| Year |
Citation |
Score |
| 2024 |
Kenyon KH, Boonstra F, Noffs G, Morgan AT, Vogel AP, Kolbe S, Van Der Walt A. The characteristics and reproducibility of motor speech functional neuroimaging in healthy controls. Frontiers in Human Neuroscience. 18: 1382102. PMID 39171097 DOI: 10.3389/fnhum.2024.1382102 |
0.303 |
|
| 2024 |
Morgan AT, Coleman B, Vogel AP, McNeill A, Robinson PN. Speech and language classification in the human phenotype ontology. European Journal of Human Genetics : Ejhg. PMID 38951652 DOI: 10.1038/s41431-024-01635-6 |
0.396 |
|
| 2024 |
Gasparini L, Shepherd DA, Wang J, Wake M, Morgan AT. Identifying early language predictors: A replication of Gasparini et al. (2023) confirming applicability in a general population cohort. International Journal of Language & Communication Disorders. PMID 38948964 DOI: 10.1111/1460-6984.13086 |
0.362 |
|
| 2024 |
Kenyon KH, Strik M, Noffs G, Morgan A, Kolbe S, Harding IH, Vogel AP, Boonstra FMC, van der Walt A. Volumetric and diffusion MRI abnormalities associated with dysarthria in multiple sclerosis. Brain Communications. 6: fcae177. PMID 38846538 DOI: 10.1093/braincomms/fcae177 |
0.306 |
|
| 2024 |
Brignell A, Williams KJ, Reilly S, Morgan AT. Language growth in verbal autistic children from 5 to 11 years. Autism Research : Official Journal of the International Society For Autism Research. PMID 38828606 DOI: 10.1002/aur.3171 |
0.4 |
|
| 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 |
0.741 |
|
| 2024 |
Magielski J, Ruggiero SM, Xian J, Parthasarathy S, Galer P, Ganesan S, Back A, McKee J, McSalley I, Gonzalez AK, Morgan A, Donaher J, Helbig I. The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individuals. Medrxiv : the Preprint Server For Health Sciences. PMID 38712155 DOI: 10.1101/2024.04.23.24306192 |
0.478 |
|
| 2024 |
Forbes EJ, Morison LD, Lelik F, Howell T, Debono S, Goel H, Burger P, Mandel JL, Geneviève D, Amor DJ, Morgan AT. Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. e32971. PMID 38421120 DOI: 10.1002/ajmg.b.32971 |
0.446 |
|
| 2024 |
Morgan AT, Amor DJ, St John MD, Scheffer IE, Hildebrand MS. Genetic architecture of childhood speech disorder: a review. Molecular Psychiatry. PMID 38366112 DOI: 10.1038/s41380-024-02409-8 |
0.317 |
|
| 2024 |
Morison LD, Van Reyk O, Baker E, Ruaud L, Couque N, Verloes A, Amor DJ, Morgan AT. Beyond 'speech delay': Expanding the phenotype of BRPF1-related disorder. European Journal of Medical Genetics. 68: 104923. PMID 38346666 DOI: 10.1016/j.ejmg.2024.104923 |
0.488 |
|
| 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, ... ... Morgan AT, 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 |
0.732 |
|
| 2023 |
Morison LD, van Reyk O, Forbes E, Rouxel F, Faivre L, Bruinsma F, Vincent M, Jacquemont ML, Dykzeul NL, Geneviève D, Amor DJ, Morgan AT. Correction: CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European Journal of Human Genetics : Ejhg. PMID 38066173 DOI: 10.1038/s41431-023-01515-5 |
0.457 |
|
| 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 |
0.7 |
|
| 2023 |
Lauretta ML, Jarmolowicz A, Amor DJ, Best S, Morgan AT. An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of Speech. Journal of Speech, Language, and Hearing Research : Jslhr. 1-15. PMID 37713535 DOI: 10.1044/2023_JSLHR-22-00714 |
0.389 |
|
| 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 |
0.681 |
|
| 2023 |
John MS, Tripathi T, Morgan AT, Amo DJ. To speak may draw on epigenetic writing and reading: Unravelling the complexity of speech and language outcomes across chromatin-related neurodevelopmental disorders. Neuroscience and Biobehavioral Reviews. 105293. PMID 37353048 DOI: 10.1016/j.neubiorev.2023.105293 |
0.464 |
|
| 2023 |
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, ... ... Morgan AT, et al. Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. Molecular Psychiatry. PMID 36658335 DOI: 10.1038/s41380-022-01879-y |
0.353 |
|
| 2023 |
Morison LD, van Reyk O, Forbes E, Rouxel F, Faivre L, Bruinsma F, Vincent M, Jacquemont ML, Dykzeul NL, Geneviève D, Amor DJ, Morgan AT. CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European Journal of Human Genetics : Ejhg. PMID 36599938 DOI: 10.1038/s41431-022-01275-8 |
