| Year |
Citation |
Score |
| 2024 |
Thompson-Lake DGY, Liegeois FJ, Braden RO, Jackson GD, Turner SJ, Morison L, Hildebrand M, Scheffer IE, Morgan AT. Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic Variants. Neurology. Genetics. 10: e200129. PMID 38715655 DOI: 10.1212/NXG.0000000000200129 |
0.637 |
|
| 2024 |
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, et al. Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of Medical Genetics. PMID 38290825 DOI: 10.1136/jmg-2023-109702 |
0.618 |
|
| 2023 |
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, et al. Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40. Brain : a Journal of Neurology. PMID 37977818 DOI: 10.1093/brain/awad314 |
0.567 |
|
| 2023 |
Bonthrone AF, Green D, Morgan AT, Mankad K, Clark CA, Liégeois FJ. Attention and motor profiles in children with developmental coordination disorder: A neuropsychological and neuroimaging investigation. Developmental Medicine and Child Neurology. PMID 37667426 DOI: 10.1111/dmcn.15745 |
0.538 |
|
| 2023 |
Clayden JD, Hope S, Argyri F, Goksan S, Stefani A, Wei L, Liegeois FJ. The impact of multiple language exposure on cognition during childhood: evidence from the UK Millennium Cohort Study. Frontiers in Psychology. 14: 1158333. PMID 37275707 DOI: 10.3389/fpsyg.2023.1158333 |
0.325 |
|
| 2022 |
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, ... ... Liegeois F, et al. In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting . Journal of Medical Genetics. PMID 36328423 DOI: 10.1136/jmg-2022-108734 |
0.665 |
|
| 2021 |
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. Atypical development of Broca's area in a large family with inherited stuttering. Brain : a Journal of Neurology. PMID 35296891 DOI: 10.1093/brain/awab364 |
0.554 |
|
| 2021 |
Morgan A, Braden R, Wong MMK, Colin E, Amor D, Liégeois F, Srivastava S, Vogel A, Bizaoui V, Ranguin K, Fisher SE, van Bon BW. Speech and language deficits are central to SETBP1 haploinsufficiency disorder. European Journal of Human Genetics : Ejhg. PMID 33907317 DOI: 10.1038/s41431-021-00894-x |
0.681 |
|
| 2020 |
Nahum AS, Liégeois FJ. Language after childhood hemispherectomy: A systematic review. Neurology. PMID 33087498 DOI: 10.1212/WNL.0000000000011073 |
0.361 |
|
| 2020 |
Liégeois F, Elward R. Functional magnetic resonance imaging. Handbook of Clinical Neurology. 174: 265-275. PMID 32977883 DOI: 10.1016/B978-0-444-64148-9.00019-3 |
0.722 |
|
| 2020 |
Goksan S, Argyri F, Clayden JD, Liegeois F, Wei L. Early childhood bilingualism: effects on brain structure and function. F1000research. 9: 370. PMID 32528666 DOI: 10.12688/F1000Research.23216.1 |
0.552 |
|
| 2020 |
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, et al. Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation. Neurology. PMID 32345733 DOI: 10.1212/WNL.0000000000009441 |
0.625 |
|
| 2020 |
Pigdon L, Willmott C, Reilly S, Conti-Ramsden G, Liegeois F, Connelly A, Morgan AT. The neural basis of nonword repetition in children with developmental speech or language disorder: An fMRI study. Neuropsychologia. 107312. PMID 31917203 DOI: 10.1016/J.Neuropsychologia.2019.107312 |
0.719 |
|
| 2019 |
Northam GB, Morgan AT, Fitzsimmons S, Baldeweg T, Liégeois FJ. Corticobulbar Tract Injury, Oromotor Impairment and Language Plasticity in Adolescents Born Preterm. Frontiers in Human Neuroscience. 13: 45. PMID 30837853 DOI: 10.3389/fnhum.2019.00045 |
0.665 |
|
| 2019 |
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. Dorsal language stream anomalies in an inherited speech disorder. Brain : a Journal of Neurology. PMID 30796815 DOI: 10.1093/brain/awz018 |
0.706 |
|
| 2018 |
Liégeois FJ, Mei C, Pigdon L, Lee KJ, Stojanowski B, Mackay M, Morgan AT. Speech and Language Impairments After Childhood Arterial Ischemic Stroke: Does Hemisphere Matter? Pediatric Neurology. PMID 30594525 DOI: 10.1016/j.pediatrneurol.2018.11.006 |
0.553 |
|
| 2018 |
Argyropoulos GPD, Watkins KE, Belton-Pagnamenta E, Liégeois F, Saleem KS, Mishkin M, Vargha-Khadem F. Neocerebellar Crus I Abnormalities Associated with a Speech and Language Disorder Due to a Mutation in FOXP2. Cerebellum (London, England). PMID 30460543 DOI: 10.1007/S12311-018-0989-3 |
0.726 |
|
| 2018 |
Morgan AT, Murray E, Liégeois FJ. Interventions for childhood apraxia of speech. The Cochrane Database of Systematic Reviews. 5: CD006278. PMID 29845607 DOI: 10.1002/14651858.CD006278.pub3 |
0.626 |
|
| 2018 |
