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For: 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: 9.8] [Reference Citation Analysis]
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5 Crespo I, Pignatelli J, Kinare V, Méndez-Gómez HR, Esgleas M, Román MJ, Canals JM, Tole S, Vicario C. Tbr1 Misexpression Alters Neuronal Development in the Cerebral Cortex. Mol Neurobiol 2022. [PMID: 35781633 DOI: 10.1007/s12035-022-02936-x] [Reference Citation Analysis]
6 Fazel Darbandi S, Nelson AD, Pai EL, Bender KJ, Rubenstein JLR. LiCl treatment leads to long-term restoration of spine maturation and synaptogenesis in adult Tbr1 mutants. J Neurodevelop Disord 2022;14. [DOI: 10.1186/s11689-022-09421-5] [Reference Citation Analysis]
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8 Bao Z, Fang K, Miao Z, Li C, Yang C, Yu Q, Zhang C, Miao Z, Liu Y, Ji J. Human Cerebral Organoid Implantation Alleviated the Neurological Deficits of Traumatic Brain Injury in Mice. Oxid Med Cell Longev 2021;2021:6338722. [PMID: 34853630 DOI: 10.1155/2021/6338722] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
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14 Garcia-Forn M, Boitnott A, Akpinar Z, De Rubeis S. Linking Autism Risk Genes to Disruption of Cortical Development. Cells 2020;9:E2500. [PMID: 33218123 DOI: 10.3390/cells9112500] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 3.7] [Reference Citation Analysis]
15 Suliman-Lavie R, Title B, Cohen Y, Hamada N, Tal M, Tal N, Monderer-Rothkoff G, Gudmundsdottir B, Gudmundsson KO, Keller JR, Huang GJ, Nagata KI, Yarom Y, Shifman S. Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice. Nat Commun 2020;11:5836. [PMID: 33203851 DOI: 10.1038/s41467-020-19577-0] [Cited by in Crossref: 19] [Cited by in F6Publishing: 22] [Article Influence: 6.3] [Reference Citation Analysis]
16 Prem S, Millonig JH, DiCicco-Bloom E. Dysregulation of Neurite Outgrowth and Cell Migration in Autism and Other Neurodevelopmental Disorders. Adv Neurobiol 2020;25:109-53. [PMID: 32578146 DOI: 10.1007/978-3-030-45493-7_5] [Cited by in Crossref: 14] [Cited by in F6Publishing: 3] [Article Influence: 4.7] [Reference Citation Analysis]
17 Sapey-Triomphe LA, Reversat J, Lesca G, Chatron N, Bussa M, Mazoyer S, Schmitz C, Sonié S, Edery P. A de novo frameshift pathogenic variant in TBR1 identified in autism without intellectual disability. Hum Genomics 2020;14:32. [PMID: 32948248 DOI: 10.1186/s40246-020-00281-5] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
18 Becker M, Mastropasqua F, Reising JP, Maier S, Ho ML, Rabkina I, Li D, Neufeld J, Ballenberger L, Myers L, Moritz V, Kele M, Wincent J, Willfors C, Sitnikov R, Herlenius E, Anderlid BM, Falk A, Bölte S, Tammimies K. Presynaptic dysfunction in CASK-related neurodevelopmental disorders. Transl Psychiatry 2020;10:312. [PMID: 32929080 DOI: 10.1038/s41398-020-00994-0] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 4.3] [Reference Citation Analysis]
19 Hickey SL, Berto S, Konopka G. Chromatin Decondensation by FOXP2 Promotes Human Neuron Maturation and Expression of Neurodevelopmental Disease Genes. Cell Rep 2019;27:1699-1711.e9. [PMID: 31067457 DOI: 10.1016/j.celrep.2019.04.044] [Cited by in Crossref: 23] [Cited by in F6Publishing: 17] [Article Influence: 7.7] [Reference Citation Analysis]
20 Kiyama T, Long Y, Chen CK, Whitaker CM, Shay A, Wu H, Badea TC, Mohsenin A, Parker-Thornburg J, Klein WH, Mills SL, Massey SC, Mao CA. Essential Roles of Tbr1 in the Formation and Maintenance of the Orientation-Selective J-RGCs and a Group of OFF-Sustained RGCs in Mouse. Cell Rep 2019;27:900-915.e5. [PMID: 30995485 DOI: 10.1016/j.celrep.2019.03.077] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 4.7] [Reference Citation Analysis]
