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Details

Role Group Leader / Snr Princ Research Fellow
Research area Genomic Medicine

Top Publications

  • Mei, C, Hodgson, M, Reilly, S, Fern, B, Reddihough, D, Mensah, F, Pennington, L, Losche, A, Morgan, A. Oromotor dysfunction in minimally verbal children with cerebral palsy: characteristics and associated factors. Disability and Rehabilitation 44(6) : 973 -981 2022
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  • Levy, MA, McConkey, H, Kerkhof, J, Barat-Houari, M, Bargiacchi, S, Biamino, E, Bralo, MP, Cappuccio, G, Ciolfi, A, Clarke, A, et al. Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders. Human Genetics and Genomics Advances 3(1) : 100075 2022
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  • Braden, RO, Amor, DJ, Fisher, SE, Mei, C, Myers, CT, Mefford, H, Gill, D, Srivastava, S, Swanson, LC, Goel, H, et al. Severe speech impairment is a distinguishing feature of FOXP1‐related disorder. Developmental Medicine & Child Neurology 63(12) : 1417 -1426 2021
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  • Brignell, A, Krahe, M, Downes, M, Kefalianos, E, Reilly, S, Morgan, A. Interventions for children and adolescence who stutter: A systematic review, meta-analysis, and evidence map. Journal of Fluency Disorders 70: 105843 2021
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  • Morgan, A, Braden, R, Wong, MMK, Colin, E, Amor, D, Liégeois, F, Srivastava, S, Vogel, A, Bizaoui, V, Ranguin, K, et al. Speech and language deficits are central to SETBP1 haploinsufficiency disorder. European Journal of Human Genetics 29(8) : 1216 -1225 2021
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