Lottie Morison
Lottie Morison
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Top Publications
- Morison, LD, Van Reyk, O, Baker, E, Ruaud, L, Couque, N, Verloes, A, Amor, DJ, Morgan, AT. Beyond 'speech delay': Expanding the phenotype of BRPF1-related disorder.. Eur J Med Genet 68: 104923 2024 view publication
- Forbes, EJ, Morison, LD, Lelik, F, Howell, T, Debono, S, Goel, H, Burger, P, Mandel, J-L, Geneviève, D, Amor, DJ, et al. Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention.. Am J Med Genet B Neuropsychiatr Genet e32971 2024 view publication
- Morison, LD, Kennis, MGP, Rots, D, Bouman, A, Kummeling, J, Palmer, E, Vogel, AP, Liegeois, F, Brignell, A, Srivastava, S, et al. Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals.. J Med Genet 2024 view publication
- Kaspi, A, Hildebrand, MS, Jackson, VE, Braden, R, van Reyk, O, Howell, T, Debono, S, Lauretta, M, Morison, L, Coleman, M, et al. Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. 2024 view publication
- Morison, L, Meffert, E, Stampfer, M, Steiner-Wilke, I, Vollmer, B, Schulze, K, Briggs, T, Braden, R, Vogel, AP, Thompson-Lake, D, et al. Indepth characterization of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2. 2024 view publication
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