Jonathan N. Dodd

<i>WAC</i> loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome

C.L. DeSanto, Kristin D׳Aco, Gabriel C. Araujo et al. · Journal of Medical Genetics · 2015 · 54 citations

Optimizing Neurocritical Care Follow-Up Through the Integration of Neuropsychology

Jonathan N. Dodd, Trevor A. Hall, Kristin P. Guilliams et al. · Pediatric Neurology · 2018 · 42 citations · Full text

Critical Care Management, Neuropsychology, Psychiatry +6

Diffusion tensor imaging study of pediatric patients with congenital hydrocephalus: 1-year postsurgical outcomes

Francesco T. Mangano, Mekibib Altaye, Robert C. McKinstry et al. · Journal of Neurosurgery Pediatrics · 2016 · 41 citations · Full text

Neuropsychology, Pediatric Hydrocephalus, White Matter +20

Mutations in the <scp>PH</scp> Domain of <i><scp>DNM</scp>1</i> are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities

Emily Brereton, Emily Fassi, Gabriel C. Araujo et al. · Molecular Genetics & Genomic Medicine · 2018 · 26 citations · Full text

Sensitivity of the Memory Validity Profile (MVP): Raising the bar

Jonathan N. Dodd, Samantha Murphy, Christopher C. Bosworth · Child Neuropsychology · 2019 · 10 citations