Latham A

ORCID: 0000-0002-9758-713X · 2 papers in corpus
observational 2022
Genetics in medicine : official journal of the American College of Medical Genetics ·doi:10.1016/j.gim.2022.02.016

PURPOSE: This study aimed to characterize MSH6/PMS2-associated mismatch repair-deficient (MMR-D)/microsatellite instability-high (MSI-H) tumors, given revised guidelines suggesting more modest phenotypes. METHODS: Patients who consented to…

review 2022
JCO oncology practice ·doi:10.1200/op.21.00382

Pathogenic germline variants underlie up to 20% of ovarian cancer (OC) and are associated with varying degrees of risk for OC. For mutations in high-penetrance genes such as BRCA1/2, the role of risk-reducing bilateral salpingo-oophorectomy…