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Page 1
Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic GRIN2A Variants.
Thompson-Lake DGY, Liegeois FJ, Braden RO, Jackson GD, Turner SJ, Morison L, Hildebrand M, Scheffer IE, Morgan AT. Thompson-Lake DGY, et al. Among authors: liegeois fj. Neurol Genet. 2024 Feb 26;10(2):e200129. doi: 10.1212/NXG.0000000000200129. eCollection 2024 Apr. Neurol Genet. 2024. PMID: 38715655 Free PMC article.
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals.
Morison LD, Kennis MGP, Rots D, Bouman A, Kummeling J, Palmer E, Vogel AP, Liegeois F, Brignell A, Srivastava S, Frazier Z, Milnes D, Goel H, Amor DJ, Scheffer IE, Kleefstra T, Morgan AT. Morison LD, et al. Among authors: liegeois f. J Med Genet. 2024 May 21;61(6):578-585. doi: 10.1136/jmg-2023-109702. J Med Genet. 2024. PMID: 38290825 Free PMC article.
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40.
Morgan AT, Scerri TS, Vogel AP, Reid CA, Quach M, Jackson VE, McKenzie C, Burrows EL, Bennett MF, Turner SJ, Reilly S, Horton SE, Block S, Kefalianos E, Frigerio-Domingues C, Sainz E, Rigbye KA, Featherby TJ, Richards KL, Kueh A, Herold MJ, Corbett MA, Gecz J, Helbig I, Thompson-Lake DGY, Liégeois FJ, Morell RJ, Hung A, Drayna D, Scheffer IE, Wright DK, Bahlo M, Hildebrand MS. Morgan AT, et al. Among authors: liegeois fj. Brain. 2023 Dec 1;146(12):5086-5097. doi: 10.1093/brain/awad314. Brain. 2023. PMID: 37977818 Free PMC article.
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2.
Morison LD, Meffert E, Stampfer M, Steiner-Wilke I, Vollmer B, Schulze K, Briggs T, Braden R, Vogel A, Thompson-Lake D, Patel C, Blair E, Goel H, Turner S, Moog U, Riess A, Liegeois F, Koolen DA, Amor DJ, Kleefstra T, Fisher SE, Zweier C, Morgan AT. Morison LD, et al. Among authors: liegeois f. J Med Genet. 2023 Jun;60(6):597-607. doi: 10.1136/jmg-2022-108734. Epub 2022 Nov 3. J Med Genet. 2023. PMID: 36328423 Free PMC article.
Atypical development of Broca's area in a large family with inherited stuttering.
Thompson-Lake DGY, Scerri TS, Block S, Turner SJ, Reilly S, Kefalianos E, Bonthrone AF, Helbig I, Bahlo M, Scheffer IE, Hildebrand MS, Liégeois FJ, Morgan AT. Thompson-Lake DGY, et al. Among authors: liegeois fj. Brain. 2022 Apr 29;145(3):1177-1188. doi: 10.1093/brain/awab364. Brain. 2022. PMID: 35296891 Free PMC article.
Detection and genetic diversity of Mopeia virus in Mastomys natalensis from different habitats in the Limpopo National Park, Mozambique.
Mapaco L, Crespin L, Rodrigues D, Gouy de Bellocq J, Bryja J, Bourgarel M, Missé D, Caron A, Fafetine J, Cappelle J, Liégeois F. Mapaco L, et al. Among authors: liegeois f. Infect Genet Evol. 2022 Mar;98:105204. doi: 10.1016/j.meegid.2022.105204. Epub 2022 Jan 5. Infect Genet Evol. 2022. PMID: 34999003 Free article.
154 results