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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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Gasparini, L, Shepherd, D, Wang, J, Wake, M, Morgan, A.
Identifying early language predictors: A replication of Gasparini et al. (2023) confirming applicability in a general population cohort.
2024
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Koene, S, Ropers, FG, Wieland, J, Rybak, T, Wildschut, F, Berghuis, D, Morgan, A, Trelles, MP, Scheepe, JR, Bökenkamp, R, et al.
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals.
Journal of Medical Genetics
jmg-2023-109537
2023
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