Challenges and opportunities for Lynch syndrome cascade testing in the United States
Author:
Funder
NCI and UNC-CH
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s10689-024-00374-3.pdf
Reference28 articles.
1. Cohen SA, Pritchard CC, Jarvik GP (2019) Lynch Syndrome: From Screening to Diagnosis to Treatment in the Era of Modern Molecular Oncology. Annu Rev Genomics Hum Genet 20:293–307. https://doi.org/10.1146/annurev-genom-083118-015406
2. Hampel H, de la Chapelle A (Jan. 2011) The search for unaffected individuals with Lynch Syndrome: do the ends justify the means? Cancer Prev Res Phila Pa 4(1):1–5. https://doi.org/10.1158/1940-6207.CAPR-10-0345
3. Sharaf RN, Myer P, Stave CD, Diamond LC, Ladabaum U (2013) Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review. Clin Gastroenterol Hepatol Off Clin Pract J Am Gastroenterol Assoc 11(9):1093–1100. https://doi.org/10.1016/j.cgh.2013.04.044
4. Srinivasan S et al (2020) Dec., Stakeholder perspectives on overcoming barriers to cascade testing in Lynch syndrome: A qualitative study. Cancer Prev Res Phila Pa 13(12):1037–1046. https://doi.org/10.1158/1940-6207.CAPR-20-0141
5. Srinivasan S, Won NY, Dotson WD, Wright ST, Roberts MC (2020) Barriers and facilitators for cascade testing in genetic conditions: a systematic review. Eur J Hum Genet EJHG 28(12):1631–1644. https://doi.org/10.1038/s41431-020-00725-5
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