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Plos Genetics|February 6, 2023
Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoidsYoshitaka Tamaki, Jay P Ross, Paria Alipour, et al.
Neurobiology of Disease|March 10, 2005
Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in micePatrick Dion, Vijayalakshmi Shanmugam, Claudia Gaspar, et al.
Human Molecular Genetics|February 17, 2012
Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron modelsShawn J Stochmanski, Martine Therrien, Janet Laganière, et al.
Frontiers in Genetics|December 12, 2019
Investigation of the RFC1 Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel ConformationsFulya Akçimen, Jay P Ross, Cynthia V Bourassa, et al.
Neurobiology of Aging|January 1, 2013
Investigation of C9orf72 repeat expansions in Parkinson's diseaseHussein Daoud, Anne Noreau, Daniel Rochefort, et al.
European Journal of Human Genetics : EJHG|July 23, 2015
Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosumLoubna Jouan, Bouchra Ouled Amar Bencheikh, Hussein Daoud, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2020
Multiomics Analyses Identify Genes and Pathways Relevant to Essential TremorCalwing Liao, Faezeh Sarayloo, Daniel Rochefort, et al.
Science (New York, N.Y.)|May 1, 2010
Mutations in DCC cause congenital mirror movementsMyriam Srour, Jean-Baptiste Rivière, Jessica M T Pham, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 1, 2018
Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in malesAmirthagowri Ambalavanan, Boris Chaumette, Sirui Zhou, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 17, 2012
Loss of neuronal potassium/chloride cotransporter 3 (KCC3) is responsible for the degenerative phenotype in a conditional mouse model of hereditary motor and sensory neuropathy associated with agenesis of the corpus callosumMasoud Shekarabi, Randal X Moldrich, Sarah Rasheed, et al.
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