| 1 | FOXG1, LHX2
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| Hierarchical genetic interactions between FOXG1 and LHX2 regulate the formation of the cortical hem in the developing telencephalon.
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| Godbole G, Shetty AS, Roy A, D'Souza L, Chen B, Miyoshi G, Fishell G, Tole S.
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| Development 145(1). pii: dev154583. doi: 10.1242/dev.154583.
2018
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| 2 | FOXG1
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| Forkhead box G1 gene haploinsufficiency: an emerging cause of dyskinetic encephalopathy of infancy.
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| Bertossi C, Cassina M, Cappellari A, Toldo I, Nosadini M, Rigon C, Suppiej A, Sartori S.
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| Neuropediatrics 46(1):56-64. doi: 10.1055/s-0034-1395345. Epub 2015 Jan 7.
2015
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| 3 | CDKL5, EIEE2, FOXG1, MECP2, RTT, RTTL1
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| CAGE-defined promoter regions of the genes implicated in Rett Syndrome.
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| Vitezic M, Bertin N, Andersson R, Lipovich L, Kawaji H, Lassmann T, Sandelin A, Heutink P, Goldowitz D, Ha T, Zhang P, Patrizi A, Fagiolini M, Forrest AR, Carninci P, Saxena A.
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| BMC Genomics 15(1):1177. [Epub ahead of print]
2014
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| 4 | FOXG1
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| The facial neural crest controls fore- and midbrain patterning by regulating Foxg1 expression through Smad1 activity.
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| Aguiar DP, Sghari S, Creuzet S.
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| Development evelopment. 2014 2014
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| 5 | FOXG1
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| Epilepsy and outcome in FOXG1-related disorders.
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| Seltzer LE, Ma M, Ahmed S, Bertrand M, Dobyns WB, Wheless J, Paciorkowski AR.
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| Epilepsia 55(8):1292-300. doi: 10.1111/epi.12648. Epub 2014 May 16.
2014
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| 6 | FOXG1, PRKD1, RTTL1
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| 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.
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| Ellaway CJ, Ho G, Bettella E, Knapman A, Collins F, Hackett A, McKenzie F, Darmanian A, Peters GB, Fagan K, Christodoulou J.
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| Eur J Hum Genet 21(5):522-7. doi: 10.1038/ejhg.2012.208. Epub 2012 Sep 12.
2013
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| 7 | FOXG1, NCOA3
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| Transcriptional repression of AIB1 by FoxG1 leads to apoptosis in breast cancer cells.
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| Li JV, Chien CD, Garee JP, Xu J, Wellstein A, Riegel AT.
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| Mol Endocrinol 27(7):1113-27. doi: 10.1210/me.2012-1353. Epub 2013 May 9.
2013
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| 8 | FOXG1
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| Foxg1 is required to limit the formation of ciliary margin tissue and Wnt/β-catenin signalling in the developing nasal retina of the mouse.
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| Fotaki V, Smith R, Pratt T, Price DJ.
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| Dev Biol 380(2):299-313. doi: 10.1016/j.ydbio.2013.04.017. Epub 2013 Apr 24.
2013
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| 9 | DMRT3, DMRTA1, EBF2, EBF3, EYA2, FOXG1
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| Foxg1 coordinates the switch from nonradially to radially migrating glutamatergic subtypes in the neocortex through spatiotemporal repression.
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| Kumamoto T, Toma K, Gunadi, McKenna WL, Kasukawa T, Katzman S, Chen B, Hanashima C.
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| Cell Rep 3(3):931-45. doi: 10.1016/j.celrep.2013.02.023. Epub 2013 Mar 21.
2013
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| 10 | FOXG1, RTTL1
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| Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12
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| Goubau C, Devriendt K, Van der Aa N, Crepel A, Wieczorek D, Kleefstra T, Willemsen MH, Rauch A, Tzschach A, de Ravel T, Leemans P, Van Geet C, Buyse G, Freson K.
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| Eur J Hum Genet. Dec;21(12):1349-55. doi: 10.1038/ejhg.2013.86. Epub 2013 May 1. 2013
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| 11 | DEL14Q12, DEL14QP, FOXG1
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| Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus.
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| Santen GW, Sun Y, Gijsbers AC, Carré A, Holvoet M, Haeringen Av, Lesnik Oberstein SA, Tomoda A, Mabe H, Polak M, Devriendt K, Ruivenkamp CA, Bijlsma EK.
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| J Med Genet 49(6):366-72. Epub 2012 May 25. 2012
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| 12 | DEL14Q12, FOXG1
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| 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.
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| Ellaway CJ, Ho G, Bettella E, Knapman A, Collins F, Hackett A, McKenzie F, Darmanian A, Peters GB, Fagan K, Christodoulou J.
