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Morison, LD, Meffert, E, Stampfer, M, Steiner-Wilke, I, Vollmer, B, Schulze, K, Briggs, T, Braden, R, Vogel, A, Thompson-Lake, D, et al.
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2.
Journal of Medical Genetics
60(6)
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597 -607
2023
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Kaspi, A, Hildebrand, MS, Jackson, VE, Braden, R, van Reyk, O, Howell, T, Debono, S, Lauretta, M, Morison, L, Coleman, MJ, et al.
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development.
Molecular Psychiatry
28(4)
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1647 -1663
2023
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Kaspi, A, Hildebrand, MS, Jackson, VE, Braden, R, van Reyk, O, Howell, T, Debono, S, Lauretta, M, Morison, L, Coleman, MJ, et al.
Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development.
Molecular Psychiatry
28(4)
:
1664 -1666
2023
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Mountford, H, Braden, R, Morgan, A, Newbury, D.
Genetic Studies of Language Disorders.
45 -77
2022
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Morison, LD, Braden, RO, Amor, DJ, Brignell, A, van Bon, BWM, Morgan, AT.
Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments.
European Journal of Human Genetics
30(7)
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800 -811
2022
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