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PubPharm (32)
1
Polygenic background modifies penetrance of monogenic variants conferring risk for coronary artery disease, breast cancer, or colorectal cancer
enthalten in:
bioRxiv.org
| 2024
von
Fahed, A.
|
Wang, M.
|
Homburger, J.
| +14
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2
Genomic data in the All of Us Research Program
enthalten in:
Nature
| 2024
von
All of Us Research Program Genomics Investigators
|
Bick, A.
|
Metcalf, G.
| +98
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3
Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores
enthalten in:
bioRxiv.org
| 2023
von
Homburger, J.
|
Neben, C.
|
Mishne, G.
| +3
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4
Clinical Implementation of Combined Monogenic and Polygenic Risk Disclosure for Coronary Artery Disease
enthalten in:
JACC. Advances
| 2022
von
Maamari, D.
|
Brockman, D.
|
Aragam, K.
| +12
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5
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program
enthalten in:
Genome medicine
| 2022
von
Venner, E.
|
Muzny, D.
|
Smith, J.
| +19
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6
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program
enthalten in:
Genome medicine
| 2022
von
Venner, E.
|
Muzny, D.
|
Smith, J.
| +18
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7
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program
enthalten in:
Genome medicine
| 2022
von
Venner, E.
|
Muzny, D.
|
Smith, J.
| +18
Wird geladen...
8
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions
enthalten in:
Nature communications
| 2020
von
Fahed, A.
|
Wang, M.
|
Homburger, J.
| +14
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9
Burden of hereditary cancer susceptibility in unselected patients with pancreatic ductal adenocarcinoma referred for germline screening
enthalten in:
Cancer medicine
| 2020
von
Cremin, C.
|
Lee, M.
|
Hong, Q.
| +19
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10
Patient acceptance of genetic testing for familial hypercholesterolemia in the CASCADE FH Registry
enthalten in:
Journal of clinical lipidology
| 2020
von
Gidding, S.
|
Sheldon, A.
|
Neben, C.
| +6
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20
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13
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8
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3
Atrial fibrillation
3
Breast cancer
3
Coronary artery disease
3
EC 2.7.10.1
3
Genome-wide polygenic score
3
Low coverage whole genome sequencing
3
Review
3
Tumor Suppressor Protein p53
2
5688UTC01R
2
570
2
Biology
2
Biomarkers, Tumor
2
Cyp26a1 protein, mouse
2
Cyp26c1 protein, mouse
2
Cytochrome P450 Family 26
2
DNA, Ribosomal
2
EC 1.14.14.1
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Erscheinungszeitraum
13
2020-
19
2010-2019
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