Editor’s Note: Genetic counselors interpret genetic test results to guide and support patients seeking information about their personal and family health. They can take a variety of roles, from meeting with patients in a hospital or clinical care setting, to working in a diagnostic laboratory, to performing primary research. In this guest blog, Sarah Raible, MS, CGC, a senior genetic counselor and clinical director of the Center for Cornelia de Lange Syndrome and Related Diagnoses Center within the Roberts Individualized Medical Genetics Center (RIMGC) at Children’s Hospital of Philadelphia, discusses how genetic counselors’ unique contributions and insights are helping to shape the future of precision medicine.
Tag Archive: CHOPS syndrome
Take a look at who’s been in the press lately. This week we’re covering physician-endorsed parent-teen talks, the high rate of success with ultrasound-guided intravenous line placement, and how moms with postpartum depression are being helped with a social media-based parenting program.
Physician Endorsed ‘Birds and the Bees’ Parent-teen Talk may Prove Effective
New research shows that brief parent-targeted interventions in the primary care setting can increase communication between parents and their teens about sexual and alcohol behavior. This method may serve as an important strategy for parents to influence adolescent behaviors and health outcomes.
By Nancy McCann
It was no easy feat for two “superhero” clinical research coordinators (CRCs) to rise to the top of nominees at the 6th annual CRC Research Excellence @ Children’s Hospital (RE@CH) Award ceremony because they were in the company of extraordinaires.
Congratulations go out to the 2019 CRC RE@CH Award winners Katherine Kellom, a qualitative methods program manager at CHOP’s PolicyLab, and Lindsay Waqar, MPH, CCRC, a clinical research coordinator in the Division of Rheumatology. Their nominating principal investigators were Meredith Matone, DrPH, MHS, and Pamela Weiss, MD, MSCE, respectively.
Scientific minds are imagining. Sophisticated machines are harnessing genetic data. An invisible universe of microbes is revealing new insights into disease. Discoveries are changing children’s worlds. Every second of every day is filled with wonder at The Children’s Hospital of Philadelphia Research Institute.
CHOP medical geneticist and researcher Ian Krantz, MD, has been a tireless detective in his efforts to find out what genetic syndrome could be behind Leta’s constellation of symptoms.