Angela Morgan
Affiliations: | University College London, London, United Kingdom |
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| Forbes EJ, Morison LD, Lelik F, et al. (2024) Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. e32971 |
| Morison LD, Kennis MGP, Rots D, et al. (2024) Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of Medical Genetics |
| Morison LD, van Reyk O, Forbes E, et al. (2023) Correction: CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European Journal of Human Genetics : Ejhg |
| Morgan AT, Scerri TS, Vogel AP, et al. (2023) Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40. Brain : a Journal of Neurology |
| Lauretta ML, Jarmolowicz A, Amor DJ, et al. (2023) An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of Speech. Journal of Speech, Language, and Hearing Research : Jslhr. 1-15 |
| Bonthrone AF, Green D, Morgan AT, et al. (2023) Attention and motor profiles in children with developmental coordination disorder: A neuropsychological and neuroimaging investigation. Developmental Medicine and Child Neurology |
| John MS, Tripathi T, Morgan AT, et al. (2023) To speak may draw on epigenetic writing and reading: Unravelling the complexity of speech and language outcomes across chromatin-related neurodevelopmental disorders. Neuroscience and Biobehavioral Reviews. 105293 |
| Kaspi A, Hildebrand MS, Jackson VE, et al. (2023) Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. Molecular Psychiatry |
| Morison LD, van Reyk O, Forbes E, et al. (2023) CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European Journal of Human Genetics : Ejhg |
| St John M, van Reyk O, Koolen DA, et al. (2022) Expanding the speech and language phenotype in Koolen-de Vries syndrome: late onset and periodic stuttering a novel feature. European Journal of Human Genetics : Ejhg |