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| Eur J Hum Genet ur J Hum Genet. 2012 Sep 12. doi: 10.1038/ejhg.2012.208. [Epub ahead of print]
2012
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| 13 | FOXG1, TLE1
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| Transducin-like enhancer of Split-1 (TLE1) combines with Forkhead box protein G1 (FoxG1) to promote neuronal survival.
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| Dastidar SG, Narayanan S, Stifani S, D'Mello SR.
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| J Biol Chem 287(18):14749-59. doi: 10.1074/jbc.M111.328336. Epub 2012 Feb 21.
2012
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| 14 | DEL14Q12, FOXG1, PRKD1
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| 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements.
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| Allou L, Lambert L, Amsallem D, Bieth E, Edery P, Destrée A, Rivier F, Amor D, Thompson E, Nicholl J, Harbord M, Nemos C, Saunier A, Moustaïne A, Vigouroux A, Jonveaux P, Philippe C.
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| Eur J Hum Genet 20(12):1216-23. doi: 10.1038/ejhg.2012.127. Epub 2012 Jun 27. 2012
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| 15 | FOXG1, SIX3
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| Six3 cooperates with Hedgehog signaling to specify ventral telencephalon by promoting early expression of Foxg1a and repressing Wnt signaling.
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| Carlin D, Sepich D, Grover VK, Cooper MK, Solnica-Krezel L, Inbal A.
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| Development 139(14):2614-24. doi: 10.1242/dev.076018.
2012
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| 16 | FOXG1
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| Foxg1 has an essential role in postnatal development of the dentate gyrus.
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| Tian C, Gong Y, Yang Y, Shen W, Wang K, Liu J, Xu B, Zhao J, Zhao C.
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| J Neurosci 32(9):2931-49. doi: 10.1523/JNEUROSCI.5240-11.2012.
2012
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| 17 | FOXG1, RTTL1
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| FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome.
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| Takahashi S, Matsumoto N, Okayama A, Suzuki N, Araki A, Okajima K, Tanaka H, Miyamoto A.
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| Clin Genet. Dec;82(6):569-73. doi: 10.1111/j.1399-0004.2011.01819.x. Epub 2011 Dec 16. 2012
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| 18 | DEL14Q12, FOXG1, RTTL1
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| The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
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| Kortüm F, Das S, Flindt M, Morris-Rosendahl DJ, Stefanova I, Goldstein A, Horn D, Klopocki E, Kluger G, Martin P, Rauch A, Roumer A, Saitta S, Walsh LE, Wieczorek D, Uyanik G, Kutsche K, Dobyns WB.
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| J Med Genet 48(6):396-406. Epub 2011 Mar 25.
2011
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| 19 | FOXG1
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| FoxG1 promotes the survival of postmitotic neurons.
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| Dastidar SG, Landrieu PM, D'Mello SR.
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| J Neurosci 31(2):402-13.
2011
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| 20 | FOXG1, RTTL1
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| A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localization.
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| Le Guen T, Fichou Y, Nectoux J, Bahi-Buisson N, Rivier F, Boddaert N, Diebold B, Héron D, Chelly J, Bienvenu T.
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| Hum Mutat 32(2):E2026-35. doi: 10.1002/humu.21422. Epub 2010 Dec 7.
2011
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| 21 | DUP14QP, FOXG1, UPD14M
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| West syndrome associated with mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14.
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| Tohyama J, Yamamoto T, Hosoki K, Nagasaki K, Akasaka N, Ohashi T, Kobayashi Y, Saitoh S.
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| Am J Med Genet A 155A(10):2584-8. doi: 10.1002/ajmg.a.34224. Epub 2011 Sep 9.
2011
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| 22 | DUP14QP, FOXG1
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| Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.
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| Brunetti-Pierri N, Paciorkowski AR, Ciccone R, Mina ED, Bonaglia MC, Borgatti R, Schaaf CP, Sutton VR, Xia Z, Jelluma N, Ruivenkamp C, Bertrand M, de Ravel TJ, Jayakar P, Belli S, Rocchetti K, Pantaleoni C, D'Arrigo S, Hughes J, Cheung SW, Zuffardi O, Stankiewicz P.
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| Eur J Hum Genet 19(1):102-7. Epub 2010 Aug 25.
2011
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| 23 | EMX2, FOXG1
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| Emx2 and Foxg1 inhibit gliogenesis and promote neuronogenesis.
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| Brancaccio M, Pivetta C, Granzotto M, Filippis C, Mallamaci A.
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| Stem Cells 28(7):1206-18.
2010
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| 24 | FOXG1, RTTL1
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| Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
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| Mencarelli MA, Spanhol-Rosseto A, Artuso R, Rondinella D, De Filippis R, Bahi-Buisson N, Nectoux J, Rubinsztajn R, Bienvenu T, Moncla A, Chabrol B, Villard L, Krumina Z, Armstrong J, Roche A, Pineda M, Gak E, Mari F, Ariani F, Renieri A.
