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Tochigi M, Iwamoto K, Bundo M, Sasaki T, Kato N, Kato T. “Gene Expression Profiling of Major Depression and Suicide in the Prefrontal Cortex of Postmortem Brains.” Neuroscience Research (February 2008): 184-191.

Kirshenbaum GS, Clapcote SJ, Petersen J, Vilsen B, Ralph MR, Roder JC. “Genetic Suppression of Agrin Reduces Mania-Like Behavior in Na+, K+-ATPase a3 Mutant Mice.” Genes Brain and Behavior (June 2012): 436-443.

Kirshenbaum GS, Dachtler J, Roder JC, Clapcote SJ. “Characterization of Cognitive Deficits in Mice with an Alternating Hemiplegia-linked Mutation.” Behavioral Neuroscience (2015): 822–831.

Kirshenbaum GS, Dachtler J, Roder JC, Clapcote SJ. “Transgenic Rescue of Phenotypic Deficits in a Mouse Model of Alternating Hemiplegia of Childhood.” Neurogenetics (2016): 57–63.
Kirshenbaum, GS, Dawson, N, Mullins, JG, Johnston, TH, Drinkhill, MJ, Edwards, IJ, Fox SH, Pratt, JA, Brotchie, JM, Roder, JC, Clapcote, SJ. “Alternating Hemiplegia of Childhood-Related Neural and Behavioural Phenotypes in Na+K+-ATPase a3 Missense Mutant Mice.” PLos ONE 2013; 8(3).

Kirshenbaum GS, Idris NF, Dachtler J, Roder JC, Clapcote SJ. “Deficits in Social Behavioral Tests in a Mouse Model of Alternating Hemiplegia of Childhood.” J Neurogenet. 2016 Mar 30; 8(3): 42-49.

Kirshenbaum GS, Saltzman K, Rose B, Petersen J, Vilsen B, Roder JC. “Decreased Neuronal Na+, K+ -ATPase Activity in Atp1a3 Heterozygous Mice Increases Susceptibility to Depression-like Endophenotypes by Chronic Variable Stress.” Genes Brain Behav. 2011 Jul; 10(5): 542550.

Brashear A, Cook JF, Hill DF, Amonsah A, Snively BM, Light L, Boggs N, Suerken CK, Stacy M, Ozelius L, Sweadner KJ, McCall WV. “Psychiatric Disorders in Rapid-Onset Dystonia Parkinsonism.” Neurology (September 11, 2012): 1168-1173.

Chaumette B, Ferrafiat V, Ambalavanan A, Goldenberg A, Dionne-Laporte A, Spiegelman D, Dion PA, Gerardin P, Laurent C, Cohen D, Rapoport J, Rouleau GA. “Missense Variants in ATP1A3 and FXYD Gene Family are Associated with Childhood-onset Schizophrenia.” Molecular Psychiatry. 2018 Jun 12. Abstract: https://www.nature.com/articles/s41380-018-0103-8

Holm TH, Isaksen TJ, Clerup S, Heuck A, Nissen P, Lykke-Hartmann K. “Cognitive Deficits Caused by a Disease-Mutation in the a3 Na(+)/K(+)-ATPase Isoform.” Scientific Reports (August 23, 2016).

Hunanyan Aresn, Fainberg N, Linabarger M, Arehart E, Leonard A, Adil S, Mikati M. “Knock-in Mouse Model of Alternating Hemiplegia of Childhood: Behavioral and Electrophysiologic Characterization.” Epilepsia. 2015 Jan; 56(1): 82-93.