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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|November 6, 2019
Molecular Mechanisms and Therapeutics for SBMA/Kennedy's DiseaseFrederick J Arnold, Diane E MerryScience (New York, N.Y.)|February 5, 2026
Pinpointing protein as the problemFrederick J Arnold, Albert R La SpadaScientific Reports|January 16, 2019
Impaired Nuclear Export of Polyglutamine-Expanded Androgen Receptor in Spinal and Bulbar Muscular AtrophyFrederick J Arnold, Anna Pluciennik, Diane E MerryJCI Insight|March 7, 2024
Differentially disrupted spinal cord and muscle energy metabolism in spinal and bulbar muscular atrophyDanielle DeBartolo, Frederick J Arnold, Yuhong Liu, et al.International Journal of Molecular Sciences|June 19, 2024
Revisiting Glutamate Excitotoxicity in Amyotrophic Lateral Sclerosis and Age-Related NeurodegenerationFrederick J Arnold, Alexandra F Putka, Urmimala Raychaudhuri, et al.Nature Communications|February 3, 2023
Alternative polyadenylation transcriptome-wide association study identifies APA-linked susceptibility genes in brain disordersYa Cui, Frederick J Arnold, Fanglue Peng, et al.The Journal of Clinical Investigation|November 10, 2020
Deubiquitinase USP7 contributes to the pathogenicity of spinal and bulbar muscular atrophyAnna Pluciennik, Yuhong Liu, Elana Molotsky, et al.Nature Genetics|January 14, 2025
Multi-omic quantitative trait loci link tandem repeat size variation to gene regulation in human brainYa Cui, Frederick J Arnold, Jason Sheng Li, et al.Acta Neuropathologica Communications|October 16, 2023
Senataxin helicase, the causal gene defect in ALS4, is a significant modifier of C9orf72 ALS G4C2 and arginine-containing dipeptide repeat toxicityCraig L Bennett, Somasish Dastidar, Frederick J Arnold, et al.Biorxiv : the Preprint Server for Biology|February 8, 2024
TDP-43 dysregulation of polyadenylation site selection is a defining feature of RNA misprocessing in ALS/FTD and related disordersFrederick J Arnold, Ya Cui, Sebastian Michels, et al.Pageof 2