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Plos One|February 25, 2012
Mutant TDP-43 and FUS cause age-dependent paralysis and neurodegeneration in C. elegansAlexandra Vaccaro, Arnaud Tauffenberger, Dina Aggad, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 19, 2021
Genetics of primary lateral sclerosisVincenzo Silani, Philippe Corcia, Matthew B Harms, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 15, 2008
Lithium response and genetic variation in the CREB family of genesFiroza Mamdani, Martin Alda, Paul Grof, et al.Pediatric Neurology|August 1, 2014
Vanishing white matter disease in French-Canadian patients from QuebecMarie-Ève Robinson, Elsa Rossignol, Bernard Brais, et al.Human Molecular Genetics|June 5, 2003
Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform molesOsman El-Maarri, Muhieddine Seoud, Philippe Coullin, et al.Neuroscience Letters|May 8, 2020
Characterization of human iPSC-derived astrocytes with potential for disease modeling and drug discoveryVincent Soubannier, Gilles Maussion, Mathilde Chaineau, et al.European Journal of Human Genetics : EJHG|January 20, 2005
Patients with familial biparental hydatidiform moles have normal methylation at imprinted genesOsman El-Maarri, Muhieddine Seoud, Jean-Baptiste Rivière, et al.Brain Stimulation|November 1, 2011
Neurophysiological investigation of congenital mirror movements in a patient with agenesis of the corpus callosumJean-François Lepage, Vincent Beaulé, Myriam Srour, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 18, 2013
Genetic and epigenetic studies of amyotrophic lateral sclerosisAmmar Al-Chalabi, Shin Kwak, Mark Mehler, et al.Neurology|July 15, 2018
Valproic acid is protective in cellular and worm models of oculopharyngeal muscular dystrophyAida Abu-Baker, Alex Parker, Siriram Ramalingam, et al.Pageof 11