Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Erin G. Sutcliffe"'
Autor:
Erin G. Sutcliffe, Jessica L. Mester, Lisa R. Susswein, Maegan E. Roberts, Megan L. Marshall, Kathleen S. Hruska
Publikováno v:
Cancer Genetics. :86-89
Mosaic variants are regularly detected on hereditary cancer genetic tests. While some of these variants may be constitutional, the majority are likely limited to blood lineages. In the present study, we correlate clinical histories from individuals w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::196417f0a48d77af660d11d9c0525643
https://doi.org/10.1016/j.cancergen.2022.07.004
https://doi.org/10.1016/j.cancergen.2022.07.004
Autor:
Amanda Bartenbaker Thompson, Erin G. Sutcliffe, Kevin Arvai, Maegan E. Roberts, Lisa R. Susswein, Megan L. Marshall, Rebecca Torene, Kristen J. Vogel Postula, Kathleen S. Hruska, Shaochun Bai
Publikováno v:
Familial Cancer. 21:415-422
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6131065a102437588df7063fdcfbe583
https://doi.org/10.1007/s10689-021-00285-7
https://doi.org/10.1007/s10689-021-00285-7
Autor:
Amanda Bartenbaker, Thompson, Erin G, Sutcliffe, Kevin, Arvai, Maegan E, Roberts, Lisa R, Susswein, Megan L, Marshall, Rebecca, Torene, Kristen J Vogel, Postula, Kathleen S, Hruska, Shaochun, Bai
Publikováno v:
Familial cancer. 21(4)
We aimed to determine whether monoallelic MUTYH pathogenic and likely pathogenic variants (PVs) are associated with colorectal, breast, and endometrial cancer. Cases were individuals with colorectal, female breast, or endometrial cancer who reported
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::805ba9dbe71a848f36a3c7900d650b33
https://pubmed.ncbi.nlm.nih.gov/34981295
https://pubmed.ncbi.nlm.nih.gov/34981295
Autor:
Kevin J. Arvai, Erin G. Sutcliffe, Lisa R. Susswein, Amy R. Stettner, Sheila R. Solomon, Patricia D. Murphy, Maegan E. Roberts, Kathleen S. Hruska, Rachel T. Klein, Megan L. Marshall, Stacey A. Miller
Publikováno v:
Cancer genetics.
Purpose Although CHEK2 is a well-established cancer gene, questions remain including whether risks vary substantially between different variants and whether biallelic carriers have higher risks than heterozygotes. We report on a cohort of individuals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f7f30e55fd27e61a648598f0318a892
https://pubmed.ncbi.nlm.nih.gov/32805687
https://pubmed.ncbi.nlm.nih.gov/32805687