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For: Deriziotis P, Fisher SE. Neurogenomics of speech and language disorders: the road ahead. Genome Biol 2013;14:204. [PMID: 23597266 DOI: 10.1186/gb-2013-14-4-204] [Cited by in Crossref: 24] [Cited by in F6Publishing: 21] [Article Influence: 2.7] [Reference Citation Analysis]
Number Citing Articles
1 Pak LA, Savostyanov KV, Kuzenkova LM, Pushkov AA, Zhanin IS, Uvakina EV. Molecular genetic diagnosis of speech disorders in children. Nevrol ž im L O Badalâna 2022;3:7-13. [DOI: 10.46563/2686-8997-2022-3-1-7-13] [Reference Citation Analysis]
2 Josserand M, Allassonnière-Tang M, Pellegrino F, Dediu D. Interindividual Variation Refuses to Go Away: A Bayesian Computer Model of Language Change in Communicative Networks. Front Psychol 2021;12:626118. [PMID: 34234707 DOI: 10.3389/fpsyg.2021.626118] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Benito-Aragón C, Gonzalez-Sarmiento R, Liddell T, Diez I, d'Oleire Uquillas F, Ortiz-Terán L, Bueichekú E, Chow HM, Chang SE, Sepulcre J. Neurofilament-lysosomal genetic intersections in the cortical network of stuttering. Prog Neurobiol 2020;184:101718. [PMID: 31669185 DOI: 10.1016/j.pneurobio.2019.101718] [Cited by in Crossref: 18] [Cited by in F6Publishing: 14] [Article Influence: 6.0] [Reference Citation Analysis]
4 Paquette S, Li HC, Corrow SL, Buss SS, Barton JJS, Schlaug G. Developmental Perceptual Impairments: Cases When Tone-Deafness and Prosopagnosia Co-occur. Front Hum Neurosci 2018;12:438. [PMID: 30425629 DOI: 10.3389/fnhum.2018.00438] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
5 Wanke KA, Devanna P, Vernes SC. Understanding Neurodevelopmental Disorders: The Promise of Regulatory Variation in the 3'UTRome. Biol Psychiatry 2018;83:548-57. [PMID: 29289333 DOI: 10.1016/j.biopsych.2017.11.006] [Cited by in Crossref: 29] [Cited by in F6Publishing: 30] [Article Influence: 5.8] [Reference Citation Analysis]
6 Gialluisi A, Guadalupe T, Francks C, Fisher SE. Neuroimaging genetic analyses of novel candidate genes associated with reading and language. Brain and Language 2017;172:9-15. [DOI: 10.1016/j.bandl.2016.07.002] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
7 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: 8.4] [Reference Citation Analysis]
8 Peretz I, Vuvan DT. Prevalence of congenital amusia. Eur J Hum Genet 2017;25:625-30. [PMID: 28224991 DOI: 10.1038/ejhg.2017.15] [Cited by in Crossref: 70] [Cited by in F6Publishing: 74] [Article Influence: 14.0] [Reference Citation Analysis]
9 Negwer M, Schubert D. Talking Convergence: Growing Evidence Links FOXP2 and Retinoic Acid in Shaping Speech-Related Motor Circuitry. Front Neurosci 2017;11. [DOI: 10.3389/fnins.2017.00019] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
10 Tager-Flusberg H. Risk Factors Associated With Language in Autism Spectrum Disorder: Clues to Underlying Mechanisms. J Speech Lang Hear Res 2016;59:143-54. [PMID: 26502110 DOI: 10.1044/2015_JSLHR-L-15-0146] [Cited by in Crossref: 57] [Cited by in F6Publishing: 63] [Article Influence: 9.5] [Reference Citation Analysis]
11 Peretz I. Neurobiology of Congenital Amusia. Trends in Cognitive Sciences 2016;20:857-67. [DOI: 10.1016/j.tics.2016.09.002] [Cited by in Crossref: 81] [Cited by in F6Publishing: 82] [Article Influence: 13.5] [Reference Citation Analysis]