0.475 |
|
| 2022 |
St John M, van Reyk O, Koolen DA, de Vries BBA, Amor DJ, Morgan AT. Expanding the speech and language phenotype in Koolen-de Vries syndrome: late onset and periodic stuttering a novel feature. European Journal of Human Genetics : Ejhg. PMID 36529818 DOI: 10.1038/s41431-022-01230-7 |
0.433 |
|
| 2022 |
Gasparini L, Shepherd DA, Bavin EL, Eadie P, Reilly S, Morgan AT, Wake M. Using machine-learning methods to identify early-life predictors of 11-year language outcome. Journal of Child Psychology and Psychiatry, and Allied Disciplines. PMID 36478310 DOI: 10.1111/jcpp.13733 |
0.4 |
|
| 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, ... ... Morgan AT, 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 |
0.755 |
|
| 2022 |
Eising E, Mirza-Schreiber N, de Zeeuw EL, Wang CA, Truong DT, Allegrini AG, Shapland CY, Zhu G, Wigg KG, Gerritse ML, Molz B, Alagöz G, Gialluisi A, Abbondanza F, Rimfeld K, ... ... Morgan AT, et al. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America. 119: e2202764119. PMID 35998220 DOI: 10.1073/pnas.2202764119 |
0.53 |
|
| 2022 |
St John M, Amor DJ, Morgan AT. Speech and language development and genotype-phenotype correlation in 49 individuals with KAT6A syndrome. American Journal of Medical Genetics. Part A. PMID 35892268 DOI: 10.1002/ajmg.a.62899 |
0.414 |
|
| 2022 |
Mountford HS, Braden R, Newbury DF, Morgan AT. The Genetic and Molecular Basis of Developmental Language Disorder: A Review. Children (Basel, Switzerland). 9. PMID 35626763 DOI: 10.3390/children9050586 |
0.309 |
|
| 2022 |
Morison LD, Braden RO, Amor DJ, Brignell A, van Bon BWM, Morgan AT. Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments. European Journal of Human Genetics : Ejhg. PMID 35437318 DOI: 10.1038/s41431-022-01079-w |
0.437 |
|
| 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 |
0.688 |
|
| 2021 |
Holm A, Sanchez K, Crosbie S, Morgan A, Dodd B. Is children's speech development changing? Preliminary evidence from Australian English-speaking 3-year-olds. International Journal of Speech-Language Pathology. 1-10. PMID 34779320 DOI: 10.1080/17549507.2021.1991474 |
0.419 |
|
| 2021 |
Braden RO, Amor DJ, Fisher SE, Mei C, Myers CT, Mefford H, Gill D, Srivastava S, Swanson LC, Goel H, Scheffer IE, Morgan AT. Severe speech impairment is a distinguishing feature of FOXP1-related disorder. Developmental Medicine and Child Neurology. PMID 34109629 DOI: 10.1111/dmcn.14955 |
0.462 |
|
| 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 |
0.776 |
|
| 2021 |
Chenausky KV, Brignell A, Morgan AT, Norton AC, Tager-Flusberg HB, Schlaug G, Guenther FH. A Modeling-Guided Case Study of Disordered Speech in Minimally Verbal Children With Autism Spectrum Disorder. American Journal of Speech-Language Pathology. 1-16. PMID 33852328 DOI: 10.1044/2021_AJSLP-20-00121 |
0.391 |
|
| 2021 |
Brignell A, Gu C, Holm A, Carrigg B, Sheppard DA, Amor DJ, Morgan AT. Correction: Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome. European Journal of Human Genetics : Ejhg. PMID 33723356 DOI: 10.1038/s41431-021-00855-4 |
0.356 |
|
| 2021 |
Braden MSpPath RO, Boyce JO, Stutterd CA, Pope K, Goel H, Leventer RJ, Scheffer IE, Morgan AT. Speech, Language and Oromotor Skills in Patients with Polymicrogyria. Neurology. PMID 33589534 DOI: 10.1212/WNL.0000000000011698 |
0.412 |
|
| 2020 |
Brignell A, Gu C, Holm A, Carrigg B, Sheppard DA, Amor DJ, Morgan AT. Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome. European Journal of Human Genetics : Ejhg. PMID 33293697 DOI: 10.1038/s41431-020-00761-1 |
0.416 |
|
| 2020 |
Chenausky KV, Brignell A, Morgan A, Gagné D, Norton A, Tager-Flusberg H, Schlaug G, Shield A, Green JR. Factor analysis of signs of childhood apraxia of speech. Journal of Communication Disorders. 87: 106033. PMID 32877838 DOI: 10.1016/J.Jcomdis.2020.106033 |
0.389 |
|
| 2020 |
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. 1-9. PMID 32744922 DOI: 10.1080/09638288.2020.1788179 |
0.404 |
|
| 2020 |
Mei C, Reilly S, Bickerton M, Mensah F, Turner S, Kumaranayagam D, Pennington L, Reddihough D, Morgan AT. Speech in children with cerebral palsy. Developmental Medicine and Child Neurology. PMID 32588921 DOI: 10.1111/Dmcn.14592 |
