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Acta Neuropathologica|October 29, 2018
C9orf72-FTD/ALS pathogenesis: evidence from human neuropathological studiesSarat C Vatsavayai, Alissa L Nana, Jennifer S Yokoyama, et al.Brain Research Bulletin|March 14, 2007
Abnormal cortical synaptic plasticity in a mouse model of Huntington's diseaseDamian M Cummings, Austen J Milnerwood, Glenn M Dallérac, et al.Brain Research Bulletin|March 14, 2007
Progressive CAG expansion in the brain of a novel R6/1-89Q mouse model of Huntington's disease with delayed phenotypic onsetSarat C Vatsavayai, Glenn M Dallérac, Austen J Milnerwood, et al.Human Molecular Genetics|August 15, 2006
Aberrant cortical synaptic plasticity and dopaminergic dysfunction in a mouse model of Huntington's diseaseDamian M Cummings, Austen J Milnerwood, Glenn M Dallérac, et al.Human Molecular Genetics|April 8, 2006
Early development of aberrant synaptic plasticity in a mouse model of Huntington's diseaseAusten J Milnerwood, Damian M Cummings, Glenn M Dallérac, et al.Frontiers in Neuroscience|October 18, 2023
Loss of TDP-43 function contributes to genomic instability in amyotrophic lateral sclerosisMinggang Fang, Sara K Deibler, Alissa L Nana, et al.Elife|January 11, 2017
Suppression of C9orf72 RNA repeat-induced neurotoxicity by the ALS-associated RNA-binding protein Zfp106Barbara Celona, John von Dollen, Sarat C Vatsavayai, et al.Neuro-Degenerative Diseases|April 15, 2015
Dysfunctional Dopaminergic Neurones in Mouse Models of Huntington's Disease: A Role for SK3 ChannelsGlenn M Dallérac, Grégoire Levasseur, Sarat C Vatsavayai, et al.Acta Neuropathologica|December 5, 2022
Tuberous sclerosis complex is associated with a novel human tauopathyJi-Hye L Hwang, Olga S Perloff, Stephanie E Gaus, et al.Biorxiv : the Preprint Server for Biology|September 15, 2025
Cryptic splicing in synaptic and membrane excitability genes links TDP-43 loss to neuronal dysfunctionCaiwei Guo, Kuchuan Chen, Sarat C Vatsavayai, et al.Pageof 2