Fletcher O

ORCID: 0000-0001-9387-7116 · 2 papers in corpus

2024

Germline copy number variants and endometrial cancer risk.

Human genetics ·doi:10.1007/s00439-024-02707-9

Known risk loci for endometrial cancer explain approximately one third of familial endometrial cancer. However, the association of germline copy number variants (CNVs) with endometrial cancer risk remains relatively unknown. We conducted a …

2016

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

Gynecologic Oncology ·doi:10.1016/j.ygyno.2015.04.034

ObjectiveClinical genetic testing is commercially available for rs61764370, an inherited variant residing in a KRAS 3' UTR microRNA binding site, based on suggested associations with increased ovarian and breast cancer risk as well as with …