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PubPharm (186)
1
Applying health equity implementation science frameworks to population genetic screening
enthalten in:
bioRxiv.org
| 2024
von
Rao, N.
|
Fullerton, S.
|
Shirts, B.
| +2
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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
Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients
enthalten in:
European journal of human genetics : EJHG
| 2024
von
Rao, N.
|
King, K.
|
Kaganovsky, J.
| +6
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4
ClinGen guidance for use of the PP1/BS4 co-segregation and PP4 phenotype specificity criteria for sequence variant pathogenicity classification
enthalten in:
American journal of human genetics
| 2024
von
Biesecker, L.
|
Byrne, A.
|
Harrison, S.
| +6
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5
Most people share genetic test results with relatives even if the findings are normal : Family communication in a diverse population
enthalten in:
Genetics in medicine : official journal of the American College of Medical Genetics
| 2023
von
Hunter, J.
|
Riddle, L.
|
Joseph, G.
| +78
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6
Assigning credit where it’s due: An information content score to capture the clinical value of Multiplexed Assays of Variant Effect
enthalten in:
bioRxiv.org
| 2023
von
Ranola, J.
|
Horton, C.
|
Pesaran, T.
| +3
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7
Assigning credit where it's due : An information content score to capture the clinical value of Multiplexed Assays of Variant Effect
enthalten in:
bioRxiv : the preprint server for biology
| 2023
von
Ranola, J.
|
Horton, C.
|
Pesaran, T.
| +3
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8
Multiplexing Mutation Rate Assessment: Determining Pathogenicity of Msh2 Variants in
S. cerevisiae
enthalten in:
bioRxiv.org
| 2023
von
Ollodart, A.
|
Yeh, C.
|
Miller, A.
| +3
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9
Exploring Stakeholders' Perspectives on Implementing Universal Germline Testing for Colorectal Cancer : Findings From a Clinical Practice Survey
enthalten in:
JCO precision oncology
| 2023
von
Rodgers-Fouche, L.
|
Arora, S.
|
Ricker, C.
| +13
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10
Risk management actions following genetic testing in the Cancer Health Assessments Reaching Many (CHARM) Study : A prospective cohort study
enthalten in:
Cancer medicine
| 2023
von
Guo, B.
|
Knerr, S.
|
Kauffman, T.
| +82
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Familial cancer
11
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Schizophrenia research
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bioRxiv.org
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Journal of pathology informatics
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American journal of clinical pathology
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American journal of human genetics
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Lynch syndrome
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7
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VUS
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570
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BRCA1 Protein
6
BRCA1 protein, human
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Biology
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family studies
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variant classification
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BRCA2 Protein
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BRCA2 protein, human
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