Seizures in Fragile X Syndrome: Associations and Longitudinal Analysis of a Large Clinic-Based Cohort
Berry-Kravis, Elizabeth, Filipink, Robyn A, Frye, Richard E, Golla, Sailaja, Morris, Stephanie M, Andrews, Howard, Choo, Tse-Hwei, Kaufmann, Walter E
Published in Frontiers in pediatrics (30.12.2021)
Published in Frontiers in pediatrics (30.12.2021)
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Journal Article
SARS-CoV-2 screening testing in schools for children with intellectual and developmental disabilities
Sherby, Michael R, Walsh, Tyler J, Lai, Albert M, Neidich, Julie A, Balls-Berry, Joyce E, Morris, Stephanie M, Head, Richard, Prener, Christopher G, Newland, Jason G, Gurnett, Christina A
Published in Journal of neurodevelopmental disorders (01.12.2021)
Published in Journal of neurodevelopmental disorders (01.12.2021)
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Journal Article
Neurodevelopmental disorders in children with neurofibromatosis type 1
Vogel, Alecia C, Gutmann, David H, Morris, Stephanie M
Published in Developmental medicine and child neurology (01.11.2017)
Published in Developmental medicine and child neurology (01.11.2017)
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Journal Article
Nonoptic pathway tumors in children with neurofibromatosis type 1
Mahdi, Jasia, Goyal, Manu S, Griffith, Jennifer, Morris, Stephanie M, Gutmann, David H
Published in Neurology (25.08.2020)
Published in Neurology (25.08.2020)
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Journal Article
Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT)
Morris, Stephanie M, Acosta, Maria T, Garg, Shruti, Green, Jonathan, Huson, Susan, Legius, Eric, North, Kathryn N, Payne, Jonathan M, Plasschaert, Ellen, Frazier, Thomas W, Weiss, Lauren A, Zhang, Yi, Gutmann, David H, Constantino, John N
Published in JAMA psychiatry (Chicago, Ill.) (01.12.2016)
Published in JAMA psychiatry (Chicago, Ill.) (01.12.2016)
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Journal Article
Predictors of patient return to a tertiary neurofibromatosis subspecialty clinic
Rosen, Kyra L., Cobb, Olivia, Gavney, Deann, Morris, Stephanie M., Gutmann, David H.
Published in The Journal of pediatrics (01.09.2022)
Published in The Journal of pediatrics (01.09.2022)
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Journal Article
Adaptive functioning in children with neurofibromatosis type 1: relationship to cognition, behavior, and magnetic resonance imaging
Eby, Noah S, Griffith, Jennifer L, Gutmann, David H, Morris, Stephanie M
Published in Developmental medicine and child neurology (01.08.2019)
Published in Developmental medicine and child neurology (01.08.2019)
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Journal Article
Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis
Wegscheid, Michelle L., Anastasaki, Corina, Hartigan, Kelly A., Cobb, Olivia M., Papke, Jason B., Traber, Jennifer N., Morris, Stephanie M., Gutmann, David H.
Published in Cell reports (Cambridge) (06.07.2021)
Published in Cell reports (Cambridge) (06.07.2021)
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Journal Article
A multi-institutional study of brainstem gliomas in children with neurofibromatosis type 1
Mahdi, Jasia, Shah, Amish C, Sato, Aimee, Morris, Stephanie M, McKinstry, Robert C, Listernick, Robert, Packer, Roger J, Fisher, Michael J, Gutmann, David H
Published in Neurology (18.04.2017)
Published in Neurology (18.04.2017)
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Journal Article
Sorting nexin 27 (SNX27) variants associated with seizures, developmental delay, behavioral disturbance, and subcortical brain abnormalities
Parente, Daniel J., Morris, Stephanie M., McKinstry, Robert C., Brandt, Tracy, Gabau, Elisabeth, Ruiz, Anna, Shinawi, Marwan
Published in Clinical genetics (01.03.2020)
Published in Clinical genetics (01.03.2020)
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Journal Article
Stroke Mimics Are Not Benign in Immunocompromised Children
Mahdi, Jasia, Bach, Alicia, Smith, Alyssa E., Tomko, Stuart R., Fields, Melanie E., Griffith, Jennifer L., Morris, Stephanie M., Guerriero, Réjean M., Noetzel, Michael J., Guilliams, Kristin P., Agner, Shannon C.
Published in Stroke (1970) (01.10.2022)
Published in Stroke (1970) (01.10.2022)
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Journal Article
Latent Class Analysis Identifies Distinctive Behavioral Subtypes in Children with Fragile X Syndrome
Kaufmann, Walter E., Raspa, Melissa, Bann, Carla M., Gable, Julia M., Harris, Holly K., Budimirovic, Dejan B., Lozano, Reymundo
Published in Journal of autism and developmental disorders (01.02.2024)
Published in Journal of autism and developmental disorders (01.02.2024)
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Journal Article
Autism in neurofibromatosis type 1: misuse of covariance to dismiss autistic trait burden
Morris, Stephanie M, Acosta, Maria T, Garg, Shruti, Green, Jonathan, Legius, Eric, North, Kathryn, Payne, Jonathan M, Weiss, Lauren A, Constantino, John N, Gutmann, David H
Published in Developmental medicine and child neurology (01.02.2021)
Published in Developmental medicine and child neurology (01.02.2021)
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Journal Article
Familial Lipomas Without Classic Neurofibromatosis-1 Caused by a Missense Germline NF1 Mutation
Ramirez, Erika, Morris, Stephanie M, Turner, Tychele N, Gutmann, David H
Published in Neurology. Genetics (01.06.2021)
Published in Neurology. Genetics (01.06.2021)
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Journal Article
Children with 5'-end NF1 gene mutations are more likely to have glioma
Anastasaki, Corina, Morris, Stephanie M, Gao, Feng, Gutmann, David H
Published in Neurology. Genetics (01.10.2017)
Published in Neurology. Genetics (01.10.2017)
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Journal Article