Stephanie Morris

Research output

Research output per year 2016 2017 2021 2022 2024

• 19 Article
• 1 Letter
• 1 Review article

Research output per year

Research output per year

Search results

• 2024

  Latent Class Analysis Identifies Distinctive Behavioral Subtypes in Children with Fragile X Syndrome

  FORWARD Consortium, Feb 2024, In: Journal of Autism and Developmental Disorders. 54, 2, p. 725-737 13 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Fragile X Syndrome 100%
  • Latent Class Analysis 86%
  • Checklist 50%
  • Child 33%
  • clinical management 27%
• 2022

  Dose-dependent seizure control with MEK inhibitor therapy for progressive glioma in a child with neurofibromatosis type 1

  Cantor, E., Meyer, A., Morris, S. M., Weisenberg, J. L. Z. & Brossier, N. M., Nov 2022, In: Child's Nervous System. 38, 11, p. 2245-2249 5 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Neurofibromatosis 1 100%
  • AZD 6244 90%
  • Mitogen-Activated Protein Kinase Kinases 89%
  • Glioma 75%
  • Seizures 63%

• Predictors of Patient Return to a Tertiary Neurofibromatosis Subspecialty Clinic

  Rosen, K. L., Cobb, O., Gavney, D., Morris, S. M. & Gutmann, D. H., Sep 2022, In: Journal of Pediatrics. 248, p. 94-99.e1

  Research output: Contribution to journal › Article › peer-review

  • Neurofibromatoses 100%
  • Logistic Models 51%
  • Neurofibromatosis 1 23%
  • Child Care 20%
  • Electronic Health Records 20%

• Stroke Mimics Are Not Benign in Immunocompromised Children

  Mahdi, J., Bach, A., Smith, A. E., Tomko, S. R., Fields, M. E., Griffith, J. L., Morris, S. M., Guerriero, R. M., Noetzel, M. J., Guilliams, K. P. & Agner, S. C., Oct 1 2022, In: Stroke. 53, 10, p. E442-E443

  Research output: Contribution to journal › Article › peer-review

  Open Access
• 2021

  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

  Open Access

• Familial Lipomas Without Classic Neurofibromatosis-1 Caused by a Missense Germline NF1 Mutation

  Ramirez, E., Morris, S. M., Turner, T. N. & Gutmann, D. H., Jun 26 2021, In: Neurology: Genetics. 7, 3, e582.

  Research output: Contribution to journal › Article › peer-review

  Open Access

• 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 Access

  • Organoids 100%
  • Neurofibromatosis 1 92%
  • Developmental 92%
  • Cytokine Receptors 92%
  • Neurogenesis 80%

• Predictive Modeling for Clinical Features Associated With Neurofibromatosis Type 1

  Morris, S. M., Gupta, A., Kim, S., Foraker, R. E., Gutmann, D. H. & Payne, P. R. O., Dec 1 2021, In: Neurology: Clinical Practice. 11, 6, p. E497-E505

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Neurofibromatosis 1 100%
  • Optic Nerve Glioma 82%
  • Machine Learning 46%
  • Attention Deficit Disorder with Hyperactivity 41%
  • Electronic Health Records 27%

• 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

  • SARS Virus 100%
  • Disabled Children 81%
  • Intellectual Disability 64%
  • Students 19%
  • Pandemics 8%

• Seizures in Fragile X Syndrome: Associations and Longitudinal Analysis of a Large Clinic-Based Cohort

  The FORWARD Consortium, Dec 30 2021, In: Frontiers in Pediatrics. 9, 736255.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Fragile X Syndrome 100%
  • Seizures 59%
  • Anticonvulsants 13%
  • Epilepsy 11%
  • Levetiracetam 9%
• 2020

  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 journal › Article › peer-review

  • Neurofibromatosis 1 100%
  • Natural History 38%
  • Child 35%
  • Neoplasms 26%
  • Brain Stem 9%

• 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

  • Sorting Nexins 100%
  • Seizures 46%
  • Brain 29%
  • Neuronal Plasticity 16%
  • White Matter 15%
• 2019

  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

  • Neurofibromatosis 1 100%
  • Psychological Adaptation 94%
  • Cognition 64%
  • Magnetic Resonance Imaging 54%
  • Executive Function 42%
• 2018

  A genotype–phenotype correlation for quantitative autistic trait burden in neurofibromatosis 1

  Morris, S. M. & Gutmann, D. H., 2018, In: Neurology. 90, 8, p. 377-379 3 p.

