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Dorsal language stream anomalies in an inherited speech disorder.
Liégeois FJ, Turner SJ, Mayes A, Bonthrone AF, Boys A, Smith L, Parry-Fielder B, Mandelstam S, Spencer-Smith M, Bahlo M, Scerri TS, Hildebrand MS, Scheffer IE, Connelly A, Morgan AT. Liégeois FJ, et al. Among authors: connelly a. Brain. 2019 Apr 1;142(4):966-977. doi: 10.1093/brain/awz018. Brain. 2019. PMID: 30796815
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: connelly a. Sci Rep. 2016 Oct 13;6:35192. doi: 10.1038/srep35192. Sci Rep. 2016. PMID: 27734906 Free PMC article.
A Brain Marker for Developmental Speech Disorders.
Morgan AT, Su M, Reilly S, Conti-Ramsden G, Connelly A, Liégeois FJ. Morgan AT, et al. Among authors: connelly a. J Pediatr. 2018 Jul;198:234-239.e1. doi: 10.1016/j.jpeds.2018.02.043. Epub 2018 Apr 25. J Pediatr. 2018. PMID: 29705112
Grey matter volume in developmental speech and language disorder.
Pigdon L, Willmott C, Reilly S, Conti-Ramsden G, Gaser C, Connelly A, Morgan AT. Pigdon L, et al. Among authors: connelly a. Brain Struct Funct. 2019 Dec;224(9):3387-3398. doi: 10.1007/s00429-019-01978-7. Epub 2019 Nov 15. Brain Struct Funct. 2019. PMID: 31732792
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation.
Hildebrand MS, Jackson VE, Scerri TS, Van Reyk O, Coleman M, Braden RO, Turner S, Rigbye KA, Boys A, Barton S, Webster R, Fahey M, Saunders K, Parry-Fielder B, Paxton G, Hayman M, Coman D, Goel H, Baxter A, Ma A, Davis N, Reilly S, Delatycki M, Liégeois FJ, Connelly A, Gecz J, Fisher SE, Amor DJ, Scheffer IE, Bahlo M, Morgan AT. Hildebrand MS, et al. Among authors: connelly a. Neurology. 2020 May 19;94(20):e2148-e2167. doi: 10.1212/WNL.0000000000009441. Epub 2020 Apr 28. Neurology. 2020. PMID: 32345733
295 results