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Molecular Neurobiology|October 14, 2018
Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor CasesJean-François Schmouth, Gabrielle Houle, Amirthagowri Ambalavanan, et al.Sleep Medicine|August 24, 2015
Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndromeZiv Gan-Or, Sirui Zhou, Amirthagowri Ambalavanan, et al.Communications Biology|September 12, 2019
Social and non-social autism symptoms and trait domains are genetically dissociableVarun Warrier, Roberto Toro, Hyejung Won, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 4, 2017
Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian populationGabrielle Houle, Jean-François Schmouth, Claire S Leblond, et al.Journal of Medicinal Chemistry|August 1, 1981
Synthesis and antiviral activity of certain 9-beta-D-ribofuranosylpurine-6-carboxamidesJ D Westover, G R Revankar, R K Robins, et al.Journal of the American College of Cardiology|July 2, 2013
Survival after shock therapy in implantable cardioverter-defibrillator and cardiac resynchronization therapy-defibrillator recipients according to rhythm shocked. The ALTITUDE survival by rhythm studyBrian D Powell, Leslie A Saxon, John P Boehmer, et al.Canadian Journal of Public Health = Revue Canadienne De Sante Publique|November 13, 2001
Improving the time to diagnosis after an abnormal screening mammogramI A Olivotto, M J Borugian, L Kan, et al.Neurobiology of Aging|October 24, 2015
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosisClaire S Leblond, Ziv Gan-Or, Dan Spiegelman, et al.Neurology. Genetics|December 26, 2018
No rare deleterious variants from STK32B, PPARGC1A, and CTNNA3 are associated with essential tremorGabrielle Houle, Amirthagowri Ambalavanan, Jean-François Schmouth, et al.Scientific Reports|January 16, 2019
Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutationsLaura Gouder, Aline Vitrac, Hany Goubran-Botros, et al.Pageof 29