12 Chabout J, Sarkar A, Patel SR, Radden T, Dunson DB, Fisher SE, Jarvis ED. A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice. Front Behav Neurosci 2016;10:197. [PMID: 27812326 DOI: 10.3389/fnbeh.2016.00197] [Cited by in Crossref: 60] [Cited by in F6Publishing: 64] [Article Influence: 10.0] [Reference Citation Analysis]
13 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: 2.7] [Reference Citation Analysis]
14 Gingras B, Honing H, Peretz I, Trainor LJ, Fisher SE. Defining the biological bases of individual differences in musicality. Philos Trans R Soc Lond B Biol Sci 2015;370:20140092. [PMID: 25646515 DOI: 10.1098/rstb.2014.0092] [Cited by in Crossref: 42] [Cited by in F6Publishing: 43] [Article Influence: 7.0] [Reference Citation Analysis]
15 Fisher SE. A Molecular Genetic Perspective on Speech and Language. Neurobiology of Language 2016. [DOI: 10.1016/b978-0-12-407794-2.00002-x] [Cited by in Crossref: 2] [Article Influence: 0.3] [Reference Citation Analysis]
16 Karikari TK, Aleksic J. Neurogenomics: An opportunity to integrate neuroscience, genomics and bioinformatics research in Africa. Appl Transl Genom 2015;5:3-10. [PMID: 26937352 DOI: 10.1016/j.atg.2015.06.004] [Cited by in Crossref: 17] [Cited by in F6Publishing: 21] [Article Influence: 2.4] [Reference Citation Analysis]
17 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: 6.4] [Reference Citation Analysis]
18 Barnett CP, van Bon BWM. Monogenic and chromosomal causes of isolated speech and language impairment. J Med Genet 2015;52:719-29. [DOI: 10.1136/jmedgenet-2015-103161] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 2.0] [Reference Citation Analysis]
19 Graham SA, Deriziotis P, Fisher SE. Insights into the genetic foundations of human communication. Neuropsychol Rev 2015;25:3-26. [PMID: 25597031 DOI: 10.1007/s11065-014-9277-2] [Cited by in Crossref: 23] [Cited by in F6Publishing: 15] [Article Influence: 3.3] [Reference Citation Analysis]
20 Aitken KJ. The sound of one hand clapping: overdetermination and the pansensory nature of communication. Behav Brain Sci 2014;37:546-7; discussion 577-604. [PMID: 25514936 DOI: 10.1017/S0140525X13003944] [Reference Citation Analysis]
21 Deriziotis P, O'Roak BJ, Graham SA, Estruch SB, Dimitropoulou D, Bernier RA, Gerdts J, Shendure J, Eichler EE, Fisher SE. De novo TBR1 mutations in sporadic autism disrupt protein functions. Nat Commun 2014;5:4954. [PMID: 25232744 DOI: 10.1038/ncomms5954] [Cited by in Crossref: 88] [Cited by in F6Publishing: 89] [Article Influence: 11.0] [Reference Citation Analysis]
22 Hoogman M, Guadalupe T, Zwiers MP, Klarenbeek P, Francks C, Fisher SE. Assessing the effects of common variation in the FOXP2 gene on human brain structure. Front Hum Neurosci 2014;8:473. [PMID: 25013396 DOI: 10.3389/fnhum.2014.00473] [Cited by in Crossref: 29] [Cited by in F6Publishing: 32] [Article Influence: 3.6] [Reference Citation Analysis]
23 Deriziotis P, Graham SA, Estruch SB, Fisher SE. Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer. J Vis Exp 2014. [PMID: 24893771 DOI: 10.3791/51438] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 1.8] [Reference Citation Analysis]
24 Worthey EA, Raca G, Laffin JJ, Wilk BM, Harris JM, Jakielski KJ, Dimmock DP, Strand EA, Shriberg LD. Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech. J Neurodev Disord 2013;5:29. [PMID: 24083349 DOI: 10.1186/1866-1955-5-29] [Cited by in Crossref: 55] [Cited by in F6Publishing: 55] [Article Influence: 6.1] [Reference Citation Analysis]