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Sweney MT, Silver K, Gerard-Blanluet M, Pedespan JM, Renault F, Arzimanoglou A, Schlesinger-Massart M, Lewelt AJ, Reyna SP, Swoboda KJ. “Alternating Hemiplegia of Childhood: Early Characteristics and Evolution of a Neurodevelopmental Syndrome.” Pediatrics 123, no. 3 (March 2009): e534-541.

Kirshenbaum GS, Clapcote SJ, Duffy S, Burgess CR, Petersen J, Jarowek KJ, Yucel YH, Cortez MA, Snead OC 3rd, Vilsen B, Peever, JH, Ralph MR, Roder JC. “Mania-like Behavior Induced by Genetic Dysfunction of the Neuron-specific Na+,K+-ATPase α3 Sodium Pump.” Proc Natl Acad Sci U S A. 2011 Nov 1; 108(44): 18144-18149.

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).