Low frequency of structured documentation for cancer genetic testing in a large electronic health record dataset: A brief report using All of Us Research data.
Annually, over two million individuals in the United States are diagnosed with cancer, with 10–20% attributed to hereditary cancer syndromes. Genetic testing for pathogenic variants is a standard component of cancer care guided by tumor pathology and family history. Despite this, access to and compl...
| Published in: | Journal of Genetic Counseling Vol. 34; no. 2; pp. 1 - 8 |
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| Main Authors: | , , , |
| Format: | research tables/charts Journal Article |
| Published: |
Wiley-Blackwell
Apr2025
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| Online Access: | View this record in EBSCOhost |