Sherin Shaaban, MD, PhD, FACMG
Associate Professor of Pathology/Medical director of pharmacogenetics and molecular genetics
University of Utah
Salt Lake City, Utah, United States
Hannah Wollenzien, PhD (she/her/hers)
Assistant Clinical Laboratory Director
Sanford Health
Sioux Falls, South Dakota, United States
Description: The continued growth of knowledge on germline variation and how it can impart certain health risks has prompted the availability of genetic testing as a preventive medicine intervention. Notable examples include the optional return of ACMG secondary findings during clinical exome/genome testing, pharmacogenomic testing, and polygenic risk score testing. Although all these forms of testing are currently available for providers through traditional clinical workflows, this session is aimed at reviewing how these forms of testing can be leveraged for more innovative genomic screening in the context of larger preventative medicine programs.
If this session topic is of interest to you, please consider looking at the following course on AMP EDucation (AMPED™ Online)
Title: Germline Testing in Cancer Patients: Molecular Diagnostic Considerations and Clinical Implications
Please Click Here to Learn More.
Breakout Speaker: David T Miller, MD, PhD (he/him/his) – Boston Children's Hospital
Breakout Speaker: Anna C F Lewis, PhD (she/her/hers) – Brigham and Women's Hospital
Breakout Speaker: Peter H. O'Donnell, MD – The University of Chicago