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For: 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. Eur J Hum Genet 2016;24:302-6. [PMID: 26173965 DOI: 10.1038/ejhg.2015.149] [Cited by in Crossref: 45] [Cited by in F6Publishing: 47] [Article Influence: 5.6] [Reference Citation Analysis]
Number Citing Articles
1 Liu N, Li H, Li M, Gao Y, Yan H. Prenatally diagnosed 16p11.2 copy number variations by SNP Array: A retrospective case series. Clin Chim Acta 2023;538:15-21. [PMID: 36374846 DOI: 10.1016/j.cca.2022.10.016] [Reference Citation Analysis]
2 O'Brien AM, Perrachione TK, Wisman Weil L, Sanchez Araujo Y, Halverson K, Harris A, Ostrovskaya I, Kjelgaard M, Kenneth Wexler, Tager-Flusberg H, Gabrieli JDE, Qi Z. Altered engagement of the speech motor network is associated with reduced phonological working memory in autism. Neuroimage Clin 2022;37:103299. [PMID: 36584426 DOI: 10.1016/j.nicl.2022.103299] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Jiménez-Romero MS, Fernández-Urquiza M, Benítez-Burraco A. Language and Communication Deficits in Chromosome 16p11.2 Deletion Syndrome. J Speech Lang Hear Res 2022;65:4724-40. [PMID: 36410413 DOI: 10.1044/2022_JSLHR-22-00160] [Reference Citation Analysis]
4 St John M, Amor DJ, Morgan AT. Speech and language development and genotype-phenotype correlation in 49 individuals with KAT6A syndrome. Am J Med Genet A 2022;188:3389-400. [PMID: 35892268 DOI: 10.1002/ajmg.a.62899] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Chenausky KV, Maffei M, Tager-flusberg H, Green JR. Review of methods for conducting speech research with minimally verbal individuals with autism spectrum disorder. Augmentative and Alternative Communication 2022. [DOI: 10.1080/07434618.2022.2120071] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 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. Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. Mol Psychiatry 2022. [PMID: 36117209 DOI: 10.1038/s41380-022-01764-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Chenausky KV, Tager-Flusberg H. The importance of deep speech phenotyping for neurodevelopmental and genetic disorders: a conceptual review. J Neurodev Disord 2022;14:36. [PMID: 35690736 DOI: 10.1186/s11689-022-09443-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
8 Kaspi A, Hildebrand MS, Jackson VE, Braden R, van Reyk O, Howell T, Debono S, Lauretta M, Morison L, Coleman M, 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. Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development.. [DOI: 10.1101/2022.05.15.22274630] [Reference Citation Analysis]
9 Mountford HS, Braden R, Newbury DF, Morgan AT. The Genetic and Molecular Basis of Developmental Language Disorder: A Review. Children (Basel) 2022;9:586. [PMID: 35626763 DOI: 10.3390/children9050586] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 O'farrell C, Mccabe P, Purcell A, Heard R. The Adult Perceptual Limen of Syllable Segregation in Typically Developing Paediatric Speech. Front Commun 2022;7:839415. [DOI: 10.3389/fcomm.2022.839415] [Reference Citation Analysis]
11 Chenausky KV, Gagné D, Stipancic KL, Shield A, Green JR. The Relationship Between Single-Word Speech Severity and Intelligibility in Childhood Apraxia of Speech. J Speech Lang Hear Res 2022;65:843-57. [PMID: 35133873 DOI: 10.1044/2021_JSLHR-21-00213] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Jacquemont S, Huguet G, Klein M, Chawner SJRA, Donald KA, van den Bree MBM, Sebat J, Ledbetter DH, Constantino JN, Earl RK, McDonald-McGinn DM, van Amelsvoort T, Swillen A, O'Donnell-Luria AH, Glahn DC, Almasy L, Eichler EE, Scherer SW, Robinson E, Bassett AS, Martin CL, Finucane B, Vorstman JAS, Bearden CE, Gur RE; Genes to Mental Health Network. Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology. Am J Psychiatry 2022;179:189-203. [PMID: 35236119 DOI: 10.1176/appi.ajp.2021.21040432] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 11.0] [Reference Citation Analysis]
13 Kent RD, Kim Y, Chen LM. Oral and Laryngeal Diadochokinesis Across the Life Span: A Scoping Review of Methods, Reference Data, and Clinical Applications. J Speech Lang Hear Res 2021;:1-50. [PMID: 34958599 DOI: 10.1044/2021_JSLHR-21-00396] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
14 Peter B, Davis J, Cotter S, Belter A, Williams E, Stumpf M, Bruce L, Eng L, Kim Y, Finestack L, Stoel-Gammon C, Williams D, Scherer N, VanDam M, Potter N. Toward Preventing Speech and Language Disorders of Known Genetic Origin: First Post-Intervention Results of Babble Boot Camp in Children With Classic Galactosemia. Am J Speech Lang Pathol 2021;30:2616-34. [PMID: 34665663 DOI: 10.1044/2021_AJSLP-21-00098] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