21 Kim Y, An JY. Spatio-Temporal Roles of ASD-Associated Variants in Human Brain Development. Genes (Basel) 2020;11:E535. [PMID: 32403330 DOI: 10.3390/genes11050535] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
22 Medvedeva VP, Rieger MA, Vieth B, Mombereau C, Ziegenhain C, Ghosh T, Cressant A, Enard W, Granon S, Dougherty JD, Groszer M. Altered social behavior in mice carrying a cortical Foxp2 deletion. Hum Mol Genet 2019;28:701-17. [PMID: 30357341 DOI: 10.1093/hmg/ddy372] [Cited by in Crossref: 19] [Cited by in F6Publishing: 24] [Article Influence: 6.3] [Reference Citation Analysis]
23 Nambot S, Faivre L, Mirzaa G, Thevenon J, Bruel AL, Mosca-Boidron AL, Masurel-Paulet A, Goldenberg A, Le Meur N, Charollais A, Mignot C, Petit F, Rossi M, Metreau J, Layet V, Amram D, Boute-Bénéjean O, Bhoj E, Cousin MA, Kruisselbrink TM, Lanpher BC, Klee EW, Fiala E, Grange DK, Meschino WS, Hiatt SM, Cooper GM, Olivié H, Smith WE, Dumas M, Lehman A, Inglese C, Nizon M, Guerrini R, Vetro A, Kaplan ES, Miramar D, Van Gils J, Fergelot P, Bodamer O, Herkert JC, Pajusalu S, Õunap K, Filiano JJ, Smol T, Piton A, Gérard B, Chantot-Bastaraud S, Bienvenu T, Li D, Juusola J, Devriendt K, Bilan F, Poé C, Chevarin M, Jouan T, Tisserant E, Rivière JB, Tran Mau-Them F, Philippe C, Duffourd Y, Dobyns WB, Hevner R, Thauvin-Robinet C; CAUSES Study. De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature. Eur J Hum Genet 2020;28:770-82. [PMID: 32005960 DOI: 10.1038/s41431-020-0571-6] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 5.3] [Reference Citation Analysis]
24 Co M, Anderson AG, Konopka G. FOXP transcription factors in vertebrate brain development, function, and disorders. Wiley Interdiscip Rev Dev Biol 2020;9:e375. [PMID: 31999079 DOI: 10.1002/wdev.375] [Cited by in Crossref: 25] [Cited by in F6Publishing: 28] [Article Influence: 8.3] [Reference Citation Analysis]
25 Wang Y, Zeng C, Li J, Zhou Z, Ju X, Xia S, Li Y, Liu A, Teng H, Zhang K, Shi L, Bi C, Xie W, He X, Jia Z, Jiang Y, Cai T, Wu J, Xia K, Sun ZS. PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior. Cell Rep 2018;24:2029-41. [PMID: 30134165 DOI: 10.1016/j.celrep.2018.07.061] [Cited by in Crossref: 41] [Cited by in F6Publishing: 43] [Article Influence: 13.7] [Reference Citation Analysis]
26 Lambert J, Haigh J, Nord A. Gene regulatory networks controlling neuronal development. Patterning and Cell Type Specification in the Developing CNS and PNS 2020. [DOI: 10.1016/b978-0-12-814405-3.00027-8] [Reference Citation Analysis]
27 Becker M, Mastropasqua F, Reising JP, Maier S, Ho M, Rabkina I, Li D, Neufeld J, Ballenberger L, Myers L, Moritz V, Kele M, Wincent J, Willfors C, Sitnikov R, Herlenius E, Anderlid B, Falk A, Bölte S, Tammimies K. Presynaptic dysfunction in CASK-related neurodevelopmental disorders.. [DOI: 10.1101/863308] [Reference Citation Analysis]
28 Song J, Yang X, Zhou Y, Chen L, Zhang X, Liu Z, Niu W, Zhan N, Fan X, Khan AA, Kuang Y, Song L, He G, Li W. Dysregulation of neuron differentiation in an autistic savant with exceptional memory. Mol Brain 2019;12:91. [PMID: 31699123 DOI: 10.1186/s13041-019-0507-7] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]
29 Yook C, Kim K, Kim D, Kang H, Kim SG, Kim E, Kim SY. A TBR1-K228E Mutation Induces Tbr1 Upregulation, Altered Cortical Distribution of Interneurons, Increased Inhibitory Synaptic Transmission, and Autistic-Like Behavioral Deficits in Mice. Front Mol Neurosci 2019;12:241. [PMID: 31680851 DOI: 10.3389/fnmol.2019.00241] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 3.3] [Reference Citation Analysis]
