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For: 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: 3.2] [Reference Citation Analysis]
Number Citing Articles
1 Macciardi F, Martini F. The Neanderthal brain: Biological and cognitive evolution. Updating Neanderthals 2022. [DOI: 10.1016/b978-0-12-821428-2.00008-1] [Reference Citation Analysis]
2 Lampis V, Ventura R, Di Segni M, Marino C, D'Amato FR, Mascheretti S. Animal models of developmental dyslexia: Where we are and what we are missing. Neurosci Biobehav Rev 2021;131:1180-97. [PMID: 34699847 DOI: 10.1016/j.neubiorev.2021.10.022] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
3 Sanjuán J, Castro-Martínez XH, García-Martí G, González-Fernández J, Sanz-Requena R, Haro JM, Meana JJ, Martí-Bonmatí L, Nacher J, Sebastiá-Ortega N, Gilabert-Juan J, Moltó MD. FOXP2 expression and gray matter density in the male brains of patients with schizophrenia. Brain Imaging Behav 2021;15:1403-11. [PMID: 32734433 DOI: 10.1007/s11682-020-00339-x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
4 den Hoed J, Devaraju K, Fisher SE. Molecular networks of the FOXP2 transcription factor in the brain. EMBO Rep 2021;22:e52803. [PMID: 34260143 DOI: 10.15252/embr.202152803] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
5 Du J, Palaniyappan L, Liu Z, Cheng W, Gong W, Zhu M, Wang J, Zhang J, Feng J. The genetic determinants of language network dysconnectivity in drug-naïve early stage schizophrenia. NPJ Schizophr 2021;7:18. [PMID: 33658499 DOI: 10.1038/s41537-021-00141-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 5.5] [Reference Citation Analysis]
6 Vilor-Tejedor N, Ikram MA, Roshchupkin GV, Cáceres A, Alemany S, Vernooij MW, Niessen WJ, van Duijn CM, Sunyer J, Adams HH, González JR. Independent Multiple Factor Association Analysis for Multiblock Data in Imaging Genetics. Neuroinformatics 2019;17:583-92. [PMID: 30903541 DOI: 10.1007/s12021-019-09416-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
7 Uddén J, Hultén A, Bendtz K, Mineroff Z, Kucera KS, Vino A, Fedorenko E, Hagoort P, Fisher SE. Toward Robust Functional Neuroimaging Genetics of Cognition. J Neurosci 2019;39:8778-87. [PMID: 31570534 DOI: 10.1523/JNEUROSCI.0888-19.2019] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 3.3] [Reference Citation Analysis]
8 Torres-Ruiz R, Benítez-Burraco A, Martínez-Lage M, Rodríguez-Perales S, García-Bellido P. Functional characterization of two enhancers located downstream FOXP2. BMC Med Genet 2019;20:65. [PMID: 31046704 DOI: 10.1186/s12881-019-0810-2] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
9 Zhang S, Zhao J, Guo Z, Jones JA, Liu P, Liu H. The Association Between Genetic Variation in FOXP2 and Sensorimotor Control of Speech Production. Front Neurosci 2018;12:666. [PMID: 30294257 DOI: 10.3389/fnins.2018.00666] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
10 Vilor-Tejedor N, Alemany S, Cáceres A, Bustamante M, Pujol J, Sunyer J, González JR. Strategies for integrated analysis in imaging genetics studies. Neurosci Biobehav Rev 2018;93:57-70. [PMID: 29944960 DOI: 10.1016/j.neubiorev.2018.06.013] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.4] [Reference Citation Analysis]
11 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: 2.3] [Reference Citation Analysis]
12 Uddén J, Snijders TM, Fisher SE, Hagoort P. A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus. Brain and Language 2017;172:16-21. [DOI: 10.1016/j.bandl.2016.02.003] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 2.3] [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 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]
15 Mozzi A, Riva V, Forni D, Sironi M, Marino C, Molteni M, Riva S, Guerini FR, Clerici M, Cagliani R, Mascheretti S. A common genetic variant in FOXP2 is associated with language-based learning (dis)abilities: Evidence from two Italian independent samples. Am J Med Genet B Neuropsychiatr Genet 2017;174:578-86. [PMID: 28436202 DOI: 10.1002/ajmg.b.32546] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 2.0] [Reference Citation Analysis]