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| J Med Genet 47(1):49-53. Epub 2009 Jul 2.
2010
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| 25 | FOXG1, RTTL1
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| Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females.
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| Philippe C, Amsallem D, Francannet C, Lambert L, Saunier A, Verneau F, Jonveaux P.
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| J Med Genet 47(1):59-65. Epub 2009 Jun 29.
2010
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| 26 | BMI1, FOXG1
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| Bmi-1 cooperates with Foxg1 to maintain neural stem cell self-renewal in the forebrain.
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| Fasano CA, Phoenix TN, Kokovay E, Lowry N, Elkabetz Y, Dimos JT, Lemischka IR, Studer L, Temple S.
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| Genes Dev 23(5):561-74. 2009
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| 27 | DEL14QD, DEL14QP, FOXG1, RG14, RPGRIP1
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| The ring 14 syndrome: clinical and molecular definition.
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| Zollino M, Seminara L, Orteschi D, Gobbi G, Giovannini S, Della Giustina E, Frattini D, Scarano A, Neri G.
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| Am J Med Genet A 149A(6):1116-24. 2009
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| 28 | DEL14QP, FOXG1, RTTL1
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| Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature.
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| Jacob FD, Ramaswamy V, Andersen J, Bolduc FV.
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| Eur J Hum Genet 17(12):1577-81. Epub 2009 Jul 22. Review.PMID: 19623215 2009
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| 29 | DUP14QP, FOXG1
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| 4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment.
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| Yeung A, Bruno D, Scheffer IE, Carranza D, Burgess T, Slater HR, Amor DJ.
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| Eur J Med Genet 52(6):440-2. Epub 2009 Sep 20.PMID: 19772934 2009
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| 30 | FOXD1, FOXG1
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| Functional mode of FoxD1/CBF2 for the establishment of temporal retinal specificity in the developing chick retina.
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| Takahashi H, Sakuta H, Shintani T, Noda M.
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| Dev Biol 331(2):300-10. Epub 2009 May 18.
2009
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| 31 | FOXG1, RTTL1
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| FOXG1 is responsible for the congenital variant of Rett syndrome.
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| Ariani F, Hayek G, Rondinella D, Artuso R, Mencarelli MA, Spanhol-Rosseto A, Pollazzon M, Buoni S, Spiga O, Ricciardi S, Meloni I, Longo I, Mari F, Broccoli V, Zappella M, Renieri A.
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| Am J Hum Genet 83(1):89-93. Epub 2008 Jun 19. 2008
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| 32 | AR, FOXG1
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| FoxG1, a member of the forkhead family, is a corepressor of the androgen receptor.
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| Obendorf M, Meyer R, Henning K, Mitev YA, Schröder J, Patchev VK, Wolf SS.
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| J Steroid Biochem Mol Biol 104(3-5):195-207. Epub 2007 Mar 23.
2007
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| 33 | FOXG1
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| Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly.
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| Shoichet SA, Kunde SA, Viertel P, Schell-Apacik C, von Voss H, Tommerup N, Ropers HH, Kalscheuer VM.
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| Hum Genet 117(6):536-44. Epub 2005 Aug 17. 2005
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| 34 | FOXG1, KDM5B, PAX9
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| Human PLU-1 Has transcriptional repression properties and interacts with the developmental transcription factors BF-1 and PAX9.
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| Tan K, Shaw AL, Madsen B, Jensen K, Taylor-Papadimitriou J, Freemont PS.
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| J Biol Chem 278(23):20507-13. Epub 2003 Mar 25. 2003
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| 35 | FOXG1, SIK2
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| The new serine-threonine kinase, Qik, is a target of the Qin oncogene.
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| Xia Y, Zhang Z, Kruse U, Vogt PK, Li J.
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| Biochem Biophys Res Commun 276(2):564-70. 2000
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| 36 | FOXG1
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| The oncogene qin codes for a transcriptional repressor.
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| Li J, et al.
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| Cancer Res 55 : 5540-5544. 1995
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| 37 | FOXG1
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| The genes for human brain factor 1 and 2, members of the fork head gene family, are clustered on chromosome 14q.
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| Wiese S, et al.
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| Biochim Biophys Acta 1262 : 105-112. 1995
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| 38 | FOXG1
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| The human homologue of the retroviral oncogene qin maps to chromosome 14q13.
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| Kastury K, et al.
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| Proc Natl Acad Sci U S A 91 : 3616-3618. 1994
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| 39 | FOXG1
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| Human brain factor 1, a new member of the fork head gene family.
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| Murphy DB, et al.
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| Genomics 21 : 551-557. 1994
|