Citations (21)
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Ting Lu, Jie Yang, Lijun Luo & Dongsheng Wei. (2022) FUS mutations in Asian amyotrophic lateral sclerosis patients: a case report and literature review of genotype-phenotype correlations. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 23:7-8, pages 580-584.
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Zhang-Yu Zou, Chun-Hui Che, Shu-Yan Feng, Xiu-Ying Fang, Hua-Pin Huang & Chang-Yun Liu. (2021) Novel FUS mutation Y526F causing rapidly progressive familial amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 22:1-2, pages 73-79.
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Jianing Lin, Weineng Chen, Pian Huang, Youna Xie, Minying Zheng & Xiaoli Yao. (2021) The distinct manifestation of young-onset amyotrophic lateral sclerosis in China. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 22:1-2, pages 30-37.
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Articles from other publishers (18)
Siwei Chu, Xinyi Xie, Carla Payan & Ursula Stochaj. (2023) Valosin containing protein (VCP): initiator, modifier, and potential drug target for neurodegenerative diseases. Molecular Neurodegeneration 18:1.
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Alberto A Zambon, Veronica Pini, Luca Bosco, Yuri M Falzone, Pinki Munot, Francesco Muntoni & Stefano C Previtali. (2023)
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Maurizio GrassanoGiorgia BrodiniGiovanni De MarcoFederico CasaleGiuseppe FudaPaolina SalamoneMaura BrunettiLuca SbaizSalvatore GallonePaolo CugnascoAlessandro BombaciRosario VastaUmberto ManeraAntonio CanosaCristina MogliaAndrea CalvoBryan J. TraynorAdriano Chio. (2022) Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis. Neurology Genetics 8:5.
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Ilaria Martinelli, Elisabetta Zucchi, Viviana Pensato, Cinzia Gellera, Bryan J Traynor, Giulia Gianferrari, Adriano Chiò & Jessica Mandrioli. (2022) G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlation. Neurobiology of Aging 118, pages 124-128.
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Fanxi Xu, Sen Huang, Xu-Ying Li, Jianing Lin, Xiuli Feng, Shu Xie, Zhanjun Wang, Xian Li, Junge Zhu, Hong Lai, Yanming Xu, Xusheng Huang, Xiaoli Yao & Chaodong Wang. (2022) Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China. BMC Medical Genomics 15:1.
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Brigid K. Jensen, Kevin J. McAvoy, Nicolette M. Heinsinger, Angelo C. Lepore, Hristelina Ilieva, Aaron R. Haeusler, Davide Trotti & Piera Pasinelli. (2022) Targeting TNFα produced by astrocytes expressing amyotrophic lateral sclerosis‐linked mutant fused in sarcoma prevents neurodegeneration and motor dysfunction in mice. Glia 70:7, pages 1426-1449.
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Hyoung Won Choi. (2021) Fasciculations in Children. Pediatric Neurology 125, pages 40-47.
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Kathryn Volkening, Sali M. K. Farhan, Jessica Kao, Cheryl Leystra-Lantz, Lee Cyn Ang, Adam McIntyre, Jian Wang, Robert A. Hegele & Michael J. Strong. (2021) Evidence of synergism among three genetic variants in a patient with LMNA-related lipodystrophy and amyotrophic lateral sclerosis leading to a remarkable nuclear phenotype. Molecular and Cellular Biochemistry 476:7, pages 2633-2650.
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L. Chen. (2021) FUS mutation is probably the most common pathogenic gene for JALS, especially sporadic JALS. Revue Neurologique 177:4, pages 333-340.
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Li Chen, Yali Wang & Jie Xie. (2020) 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. Frontiers in Cellular Neuroscience 14.
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Vincent Picher-Martel, Francis BrunetNicolas Dupré & Nicolas Chrestian. (2020) The Occurrence of FUS Mutations in Pediatric Amyotrophic Lateral Sclerosis: A Case Report and Review of the Literature. Journal of Child Neurology 35:8, pages 556-562.
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Owen Connolly, Laura Le Gall, Gavin McCluskey, Colette G Donaghy, William J Duddy & Stephanie Duguez. (2020) A Systematic Review of Genotype–Phenotype Correlation across Cohorts Having Causal Mutations of Different Genes in ALS. Journal of Personalized Medicine 10:3, pages 58.
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Zhi-Jun Liu, Hui-Xia Lin, Qiao Wei, Qi-Jie Zhang, Cong-Xin Chen, Qing-Qing Tao, Gong-Lu Liu, Wang Ni, Aaron D Gitler, Hong-Fu Li & Zhi-Ying Wu. (2019) Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis. Aging and disease 10:6, pages 1199.
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Xiaolu Liu, Ji He, Fen-Biao Gao, Aaron D. Gitler & Dongsheng Fan. (2018) The epidemiology and genetics of Amyotrophic lateral sclerosis in China. Brain Research 1693, pages 121-126.
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