Background Reducing ultraviolet radiation (UV) exposure and improving early detection
may reduce melanoma incidence, mortality and health system costs. This study aims to …

Purpose Genetic testing for gene mutations which elevate risk for breast cancer is
particularly important for women diagnosed at a young age. Differences remain in access …

In “A Framework for Unrestricted Prenatal Whole-Genome Sequencing: Respecting and
Enhancing the Autonomy of Prospective Parents,” Chen and Wasserman (2017) argue in …

Aim: As genomic medicine reaches more diverse populations, there is an increased need for
healthcare interpreters who understand and can effectively interpret genomics concepts …

Biostatistics for Clinical and Public Health Research provides a concise overview of
statistical analysis methods. Use of SAS and Stata statistical software is illustrated in full …

Personalized polygenic risk information may be used to guide risk-based melanoma
prevention and early detection at a population scale, but research on communicating this …

PURPOSE: Tumor genomic testing (TGT) has become increasingly adopted as part of
standard cancer care for many cancers. Despite national guidelines around patient …

Objective This study sought to evaluate the experiences of individuals who chose to
participate in a study and receive prenatal genomic sequencing (pGS) for fetuses with …

Background Genetic testing can help determine the risk of many cancers and guide cancer
prevention and treatment plans. Despite increasing concern about disparities in precision …

Informed consent is crucial for participant understanding, engagement, and partnering for
research. However, current written informed consents have significant limitations …