Frederique Liegeois

Affiliations: 
Institute of Child Health University College London, London, United Kingdom 
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"Frederique Liegeois"
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Children

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Merina T Su grad student 2011-2016 UCL
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Thompson-Lake DGY, Liegeois FJ, Braden RO, et al. (2024) Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic Variants. Neurology. Genetics. 10: e200129
Morison LD, Kennis MGP, Rots D, et al. (2024) Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of Medical Genetics
Morgan AT, Scerri TS, Vogel AP, et al. (2023) Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40. Brain : a Journal of Neurology
Bonthrone AF, Green D, Morgan AT, et al. (2023) Attention and motor profiles in children with developmental coordination disorder: A neuropsychological and neuroimaging investigation. Developmental Medicine and Child Neurology
Clayden JD, Hope S, Argyri F, et al. (2023) The impact of multiple language exposure on cognition during childhood: evidence from the UK Millennium Cohort Study. Frontiers in Psychology. 14: 1158333
Morison LD, Meffert E, Stampfer M, et al. (2022) In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting . Journal of Medical Genetics
Thompson-Lake DGY, Scerri TS, Block S, et al. (2021) Atypical development of Broca's area in a large family with inherited stuttering. Brain : a Journal of Neurology
Morgan A, Braden R, Wong MMK, et al. (2021) Speech and language deficits are central to SETBP1 haploinsufficiency disorder. European Journal of Human Genetics : Ejhg
Nahum AS, Liégeois FJ. (2020) Language after childhood hemispherectomy: A systematic review. Neurology
Liégeois F, Elward R. (2020) Functional magnetic resonance imaging. Handbook of Clinical Neurology. 174: 265-275
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