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EFO_0001645
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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)
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
PGP000686
1
1
Christiansen MR
Abdominal Obesity Genetic Variants Predict Waist Circumference Regain After Weight Loss.
Diabetes
01/10/2023
10.2337/db23-0131
37494631
PGP000583
0
1
Dueñas N
Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome.
J Med Genet
15/06/2023
10.1136/jmg-2023-109344
37321833
PGP000256
1
1
Gafni A
Ability of known colorectal cancer susceptibility SNPs to predict colorectal cancer risk: A cohort study within the UK Biobank.
PLoS One
15/09/2021
10.1371/journal.pone.0251469
34525106
PGP000216
1
1
Brentnall AR
A case-control evaluation of 143 single nucleotide polymorphisms for breast cancer risk stratification with classical factors and mammographic density.
Int J Cancer
13/07/2019
10.1002/ijc.32541
31251818
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
PGP000587
0
1
Luo M
Accelerometer-measured intensity-specific physical activity, genetic risk and incident type 2 diabetes: a prospective cohort study.
Br J Sports Med
05/06/2023
10.1136/bjsports-2022-106653
37277158
PGP000028
1
1
Abraham G
Accurate and robust genomic prediction of celiac disease using statistical learning.
PLoS Genet
13/02/2014
10.1371/journal.pgen.1004137
24550740
PGP000417
0
1
Dite GS
A combined clinical and genetic model for predicting risk of ovarian cancer.
Eur J Cancer Prev
27/10/2022
10.1097/cej.0000000000000771
36503897
PGP000091
0
1
Ferrat LA
A combined risk score enhances prediction of type 1 diabetes among susceptible children.
Nat Med
07/08/2020
10.1038/s41591-020-0930-4
32770166
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
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
PGP000037
1
1
Lakeman IMM
Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families.
J Med Genet
11/06/2019
10.1136/jmedgenet-2019-106072
31186341
PGP000036
1
1
Zhang X
Addition of a polygenic risk score, mammographic density, and endogenous hormones to existing breast cancer risk prediction models: A nested case-control study.
PLoS Med
04/09/2018
10.1371/journal.pmed.1002644
30180161
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
PGP000552
0
1
Mantovani A
Adverse effect of PNPLA3 p.I148M genetic variant on kidney function in middle-aged individuals with metabolic dysfunction.
Aliment Pharmacol Ther
22/03/2023
10.1111/apt.17477
36947711
PGP000315
0
1
Hämmerle M
A Family and a Genome-Wide Polygenic Risk Score Are Independently Associated With Stroke in a Population-Based Study.
Stroke
07/04/2022
10.1161/strokeaha.121.036551
35387493
PGP000139
1
2
Karunamuni RA
African-specific improvement of a polygenic hazard score for age at diagnosis of prostate cancer.
Int J Cancer
24/09/2020
10.1002/ijc.33282
32930425
PGP000493
4
4
Li J
Age and Genetic Risk Score and Rates of Blood Lipid Changes in China.
JAMA Netw Open
01/03/2023
10.1001/jamanetworkopen.2023.5565
36988954
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
PGP000549
1
1
Fernández-Rhodes L
A Gene-Acculturation Study of Obesity Among US Hispanic/Latinos: The Hispanic Community Health Study/Study of Latinos.
Psychosom Med
15/03/2023
10.1097/psy.0000000000001193
36917487
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
PGP000241
1
1
Wang M
A genome-wide association and polygenic risk score study on abnormal electrocardiogram in a Chinese population.
Sci Rep
25/02/2021
10.1038/s41598-021-84135-7
33633301
PGP000156
1
1
Du Z
A genome-wide association study of prostate cancer in Latinos.
Int J Cancer
03/07/2019
10.1002/ijc.32525
31226226
PGP000519
0
1
Thomas NJ
Age of Diagnosis Does Not Alter the Presentation or Progression of Robustly Defined Adult-Onset Type 1 Diabetes.
Diabetes Care
01/06/2023
10.2337/dc22-2159
36802355
PGP000199
0
1
Ferreira MAR
Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
PLoS Genet
30/06/2020
10.1371/journal.pgen.1008725
32603359
PGP000638
1
1
Ma Y
Air pollution, genetic susceptibility, and the risk of atrial fibrillation: A large prospective cohort study.
Proc Natl Acad Sci U S A
31/07/2023
10.1073/pnas.2302708120
37523535
PGP000623
2
2
Cañadas-Garre M
Albuminuria-Related Genetic Biomarkers: Replication and Predictive Evaluation in Individuals with and without Diabetes from the UK Biobank.
Int J Mol Sci
07/07/2023
10.3390/ijms241311209
37446387
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
—
PGP000069
1
1
Hsu L
A model to determine colorectal cancer risk using common genetic susceptibility loci.
Gastroenterology
13/02/2015
10.1053/j.gastro.2015.02.010
25683114
PGP000341
1
1
Vujkovic M
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.
Nat Genet
02/06/2022
10.1038/s41588-022-01078-z
35654975
PGP000466
3
3
Patel AP
A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.
Nat Med
06/07/2023
10.1038/s41591-023-02429-x
37414900
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
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
PGP000578
1
1
Tomassen J
Amyloid-β and APOE genotype predict memory decline in cognitively unimpaired older individuals independently of Alzheimer's disease polygenic risk score.
BMC Neurol
15/12/2022
10.1186/s12883-022-02925-6
36522743
PGP000126
1
1
Pirruccello JP
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.
Nat Commun
07/05/2020
10.1038/s41467-020-15823-7
32382064
PGP000282
1
1
Wu Q
An early prediction model for gestational diabetes mellitus based on genetic variants and clinical characteristics in China.
Diabetol Metab Syndr
24/01/2022
10.1186/s13098-022-00788-y
35073990
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
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
PGP000489
82
82
Zhang H
A new method for multiancestry polygenic prediction improves performance across diverse populations.
Nat Genet
25/09/2023
10.1038/s41588-023-01501-z
37749244
PGP000498
1
1
Clark R
A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration.
EBioMedicine
11/04/2023
10.1016/j.ebiom.2023.104551
37055258
PGP000045
4
4
Johnson L
An Examination of the Relationship between Lipid Levels and Associated Genetic Markers across Racial/Ethnic Populations in the Multi-Ethnic Study of Atherosclerosis.
PLoS One
07/05/2015
10.1371/journal.pone.0126361
25951326
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
PGP000547
3
3
Bui A
A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort.
Front Genet
31/05/2023
10.3389/fgene.2023.1141010
37323656
PGP000504
0
1
Duschek E
A polygenic and family risk score are both independently associated with risk of type 2 diabetes in a population-based study.
Sci Rep
23/03/2023
10.1038/s41598-023-31496-w
36959271
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
PGP000385
0
2
Zhang J
A polygenic risk score and age of diagnosis of COPD.
Eur Respir J
15/09/2022
10.1183/13993003.01954-2021
35115341
PGP000153
0
1
Manousaki D
A Polygenic Risk Score as a Risk Factor for Medication-Associated Fractures.
J Bone Miner Res
20/07/2020
10.1002/jbmr.4104
32511779
PGP000645
1
1
Schwantes-An TH
A polygenic risk score for alcohol-associated cirrhosis among heavy drinkers with European ancestry.
Hepatol Commun
10/05/2024
10.1097/hc9.0000000000000431
38727677
PGP000503
6
6
Sofer T
A polygenic risk score for Alzheimer's disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S.
Alzheimers Res Ther
30/08/2023
10.1186/s13195-023-01298-3
37649099
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