Factors Influencing Clinical Follow-Up for Individuals with a Personal History of Breast and/or Ovarian Cancer and Previous Uninformative BRCA1 and BRCA2 Testing
Author:
Funder
GeneDx
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://link.springer.com/article/10.1007/s10897-018-0241-9/fulltext.html
Reference24 articles.
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3. Castera, L., Krieger, S., Rousselin, A., Legros, A., Baumann, J. J., Bruet, O., et al. (2014). Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes. European Journal of Human Genetics, 22(11), 1305–1313. https://doi.org/10.1038/ejhg.2014.16 .
4. Bakos, A. D., Hutson, S. P., Loud, J. T., Peters, J. A., Giusti, R. M., & Greene, M. H. (2008). BRCA mutation-negative women from hereditary breast and ovarian cancer families: A qualitative study of the BRCA-negative experience. Health Expectations, 11(3), 220–231. https://doi.org/10.1111/j.1369-7625.2008.00494.x .
5. Buchberg, M. K., Fletcher, F. E., Vidrine, D. J., Levison, J., Peters, M. Y., Hardwicke, R., Yu, X., & Bell, T. K. (2015). A mixed-methods approach to understanding barriers to postpartum retention in care among low-income, HIV-infected women. AIDS Patient Care and STDs, 29, 126–132. https://doi.org/10.1089/apc.2014.0227 .
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2. Uptake of genetic counseling and multi‐gene panel testing among women in the Intermountain West with previous negative BRCA1 and BRCA2 results contacted for updated testing;Journal of Genetic Counseling;2021-09-27
3. Outcomes of retesting in patients with previously uninformative cancer genetics evaluations;Familial Cancer;2021-09-21
4. Out‐of‐pocket and private pay in clinical genetic testing: A scoping review;Clinical Genetics;2021-06-21
5. Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiences;Hereditary Cancer in Clinical Practice;2021-01-19
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