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Article
Our Mission and Strategic Plan
The Abigail Wexner Research Institute at Nationwide Children's Hospital is dedicated to enhancing the health of children by engaging in high-quality, cutting-edge research according to the highest scientific and ethical standards.
Article
Moscato Lab
The Moscato Lab, led by Emily Moscato, PhD, focuses on designing, testing and implementing equitable behavioral interventions to improve quality of life and neurodevelopmental trajectories for young children with chronic conditions impacting the central nervous system.
Article
Mo Lab
The Mo Lab investigates how genetic mutations lead to autism and intellectual disability by studying their impact on brain development.
Article
Stottmann Lab
The long-term goals of the Stottmann Lab are to understand the genes and molecular mechanisms guiding normal development of both the brain and face.
Article
Wedemeyer Lab
The Wedemeyer Laboratory seeks to apply state of the art genomics technologies to better understand common neurosurgical disease processes in children and improve the overall neurosurgical care for the children in our community.
Article
Community Provider Corner
- Ask A Pediatric Specialist
- Free Virtual Learning From Project ECHO
- Support School Readiness During Literacy Month
- Diabetes Management Education – Professional Accreditation
- Neuroimmune Family Education Day
- 38th Annual Celiac Conference
- Living with Epilepsy Conference
Specialty
Neuro-Oncology
Our highly experienced and internationally recognized team of pediatric neuro-oncologists, neurosurgeons and neuroradiologists will care for your child by providing the most advanced and innovative treatments, while at the same time, paying careful attention to all the needs and concerns of your child and family.
Specialty
Innovative Infant Feeding Disorders Program
The Innovative Infant Feeding Disorders Program works to prevent, predict, diagnose and treat feeding-related disorders for infants. Dedicated to improving outcomes, our expert team focuses on personalized, feeding management strategies based on the latest clinical and transitional research.
Condition
Marfan Syndrome
Marfan Syndrome is an inherited disorder of connective tissue caused by genetic mutations that result in the dysregulation of the proteins of the extracellular matrix (fibrillin). The diagnosis is based on signs, family history, and results of diagnostic tests.