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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
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Verhoef, E, Allegrini, AG, Jansen, PR, Lange, K, Wang, CA, Morgan, AT, Ahluwalia, TS, Symeonides, C, group, EW, Eising, E, et al.
Genome-wide analyses of vocabulary size in infancy and toddlerhood: associations with Attention-Deficit/Hyperactivity Disorder and cognition-related traits.
2024
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Gasparini, L, Shepherd, D, Bavin, EL, Eadie, P, Reilly, S, Morgan, A, Wake, M.
Using machine-learning methods to identify early-life predictors of 11-year language outcome.
2024
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John, MS, Reyk, OV, Koolen, D, de Vries, B, Amor, D, Morgan, A.
Expanding the speech and language phenotype in Koolen-de Vries syndrome: late onset and periodic stuttering a novel feature.
2024
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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.
2024
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