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Paper Details

Association of genetic and sulcal traits with executive function in congenital heart disease.
Ann Clin Transl Neurol
0
2024
CHD, Persons, apolipoprotein E, biventricular, congenital heart disease, executive dysfunction, executive function impairment, impairments to executive function, neurodevelopmental, neurodevelopmental disabilities, participant, single-ventricle CHD, single-ventricle heart disease, sulcal, tetralogy of Fallot
Author NameAffiliation
Martina BruecknerYale University School of Medicine
Martina BruecknerYale University School of Medicine
Bruce D GelbMindich Child Health and Development Institute and Department of Pediatrics, Icahn School of Medicine at Mount Sinai
Bruce D GelbMindich Child Health and Development Institute and Department of Pediatrics, Icahn School of Medicine at Mount Sinai
Elizabeth GoldmuntzChildren's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Donald J HaglerCenter for Multimodal Imaging and Genetics, University of California San Diego
Donald J HaglerUniversity of California San Diego
Sarah U MortonHarvard Medical School
Sarah U MortonBoston Children's Hospital
Sarah U MortonBoston Children's Hospital
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