Kerry, Michele, & Darin, will be seeking feedback on wording and flow/ordering of an interview guide. The interview will be with individuals at risk for Huntington’s Disease, individuals with HD, and/or family members/caregivers.
Page not found
Wendy Uhlmann, Scott Roberts, and Ray De Vries will serve as panelists on Monday, September 11th for FINDING COMMON GROUND: A Conversation on Genetics and Religion at the Ann Arbor Downtown Library.
More information can be found here.
Sarah Hawley's perspective piece, "Half of women with early-stage breast cancer consider prophylactic double mastectomy" was recently published in Healio ITJ (in the journals).
Full article can be found here.
Christina Hunter Chapman, M.D., M.S.
Assistant Professor of Radiation Oncology
Title: African Americans and Tailored Cancer Screening: Evidence and Ethics
Abstract: Dr. Chapman will discuss the elevated cancer mortality that African Americans experience and the ethical barriers to consideration of tailored cancer screening strategies that have the potential to reduce this disparity.
Brian Zikmund-Fisher presented the Berguer Lecture on Ethics, "Communicating Everything Important Poorly vs. One Critical Thing Well" in Danto Auditorium, Frankel Cardiovascular Center on Friday, January 26th 4 - 5 pm.
The Genetics in Primary Care Institute recently launched its new website, featuring co-chairperson Beth Tarini, M.D., assistant professor of pediatrics at the University of Michigan’s C.S. Mott Children’s Hospital.
Along with Robert Saul, M.D., Tarini co-chairs the Institute, which aims to take genetic advances made during the last decade and help make them useful in the practice of primary care pediatrics.
The new website, www.geneticsinprimarycare.org, features information for primary care providers related to genetics testing, ethical, legal and social issues, patient communication and family history.
Tarini’s research focuses on the communication process and the health outcomes associated with genetic testing in pediatrics. She is particularly interested in pediatric population-based screening programs, such as newborn screening. Through her research, Tarini seeks to optimize communication about genetic testing between parents and providers in an effort to maximize health and minimize harm.