Morgan AT, Su M, Reilly S, Conti-Ramsden G, Connelly A, Liégeois FJ. A Brain Marker for Developmental Speech Disorders. The Journal of Pediatrics. PMID 29705112 DOI: 10.1016/j.jpeds.2018.02.043 |
0.769 |
|
| 2016 |
Liégeois FJ, Hildebrand MS, Bonthrone A, Turner SJ, Scheffer IE, Bahlo M, Connelly A, Morgan AT. Early neuroimaging markers of FOXP2 intragenic deletion. Scientific Reports. 6: 35192. PMID 27734906 DOI: 10.1038/srep35192 |
0.639 |
|
| 2016 |
Morgan A, Bonthrone A, Liégeois FJ. Brain basis of childhood speech and language disorders: are we closer to clinically meaningful MRI markers? Current Opinion in Pediatrics. PMID 27662370 DOI: 10.1097/Mop.0000000000000420 |
0.687 |
|
| 2015 |
Liégeois FJ, Butler J, Morgan AT, Clayden JD, Clark CA. Anatomy and lateralization of the human corticobulbar tracts: an fMRI-guided tractography study. Brain Structure & Function. PMID 26411871 DOI: 10.1007/S00429-015-1104-X |
0.735 |
|
| 2014 |
Liégeois F, Mayes A, Morgan A. Neural Correlates of Developmental Speech and Language Disorders: Evidence from Neuroimaging. Current Developmental Disorders Reports. 1: 215-227. PMID 25057455 DOI: 10.1007/S40474-014-0019-1 |
0.702 |
|
| 2013 |
Pahs G, Rankin P, Helen Cross J, Croft L, Northam GB, Liegeois F, Greenway S, Harrison S, Vargha-Khadem F, Baldeweg T. Asymmetry of planum temporale constrains interhemispheric language plasticity in children with focal epilepsy. Brain : a Journal of Neurology. 136: 3163-75. PMID 24022474 DOI: 10.1093/Brain/Awt225 |
0.692 |
|
| 2012 |
Northam GB, Liégeois F, Tournier JD, Croft LJ, Johns PN, Chong WK, Wyatt JS, Baldeweg T. Interhemispheric temporal lobe connectivity predicts language impairment in adolescents born preterm. Brain : a Journal of Neurology. 135: 3781-98. PMID 23144265 DOI: 10.1093/Brain/Aws276 |
0.546 |
|
| 2012 |
Northam GB, Liégeois F, Chong WK, Baker K, Tournier JD, Wyatt JS, Baldeweg T, Morgan A. Speech and oromotor outcome in adolescents born preterm: relationship to motor tract integrity. The Journal of Pediatrics. 160: 402-408.e1. PMID 22000302 DOI: 10.1016/J.Jpeds.2011.08.055 |
0.623 |
|
| 2012 |
Liégeois FJ, Morgan AT. Neural bases of childhood speech disorders: lateralization and plasticity for speech functions during development. Neuroscience and Biobehavioral Reviews. 36: 439-58. PMID 21827785 DOI: 10.1016/j.neubiorev.2011.07.011 |
0.667 |
|
| 2012 |
Morgan A, Liégeois F, Vargha-Khadem F. Motor speech profile in relation to site of brain pathology: A developmental perspective Speech Motor Control: New Developments in Basic and Applied Research. DOI: 10.1093/acprof:oso/9780199235797.003.0006 |
0.676 |
|
| 2011 |
Northam GB, Liégeois F, Chong WK, Wyatt JS, Baldeweg T. Total brain white matter is a major determinant of IQ in adolescents born preterm. Annals of Neurology. 69: 702-11. PMID 21391229 DOI: 10.1002/Ana.22263 |
0.332 |
|
| 2011 |
Liegeois F, Morgan A, Connolly A, Vargha-Khadem F. 2PS1.1 Dissecting the neural networks involved in articulation through structural and functional brain imaging: FOXP2 and the KE family European Journal of Paediatric Neurology. 15: S3. DOI: 10.1016/S1090-3798(11)70013-7 |
0.66 |
|
| 2010 |
Morgan AT, Liégeois F. Re-thinking diagnostic classification of the dysarthrias: a developmental perspective. Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (Ialp). 62: 120-6. PMID 20424467 DOI: 10.1159/000287210 |
0.642 |
|
| 2007 |
Morgan AT, Liegeois F, Occomore L. Electropalatography treatment for articulation impairment in children with dysarthria post-traumatic brain injury Brain Injury. 21: 1183-1193. PMID 17896211 DOI: 10.1080/02699050701649573 |
0.547 |
|
| 2003 |
Liégeois F, Baldeweg T, Connelly A, Gadian DG, Mishkin M, Vargha-Khadem F. Language fMRI abnormalities associated with FOXP2 gene mutation. Nature Neuroscience. 6: 1230-7. PMID 14555953 DOI: 10.1038/Nn1138 |
0.7 |
|
| 2002 |
Liégeois F, de Schonen S. Picture naming in young children: a developmental study on interhemispheric collaboration. Brain and Cognition. 49: 123-37. PMID 12027398 DOI: 10.1006/Brcg.2001.1491 |
0.323 |
|
| 2001 |
Baldeweg T, Liegeois F, Salmond C, Vargha-Khadem F, Holloway V, Gadian D, Connelly A. A direct test for lateralisation of language activation using fMRI: comparison with the Wada test Neuroimage. 13: 500. DOI: 10.1016/S1053-8119(01)91843-9 |
0.743 |
|
| 2000 |
Holloway V, Liegeois F, Baldeweg T, Gadian DG, Vargha-Khadem F, Connelly A. Language lateralisation using fMRI in children undergoing Wada testing Neuroimage. 11: S290. DOI: 10.1016/S1053-8119(00)91222-9 |
0.671 |
|
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