15 Mountford HS, Hill A, Barnett AL, Newbury DF. Genome-Wide Association Study of Motor Coordination. Front Hum Neurosci 2021;15:669902. [PMID: 34177493 DOI: 10.3389/fnhum.2021.669902] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
16 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. Dev Med Child Neurol 2021. [PMID: 34109629 DOI: 10.1111/dmcn.14955] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
17 Chung WK, Roberts TP, Sherr EH, Snyder LG, Spiro JE. 16p11.2 deletion syndrome. Curr Opin Genet Dev 2021;68:49-56. [PMID: 33667823 DOI: 10.1016/j.gde.2021.01.011] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
18 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. J Commun Disord 2020;87:106033. [PMID: 32877838 DOI: 10.1016/j.jcomdis.2020.106033] [Cited by in Crossref: 6] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
19 Kim SH, Green-Snyder L, Lord C, Bishop S, Steinman KJ, Bernier R, Hanson E, Goin-Kochel RP, Chung WK. Language characterization in 16p11.2 deletion and duplication syndromes. Am J Med Genet B Neuropsychiatr Genet 2020;183:380-91. [PMID: 32652891 DOI: 10.1002/ajmg.b.32809] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 3.7] [Reference Citation Analysis]
20 Agarwalla S, Arroyo NS, Long NE, O'Brien WT, Abel T, Bandyopadhyay S. Male-specific alterations in structure of isolation call sequences of mouse pups with 16p11.2 deletion. Genes Brain Behav 2020;19:e12681. [PMID: 32558237 DOI: 10.1111/gbb.12681] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.7] [Reference Citation Analysis]
21 Mei C, Reilly S, Bickerton M, Mensah F, Turner S, Kumaranayagam D, Pennington L, Reddihough D, Morgan AT. Speech in children with cerebral palsy. Dev Med Child Neurol 2020;62:1374-82. [PMID: 32588921 DOI: 10.1111/dmcn.14592] [Cited by in Crossref: 9] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis]
22 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. Int J Lang Commun Disord 2020;55:537-46. [PMID: 32374456 DOI: 10.1111/1460-6984.12536] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
23 Rakhlin N, Landi N, Lee M, Magnuson JS, Naumova OY, Ovchinnikova IV, Grigorenko EL. Cohesion of Cortical Language Networks During Word Processing Is Predicted by a Common Polymorphism in the SETBP1 Gene. New Directions for Child and Adolescent Development 2020;2020:131-155. [DOI: 10.1002/cad.20331] [Reference Citation Analysis]
24 Au PYB, Eaton A, Dyment DA. Genetic mechanisms of neurodevelopmental disorders. Handb Clin Neurol 2020;173:307-26. [PMID: 32958182 DOI: 10.1016/B978-0-444-64150-2.00024-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
25 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 Phoniatr Logop 2019;71:203-15. [PMID: 31330526 DOI: 10.1159/000500554] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
26 Hinkley LBN, Dale CL, Luks TL, Findlay AM, Bukshpun P, Pojman N, Thieu T, Chung WK, Berman J, Roberts TPL, Mukherjee P, Sherr EH, Nagarajan SS. Sensorimotor Cortical Oscillations during Movement Preparation in 16p11.2 Deletion Carriers. J Neurosci 2019;39:7321-31. [PMID: 31270155 DOI: 10.1523/JNEUROSCI.3001-17.2019] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
27 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 2019;4:239694151985633. [DOI: 10.1177/2396941519856333] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 5.3] [Reference Citation Analysis]
28 Peter B, Dougherty MJ, Reed EK, Edelman E, Hanson K. Perceived Gaps in Genetics Training Among Audiologists and Speech-Language Pathologists: Lessons From a National Survey. Am J Speech Lang Pathol 2019;28:408-23. [PMID: 31091132 DOI: 10.1044/2018_AJSLP-18-0069] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
29 Peter B, Dinu V, Liu L, Huentelman M, Naymik M, Lancaster H, Vose C, Schrauwen I. Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects. Behav Genet 2019;49:399-414. [DOI: 10.1007/s10519-019-09957-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.8] [Reference Citation Analysis]
30 Redaelli S, Maitz S, Crosti F, Sala E, Villa N, Spaccini L, Selicorni A, Rigoldi M, Conconi D, Dalprà L, Roversi G, Bentivegna A. Refining the Phenotype of Recurrent Rearrangements of Chromosome 16. Int J Mol Sci 2019;20:E1095. [PMID: 30836598 DOI: 10.3390/ijms20051095] [Cited by in Crossref: 27] [Cited by in F6Publishing: 27] [Article Influence: 6.8] [Reference Citation Analysis]
31 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 2019;142:966-77. [DOI: 10.1093/brain/awz018] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 3.3] [Reference Citation Analysis]