0.331 |
|
| 2020 |
St John M, Columbus G, Brignell A, Carew P, Skeat J, Reilly S, Morgan AT. Predicting speech-sound disorder outcomes in school-age children with hearing loss: The VicCHILD experience. International Journal of Language & Communication Disorders. PMID 32374456 DOI: 10.1111/1460-6984.12536 |
0.431 |
|
| 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, ... ... Morgan AT, et al. Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation. Neurology. PMID 32345733 DOI: 10.1212/WNL.0000000000009441 |
0.741 |
|
| 2020 |
Unicomb R, Kefalianos E, Reilly S, Cook F, Morgan A. Prevalence and features of comorbid stuttering and speech sound disorder at age 4 years. Journal of Communication Disorders. 84: 105976. PMID 32092590 DOI: 10.1016/J.Jcomdis.2020.105976 |
0.477 |
|
| 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 |
0.767 |
|
| 2019 |
Chenausky K, Brignell A, Morgan A, Tager-Flusberg H. Motor speech impairment predicts expressive language in minimally verbal, but not low verbal, individuals with autism spectrum disorder. Autism & Developmental Language Impairments. 4. PMID 35155816 DOI: 10.1177/2396941519856333 |
0.458 |
|
| 2019 |
Sanchez K, Spittle AJ, Boyce JO, Leembruggen L, Mantelos A, Mills S, Mitchell N, Neil E, John MS, Treloar J, Morgan AT. Conversational Language in 3-Year-Old Children Born Very Preterm and at Term. Journal of Speech, Language, and Hearing Research : Jslhr. 1-10. PMID 31855605 DOI: 10.1044/2019_JSLHR-19-00153 |
0.409 |
|
| 2019 |
Bowman-Smart H, Gyngell C, Morgan A, Savulescu J. The moral case for sign language education. Monash Bioethics Review. PMID 31760625 DOI: 10.1007/S40592-019-00101-0 |
0.431 |
|
| 2019 |
Pigdon L, Willmott C, Reilly S, Conti-Ramsden G, Gaser C, Connelly A, Morgan AT. Grey matter volume in developmental speech and language disorder. Brain Structure & Function. PMID 31732792 DOI: 10.1007/S00429-019-01978-7 |
0.482 |
|
| 2019 |
Pigdon L, Willmott C, Reilly S, Conti-Ramsden G, Morgan AT. What predicts nonword repetition performance? Child Neuropsychology : a Journal On Normal and Abnormal Development in Childhood and Adolescence. 1-16. PMID 31581884 DOI: 10.1080/09297049.2019.1674799 |
0.401 |
|
| 2019 |
Sanchez K, Boyce JO, Mei C, St John M, Smith J, Leembruggen L, Mills S, Spittle AJ, Morgan AT. Communication in children born very preterm: a prospective cohort study. Developmental Medicine and Child Neurology. PMID 31538339 DOI: 10.1111/dmcn.14360 |
0.342 |
|
| 2019 |
Turner SJ, Vogel AP, Parry-Fielder B, Campbell R, Scheffer IE, Morgan AT. Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of Speech. Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (Ialp). 1-13. PMID 31330526 DOI: 10.1159/000500554 |
0.381 |
|
| 2019 |
Boyce JO, Sanchez K, Amor DJ, Reilly S, Da Costa A, Kilpatrick N, Morgan AT. Exploring the speech and language of individuals with non-syndromic submucous cleft palate: a preliminary report. International Journal of Language & Communication Disorders. PMID 31045304 DOI: 10.1111/1460-6984.12474 |
0.375 |
|
| 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 |
0.757 |
|
| 2019 |
St John M, Ponchard C, van Reyk O, Mei C, Pigdon L, Amor DJ, Morgan AT. Speech and language in children with Klinefelter syndrome. Journal of Communication Disorders. 78: 84-96. PMID 30822601 DOI: 10.1016/j.jcomdis.2019.02.003 |
0.405 |
|
| 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 |
0.788 |
|
| 2019 |
Braden RO, Leventer RJ, Jansen A, Scheffer IE, Morgan AT. Speech and language in bilateral perisylvian polymicrogyria: a systematic review. Developmental Medicine and Child Neurology. PMID 30680716 DOI: 10.1111/dmcn.14153 |
0.434 |
|
| 2019 |
Chenausky K, Brignell A, Morgan A, Tager-Flusberg H. Motor speech impairment predicts expressive language in minimally verbal, but not low verbal, individuals with autism spectrum disorder Autism & Developmental Language Impairments. 4: 239694151985633. DOI: 10.1177/2396941519856333 |
0.476 |
|
| 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 |
0.689 |
|
| 2018 |
