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For: Wong LC, Singh S, Wang HP, Hsu CJ, Hu SC, Lee WT. FOXG1-Related Syndrome: From Clinical to Molecular Genetics and Pathogenic Mechanisms. Int J Mol Sci 2019;20:E4176. [PMID: 31454984 DOI: 10.3390/ijms20174176] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 4.7] [Reference Citation Analysis]
Number Citing Articles
1 Jang HN, Kim T, Jung AY, Lee BH, Yum MS, Ko TS. Identification of FOXG1 mutations in infantile hypotonia and postnatal microcephaly. Medicine (Baltimore) 2021;100:e27949. [PMID: 34964776 DOI: 10.1097/MD.0000000000027949] [Reference Citation Analysis]
2 Yang H, Ryu J, Lim C, Choi JW, Park YJ, Jang SW, Shim S. SOXE group transcription factors regulates the expression of FoxG1 during inner ear development. Biochem Biophys Res Commun 2022;623:96-103. [PMID: 35878429 DOI: 10.1016/j.bbrc.2022.07.048] [Reference Citation Analysis]
3 Pecora G, Sortino V, Brafa Musicoro V, Salomone G, Pizzo F, Costanza G, Falsaperla R, Zanghì A, Praticò AD. FOXG1 Gene and Its Related Phenotypes. Journal of Pediatric Neurology. [DOI: 10.1055/s-0041-1727270] [Reference Citation Analysis]
4 Waite AJ, Millar D, Clarke A. The generation of an induced pluripotent stem cell line (DCGi001-A) from an individual with FOXG1 syndrome carrying the c.460dupG (p.Glu154fs) variation in the FOXG1 gene. Stem Cell Res 2020;49:102018. [PMID: 33096386 DOI: 10.1016/j.scr.2020.102018] [Reference Citation Analysis]
5 Dai S, Li J, Zhang H, Chen X, Guo M, Chen Z, Chen Y. Structural Basis for DNA Recognition by FOXG1 and the Characterization of Disease-causing FOXG1 Mutations. J Mol Biol 2020;432:6146-56. [PMID: 33058871 DOI: 10.1016/j.jmb.2020.10.007] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
6 Fardghassemi Y, Parker JA. Overexpression of FKH-2/FOXG1 is neuroprotective in a C. elegans model of Machado-Joseph disease. Exp Neurol 2021;337:113544. [PMID: 33290777 DOI: 10.1016/j.expneurol.2020.113544] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Fahmi M, Yasui G, Seki K, Katayama S, Kaneko-Kawano T, Inazu T, Kubota Y, Ito M. In Silico Study of Rett Syndrome Treatment-Related Genes, MECP2, CDKL5, and FOXG1, by Evolutionary Classification and Disordered Region Assessment. Int J Mol Sci 2019;20:E5593. [PMID: 31717404 DOI: 10.3390/ijms20225593] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
8 Akaba Y, Takahashi S, Takeguchi R, Tanaka R, Nabatame S, Saitsu H, Matsumoto N. Phenotypic overlap between pyruvate dehydrogenase complex deficiency and FOXG1 syndrome. Clin Case Rep 2021;9:1711-5. [PMID: 33768920 DOI: 10.1002/ccr3.3883] [Reference Citation Analysis]
9 Sharma A, Madaan P, Vyas S, Sankhyan N. FOXG1 variant presenting as unexplained irritability and peculiar crying spells. Seizure 2021;93:32-3. [PMID: 34656939 DOI: 10.1016/j.seizure.2021.10.006] [Reference Citation Analysis]
10 Lottini G, Baggiani M, Chesi G, D'Orsi B, Quaranta P, Lai M, Pancrazi L, Onorati M, Pistello M, Freer G, Costa M. Zika virus induces FOXG1 nuclear displacement and downregulation in human neural progenitors. Stem Cell Reports 2022:S2213-6711(22)00261-2. [PMID: 35714598 DOI: 10.1016/j.stemcr.2022.05.008] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Wilpert NM, Marguet F, Maillard C, Guimiot F, Martinovic J, Drunat S, Attié-Bitach T, Razavi F, Tessier A, Capri Y, Laquerrière A, Bahi-Buisson N. Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndrome. Eur J Med Genet 2021;64:104282. [PMID: 34284163 DOI: 10.1016/j.ejmg.2021.104282] [Reference Citation Analysis]
12 Miyoshi G, Ueta Y, Natsubori A, Hiraga K, Osaki H, Yagasaki Y, Kishi Y, Yanagawa Y, Fishell G, Machold RP, Miyata M. FoxG1 regulates the formation of cortical GABAergic circuit during an early postnatal critical period resulting in autism spectrum disorder-like phenotypes. Nat Commun 2021;12:3773. [PMID: 34145239 DOI: 10.1038/s41467-021-23987-z] [Reference Citation Analysis]
13 Xiol C, Heredia M, Pascual-Alonso A, Oyarzabal A, Armstrong J. Technological Improvements in the Genetic Diagnosis of Rett Syndrome Spectrum Disorders. Int J Mol Sci 2021;22:10375. [PMID: 34638716 DOI: 10.3390/ijms221910375] [Reference Citation Analysis]
14 Santos-Terra J, Deckmann I, Fontes-Dutra M, Schwingel GB, Bambini-Junior V, Gottfried C. Transcription factors in neurodevelopmental and associated psychiatric disorders: A potential convergence for genetic and environmental risk factors. Int J Dev Neurosci 2021. [PMID: 34240460 DOI: 10.1002/jdn.10141] [Reference Citation Analysis]
15 Li H, Li QQ, Hong Y. Global gene expression signatures in response to citrate-coated silver nanoparticles exposure. Toxicology 2021;461:152898. [PMID: 34403730 DOI: 10.1016/j.tox.2021.152898] [Reference Citation Analysis]
16 Tascini G, Dell'Isola GB, Mencaroni E, Di Cara G, Striano P, Verrotti A. Sleep Disorders in Rett Syndrome and Rett-Related Disorders: A Narrative Review. Front Neurol 2022;13:817195. [PMID: 35299616 DOI: 10.3389/fneur.2022.817195] [Reference Citation Analysis]