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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)
PGP000346
1
1
Lai D
Gene-based polygenic risk scores analysis of alcohol use disorder in African Americans.
Transl Psychiatry
05/07/2022
10.1038/s41398-022-02029-2
35790736
PGP000084
6
6
Barr PB
Using polygenic scores for identifying individuals at increased risk of substance use disorders in clinical and population samples.
Transl Psychiatry
18/06/2020
10.1038/s41398-020-00865-8
32555147
PGP000174
1
1
Guffanti G
Depression genetic risk score is associated with anhedonia-related markers across units of analysis.
Transl Psychiatry
19/09/2019
10.1038/s41398-019-0566-7
31537779
PGP000397
1
1
Huynh-Le MP
Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score.
Prostate Cancer Prostatic Dis
12/02/2022
10.1038/s41391-022-00497-7
35152271
PGP000219
0
1
Huynh-Le MP
Common genetic and clinical risk factors: association with fatal prostate cancer in the Cohort of Swedish Men.
Prostate Cancer Prostatic Dis
15/03/2021
10.1038/s41391-021-00341-4
33723363
PGP000150
1
2
Karunamuni RA
Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer.
Prostate Cancer Prostatic Dis
08/01/2021
10.1038/s41391-020-00311-2
33420416
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
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
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
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
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
PGP000677
0
4
Renier TJ
Elucidating pathways to pediatric obesity: a study evaluating obesity polygenic risk scores related to appetitive traits in children.
Int J Obes (Lond)
22/09/2023
10.1038/s41366-023-01385-3
37736781
PGP000195
1
0
Ferreira MA
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.
Nat Genet
30/10/2017
10.1038/ng.3985
29083406
PGP000223
1
1
Lotta LA
Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance.
Nat Genet
14/11/2016
10.1038/ng.3714
27841877
PGP000010
1
1
Läll K
Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores.
Genet Med
11/08/2016
10.1038/gim.2016.103
27513194
PGP000032
0
1
Pashayan N
Implications of polygenic risk-stratified screening for prostate cancer on overdiagnosis.
Genet Med
08/01/2015
10.1038/gim.2014.192
25569441
PGP000031
1
1
Pashayan N
Reducing overdiagnosis by polygenic risk-stratified screening: findings from the Finnish section of the ERSPC.
Br J Cancer
20/08/2015
10.1038/bjc.2015.289
26291059
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
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
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
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
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
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
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
PGP000191
1
1
He CY
Performance of common genetic variants in risk prediction for colorectal cancer in Chinese: A two-stage and multicenter study.
Genomics
02/02/2021
10.1016/j.ygeno.2021.01.025
33545268
PGP000679
130
130
Gunn S
Comparison of Methods for Building Polygenic Scores for Diverse Populations.
HGG Adv
25/09/2024
10.1016/j.xhgg.2024.100355
39323095
PGP000193
5
5
Polfus LM
Genetic discovery and risk characterization in type 2 diabetes across diverse populations.
HGG Adv
09/03/2021
10.1016/j.xhgg.2021.100029
34604815
PGP000604
158
158
Truong B
Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases.
Cell Genom
12/03/2024
10.1016/j.xgen.2024.100523
38508198
PGP000463
2
2
Kleeman SO
Cystatin C is glucocorticoid responsive, directs recruitment of Trem2+ macrophages, and predicts failure of cancer immunotherapy.
Cell Genom
23/06/2023
10.1016/j.xgen.2023.100347
37601967
PGP000592
1
1
Wu Y
150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility.
Cell Genom
05/06/2023
10.1016/j.xgen.2023.100326
37492107
PGP000262
18
18
Wang Y
Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts.
Cell Genom
04/01/2023
10.1016/j.xgen.2022.100241
36777179
PGP000703
20
20
Tsuo K
Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity.
Cell Genom
08/11/2022
10.1016/j.xgen.2022.100212
36778051
PGP000271
5
5
Mars N
Genome-wide risk prediction of common diseases across ancestries in one million people.
Cell Genom
13/04/2022
10.1016/j.xgen.2022.100118
35591975
PGP000051
26
26
Xu Y
Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease
Cell Genom
12/01/2022
10.1016/j.xgen.2021.100086
35072137
PGP000265
1
1
Bonfiglio F
GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome.
Cell Genom
08/12/2021
10.1016/j.xgen.2021.100069
34957435
PGP000273
1
1
Haas ME
Machine learning enables new insights into genetic contributions to liver fat accumulation.
Cell Genom
01/12/2021
10.1016/j.xgen.2021.100066
34957434
PGP000422
1
4
Vanhoye X
A new 165-SNP low-density lipoprotein cholesterol polygenic risk score based on next generation sequencing outperforms previously published scores in routine diagnostics of familial hypercholesterolemia.
Transl Res
15/12/2022
10.1016/j.trsl.2022.12.002
36528340
PGP000597
0
1
Shi Z
Cancer-associated thrombosis by cancer sites and inherited factors in a prospective population-based cohort.
Thromb Res
26/06/2023
10.1016/j.thromres.2023.06.023
37419004
PGP000523
1
1
Lin J
Association of time spent in outdoor light and genetic susceptibility with the risk of type 2 diabetes.
Sci Total Environ
16/05/2023
10.1016/j.scitotenv.2023.164253
37201819
PGP000657
1
1
Cao Z
Polygenic risk score for Parkinson's disease and olfaction among middle-aged to older women.
Parkinsonism Relat Disord
17/08/2023
10.1016/j.parkreldis.2023.105815
37611509
PGP000352
1
1
Waksmunski AR
Glaucoma genetic risk scores in the Million Veteran Program.
Ophthalmology
16/06/2022
10.1016/j.ophtha.2022.06.012
35718050
PGP000299
1
1
Zekavat SM
Photoreceptor Layer Thinning Is an Early Biomarker for Age-Related Macular Degeneration: Epidemiologic and Genetic Evidence from UK Biobank OCT Data.
Ophthalmology
08/02/2022
10.1016/j.ophtha.2022.02.001
35149155
PGP000225
1
1
Qassim A
An Intraocular Pressure Polygenic Risk Score Stratifies Multiple Primary Open-Angle Glaucoma Parameters Including Treatment Intensity.
Ophthalmology
07/01/2020
10.1016/j.ophtha.2019.12.025
32081492
PGP000588
0
1
Marshall HN
High Polygenic Risk Is Associated with Earlier Trabeculectomy in Patients with Primary Open-Angle Glaucoma.
Ophthalmol Glaucoma
13/07/2022
10.1016/j.ogla.2022.06.009
35842105
PGP000374
0
1
Zaccardi F
Self-reported walking pace, polygenic risk scores and risk of coronary artery disease in UK biobank.
Nutr Metab Cardiovasc Dis
02/09/2022
10.1016/j.numecd.2022.08.021
36163213
PGP000649
1
1
Lawingco T
Genetic variants in glutamate-, Aβ-, and tau-related pathways determine polygenic risk for Alzheimer's disease.
Neurobiol Aging
12/11/2020
10.1016/j.neurobiolaging.2020.11.009
33303219
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
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
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