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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Research output
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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., 2020, (Accepted/In press) In: Developmental Medicine and Child Neurology.Research output: Contribution to journal › Letter › peer-review
1 Scopus citations -
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
1 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
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Adaptive functioning in children with neurofibromatosis type 1: relationship to cognition, behavior, and magnetic resonance imaging
Eby, N. S., Griffith, J. L., Gutmann, D. H. & Morris, S. M., Aug 2019, In: Developmental Medicine and Child Neurology. 61, 8, p. 972-978 7 p.Research output: Contribution to journal › Article › peer-review
5 Scopus citations -
A genotype–phenotype correlation for quantitative autistic trait burden in neurofibromatosis 1
Morris, S. M. & Gutmann, D. H., Jan 1 2018, In: Neurology. 90, 8, p. 377-379 3 p.Research output: Contribution to journal › Article › peer-review
8 Scopus citations