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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)
PGP000428
1
1
Nyberg T
CanRisk-Prostate: A Comprehensive, Externally Validated Risk Model for the Prediction of Future Prostate Cancer.
J Clin Oncol
09/12/2022
10.1200/jco.22.01453
36493335
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
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
PGP000425
0
1
Olsen CM
Risk Factors Associated With First and Second Primary Melanomas in a High-Incidence Population.
JAMA Dermatol
01/01/2023
10.1001/jamadermatol.2022.4975
36416830
PGP000424
1
1
Olsen CM
Does polygenic risk influence associations between sun exposure and melanoma? A prospective cohort analysis.
Br J Dermatol
17/12/2019
10.1111/bjd.18703
31747047
PGP000423
6
6
Bakker MK
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.
Stroke
19/01/2023
10.1161/strokeaha.122.040715
36655558
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
PGP000421
1
1
Wang J
Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically.
Arterioscler Thromb Vasc Biol
20/10/2016
10.1161/atvbaha.116.308027
27765764
PGP000420
1
1
Trinder M
Risk of Premature Atherosclerotic Disease in Patients With Monogenic Versus Polygenic Familial Hypercholesterolemia.
J Am Coll Cardiol
01/07/2019
10.1016/j.jacc.2019.05.043
31345425
PGP000419
1
1
Lamri A
The genetic risk of gestational diabetes in South Asian women.
Elife
22/11/2022
10.7554/elife.81498
36412575
PGP000418
1
1
Pieri K
Polygenic risk in Type III hyperlipidaemia and risk of cardiovascular disease: An epidemiological study in UK Biobank and Oxford Biobank.
Int J Cardiol
19/11/2022
10.1016/j.ijcard.2022.11.024
36410544
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
PGP000416
1
2
Robinson JR
Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.
Obesity (Silver Spring)
13/11/2022
10.1002/oby.23561
36372681
PGP000415
4
4
Jee YH
Polygenic risk scores for prediction of breast cancer in Korean women.
Int J Epidemiol
07/11/2022
10.1093/ije/dyac206
36343017
PGP000414
1
1
Xin J
Risk assessment for colorectal cancer via polygenic risk score and lifestyle exposure: a large-scale association study of East Asian and European populations.
Genome Med
24/01/2023
10.1186/s13073-023-01156-9
36694225
PGP000413
14
14
Namba S
Common germline risk variants impact somatic alterations and clinical features across cancers.
Cancer Res
26/10/2022
10.1158/0008-5472.can-22-1492
36286845
PGP000412
2
2
Kachuri L
Genetically adjusted PSA levels for prostate cancer screening.
Nat Med
01/06/2023
10.1038/s41591-023-02277-9
37264206
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
PGP000410
20
20
Saunders GRB
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
07/12/2022
10.1038/s41586-022-05477-4
36477530
PGP000409
2
2
Aragam KG
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.
Nat Genet
06/12/2022
10.1038/s41588-022-01233-6
36474045
PGP000408
0
1
Borg SÁ
Subclinical atherosclerosis determined by coronary artery calcium deposition in patients with clinical familial hypercholesterolemia.
Atheroscler Plus
11/11/2022
10.1016/j.athplu.2022.10.002
36643796
PGP000407
1
1
Downie ML
Shared genetic risk across different presentations of gene test-negative idiopathic nephrotic syndrome.
Pediatr Nephrol
10/11/2022
10.1007/s00467-022-05789-7
36357634
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
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
PGP000404
1
1
Teleka S
Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men.
Sci Rep
31/10/2022
10.1038/s41598-022-23225-6
36316463
PGP000403
0
1
Siggs OM
Association of High Polygenic Risk With Visual Field Worsening Despite Treatment in Early Primary Open-Angle Glaucoma.
JAMA Ophthalmol
10/11/2022
10.1001/jamaophthalmol.2022.4688
36355370
PGP000402
1
1
Chen Y
Cardiometabolic diseases, polygenic risk score, APOE genotype, and risk of incident dementia: A population-based prospective cohort study.