Boyce JO, Kilpatrick N, Teixeira RP, Morgan AT. Say 'ahh'… assessing structural and functional palatal issues in children. Archives of Disease in Childhood. Education and Practice Edition. PMID 30567832 DOI: 10.1136/archdischild-2018-316320 |
0.464 |
|
| 2018 |
Sanchez K, Spittle AJ, Cheong JL, Thompson DK, Doyle LW, Anderson PJ, Morgan AT. Language in 2-year-old children born preterm and term: a cohort study. Archives of Disease in Childhood. PMID 30470685 DOI: 10.1136/archdischild-2018-315843 |
0.397 |
|
| 2018 |
Brignell A, May T, Morgan AT, Williams K. Predictors and growth in receptive vocabulary from 4 to 8 years in children with and without autism spectrum disorder: A population-based study. Autism : the International Journal of Research and Practice. 1362361318801617. PMID 30458626 DOI: 10.1177/1362361318801617 |
0.311 |
|
| 2018 |
Brignell A, Chenausky KV, Song H, Zhu J, Suo C, Morgan AT. Communication interventions for autism spectrum disorder in minimally verbal children. The Cochrane Database of Systematic Reviews. 11: CD012324. PMID 30395694 DOI: 10.1002/14651858.CD012324.pub2 |
0.301 |
|
| 2018 |
Wilson DR, Loxton NJ, O'Shannessy D, Sheeran N, Morgan A. Similarities and differences in revised reinforcement sensitivities across eating disorder subtypes. Appetite. PMID 30359629 DOI: 10.1016/J.Appet.2018.10.023 |
0.311 |
|
| 2018 |
Brignell A, St John M, Boys A, Bruce A, Dinale C, Pigdon L, Hildebrand MS, Amor DJ, Morgan AT. Characterization of speech and language phenotype in children with NRXN1 deletions. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30358070 DOI: 10.1002/ajmg.b.32664 |
0.494 |
|
| 2018 |
Wearne T, Anderson V, Catroppa C, Morgan A, Ponsford J, Tate R, Ownsworth T, Togher L, Fleming J, Douglas J, Docking K, Sigmundsdottir L, Francis H, Honan C, McDonald S. Psychosocial functioning following moderate-to-severe pediatric traumatic brain injury: recommended outcome instruments for research and remediation studies. Neuropsychological Rehabilitation. 1-15. PMID 30296904 DOI: 10.1080/09602011.2018.1531768 |
0.316 |
|
| 2018 |
Morgan AT, Webster R. Aetiology of childhood apraxia of speech: A clinical practice update for paediatricians. Journal of Paediatrics and Child Health. 54: 1090-1095. PMID 30294994 DOI: 10.1111/jpc.14150 |
0.329 |
|
| 2018 |
Mürner-Lavanchy IM, Kelly CE, Reidy N, Doyle LW, Lee KJ, Inder T, Thompson DK, Morgan AT, Anderson PJ. White matter microstructure is associated with language in children born very preterm. Neuroimage. Clinical. 20: 808-822. PMID 30268990 DOI: 10.1016/J.Nicl.2018.09.020 |
0.377 |
|
| 2018 |
Ttofari Eecen K, Eadie P, Morgan AT, Reilly S. Validation of Dodd's Model for Differential Diagnosis of childhood speech sound disorders: a longitudinal community cohort study. Developmental Medicine and Child Neurology. PMID 30151900 DOI: 10.1111/dmcn.13993 |
0.328 |
|
| 2018 |
Boyce JO, Kilpatrick N, Morgan AT. Speech and language characteristics in individuals with nonsyndromic submucous cleft palate-A systematic review. Child: Care, Health and Development. PMID 30136310 DOI: 10.1111/cch.12613 |
0.404 |
|
| 2018 |
Kurth F, Luders E, Pigdon L, Conti-Ramsden G, Reilly S, Morgan AT. Altered gray matter volumes in language-associated regions in children with developmental language disorder and speech sound disorder. Developmental Psychobiology. PMID 30101474 DOI: 10.1002/dev.21762 |
0.429 |
|
| 2018 |
Boyce JO, Kilpatrick N, Reilly S, Da Costa A, Morgan AT. Receptive and expressive language characteristics of school-aged children with non-syndromic cleft lip and/or palate. International Journal of Language & Communication Disorders. PMID 29968398 DOI: 10.1111/1460-6984.12406 |
0.358 |
|
| 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 |
0.745 |
|
| 2018 |
Brignell A, Williams K, Jachno K, Prior M, Reilly S, Morgan AT. Patterns and Predictors of Language Development from 4 to 7 Years in Verbal Children With and Without Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 29705923 DOI: 10.1007/s10803-018-3565-2 |
0.416 |
|
| 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 |
0.777 |
|
| 2018 |
