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For: Ma L, Shi Y, Chen Z, Li S, Zhang J. A novel SETX gene mutation associated with Juvenile amyotrophic lateral sclerosis. Brain Behav 2018;8:e01066. [PMID: 30052327 DOI: 10.1002/brb3.1066] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
Number Citing Articles
1 Lei L, Chen H, Lu Y, Zhu W, Ouyang Y, Duo J, Chen Z, Da Y. Unusual electrophysiological findings in a Chinese ALS 4 family with SETX-L389S mutation: a three-year follow-up. J Neurol 2021;268:1050-8. [PMID: 32997296 DOI: 10.1007/s00415-020-10246-2] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Chen L. FUS mutation is probably the most common pathogenic gene for JALS, especially sporadic JALS. Rev Neurol (Paris) 2021;177:333-40. [PMID: 33036763 DOI: 10.1016/j.neurol.2020.06.010] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Provasek VE, Mitra J, Malojirao VH, Hegde ML. DNA Double-Strand Breaks as Pathogenic Lesions in Neurological Disorders. Int J Mol Sci 2022;23:4653. [PMID: 35563044 DOI: 10.3390/ijms23094653] [Reference Citation Analysis]
4 Choi HW. Fasciculations in Children. Pediatr Neurol 2021;125:40-7. [PMID: 34628142 DOI: 10.1016/j.pediatrneurol.2021.08.008] [Reference Citation Analysis]
5 Chen L, Wang Y, Xie J. A Human iPSC Line Carrying a de novo Pathogenic FUS Mutation Identified in a Patient With Juvenile ALS Differentiated Into Motor Neurons With Pathological Characteristics. Front Cell Neurosci 2020;14:273. [PMID: 33093822 DOI: 10.3389/fncel.2020.00273] [Reference Citation Analysis]
6 Hadjinicolaou A, Ngo KJ, Conway DY, Provias JP, Baker SK, Brady LI, Bennett CL, La Spada AR, Fogel BL, Yoon G. De novo pathogenic variant in SETX causes a rapidly progressive neurodegenerative disorder of early childhood-onset with severe axonal polyneuropathy. Acta Neuropathol Commun 2021;9:194. [PMID: 34922620 DOI: 10.1186/s40478-021-01277-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Balliu B, Durrant M, Goede O, Abell N, Li X, Liu B, Gloudemans MJ, Cook NL, Smith KS, Knowles DA, Pala M, Cucca F, Schlessinger D, Jaiswal S, Sabatti C, Lind L, Ingelsson E, Montgomery SB. Genetic regulation of gene expression and splicing during a 10-year period of human aging. Genome Biol 2019;20:230. [PMID: 31684996 DOI: 10.1186/s13059-019-1840-y] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 4.7] [Reference Citation Analysis]
8 Ma L, Shi Y, Chen Z, Li S, Zhang J. A novel SETX gene mutation associated with Juvenile amyotrophic lateral sclerosis. Brain Behav 2018;8:e01066. [PMID: 30052327 DOI: 10.1002/brb3.1066] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]