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The Journal of Clinical Investigation|February 11, 2014
ALS-associated mutation FUS-R521C causes DNA damage and RNA splicing defectsHaiyan Qiu, Sebum Lee, Yulei Shang, et al.Journal of Molecular Biology|January 23, 2023
Phase Separation in Biology and Disease; Current Perspectives and Open QuestionsSteven Boeynaems, Shasha Chong, Jörg Gsponer, et al.Acta Neuropathologica|March 31, 2023
C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTDPedro Ervilha Pereira, Nika Schuermans, Antoon Meylemans, et al.Neuron|October 8, 2019
CRISPR-Cas9 Screens Identify the RNA Helicase DDX3X as a Repressor of C9ORF72 (GGGGCC)n Repeat-Associated Non-AUG TranslationWeiwei Cheng, Shaopeng Wang, Zhe Zhang, et al.Molecular Cell|March 3, 2018
FUS Regulates Activity of MicroRNA-Mediated Gene SilencingTao Zhang, Yen-Ching Wu, Patrick Mullane, et al.Neuron|March 4, 2019
RNA Binding Antagonizes Neurotoxic Phase Transitions of TDP-43Jacob R Mann, Amanda M Gleixner, Jocelyn C Mauna, et al.Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
FUS Mislocalization Rewires a Cortical Gene Network to Drive Cognitive and Behavioral Impairment in ALSRaphaelle Cassel, Félicie Lorenc, Aurélie Bombardier, et al.Science Translational Medicine|September 4, 2020
<i>C9orf72</i> poly(GR) aggregation induces TDP-43 proteinopathyCasey N Cook, Yanwei Wu, Hana M Odeh, et al.Cell|April 21, 2018
Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like DomainsLin Guo, Hong Joo Kim, Hejia Wang, et al.JCI Insight|July 22, 2021
Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentationDanique Beijer, Hong Joo Kim, Lin Guo, et al.Pageof 19