Reilly S, Cini E, Gold L, Goldfeld S, Law J, Levickis P, Mensah F, Morgan A, Nicholson JM, Le HND, Pezic A, Tomblin B, Wake M, Wardrop L. Data resource profile: The Child LAnguage REpository (CLARE). International Journal of Epidemiology. PMID 29562305 DOI: 10.1093/Ije/Dyy034 |
0.411 |
|
| 2018 |
Eising E, Carrion-Castillo A, Vino A, Strand EA, Jakielski KJ, Scerri TS, Hildebrand MS, Webster R, Ma A, Mazoyer B, Francks C, Bahlo M, Scheffer IE, Morgan AT, Shriberg LD, et al. A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development. Molecular Psychiatry. PMID 29463886 DOI: 10.1038/S41380-018-0020-X |
0.392 |
|
| 2018 |
Mei C, Fedorenko E, Amor DJ, Boys A, Hoeflin C, Carew P, Burgess T, Fisher SE, Morgan AT. Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion. European Journal of Human Genetics : Ejhg. PMID 29445122 DOI: 10.1038/S41431-018-0102-X |
0.46 |
|
| 2018 |
Brignell A, Morgan AT, Woolfenden S, Klopper F, May T, Sarkozy V, Williams K. A systematic review and meta-analysis of the prognosis of language outcomes for individuals with autism spectrum disorder Autism & Developmental Language Impairments. 3: 239694151876761. DOI: 10.1177/2396941518767610 |
0.431 |
|
| 2018 |
Dodd B, Ttofari-Eecen K, Brommeyer K, Ng K, Reilly S, Morgan A. Delayed and disordered development of articulation and phonology between four and seven years Child Language Teaching and Therapy. 34: 87-99. DOI: 10.1177/0265659017735958 |
0.384 |
|
| 2017 |
Morgan AT, Haaften LV, van Hulst K, Edley C, Mei C, Tan TY, Amor D, Fisher SE, Koolen DA. Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia. European Journal of Human Genetics : Ejhg. PMID 29225339 DOI: 10.1038/S41431-017-0035-9 |
0.492 |
|
| 2017 |
Luders E, Kurth F, Pigdon L, Conti-Ramsden G, Reilly S, Morgan AT. Atypical Callosal Morphology in Children with Speech Sound Disorder. Neuroscience. PMID 29102664 DOI: 10.1016/j.neuroscience.2017.10.039 |
0.489 |
|
| 2017 |
Honan CA, McDonald S, Tate R, Ownsworth T, Togher L, Fleming J, Anderson V, Morgan A, Catroppa C, Douglas J, Francis H, Wearne T, Sigmundsdottir L, Ponsford J. Outcome instruments in moderate-to-severe adult traumatic brain injury: recommendations for use in psychosocial research. Neuropsychological Rehabilitation. 1-21. PMID 28671050 DOI: 10.1080/09602011.2017.1339616 |
0.328 |
|
| 2017 |
Morgan A, Ttofari Eecen K, Pezic A, Brommeyer K, Mei C, Eadie P, Reilly S, Dodd B. Who to Refer for Speech Therapy at 4 Years of Age Versus Who to "Watch and Wait"? The Journal of Pediatrics. PMID 28343655 DOI: 10.1016/J.Jpeds.2017.02.059 |
0.418 |
|
| 2017 |
Turner SJ, Brown A, Arpone M, Anderson V, Morgan AT, Scheffer IE. Dysarthria and broader motor speech deficits in Dravet syndrome. Neurology. PMID 28148630 DOI: 10.1212/WNL.0000000000003635 |
0.398 |
|
| 2017 |
Luders E, Kurth F, Pigdon L, Conti-Ramsden G, Reilly S, Morgan A. Atypical Callosal Morphology in Developmental Language Disorder European Psychiatry. 41: S628-S628. DOI: 10.1016/j.eurpsy.2017.01.1020 |
0.451 |
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| 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 |
0.736 |
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| 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 |
0.78 |
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| 2016 |
Duenser A, Ward L, Stefani A, Smith D, Freyne J, Morgan A, Dodd B. Feasibility of Technology Enabled Speech Disorder Screening. Studies in Health Technology and Informatics. 227: 21-7. PMID 27440284 |
0.378 |
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| 2016 |
Brignell A, Williams K, Prior M, Donath S, Reilly S, Bavin EL, Eadie P, Morgan AT. Parent-reported patterns of loss and gain in communication in 1- to 2-year-old children are not unique to autism spectrum disorder. Autism : the International Journal of Research and Practice. PMID 27178996 DOI: 10.1177/1362361316644729 |
0.407 |
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| 2015 |
Mei C, Reilly S, Reddihough D, Mensah F, Pennington L, Morgan A. Language outcomes of children with cerebral palsy aged 5 years and 6 years: a population-based study. Developmental Medicine and Child Neurology. PMID 26566585 DOI: 10.1111/Dmcn.12957 |
0.424 |
