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Publications
PGS Publication/Study ID
(PGP)
PGS Developed
PGS Evaluated
First Author
Title
Journal Name
Publication Date
Digital object identifier
(doi)
PubMed ID
(PMID)
PGP000557
1
1
Tan Q
Gene-environment interaction in long-term effects of polychlorinated biphenyls exposure on glucose homeostasis and type 2 diabetes: The modifying effects of genetic risk and lifestyle.
J Hazard Mater
01/06/2023
10.1016/j.jhazmat.2023.131757
37276697
PGP000215
1
2
Bianco C
Non-invasive stratification of hepatocellular carcinoma risk in non-alcoholic fatty liver using polygenic risk scores.
J Hepatol
25/11/2020
10.1016/j.jhep.2020.11.024
33248170
PGP000258
1
1
Whitfield JB
A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers.
J Hepatol
13/10/2021
10.1016/j.jhep.2021.10.005
34656649
PGP000395
1
1
Valenti L
Clinical and genetic determinants of the fatty liver-coagulation balance interplay in individuals with metabolic dysfunction.
JHEP Rep
25/09/2022
10.1016/j.jhepr.2022.100598
36313186
PGP000151
3
3
Cust AE
Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies.
J Invest Dermatol
08/06/2018
10.1016/j.jid.2018.05.023
29890168
PGP000451
6
6
Al-Janabi A
Atopic polygenic risk score is associated with paradoxical eczema developing in psoriasis patients treated with biologics.
J Invest Dermatol
15/02/2023
10.1016/j.jid.2023.01.021
36804406
PGP000558
1
1
Vasavda C
A Polygenic Risk Score for Predicting Racial and Genetic Susceptibility to Prurigo Nodularis.
J Invest Dermatol
26/05/2023
10.1016/j.jid.2023.04.033
37245863
PGP000358
1
1
Lahey BB
Associations of polygenic risk for attention-deficit/hyperactivity disorder with general and specific dimensions of childhood psychological problems and facets of impulsivity.
J Psychiatr Res
14/06/2022
10.1016/j.jpsychires.2022.06.019
35752070
PGP000584
1
1
Forthman KL
Transdiagnostic behavioral and genetic contributors to repetitive negative thinking: A machine learning approach.
J Psychiatr Res
05/05/2023
10.1016/j.jpsychires.2023.05.039
37178517
PGP000522
1
1
Wu Q
Sleep patterns, genetic susceptibility, and risk of new-onset gout: The UK Biobank prospective cohort study.
J Psychosom Res
18/05/2023
10.1016/j.jpsychores.2023.111381
37244070
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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