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Combining copy number, methylation markers, and mutations as a panel for endometrial cancer detection via intravaginal tampon collection

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Year: 2019
Type: article
Study design: Observational Study
Source: Gynecologic Oncology
DOI: 10.1016/j.ygyno.2019.11.028
Authors: Ajleeta Sangtani, Chen Wang, Amy Weaver, Nicole L. Hoppman, Sarah E. Kerr, Alexej Abyzov, Viji Shridhar, Julie Staub, Jean-Pierre A. Kocher, Jesse S. Voss, Karl C. Podratz, Nicolas Wentzensen, John B. Kisiel, Mark E. Sherman, Jamie N. Bakkum-Gamez
Institutions: Mayo Clinic, National Cancer Institute, Mayo Clinic in Florida
Language: English

Topic: Cancer Genomics and Diagnostics
Subfield: Cancer Research
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green

Funders: National Institutes of Health, National Cancer Institute, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: Detection of somatic, subclonal and mosaic CNVs from sequencing, G6433449787, G9000230084, Mayo Clinic Comprehensive Cancer Center Support Grant, G920212055
OpenAlex ID: W2990629088
FWCI: 0.968
Cites: 30
Cited by: 39
Related to: 10
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