30 Bruel AL, Nambot S, Quéré V, Vitobello A, Thevenon J, Assoum M, Moutton S, Houcinat N, Lehalle D, Jean-Marçais N, Chevarin M, Jouan T, Poë C, Callier P, Tisserand E, Philippe C, Them FTM, Duffourd Y, Faivre L, Thauvin-Robinet C; Orphanomix Physician’s Group. Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing. Eur J Hum Genet 2019;27:1519-31. [PMID: 31231135 DOI: 10.1038/s41431-019-0442-1] [Cited by in Crossref: 26] [Cited by in F6Publishing: 28] [Article Influence: 6.5] [Reference Citation Analysis]
31 Zhao W, Tan J, Zhu T, Ou J, Li Y, Shen L, Wu H, Han L, Liu Y, Jia X, Bai T, Li H, Ke X, Zhao J, Zou X, Hu Z, Guo H, Xia K. Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development. J Genet Genomics 2019;46:247-57. [PMID: 31196716 DOI: 10.1016/j.jgg.2019.04.002] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 2.8] [Reference Citation Analysis]
32 Wikenius E, Myhre AM, Page CM, Moe V, Smith L, Heiervang ER, Undlien DE, LeBlanc M. Prenatal maternal depressive symptoms and infant DNA methylation: a longitudinal epigenome-wide study. Nord J Psychiatry 2019;73:257-63. [PMID: 31070508 DOI: 10.1080/08039488.2019.1613446] [Cited by in Crossref: 16] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
33 Kroeze Y, Oti M, van Beusekom E, Cooijmans RHM, van Bokhoven H, Kolk SM, Homberg JR, Zhou H. Transcriptome Analysis Identifies Multifaceted Regulatory Mechanisms Dictating a Genetic Switch from Neuronal Network Establishment to Maintenance During Postnatal Prefrontal Cortex Development. Cereb Cortex 2018;28:833-51. [PMID: 28108491 DOI: 10.1093/cercor/bhw407] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 2.8] [Reference Citation Analysis]
34 Co M, Hickey SL, Kulkarni A, Harper M, Konopka G. Cortical Foxp2 supports behavioral flexibility and developmental dopamine D1 receptor expression.. [DOI: 10.1101/624973] [Reference Citation Analysis]
35 Inglese CN, Elliott AM, Lehman A; CAUSES Study. New developmental syndromes: Understanding the family experience. J Genet Couns 2019;28:202-12. [DOI: 10.1002/jgc4.1121] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 4.3] [Reference Citation Analysis]
36 Estruch SB, Graham SA, Quevedo M, Vino A, Dekkers DHW, Deriziotis P, Sollis E, Demmers J, Poot RA, Fisher SE. Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders. Hum Mol Genet 2018;27:1212-27. [PMID: 29365100 DOI: 10.1093/hmg/ddy035] [Cited by in Crossref: 27] [Cited by in F6Publishing: 32] [Article Influence: 6.8] [Reference Citation Analysis]
37 Horváth G, Otrokocsi L, Beko K, Baranyi M, Kittel Á, Fritz-Ruenes PA, Sperlágh B. P2X7 Receptors Drive Poly(I:C) Induced Autism-like Behavior in Mice. J Neurosci 2019;39:2542-61. [PMID: 30683682 DOI: 10.1523/JNEUROSCI.1895-18.2019] [Cited by in Crossref: 13] [Cited by in F6Publishing: 18] [Article Influence: 3.3] [Reference Citation Analysis]
38 Vegas N, Cavallin M, Kleefstra T, de Boer L, Philbert M, Maillard C, Boddaert N, Munnich A, Hubert L, Bery A, Besmond C, Bahi-buisson N. Mutations in TBR1 gene leads to cortical malformations and intellectual disability. European Journal of Medical Genetics 2018;61:759-64. [DOI: 10.1016/j.ejmg.2018.09.012] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 2.8] [Reference Citation Analysis]
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40 Morris G, Pahad N, Dirr HW, Fanucchi S. A conserved cation binding site in the DNA binding domain of forkhead box transcription factors regulates DNA binding by FOXP2. Archives of Biochemistry and Biophysics 2018;657:56-64. [DOI: 10.1016/j.abb.2018.09.009] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
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