-023-02107-x
37217678
PGS000080
1
1
Coleman JRI
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank.
Mol Psychiatry
23/01/2020
10.1038/s41380-019-0546-6
31969693
PGP000221
1
2
Leal LG
A polygenic biomarker to identify patients with severe hypercholesterolemia of polygenic origin.
Mol Genet Genomic Med
19/04/2020
10.1002/mgg3.1248
32307928
PGP000437
1
1
Wong CK
Melanoma risk prediction based on a polygenic risk score and clinical risk factors.
Melanoma Res
24/04/2023
10.1097/cmr.0000000000000896
37096571
PGP000280
2
2
Kujala UM
Polygenic Risk Scores and Physical Activity.
Med Sci Sports Exerc
01/07/2020
10.1249/mss.0000000000002290
32049886
PGP000058
0
1
Huynh-Le M
Polygenic hazard score predicts aggressive and fatal prostate cancer in multi-ethnic populations
medRxiv
Pre
19/11/2019
10.1101/19012237
—
PGP000517
184
184
Monti M R
Evaluation of polygenic scoring methods in five biobanks reveals greater variability between biobanks than between methods and highlights benefits of ensemble learning
medRxiv
Pre
16/11/2023
10.1101/2023.11.20.23298215
—
PGP000077
0
1
Timmerman N
Family history and polygenic risk of cardiovascular disease: independent factors associated with secondary cardiovascular manifestations in patients undergoing carotid endarterectomy
medRxiv
Pre
18/09/2019
10.1101/19006718
—
PGP000492
1
3
Thomas M T
Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity.
medRxiv
Pre
19/01/2023
10.1101/2023.01.19.23284737
—
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
—
PGP000436
1
1
Kelemen M K
Evaluating the cost-effectiveness of polygenic risk score-stratified screening for abdominal aortic aneurysm
medRxiv
Pre
20/02/2023
10.1101/2023.11.02.23297906
—
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
—
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
—
PGP000514
5
5
Hassanin E
Trans-ancestry polygenic models for the prediction of LDL blood levels: An analysis of the UK Biobank and Taiwan Biobank
medRxiv
Pre
06/08/2023
10.1101/2023.08.03.23293320
—
PGP000366
4
4
Kanoni S
Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
medRxiv
Pre
16/12/2021
10.1101/2021.12.15.21267852
—
PGP000463
2
2
Kleeman SO
Cystatin C is glucocorticoid-responsive, directs recruitment of Trem2+ macrophages and predicts failure of cancer immunotherapy
medRxiv
Pre
20/08/2021
10.1101/2021.08.17.21261668
—
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
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