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Research Affinity Groups (RAGs) are dedicated and collaborative scientific communities that reach across disciplines and the CHOP-Penn campus to share resources and delve into the most challenging problems in pediatric research. By connecting multidisciplinary investigators with common research interests on a regular basis, RAGs cross-pollinate ideas and keep members well informed on how to accomplish the best research efficiently and effectively.
Investigating the cell biological basis of disease.
Building a community of investigators conducting clinical trials at CHOP and Penn.
Investigating the fundamental mechanisms of developmental biology and translating those findings into improved care.
Exploring the possibilities for treating disorders during fetal development.
Providing an innovative program focused on the molecular genetic basis of disease.
Fostering efforts to expand and support pediatric research collaboration between investigators working in resource-limited settings worldwide.
Working to understanding the effects of behavior on children’s health.
Investigating the causes and consequences of metabolic and nutritional disorders to identify disease prevention and treatment strategies.
Bringing together CHOP mathematicians, physicists, and engineers to brainstorm emerging technology and accelerate medical innovation.
Cultivating collaborative efforts to expand the capability to develop, test, integrate, and adapt mHealth tools and approaches in pediatric research.
Supporting a diverse community of investigators and clinicians in groundbreaking basic, translational, and clinical research in mitochondrial biology and disease.
Facilitating the rapid translation of neuroscience research into clinical best practices.
Investigating the networks that regulate blood cell development in normal and diseased states.
Applying shared knowledge toward a better understanding of the immune system and its powers to protect and heal.
Building and supporting a growing community using qualitative and mixed methods approaches.
Uncovering the correct functional context of genetic variants to translate genome-wide association studies into meaningful benefits for pediatric care.