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| 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 |
0.744 |
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| 2015 |
Fedorenko E, Morgan A, Murray E, Cardinaux A, Mei C, Tager-Flusberg H, Fisher SE, Kanwisher N. A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2. European Journal of Human Genetics : Ejhg. PMID 26173965 DOI: 10.1038/Ejhg.2015.149 |
0.511 |
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| 2015 |
Turner SJ, Morgan AT, Perez ER, Scheffer IE. Erratum to: New Genes for Focal Epilepsies with Speech and Language Disorders. Current Neurology and Neuroscience Reports. 15: 578. PMID 26096512 DOI: 10.1007/s11910-015-0578-5 |
0.405 |
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| 2015 |
Reilly S, McKean C, Morgan A, Wake M. Identifying and managing common childhood language and speech impairments. Bmj (Clinical Research Ed.). 350: h2318. PMID 25976972 DOI: 10.1136/Bmj.H2318 |
0.503 |
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| 2015 |
Turner SJ, Morgan AT, Perez ER, Scheffer IE. New genes for focal epilepsies with speech and language disorders. Current Neurology and Neuroscience Reports. 15: 35. PMID 25921602 DOI: 10.1007/s11910-015-0554-0 |
0.385 |
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| 2015 |
Morgan AT, Mei C, Da Costa A, Fifer J, Lederer D, Benoit V, McMillin MJ, Buckingham KJ, Bamshad MJ, Pope K, White SM. Speech and language in a genotyped cohort of individuals with Kabuki syndrome. American Journal of Medical Genetics. Part A. 167: 1483-92. PMID 25755104 DOI: 10.1002/ajmg.a.37026 |
0.477 |
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| 2015 |
Mayes AK, Reilly S, Morgan AT. Neural correlates of childhood language disorder: a systematic review. Developmental Medicine and Child Neurology. 57: 706-17. PMID 25692930 DOI: 10.1111/dmcn.12714 |
0.476 |
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| 2015 |
Eadie P, Morgan A, Ukoumunne OC, Ttofari Eecen K, Wake M, Reilly S. Speech sound disorder at 4 years: prevalence, comorbidities, and predictors in a community cohort of children. Developmental Medicine and Child Neurology. 57: 578-84. PMID 25403868 DOI: 10.1111/Dmcn.12635 |
0.579 |
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| 2015 |
Morgan AT. Innovative assessment reveals speech production and language comprehension are dissociable skills in severe cerebral palsy. Developmental Medicine and Child Neurology. 57: 215-6. PMID 25349055 DOI: 10.1111/dmcn.12615 |
0.417 |
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| 2014 |
Reilly S, Tomblin B, Law J, McKean C, Mensah FK, Morgan A, Goldfeld S, Nicholson JM, Wake M. Specific language impairment: a convenient label for whom? International Journal of Language & Communication Disorders / Royal College of Speech & Language Therapists. 49: 416-51. PMID 25142091 DOI: 10.1111/1460-6984.12102 |
0.509 |
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| 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 |
0.774 |
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| 2014 |
Mei C, Reilly S, Reddihough D, Mensah F, Morgan A. Motor speech impairment, activity, and participation in children with cerebral palsy. International Journal of Speech-Language Pathology. 16: 427-35. PMID 24910254 DOI: 10.3109/17549507.2014.917439 |
0.476 |
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| 2013 |
Turner SJ, Hildebrand MS, Block S, Damiano J, Fahey M, Reilly S, Bahlo M, Scheffer IE, Morgan AT. Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria. American Journal of Medical Genetics. Part A. 161: 2321-6. PMID 23918746 DOI: 10.1002/ajmg.a.36055 |
0.459 |
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| 2013 |
Liégeois FJ, Mahony K, Connelly A, Pigdon L, Tournier JD, Morgan AT. Pediatric traumatic brain injury: language outcomes and their relationship to the arcuate fasciculus. Brain and Language. 127: 388-98. PMID 23756046 DOI: 10.1016/j.bandl.2013.05.003 |
0.475 |
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| 2013 |
