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Primary Care Research Network
The Nationwide Children’s Hospital Primary Care Research Network (PCRN) is a consortium of pediatric primary care practices focused on improving child health and family outcomes through high-quality research in primary care settings. Additionally, the Pediatric Primary Care Research Affinity Group (PPC-RAG) awards supplemental funding on an annual basis for collaborative projects.
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Dr. Patrick Gallagher of Yale University Named Director of Perinatal Research Center at Nationwide Children's Hospital
Patrick Gallagher, MD, from Yale University has been named the new director of the Center for Perinatal Research in the Abigail Wexner Research Institute at Nationwide Children's Hospital.
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Research and Innovation
Our team is actively engaged in clinical research that aims to help professionals and families understand more about the 22q deletion and its impact on affected children.
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Dennis Durbin, MD, MSCE, Named President of the Abigail Wexner Research Institute at Nationwide Children’s Hospital
Beginning March 1, 2022, Dennis Durbin, MD, MSCE, will become the third president of the Abigail Wexner Research Institute at Nationwide Children's Hospital. Dr. Durbin joined Nationwide Children's in 2018 as its first chief scientific officer.
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Researcher at Nationwide Childrens Hospital Secures Grant to Develop a Standard Statistical Evidence Measure to Reduce Errors in Biomedical Research
Veronica Vieland, PhD, director of the Battelle Center for Mathematical Medicine in The Research Institute at Nationwide Children’s Hospital, was recently awarded a $500,000 grant from the W.M.
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Baker Lab Staff
Learn more about principal investigator Linda Baker, MD, and her dynamic team in the Baker Lab.
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April 2010
Gene transfer of follistatin: Dr. Mendell discusses implications for muscle disease.
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January 2011
Dr. Jerry Mendell discusses dystrophin immunity in duchenne muscular dystrophy.
DISCOVERYx: The Stories Behind Discovery
Learn more about research and academic events going on at Nationwide Children's Hospital.
Article
Replacing Missing Genes
Duchenne muscular dystrophy (DMD) is the most common life-threatening childhood form of muscular dystrophy. It is characterized by progressive weakness and degeneration of skeletal muscles and caused by a mutation in the dystrophin gene.