Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
Kaneb, Hannah M, Folkmann, Andrew W, Belzil, Véronique V, Jao, Li-En, Leblond, Claire S, Girard, Simon L, Daoud, Hussein, Noreau, Anne, Rochefort, Daniel, Hince, Pascale, Szuto, Anna, Levert, Annie, Vidal, Sabrina, André-Guimont, Catherine, Camu, William, Bouchard, Jean-Pierre, Dupré, Nicolas, Rouleau, Guy A, Wente, Susan R, Dion, Patrick A
Published in Human molecular genetics (01.03.2015)
Published in Human molecular genetics (01.03.2015)
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Journal Article
Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor
Merner, Nancy D., Girard, Simon L., Catoire, Hélène, Bourassa, Cynthia V., Belzil, Véronique V., Rivière, Jean-Baptiste, Hince, Pascale, Levert, Annie, Dionne-Laporte, Alexandre, Spiegelman, Dan, Noreau, Anne, Diab, Sabrina, Szuto, Anna, Fournier, Hélène, Raelson, John, Belouchi, Majid, Panisset, Michel, Cossette, Patrick, Dupré, Nicolas, Bernard, Geneviève, Chouinard, Sylvain, Dion, Patrick A., Rouleau, Guy A.
Published in American journal of human genetics (10.08.2012)
Published in American journal of human genetics (10.08.2012)
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Journal Article
Genetic analysis of SIGMAR1 as a cause of familial ALS with dementia
Belzil, Véronique V, Daoud, Hussein, Camu, William, Strong, Michael J, Dion, Patrick A, Rouleau, Guy A
Published in European journal of human genetics : EJHG (01.02.2013)
Published in European journal of human genetics : EJHG (01.02.2013)
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Journal Article
Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis
Belzil, Véronique V, Daoud, Hussein, Desjarlais, Anne, Bouchard, Jean-Pierre, Dupré, Nicolas, Camu, William, Dion, Patrick A, Rouleau, Guy A
Published in Neurobiology of aging (01.03.2011)
Published in Neurobiology of aging (01.03.2011)
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Journal Article
Familial ALS: less common than we think?
Belzil, Véronique V, Rouleau, Guy A
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2012)
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2012)
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Journal Article
Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis
Belzil, Véronique V, St-Onge, Judith, Daoud, Hussein, Desjarlais, Anne, Bouchard, Jean-Pierre, Dupré, Nicolas, Camu, William, Dion, Patrick A, Rouleau, Guy A
Published in Journal of human genetics (01.03.2011)
Published in Journal of human genetics (01.03.2011)
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Journal Article
Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis
Belzil, Véronique V, André-Guimont, Catherine, Atallah, Marie-Renée, Daoud, Hussein, Dupré, Nicolas, Bouchard, Jean-Pierre, Camu, William, Dion, Patrick A, Rouleau, Guy A
Published in Neurobiology of aging (01.08.2012)
Published in Neurobiology of aging (01.08.2012)
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Journal Article
Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation
Camdessanché, Jean-Philippe, Belzil, Véronique V, Jousserand, Guillemette, Rouleau, Guy A, Créac'h, Christelle, Convers, Philippe, Antoine, Jean-Christophe
Published in Orphanet journal of rare diseases (05.02.2011)
Published in Orphanet journal of rare diseases (05.02.2011)
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Journal Article
SOD1 mutations: more to learn
Belzil, Véronique V, Rouleau, Guy A
Published in Canadian journal of neurological sciences (01.03.2012)
Published in Canadian journal of neurological sciences (01.03.2012)
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Journal Article
Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress
Zhang, Yong-Jie, Jansen-West, Karen, Xu, Ya-Fei, Gendron, Tania F., Bieniek, Kevin F., Lin, Wen-Lang, Sasaguri, Hiroki, Caulfield, Thomas, Hubbard, Jaime, Daughrity, Lillian, Chew, Jeannie, Belzil, Veronique V., Prudencio, Mercedes, Stankowski, Jeannette N., Castanedes-Casey, Monica, Whitelaw, Ena, Ash, Peter E. A., DeTure, Michael, Rademakers, Rosa, Boylan, Kevin B., Dickson, Dennis W., Petrucelli, Leonard
Published in Acta neuropathologica (01.10.2014)
Published in Acta neuropathologica (01.10.2014)
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Journal Article
Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood
Belzil, Veronique V., Bauer, Peter O., Prudencio, Mercedes, Gendron, Tania F., Stetler, Caroline T., Yan, Irene K., Pregent, Luc, Daughrity, Lillian, Baker, Matthew C., Rademakers, Rosa, Boylan, Kevin, Patel, Tushar C., Dickson, Dennis W., Petrucelli, Leonard
Published in Acta neuropathologica (01.12.2013)
Published in Acta neuropathologica (01.12.2013)
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Journal Article
ADAR2 mislocalization and widespread RNA editing aberrations in C9orf72-mediated ALS/FTD
Moore, Stephen, Alsop, Eric, Lorenzini, Ileana, Starr, Alexander, Rabichow, Benjamin E., Mendez, Emily, Levy, Jennifer L., Burciu, Camelia, Reiman, Rebecca, Chew, Jeannie, Belzil, Veronique V., W. Dickson, Dennis, Robertson, Janice, Staats, Kim A., Ichida, Justin K., Petrucelli, Leonard, Van Keuren-Jensen, Kendall, Sattler, Rita
Published in Acta neuropathologica (01.07.2019)
Published in Acta neuropathologica (01.07.2019)
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Journal Article
Divergent single cell transcriptome and epigenome alterations in ALS and FTD patients with C9orf72 mutation
Li, Junhao, Jaiswal, Manoj K., Chien, Jo-Fan, Kozlenkov, Alexey, Jung, Jinyoung, Zhou, Ping, Gardashli, Mahammad, Pregent, Luc J., Engelberg-Cook, Erica, Dickson, Dennis W., Belzil, Veronique V., Mukamel, Eran A., Dracheva, Stella
Published in Nature communications (15.09.2023)
Published in Nature communications (15.09.2023)
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Journal Article
ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19
Takahashi, Yuji, Fukuda, Yoko, Yoshimura, Jun, Toyoda, Atsushi, Kurppa, Kari, Moritoyo, Hiroyoko, Belzil, Veronique V., Dion, Patrick A., Higasa, Koichiro, Doi, Koichiro, Ishiura, Hiroyuki, Mitsui, Jun, Date, Hidetoshi, Ahsan, Budrul, Matsukawa, Takashi, Ichikawa, Yaeko, Moritoyo, Takashi, Ikoma, Mayumi, Hashimoto, Tsukasa, Kimura, Fumiharu, Murayama, Shigeo, Onodera, Osamu, Nishizawa, Masatoyo, Yoshida, Mari, Atsuta, Naoki, Sobue, Gen, Fifita, Jennifer A., Williams, Kelly L., Blair, Ian P., Nicholson, Garth A., Gonzalez-Perez, Paloma, Brown, Robert H., Nomoto, Masahiro, Elenius, Klaus, Rouleau, Guy A., Fujiyama, Asao, Morishita, Shinichi, Goto, Jun, Tsuji, Shoji
Published in American journal of human genetics (07.11.2013)
Published in American journal of human genetics (07.11.2013)
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Journal Article
Prognostic Factors and Epidemiology of Amyotrophic Lateral Sclerosis in Southeastern United States
Engelberg-Cook, Erica, Shah, Jaimin S., Teixeira da Silva Hucke, Andre, Vera-Garcia, Diana V., Dagher, Jany E., Donahue, Megan H., Belzil, Veronique V., Oskarsson, Björn
Published in Mayo Clinic proceedings. Innovations, quality & outcomes (01.10.2024)
Published in Mayo Clinic proceedings. Innovations, quality & outcomes (01.10.2024)
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Journal Article
A mutation in the RNF170 gene causes autosomal dominant sensory ataxia
VALDMANIS, Paul N, DUPRE, Nicolas, SAMUELS, Mark E, ROULEAU, Guy A, LACHANCE, Mathieu, STOCHMANSKI, Shawn J, BELZIL, Veronique V, DION, Patrick A, THIFFAULT, Isabelle, BRAIS, Bernard, WESTON, Lyle, SAINT-AMANT, Louis
Published in Brain (London, England : 1878) (01.02.2011)
Published in Brain (London, England : 1878) (01.02.2011)
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Journal Article
ALS and FTD: an epigenetic perspective
Belzil, Veronique V., Katzman, Rebecca B., Petrucelli, Leonard
Published in Acta Neuropathologica (01.10.2016)
Published in Acta Neuropathologica (01.10.2016)
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Journal Article
Book Review
Mechanisms of toxicity in C9FTLD/ALS
Gendron, Tania F., Belzil, Veronique V., Zhang, Yong-Jie, Petrucelli, Leonard
Published in Acta neuropathologica (01.03.2014)
Published in Acta neuropathologica (01.03.2014)
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Journal Article
RNA-mediated toxicity in neurodegenerative disease
Belzil, Veronique V., Gendron, Tania F., Petrucelli, Leonard
Published in Molecular and cellular neuroscience (01.09.2013)
Published in Molecular and cellular neuroscience (01.09.2013)
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Journal Article