Morgan A. Speech-language pathology insights into genetics and neuroscience: beyond surface behaviour. International Journal of Speech-Language Pathology. 15: 245-54. PMID 23586582 DOI: 10.3109/17549507.2013.777786 |
0.512 |
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| 2013 |
Morgan AT, Masterton R, Pigdon L, Connelly A, Liégeois FJ. Functional magnetic resonance imaging of chronic dysarthric speech after childhood brain injury: reliance on a left-hemisphere compensatory network. Brain : a Journal of Neurology. 136: 646-57. PMID 23378215 DOI: 10.1093/brain/aws355 |
0.451 |
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| 2013 |
Reidy N, Morgan A, Thompson DK, Inder TE, Doyle LW, Anderson PJ. Impaired language abilities and white matter abnormalities in children born very preterm and/or very low birth weight. The Journal of Pediatrics. 162: 719-24. PMID 23158026 DOI: 10.1016/J.Jpeds.2012.10.017 |
0.471 |
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| 2013 |
Heggie AA, Vujcich NJ, Portnof JE, Morgan AT. Tongue reduction for macroglossia in Beckwith Wiedemann syndrome: review and application of new technique. International Journal of Oral and Maxillofacial Surgery. 42: 185-91. PMID 23041202 DOI: 10.1016/j.ijom.2012.09.003 |
0.329 |
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| 2012 |
Slattery J, Morgan A, Douglas J. Early sucking and swallowing problems as predictors of neurodevelopmental outcome in children with neonatal brain injury: a systematic review. Developmental Medicine and Child Neurology. 54: 796-806. PMID 22607330 DOI: 10.1111/J.1469-8749.2012.04318.X |
0.343 |
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| 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 |
0.734 |
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| 2012 |
Shipster C, Morgan A, Dunaway D. Psychosocial, feeding, and drooling outcomes in children with Beckwith Wiedemann syndrome following tongue reduction surgery. The Cleft Palate-Craniofacial Journal. 49: 25-34. PMID 21905916 DOI: 10.1597/10-232 |
0.317 |
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| 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 |
0.769 |
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| 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 |
0.751 |
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| 2011 |
Liégeois F, Morgan AT, Connelly A, Vargha-Khadem F. Endophenotypes of FOXP2: dysfunction within the human articulatory network. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 15: 283-8. PMID 21576028 DOI: 10.1016/J.Ejpn.2011.04.006 |
0.693 |
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| 2011 |
Morgan AT, Liégeois F, Liederkerke C, Vogel AP, Hayward R, Harkness W, Chong K, Vargha-Khadem F. Role of cerebellum in fine speech control in childhood: persistent dysarthria after surgical treatment for posterior fossa tumour. Brain and Language. 117: 69-76. PMID 21334735 DOI: 10.1016/J.Bandl.2011.01.002 |
0.621 |
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| 2011 |
Barre N, Morgan A, Doyle LW, Anderson PJ. Language Abilities in Children Who Were Very Preterm and/or Very Low Birth Weight: A Meta-Analysis The Journal of Pediatrics. 158: 766-774. PMID 21146182 DOI: 10.1016/J.Jpeds.2010.10.032 |
0.456 |
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| 2011 |
Morgan AT, Skeat J. Evaluating service delivery for speech and swallowing problems following paediatric brain injury: an international survey. Journal of Evaluation in Clinical Practice. 17: 275-81. PMID 21029267 DOI: 10.1111/j.1365-2753.2010.01436.x |
0.366 |
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| 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 |
0.72 |
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| 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 |
0.722 |
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| 2010 |
White SM, Morgan A, Da Costa A, Lacombe D, Knight SJ, Houlston R, Whiteford ML, Newbury-Ecob RA, Hurst JA. The phenotype of Floating-Harbor syndrome in 10 patients. American Journal of Medical Genetics. Part A. 152: 821-9. PMID 20358590 DOI: 10.1002/Ajmg.A.33294 |
0.398 |
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| 2010 |
