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/vufind/Search/Results?lookfor=%22Christensen%2C+Kurt+D%22&type=Person&sort=year
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PubPharm (131)
1
A scalable EHR-based approach for phenotype discovery and variant interpretation for hereditary cancer genes
enthalten in:
bioRxiv.org
| 2024
von
Zeng, C.
|
Bastarache, L.
|
Tao, R.
| +30
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2
Development and utility of a clinical research informatics application for participant recruitment and workflow management for a return of results pilot trial in familial hypercholesterolemia in the Million Veteran Program
enthalten in:
JAMIA open
| 2024
von
Brunette, C.
|
Yi, T.
|
Danowski, M.
| +14
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3
Clinical impact of preemptive pharmacogenomic testing on antiplatelet therapy in a real-world setting
enthalten in:
European journal of human genetics : EJHG
| 2024
von
Massmann, A.
|
Christensen, K.
|
Van Heukelom, J.
| +10
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4
A framework evaluating the utility of multi-gene, multi-disease population-based panel testing that accounts for uncertainty in penetrance estimates
enthalten in:
bioRxiv.org
| 2024
von
Liang, J.
|
Christensen, K.
|
Green, R.
| +1
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5
Returning personalized, genetic health test results to individuals of African descent or ancestry in precision medicine research
enthalten in:
Health affairs scholar
| 2023
von
Hendricks-Sturrup, R.
|
Emmott, N.
|
Nafie, M.
| +5
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6
The GenoVA study : Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary care
enthalten in:
American journal of human genetics
| 2023
von
Vassy, J.
|
Brunette, C.
|
Lebo, M.
| +17
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7
Introducing return of results in the Million Veteran Program: Design and pilot results of the MVP-ROAR Familial Hypercholesterolemia Study
enthalten in:
bioRxiv.org
| 2023
von
Vassy, J.
|
Brunette, C.
|
Yi, T.
| +18
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8
Public perspective on medications to delay Alzheimer's disease symptoms
enthalten in:
Journal of genetic counseling
| 2023
von
Rich, M.
|
Blout Zawatsky, C.
|
Botta, J.
| +1
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9
Attitudes about pharmacogenomic testing vary by healthcare specialty
enthalten in:
Pharmacogenomics
| 2023
von
Preys, C.
|
Blout Zawatsky, C.
|
Massmann, A.
| +7
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10
Actionability of unanticipated monogenic disease risks in newborn genomic screening : Findings from the BabySeq Project
enthalten in:
American journal of human genetics
| 2023
von
Green, R.
|
Shah, N.
|
Genetti, C.
| +15
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Genetics in medicine : official journal of the ...
11
Journal of genetic counseling
7
American journal of human genetics
5
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Value in health : the journal of the Internatio...
2
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Research Support, N.I.H., Extramural
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7
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7
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5
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4
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exome sequencing
4
genetic research
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genomics
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humans
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