  Research output: Contribution to journal › Article › peer-review

• Increased prevalence of brain tumors classified as T2 hyperintensities in neurofibromatosis 1

  Griffith, J. L., Morris, S. M., Mahdi, J., Goyal, M. S., Hershey, T. & Gutmann, D. H., Aug 1 2018, In: Neurology: Clinical Practice. 8, 4, p. 283-291 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Neurofibromatosis 1 100%
  • Brain Neoplasms 76%
  • Child 28%
  • Neoplasms 26%
  • Confidence Intervals 19%
• 2017

  A 12-Year-Old Girl With Encephalopathy and Acute Flaccid Paralysis: A Neuropathological Correlation and Cohort Review

  Kim, Y. M., Orvedahl, A., Morris, S., Schmidt, R. & Mar, S., Jan 1 2017, In: Pediatric Neurology. 66, p. 5-11 7 p.

  Research output: Contribution to journal › Article › peer-review

• A multi-institutional study of brainstem gliomas in children with neurofibromatosis type 1

  Mahdi, J., Shah, A. C., Sato, A., Morris, S. M., McKinstry, R. C., Listernick, R., Packer, R. J., Fisher, M. J. & Gutmann, D. H., Apr 18 2017, In: Neurology. 88, 16, p. 1584-1589 6 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Neurofibromatosis 1 100%
  • Glioma 75%
  • Brain Stem 73%
  • Child 35%
  • Neoplasms 23%

• Children with 59-end NF1 gene mutations are more likely to have glioma

  Anastasaki, C., Morris, S. M., Gao, F. & Gutmann, D. H., Oct 1 2017, In: Neurology: Genetics. 3, 5, e192.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Neurofibromatosis 1 Genes 100%
  • Neurofibromatosis 1 77%
  • Glioma 58%
  • Mutation 35%
  • Child 27%

• Neurodevelopmental disorders in children with neurofibromatosis type 1

  Vogel, A. C., Gutmann, D. H. & Morris, S. M., Nov 2017, In: Developmental medicine and child neurology. 59, 11, p. 1112-1116 5 p.

  Research output: Contribution to journal › Review article › peer-review

  Open Access

  • Neurofibromatosis 1 100%
  • Neurodevelopmental Disorders 96%
  • Specific Learning Disorder 36%
  • Child 35%
  • Neurofibromatosis 1 Genes 32%
• 2016

  Disease burden and symptom structure of autism in neurofibromatosis type 1: A study of the international NF1-ASD consortium team (INFACT)

  Morris, S. M., Acosta, M. T., Garg, S., Green, J., Huson, S., Legius, E., North, K. N., Payne, J. M., Plasschaert, E., Frazier, T. W., Weiss, L. A., Zhang, Y., Gutmann, D. H. & Constantino, J. N., Dec 1 2016, In: JAMA psychiatry. 73, 12, p. 1276-1284 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Neurofibromatosis 1 100%
  • Autism Spectrum Disorder 84%
  • Autistic Disorder 81%
  • Attention Deficit Disorder with Hyperactivity 22%
  • Sociological Factors 9%

• Macrocephaly Is Not a Predictor of Optic Pathway Glioma Development or Treatment in Neurofibromatosis Type 1

  Morris, S. M., Monroe, C. L. & Gutmann, D. H., Dec 1 2016, In: Journal of child neurology. 31, 14, p. 1540-1545 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Optic Nerve Glioma 100%
  • Megalencephaly 93%
  • Neurofibromatosis 1 81%
  • Biomarkers 43%
  • Brain Neoplasms 20%