Liégeois F, Morgan AT, Stewart LH, Helen Cross J, Vogel AP, Vargha-Khadem F. Speech and oral motor profile after childhood hemispherectomy. Brain and Language. 114: 126-34. PMID 20096448 DOI: 10.1016/J.Bandl.2009.12.004 |
0.667 |
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| 2010 |
Morgan AT, Mageandran SD, Mei C. Incidence and clinical presentation of dysarthria and dysphagia in the acute setting following paediatric traumatic brain injury. Child: Care, Health and Development. 36: 44-53. PMID 19320903 DOI: 10.1111/j.1365-2214.2009.00961.x |
0.31 |
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| 2010 |
Morgan A. Evidence-Based Diagnosis of Speech, Language and Swallowing following Paediatric Stroke Embedding Evidence-Based Practice in Speech and Language Therapy: International Examples. 157-162. DOI: 10.1002/9780470686584.ch22 |
0.345 |
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| 2008 |
Reilly S, Morgan A. Dysphagia is prevalent in children with severe cerebral palsy Developmental Medicine and Child Neurology. 50: 567. PMID 18754892 DOI: 10.1111/J.1469-8749.2008.03049.X |
0.321 |
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| 2008 |
Morgan AT, Vogel AP. Intervention for childhood apraxia of speech. The Cochrane Database of Systematic Reviews. CD006278. PMID 18646142 DOI: 10.1002/14651858.CD006278.pub2 |
0.436 |
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| 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 |
0.664 |
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| 2006 |
Shipster C, Oliver B, Morgan A. Speech and oral motor skills in children with Beckwith Wiedemann Syndrome: Pre- and post-tongue reduction surgery Advances in Speech-Language Pathology. 8: 45-55. DOI: 10.1080/14417040500484401 |
0.437 |
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| 2006 |
Morgan A, Vogel A. Intervention for developmental apraxia of speech Cochrane Database of Systematic Reviews. DOI: 10.1002/14651858.Cd006278 |
0.397 |
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| 2004 |
Morgan A, Ward E, Murdoch B. Clinical characteristics of acute dysphagia in pediatric patients following traumatic brain injury. Journal of Head Trauma Rehabilitation. 19: 226-240. PMID 15247845 DOI: 10.1097/00001199-200405000-00004 |
0.336 |
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| 2004 |
Morgan A, Ward E, Murdoch B. Clinical progression and outcome of dysphagia following paediatric traumatic brain injury: a prospective study Brain Injury. 18: 359-376. PMID 14742150 DOI: 10.1080/02699050310001617424 |
0.366 |
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| 2003 |
Cornwell PL, Murdoch BE, Ward EC, Morgan A. Dysarthria and dysphagia as long-term sequelae in a child treated for posterior fossa tumour. Pediatric Rehabilitation. 6: 67-75. PMID 14534043 DOI: 10.1080/1363849031000139289 |
0.399 |
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| 2003 |
Cornwell PL, Murdoch BE, Ward EC, Morgan A. Dysarthria and dysphagia following treatment for a fourth ventricle choroid plexus papilloma. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 10: 506-12. PMID 12852899 DOI: 10.1016/S0967-5868(03)00077-8 |
0.378 |
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| 2003 |
Morgan A, Ward E, Murdoch B, Kennedy B, Murison R. Incidence, characteristics, and predictive factors for Dysphagia after pediatric traumatic brain injury. Journal of Head Trauma Rehabilitation. 18: 239-251. PMID 12802166 DOI: 10.1097/00001199-200305000-00002 |
0.33 |
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| 2002 |
Morgan A, Ward E, Murdoch B, Bilbie K. Acute characteristics of pediatric Dysphagia subsequent to traumatic brain injury: videofluoroscopic assessment. Journal of Head Trauma Rehabilitation. 17: 220-241. PMID 12086576 DOI: 10.1097/00001199-200206000-00004 |
0.358 |
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| 2002 |
Morgan A, Hickson L, Worrall L. The impact of hearing impairment on quality of life of older people Asia Pacific Journal of Speech, Language, and Hearing. 7: 39-53. DOI: 10.1179/136132802805576562 |
0.319 |
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