| Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development A Kaspi, MS Hildebrand, VE Jackson, R Braden, O Van Reyk, T Howell, ... Molecular psychiatry 28 (4), 1647-1663, 2023 | 39 | 2023 |
| In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2 LD Morison, E Meffert, M Stampfer, I Steiner-Wilke, B Vollmer, K Schulze, ... Journal of medical genetics 60 (6), 597-607, 2023 | 23 | 2023 |
| Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments LD Morison, RO Braden, DJ Amor, A Brignell, BWM van Bon, AT Morgan European Journal of Human Genetics 30 (7), 800-811, 2022 | 15 | 2022 |
| CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases LD Morison, O Van Reyk, E Forbes, F Rouxel, L Faivre, F Bruinsma, ... European Journal of Human Genetics 31 (7), 793-804, 2023 | 8 | 2023 |
| Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals LD Morison, MGP Kennis, D Rots, A Bouman, J Kummeling, E Palmer, ... Journal of medical genetics 61 (6), 578-585, 2024 | 5 | 2024 |
| Beyond'speech delay': Expanding the phenotype of BRPF1-related disorder LD Morison, O Van Reyk, E Baker, L Ruaud, N Couque, A Verloes, ... European Journal of Medical Genetics 68, 104923, 2024 | 4 | 2024 |
| Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention EJ Forbes, LD Morison, F Lelik, T Howell, S Debono, H Goel, P Burger, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, e32971, 2024 | 2 | 2024 |
| Adaptive functioning in children and young adults with monogenic neurodevelopmental disorders EK Baker, M St John, R Braden, LD Morison, EJ Forbes, F Lelik, ... Developmental Medicine & Child Neurology, 2025 | | 2025 |
| Speech, Language and Non‐verbal Communication in CLN2 and CLN3 Batten Disease LD Morison, IT Whiteman, AP Vogel, L Tilbrook, MC Fahey, R Braden, ... Journal of Inherited Metabolic Disease 48 (1), e12838, 2025 | | 2025 |
| Comparison of Adaptive Functioning Profiles in Children and Young People with Monogenic Neurodevelopmental Disorders EK Baker, MS John, R Braden, L Morison, E Forbes, F Lelik, S Hearps, ... INSAR 2024, 2024 | | 2024 |
| Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic GRIN2A Variants DGY Thompson-Lake, FJ Liegeois, RO Braden, GD Jackson, SJ Turner, ... Neurology: Genetics 10 (2), e200129, 2024 | | 2024 |
| P828: GenIDA, an international participatory database to better characterize comorbidities of genetic forms of intellectual disability: Novel findings of DDX3X syndrome P Burger, V Ruault, D Genevieve, E Forbes, L Morison, A Morgan, ... Genetics in Medicine Open 2, 101739, 2024 | | 2024 |
| Speech and language abilities in individuals with Kleefstra Syndrome L Morison, M Kennis, E Palmer, A Vogel, F Liegeois, A Brignell, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 453-454, 2024 | | 2024 |
| Supplementary Results LD Morison J Med Genet 578, 61, 2024 | | 2024 |
| Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development L Morison, A Kaspi, MS Hildebrand, VE Jackson, R Braden, O van Reyk, ... | | 2022 |
