Lottie Morison
Lottie Morison
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Top Publications
- Bouman, A, Gaasterland, CMW, Sloof-Enthoven, C, Draksler, TZ, Rots, D, Geelen, JM, Morison, LD, Morgan, AT, Wicher, D, Rivero, S, et al. International Clinical Evidence-based Guideline for Kleefstra Syndrome.. Genet Med 102070 2026 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. 2026 view publication
- Morgan, A, Morison, L, Reyk, OV, Forbes, E, Rouxel, F, Faivre, L, Bruinsma, F, Vincent, M, Jacquemont, M-L, Dykzeul, N, et al. CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. 2026 view publication
- Morison, LD, Vogel, AP, Christodoulou, J, Gold, WA, Verden, D, Chung, WK, Braden, R, Bredebusch, J, Kaur, S, Scheffer, IE, et al. Understanding speech and language in KIF1A-associated neurological disorder.. Eur J Hum Genet 34(1) : 78 -89 2026 view publication
- Morison, LD, Braden, R, Amor, DJ, Morgan, AT. Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2.. Am J Med Genet A 197(12) : e64190 2025 view publication
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