Latent Class Analysis Identifies Distinctive Behavioral Subtypes in Children with Fragile X Syndrome
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Published:2022-11-28
Issue:
Volume:
Page:
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ISSN:0162-3257
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Container-title:Journal of Autism and Developmental Disorders
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language:en
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Short-container-title:J Autism Dev Disord
Author:
Kaufmann Walter E.ORCID, Raspa Melissa, Bann Carla M., Gable Julia M., Harris Holly K., Budimirovic Dejan B., Lozano Reymundo, Berry-Kravis Elizabeth, Velinov Milen, Talboy Amy L, Sherman Stephanie L, Kaufmann Walter E, Schuster Marcy, Tartaglia Nicole, Filipink Robyn A, Budimirovic Dejan B, Barbouth Deborah, Lightbody Amy, Reiss Allan, Delahunty Carol M, Hagerman Randi J, Hessl David, Erickson Craig A, Feldman Gary, Picker Jonathan D, Lachiewicz Ave M, Harris Holly K, Esler Amy, Frye Richard E, Evans Patricia A, Morris Mary Ann, Haas-Givler Barbara A, Gropman Andrea L, Uy Ryan S, Buchanan Carrie, Frazier Jean A, Morris Stephanie M,
Funder
National Center on Birth Defects and Developmental Disabilities
Publisher
Springer Science and Business Media LLC
Subject
Developmental and Educational Psychology
Reference36 articles.
1. American Psychiatric Association. (2023). Diagnostic and Statistical Manual of Mental Disorders. American Psychiatric Association Publishing. https://doi.org/10.1176/appi.books.9780890425787 2. Berry-Kravis, E. M., Lindemann, L., Jønch, A. E., Apostol, G., Bear, M. F., Carpenter, R. L., Crawley, J. N., Curie, A., Des Portes, V., Hossain, F., Gasparini, F., Gomez-Mancilla, B., Hessl, D., Loth, E., Scharf, S. H., Wang, P. P., Von Raison, F., Hagerman, R., Spooren, W., & Jacquemont, S. (2018). Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome. Nature Reviews Drug Discovery, 17(4), 280–299. https://doi.org/10.1038/nrd.2017.221 3. Berry-Kravis, E., Filipink, R. A., Frye, R. E., Golla, S., Morris, S. M., Andrews, H., Choo, T. H., Kaufmann, W. E., & FORWARD Consortium. (2021). Seizures in fragile X syndrome: Associations and longitudinal analysis of a large clinic-based cohort. Frontiers in pediatrics, 9, 736255. https://doi.org/10.3389/fped.2021.736255 4. Boyle, L., & Kaufmann, W. E. (2010). The behavioral phenotype of FMR1 mutations. American journal of medical genetics Part C, Seminars in medical genetics, 154C(4), 469–476. https://doi.org/10.1002/ajmg.c.30277 5. Bruno, J. L., Romano, D., Mazaika, P., Lightbody, A. A., Hazlett, H. C., Piven, J., & Reiss, A. L. (2017). Longitudinal identification of clinically distinct neurophenotypes in young children with fragile X syndrome. Proceedings of the National Academy of Sciences of the United States of America, 114(40), 10767–10772. https://doi.org/10.1073/pnas.1620994114
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