16 Rao W, Du X, Zhang Y, Yu Q, Hui L, Yu Y, Kou C, Yin G, Zhu X, Man L, Soares JC, Zhang XY. Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population. J Neural Transm (Vienna) 2017;124:891-7. [PMID: 28421313 DOI: 10.1007/s00702-017-1723-x] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 2.2] [Reference Citation Analysis]
17 Berwick RC. A Feeling for the Phenotype. The Cambridge Companion to Chomsky 2017. [DOI: 10.1017/9781316716694.005] [Reference Citation Analysis]
18 Van der Auwera S, Wittfeld K, Shumskaya E, Bralten J, Zwiers MP, Onnink AMH, Usberti N, Hertel J, Völzke H, Völker U, Hosten N, Franke B, Grabe HJ. Predicting brain structure in population-based samples with biologically informed genetic scores for schizophrenia. Am J Med Genet 2017;174:324-32. [DOI: 10.1002/ajmg.b.32519] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 2.5] [Reference Citation Analysis]
19 Chien YL, Wu YY, Chen HI, Tsai WC, Chiu YN, Liu SK, Gau SS. The central nervous system patterning gene variants associated with clinical symptom severity of autism spectrum disorders. J Formos Med Assoc 2017;116:755-64. [PMID: 28081867 DOI: 10.1016/j.jfma.2016.11.015] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
20 Mascheretti S, De Luca A, Trezzi V, Peruzzo D, Nordio A, Marino C, Arrigoni F. Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms. Transl Psychiatry 2017;7:e987. [PMID: 28045463 DOI: 10.1038/tp.2016.240] [Cited by in Crossref: 64] [Cited by in F6Publishing: 72] [Article Influence: 10.7] [Reference Citation Analysis]
21 Mascheretti S, De Luca A, Trezzi V, Peruzzo D, Nordio A, Marino C, Arrigoni F. Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms. Transl Psychiatry 2017;7:e987. [PMID: 28045463 DOI: 10.1038/tp.2016.240] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
22 Torres-ruiz R, Benitez-burraco A, Martínez-lage M, Rodríguez-perales S, García-bellido P. Functional genetic characterization by CRISPR-Cas9 of two enhancers of FOXP2 in a child with speech and language impairment.. [DOI: 10.1101/064196] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
23 Koziol LF, Barker LA, Jansons L. Conceptualizing Developmental Language Disorders. The Linguistic Cerebellum 2016. [DOI: 10.1016/b978-0-12-801608-4.00010-4] [Reference Citation Analysis]
24 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]
25 Chandrasekaran B, Yi HG, Blanco NJ, McGeary JE, Maddox WT. Enhanced procedural learning of speech sound categories in a genetic variant of FOXP2. J Neurosci 2015;35:7808-12. [PMID: 25995468 DOI: 10.1523/JNEUROSCI.4706-14.2015] [Cited by in Crossref: 26] [Cited by in F6Publishing: 29] [Article Influence: 3.3] [Reference Citation Analysis]
26 Klein M, van der Voet M, Harich B, van Hulzen KJ, Onnink AM, Hoogman M, Guadalupe T, Zwiers M, Groothuismink JM, Verberkt A, Nijhof B, Castells-Nobau A, Faraone SV, Buitelaar JK, Schenck A, Arias-Vasquez A, Franke B; Psychiatric Genomics Consortium ADHD Working Group. Converging evidence does not support GIT1 as an ADHD risk gene. Am J Med Genet B Neuropsychiatr Genet 2015;168:492-507. [PMID: 26061966 DOI: 10.1002/ajmg.b.32327] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 2.0] [Reference Citation Analysis]
27 Kambanaros M, Michaelides M, Grohmann KK. Measuring word retrieval deficits in a multilingual child with SLI: Is there a better language? Journal of Neurolinguistics 2015;34:112-30. [DOI: 10.1016/j.jneuroling.2014.09.006] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.1] [Reference Citation Analysis]
28 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]
29 Bowers JM, Perez-Pouchoulen M, Roby CR, Ryan TE, McCarthy MM. Androgen modulation of Foxp1 and Foxp2 in the developing rat brain: impact on sex specific vocalization. Endocrinology 2014;155:4881-94. [PMID: 25247470 DOI: 10.1210/en.2014-1486] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 2.7] [Reference Citation Analysis]