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Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development.
Kaspi A, Hildebrand MS, Jackson VE, Braden R, van Reyk O, Howell T, Debono S, Lauretta M, Morison L, Coleman MJ, Webster R, Coman D, Goel H, Wallis M, Dabscheck G, Downie L, Baker EK, Parry-Fielder B, Ballard K, Harrold E, Ziegenfusz S, Bennett MF, Robertson E, Wang L, Boys A, Fisher SE, Amor DJ, Scheffer IE, Bahlo M, Morgan AT. Kaspi A, et al. Among authors: morgan at. Mol Psychiatry. 2023 Apr;28(4):1647-1663. doi: 10.1038/s41380-022-01764-8. Mol Psychiatry. 2023. PMID: 36117209 Free PMC article.
GRIN2A: an aptly named gene for speech dysfunction.
Turner SJ, Mayes AK, Verhoeven A, Mandelstam SA, Morgan AT, Scheffer IE. Turner SJ, et al. Among authors: morgan at. Neurology. 2015 Feb 10;84(6):586-93. doi: 10.1212/WNL.0000000000001228. Epub 2015 Jan 16. Neurology. 2015. PMID: 25596506 Free PMC article.
Early neuroimaging markers of FOXP2 intragenic deletion.
Liégeois FJ, Hildebrand MS, Bonthrone A, Turner SJ, Scheffer IE, Bahlo M, Connelly A, Morgan AT. Liégeois FJ, et al. Among authors: morgan at. Sci Rep. 2016 Oct 13;6:35192. doi: 10.1038/srep35192. Sci Rep. 2016. PMID: 27734906 Free PMC article.
Dysarthria and broader motor speech deficits in Dravet syndrome.
Turner SJ, Brown A, Arpone M, Anderson V, Morgan AT, Scheffer IE. Turner SJ, et al. Among authors: morgan at. Neurology. 2017 Feb 21;88(8):743-749. doi: 10.1212/WNL.0000000000003635. Epub 2017 Feb 1. Neurology. 2017. PMID: 28148630 Free PMC article.
184 results