Stephanie Morris

Assistant Professor of Neurology, Assistant Professor of Pediatrics

    • 106 Citations

    Research output per year

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    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

    • 106 Citations
    • 10 Article
    • 1 Letter
    • 1 Review article

    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 journalLetter

    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-e1059

    Research output: Contribution to journalArticle

  • 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 journalArticle

  • 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 journalArticle

    8 Scopus citations