32 St John M, Ponchard C, van Reyk O, Mei C, Pigdon L, Amor DJ, Morgan AT. Speech and language in children with Klinefelter syndrome. J Commun Disord 2019;78:84-96. [PMID: 30822601 DOI: 10.1016/j.jcomdis.2019.02.003] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 3.8] [Reference Citation Analysis]
33 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. Am J Med Genet 2018;177:700-8. [DOI: 10.1002/ajmg.b.32664] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
34 Morgan AT, Webster R. Aetiology of childhood apraxia of speech: A clinical practice update for paediatricians: Childhood apraxia of speech. J Paediatr Child Health 2018;54:1090-5. [DOI: 10.1111/jpc.14150] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 3.0] [Reference Citation Analysis]
35 Kalnak N, Stamouli S, Peyrard-Janvid M, Rabkina I, Becker M, Klingberg T, Kere J, Forssberg H, Tammimies K. Enrichment of rare copy number variation in children with developmental language disorder. Clin Genet 2018;94:313-20. [PMID: 29851021 DOI: 10.1111/cge.13389] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
36 Morgan AT, Murray E, Liégeois FJ. Interventions for childhood apraxia of speech. Cochrane Database Syst Rev 2018;5:CD006278. [PMID: 29845607 DOI: 10.1002/14651858.CD006278.pub3] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 1.2] [Reference Citation Analysis]
37 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, Fisher SE. A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development. Mol Psychiatry 2019;24:1065-78. [PMID: 29463886 DOI: 10.1038/s41380-018-0020-x] [Cited by in Crossref: 77] [Cited by in F6Publishing: 81] [Article Influence: 15.4] [Reference Citation Analysis]
38 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. Eur J Hum Genet 2018;26:676-86. [PMID: 29445122 DOI: 10.1038/s41431-018-0102-x] [Cited by in Crossref: 33] [Cited by in F6Publishing: 34] [Article Influence: 6.6] [Reference Citation Analysis]
39 Demopoulos C, Kothare H, Mizuiri D, Henderson-Sabes J, Fregeau B, Tjernagel J, Houde JF, Sherr EH, Nagarajan SS. Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions. Sci Rep 2018;8:1274. [PMID: 29352208 DOI: 10.1038/s41598-018-19751-x] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 3.8] [Reference Citation Analysis]
40 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. Eur J Hum Genet 2018;26:75-84. [PMID: 29225339 DOI: 10.1038/s41431-017-0035-9] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 3.2] [Reference Citation Analysis]
41 Björelius H, Tükel Ş. Comorbidity of Motor and Sensory Functions in Childhood Motor Speech Disorders. In: Fernandes FDM, editor. Advances in Speech-language Pathology. InTech; 2017. [DOI: 10.5772/intechopen.69710] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
42 Deriziotis P, Fisher SE. Speech and Language: Translating the Genome. Trends in Genetics 2017;33:642-56. [DOI: 10.1016/j.tig.2017.07.002] [Cited by in Crossref: 42] [Cited by in F6Publishing: 45] [Article Influence: 7.0] [Reference Citation Analysis]
43 Peter B, Lancaster H, Vose C, Fares A, Schrauwen I, Huentelman M. Two unrelated children with overlapping 6q25.3 deletions, motor speech disorders, and language delays. Am J Med Genet 2017;173:2659-69. [DOI: 10.1002/ajmg.a.38385] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 3.0] [Reference Citation Analysis]
44 Demopoulos C, Kothare H, Mizuiri D, Henderson-sabes J, Fregeau B, Tjernagel J, Houde J, Sherr EH, Nagarajan SS. Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions.. [DOI: 10.1101/165316] [Reference Citation Analysis]
45 Blackmon K, Thesen T, Green S, Ben-avi E, Wang X, Fuchs B, Kuzniecky R, Devinsky O. Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome. Cerebral Cortex 2018;28:2422-30. [DOI: 10.1093/cercor/bhx143] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 2.8] [Reference Citation Analysis]
46 Langford R, Hurrion E, Dawson PA. Genetics and pathophysiology of mammalian sulfate biology. Journal of Genetics and Genomics 2017;44:7-20. [DOI: 10.1016/j.jgg.2016.08.001] [Cited by in Crossref: 30] [Cited by in F6Publishing: 31] [Article Influence: 5.0] [Reference Citation Analysis]
47 Carrigg B, Parry L, Baker E, Shriberg LD, Ballard KJ. Cognitive, Linguistic, and Motor Abilities in a Multigenerational Family with Childhood Apraxia of Speech. Arch Clin Neuropsychol 2016;31:1006-25. [PMID: 27707700 DOI: 10.1093/arclin/acw077] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.6] [Reference Citation Analysis]
48 Gialluisi A, Visconti A, Willcutt EG, Smith SD, Pennington BF, Falchi M, DeFries JC, Olson RK, Francks C, Fisher SE. Investigating the effects of copy number variants on reading and language performance. J Neurodev Disord 2016;8:17. [PMID: 27186239 DOI: 10.1186/s11689-016-9147-8] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 2.3] [Reference Citation Analysis]