Research output per year
Research output per year
Personal profile
Research interests
Clinical focus is caring for children with Neurofibromatosis Type 1 (NF1) with specific interest in diagnosing and treating those with neurodevelopmental and behavioral disorders including autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD). Her research interests involve the deep phenotypic profiling of neurodevelopmental disabilities in NF1, identifying key genomic alterations underlying development of cognitive and behavioral impairments, and translating this comprehensive understanding into clinically useful predictive models of developmental and behavioral disability in children with NF1.
Areas of Clinical Interest
Neurofibromatosis Type 1, Neurofibromatosis Type 2, Fragile X Syndrome, Autism, ADHD, pediatric headache, seizures and developmental delay.
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Autism in neurofibromatosis type 1: misuse of covariance to dismiss autistic trait burden
Morris, S. M., Acosta, M. T., Garg, S., Green, J., Legius, E., North, K., Payne, J. M., Weiss, L. A., Constantino, J. N. & Gutmann, D. H., Feb 2021, In: Developmental Medicine and Child Neurology. 63, 2, p. 233-234 2 p.Research output: Contribution to journal › Letter › peer-review
1 Scopus citations -
Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis
Wegscheid, M. L., Anastasaki, C., Hartigan, K. A., Cobb, O. M., Papke, J. B., Traber, J. N., Morris, S. M. & Gutmann, D. H., Jul 6 2021, In: Cell Reports. 36, 1, 109315.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
SARS-CoV-2 screening testing in schools for children with intellectual and developmental disabilities
for the COMPASS-T Study Group, Dec 2021, In: Journal of neurodevelopmental disorders. 13, 1, 31.Research output: Contribution to journal › Article › peer-review
Open Access -
Nonoptic pathway tumors in children with neurofibromatosis type 1
Mahdi, J., Goyal, M. S., Griffith, J., Morris, S. M. & Gutmann, D. H., Aug 25 2020, In: Neurology. 95, 8, p. e1052-e1059Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
Sorting nexin 27 (SNX27) variants associated with seizures, developmental delay, behavioral disturbance, and subcortical brain abnormalities
Parente, D. J., Morris, S. M., McKinstry, R. C., Brandt, T., Gabau, E., Ruiz, A. & Shinawi, M., Mar 1 2020, In: Clinical Genetics. 97, 3, p. 437-446 10 p.Research output: Contribution to journal › Article › peer-review
2 Scopus citations