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For: 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: 2.9] [Reference Citation Analysis]
Number Citing Articles
1 Moreno Campos V, Benítez-Burraco A. Communication deficits in a case of a deletion in 7q31.1-q31.33 encompassing FOXP2. Clin Linguist Phon 2022;:1-14. [PMID: 35702019 DOI: 10.1080/02699206.2022.2085174] [Reference Citation Analysis]
2 Benítez-Burraco A, Fernández-Urquiza M, Jiménez-Romero MS. Language Impairment with a Partial Duplication of DOCK8. Mol Syndromol 2020;11:243-63. [PMID: 33510598 DOI: 10.1159/000511972] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Benítez-burraco A, Fernández-urquiza M, Jiménez-romero MS. Language impairment with a partial duplication of DOCK8.. [DOI: 10.1101/2020.06.16.155523] [Reference Citation Analysis]
4 Peter B, Vose C, Bruce L, Ingram D. Starting to Talk at Age 10 Years: Lessons About the Acquisition of English Speech Sounds in a Rare Case of Severe Congenital But Remediated Motor Disease of Genetic Origin. Am J Speech Lang Pathol 2019;28:1029-38. [PMID: 31298943 DOI: 10.1044/2019_AJSLP-18-0156] [Reference Citation Analysis]
5 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]
6 Chi T, Liu M, Tan X, Sun K, Jin L, Feng J. Syllable merging during ontogeny in Hipposideros larvatus. Bioacoustics 2020;29:387-98. [DOI: 10.1080/09524622.2019.1610906] [Cited by in Crossref: 2] [Article Influence: 0.5] [Reference Citation Analysis]
7 Benítez-Burraco A, Kimura R. Robust Candidates for Language Development and Evolution Are Significantly Dysregulated in the Blood of People With Williams Syndrome. Front Neurosci 2019;13:258. [PMID: 30971880 DOI: 10.3389/fnins.2019.00258] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
8 Niego A, Benítez-Burraco A. Williams Syndrome, Human Self-Domestication, and Language Evolution. Front Psychol 2019;10:521. [PMID: 30936846 DOI: 10.3389/fpsyg.2019.00521] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 4.8] [Reference Citation Analysis]
9 Benítez-burraco A, Kimura R. Robust candidates for language development and evolution are significantly dysregulated in the blood of people with Williams syndrome.. [DOI: 10.1101/488155] [Reference Citation Analysis]
10 Fisher SE. Evolution of language: Lessons from the genome. Psychon Bull Rev 2017;24:34-40. [PMID: 27432000 DOI: 10.3758/s13423-016-1112-8] [Cited by in Crossref: 28] [Cited by in F6Publishing: 29] [Article Influence: 4.7] [Reference Citation Analysis]
11 Desalle R, Tattersall I. What aDNA can (and cannot) tell us about the emergence of language and speech. Journal of Language Evolution 2018;3:59-66. [DOI: 10.1093/jole/lzx018] [Cited by in Crossref: 5] [Cited by in F6Publishing: 23] [Article Influence: 0.8] [Reference Citation Analysis]
12 Zubicaray G, Fisher SE. Genes, Brain, and Language: A brief introduction to the Special Issue. Brain Lang 2017;172:1-2. [PMID: 28867043 DOI: 10.1016/j.bandl.2017.08.003] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
13 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]
14 Berwick RC, Chomsky N. Why only us: Recent questions and answers. Journal of Neurolinguistics 2017;43:166-77. [DOI: 10.1016/j.jneuroling.2016.12.002] [Cited by in Crossref: 28] [Cited by in F6Publishing: 15] [Article Influence: 4.7] [Reference Citation Analysis]
15 Shriberg LD, Strand EA, Fourakis M, Jakielski KJ, Hall SD, Karlsson HB, Mabie HL, McSweeny JL, Tilkens CM, Wilson DL. A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker. J Speech Lang Hear Res 2017;60:S1096-117. [PMID: 28384779 DOI: 10.1044/2016_JSLHR-S-15-0296] [Cited by in Crossref: 39] [Cited by in F6Publishing: 42] [Article Influence: 6.5] [Reference Citation Analysis]
16 Berwick RC. A Feeling for the Phenotype. The Cambridge Companion to Chomsky 2017. [DOI: 10.1017/9781316716694.005] [Reference Citation Analysis]
17 Onnis L. Caregiver communication to the child as moderator and mediator of genes for language. Behav Brain Res 2017;325:197-202. [PMID: 28215549 DOI: 10.1016/j.bbr.2017.02.003] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
18 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]
19 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]
20 Rice M, Tager-flusberg H. Language Phenotypes. Innovations in Cognitive Neuroscience 2016. [DOI: 10.1007/978-1-4614-3846-5_12] [Reference Citation Analysis]