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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)
PGP000721
0
6
Sadler MC
Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medications.
Nat Commun
25/03/2025
10.1038/s41467-025-58152-3
40133288
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
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
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
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
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
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
PGP000058
0
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
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
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
PGP000723
26
26
Xiang R
Genome-wide analyses of variance in blood cell phenotypes provide new insights into complex trait biology and prediction.
Nat Commun
07/05/2025
10.1038/s41467-025-59525-4
40335489
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
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
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
PGP000080
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
PGP000658
0
1
Hu C
Genetic Predisposition, Sedentary Behavior, and Incident Coronary Artery Disease: A Prospective Chinese Cohort Study.
Med Sci Sports Exerc
30/08/2023
10.1249/mss.0000000000003277
37703277
PGP000280
2
2
Kujala UM
Polygenic Risk Scores and Physical Activity.
Med Sci Sports Exerc
01/07/2020
10.1249/mss.0000000000002290
32049886
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
—
PGP000680
4
4
Barnes DR
Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk
medRxiv
Pre
04/03/2024
10.1101/2024.02.29.24303243
—
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
—
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
—
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
PGP000622
0
1
Åberg F
Combined use of the ELF test and CLivD score improves prediction of liver-related outcomes in the general population.
Liver Int
23/07/2023
10.1111/liv.15681
37485795
PGP000505
0
1
Liu Z
Associations of serum uric acid levels with liver disease-related morbidity and mortality: A prospective cohort study of the UK Biobank.
Liver Int
29/03/2023
10.1111/liv.15564
36938749
PGP000234
0
1
Kleinstern G
Polygenic risk score and risk of monoclonal B-cell lymphocytosis in caucasians and risk of chronic lymphocytic leukemia (CLL) in African Americans.
Leukemia
20/07/2021
10.1038/s41375-021-01344-9
34285341
PGP000448
8
8
Berndt SI
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes.
Leukemia
22/10/2022
10.1038/s41375-022-01711-0
36273105
PGP000049
1
1
Dai J
Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations.
Lancet Respir Med
17/07/2019
10.1016/S2213-2600(19)30144-4
31326317
PGP000264
2
2
Moll M
Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts.
Lancet Respir Med
01/07/2020
10.1016/s2213-2600(20)30101-6
32649918
PGP000025
1
1
Belsky DW
Polygenic risk and the development and course of asthma: an analysis of data from a four-decade longitudinal study.
Lancet Respir Med
28/06/2013
10.1016/S2213-2600(13)70101-2
24429243
PGP000525
0
18
Yajnik CS
Polygenic scores of diabetes-related traits in subgroups of type 2 diabetes in India: a cohort study.
Lancet Reg Health Southeast Asia
02/05/2023
10.1016/j.lansea.2023.100182
37492423
PGP000292
0
3
Saad M
Genetic predisposition to cancer across people of different ancestries in Qatar: a population-based, cohort study.
Lancet Oncol
09/02/2022
10.1016/s1470-2045(21)00752-x
35150601
PGP000387
1
2
Qin N
Association of the interaction between mosaic chromosomal alterations and polygenic risk score with the risk of lung cancer: an array-based case-control association and prospective cohort study.
Lancet Oncol
17/10/2022
10.1016/s1470-2045(22)00600-3
36265503
PGP000235
2
2
Nalls MA
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
Lancet Neurol
01/12/2019
10.1016/s1474-4422(19)30320-5
31701892
PGP000207
1
1
van der Lee SJ
The effect of APOE and other common genetic variants on the onset of Alzheimer's disease and dementia: a community-based cohort study.
Lancet Neurol
16/03/2018
10.1016/s1474-4422(18)30053-x
29555425
PGP000003
1
1
Mega JL
Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials.
Lancet
04/03/2015
10.1016/S0140-6736(14)61730-X
25748612
PGP000200
1
1
Talmud PJ
Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study.
Lancet
22/02/2013
10.1016/s0140-6736(12)62127-8
23433573
PGP000562
3
3
Youssef O
High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases.
Lab Invest
15/01/2024
10.1016/j.labinv.2024.100325
38220043
PGP000411
1
1
Steinbrenner I
A Polygenic Score for Reduced Kidney Function and Adverse Outcomes in a Chronic Kidney Disease Cohort.
Kidney Int
05/12/2022
10.1016/j.kint.2022.11.013
36481179
PGP000124
1
1
Gorski M
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Kidney Int
30/10/2020
10.1016/j.kint.2020.09.030
33137338
PGP000495
0
2
Bakshi A
Association of polygenic scores with chronic kidney disease phenotypes in a longitudinal study of older adults.
Kidney Int
29/03/2023
10.1016/j.kint.2023.03.017
37001602
PGP000406
0
1
Gandhi GD
Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobank.
J Transl Med
03/11/2022
10.1186/s12967-022-03697-w
36329474
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