Arch Gerontol Geriatr
31/10/2022
10.1016/j.archger.2022.104853
36347157
PGP000401
0
1
Cho BPH
Association of Vascular Risk Factors and Genetic Factors With Penetrance of Variants Causing Monogenic Stroke.
JAMA Neurol
27/10/2022
10.1001/jamaneurol.2022.3832
36300346
PGP000400
0
1
Pagadala MS
Polygenic risk of any, metastatic, and fatal prostate cancer in the Million Veteran Program.
J Natl Cancer Inst
28/10/2022
10.1093/jnci/djac199
36305680
PGP000399
1
1
Fang Y
Polygenic Liability to Depression Is Associated With Multiple Medical Conditions in the Electronic Health Record: Phenome-wide Association Study of 46,782 Individuals.
Biol Psychiatry
11/06/2022
10.1016/j.biopsych.2022.06.004
35965108
PGP000398
1
1
Ghouse J
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.
Nat Genet
19/01/2023
10.1038/s41588-022-01286-7
36658437
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
PGP000396
0
1
Koraishy FM
Polygenic association of glomerular filtration rate decline in world trade center responders.
BMC Nephrol
28/10/2022
10.1186/s12882-022-02967-5
36307804
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
PGP000394
1
1
Sumpter NA
Association of Gout Polygenic Risk Score with Age at Disease Onset and Tophaceous Disease in European and Polynesian Men with Gout.
Arthritis Rheumatol
25/10/2022
10.1002/art.42393
36281732
PGP000393
514
514
Ma Y
ExPRSweb: An online repository with polygenic risk scores for common health-related exposures.
Am J Hum Genet
23/09/2022
10.1016/j.ajhg.2022.09.001
36152628
PGP000392
1
1
Miyazawa K
Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction.
Nat Genet
19/01/2023
10.1038/s41588-022-01284-9
36653681
PGP000391
3
3
Agrawal S
Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots.
Nat Commun
30/06/2022
10.1038/s41467-022-30931-2
35773277
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
PGP000389
0
1
Giardiello D
PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients.
Breast Cancer Res
21/10/2022
10.1186/s13058-022-01567-3
36271417
PGP000388
1
1
Ahmed R
Reclassification of coronary artery disease risk using genetic risk score among subjects with borderline or intermediate clinical risk.
Int J Cardiol Heart Vasc
13/10/2022
10.1016/j.ijcha.2022.101136
36275420
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
PGP000386
0
4
Saad M
Validation of Polygenic Risk Scores for Coronary Heart Disease in a Middle Eastern Cohort Using Whole Genome Sequencing.
Circ Genom Precis Med
12/10/2022
10.1161/circgen.122.003712
36252120
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
PGP000384
1
1
Parcha V
Association of a Multi-Ancestry Genome-Wide Blood Pressure Polygenic Risk Score with Adverse Cardiovascular Events.
Circ Genom Precis Med
05/11/2022
10.1161/circgen.122.003946
36334310
PGP000383
1
1
Solé-Navais P
Genetic effects on the timing of parturition and links to fetal birth weight.
Nat Genet
03/04/2023
10.1038/s41588-023-01343-9
37012456
PGP000382
6
6
Yengo L
A saturated map of common genetic variants associated with human height.
Nature
12/10/2022
10.1038/s41586-022-05275-y
36224396
PGP000381
0
6
Hao L
Development of a clinical polygenic risk score assay and reporting workflow.
Nat Med
18/04/2022
10.1038/s41591-022-01767-6
35437332
PGP000380
0
1
Chou A
Association of Prostate-Specific Antigen Levels with Prostate Cancer Risk in a Multiethnic Population: Stability over Time and Comparison with Polygenic Risk Score.
Cancer Epidemiol Biomarkers Prev
20/09/2022
10.1158/1055-9965.epi-22-0443
36126957
PGP000379
4
4
Shi Z
Reliability of Ancestry-specific Prostate Cancer Genetic Risk Score in Four Racial and Ethnic Populations.
Eur Urol Open Sci
17/09/2022
10.1016/j.euros.2022.09.001
36353656
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