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SETBP1 variants outside the degron disrupt DNA-binding and transcription independent of protein abundance to cause a heterogeneous neurodevelopmental disorder.
2024
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Mountford, HS, Braden, R, Newbury, DF, Morgan, AT.
The Genetic and Molecular Basis of Developmental Language Disorder: A Review.
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2024
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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
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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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