Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C. elegans
Therrien, Martine, Rouleau, Guy A, Dion, Patrick A, Parker, J Alex
Published in PloS one (12.12.2013)
Published in PloS one (12.12.2013)
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Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids
Tamaki, Yoshitaka, Ross, Jay P, Alipour, Paria, Castonguay, Charles-Étienne, Li, Boting, Catoire, Helene, Rochefort, Daniel, Urushitani, Makoto, Takahashi, Ryosuke, Sonnen, Joshua A, Stifani, Stefano, Dion, Patrick A, Rouleau, Guy A
Published in PLoS genetics (06.02.2023)
Published in PLoS genetics (06.02.2023)
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De novo mutations in moderate or severe intellectual disability
Hamdan, Fadi F, Srour, Myriam, Capo-Chichi, Jose-Mario, Daoud, Hussein, Nassif, Christina, Patry, Lysanne, Massicotte, Christine, Ambalavanan, Amirthagowri, Spiegelman, Dan, Diallo, Ousmane, Henrion, Edouard, Dionne-Laporte, Alexandre, Fougerat, Anne, Pshezhetsky, Alexey V, Venkateswaran, Sunita, Rouleau, Guy A, Michaud, Jacques L
Published in PLoS genetics (01.10.2014)
Published in PLoS genetics (01.10.2014)
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Global brain gene expression analysis links glutamatergic and GABAergic alterations to suicide and major depression
Sequeira, Adolfo, Mamdani, Firoza, Ernst, Carl, Vawter, Marquis P, Bunney, William E, Lebel, Veronique, Rehal, Sonia, Klempan, Tim, Gratton, Alain, Benkelfat, Chawki, Rouleau, Guy A, Mechawar, Naguib, Turecki, Gustavo
Published in PloS one (11.08.2009)
Published in PloS one (11.08.2009)
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Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes
Liao, Calwing, Laporte, Alexandre D, Spiegelman, Dan, Akçimen, Fulya, Joober, Ridha, Dion, Patrick A, Rouleau, Guy A
Published in Nature communications (01.10.2019)
Published in Nature communications (01.10.2019)
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A Population‐Based Assessment of Rates of Bone Loss at Multiple Skeletal Sites: Evidence for Substantial Trabecular Bone Loss in Young Adult Women and Men
Riggs, B Lawrence, Melton, L Joseph, Robb, Richard A, Camp, Jon J, Atkinson, Elizabeth J, McDaniel, Lisa, Amin, Shreyasee, Rouleau, Peggy A, Khosla, Sundeep
Published in Journal of bone and mineral research (01.02.2008)
Published in Journal of bone and mineral research (01.02.2008)
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FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis
Kabashi, Edor, Bercier, Valérie, Lissouba, Alexandra, Liao, Meijiang, Brustein, Edna, Rouleau, Guy A, Drapeau, Pierre
Published in PLoS genetics (01.08.2011)
Published in PLoS genetics (01.08.2011)
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The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force
Beaudin, Marie, Matilla-Dueñas, Antoni, Soong, Bing-Weng, Pedroso, Jose Luiz, Barsottini, Orlando G., Mitoma, Hiroshi, Tsuji, Shoji, Schmahmann, Jeremy D., Manto, Mario, Rouleau, Guy A, Klein, Christopher, Dupre, Nicolas
Published in Cerebellum (London, England) (01.12.2019)
Published in Cerebellum (London, England) (01.12.2019)
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Recessive mutations in >VPS13D cause childhood onset movement disorders
Gauthier, Julie, Meijer, Inge A., Lessel, Davor, Mencacci, Niccolò E., Krainc, Dimitri, Hempel, Maja, Tsiakas, Konstantinos, Prokisch, Holger, Rossignol, Elsa, Helm, Margaret H., Rodan, Lance H., Karamchandani, Jason, Carecchio, Miryam, Lubbe, Steven J., Telegrafi, Aida, Henderson, Lindsay B., Lorenzo, Kerry, Wallace, Stephanie E., Glass, Ian A., Hamdan, Fadi F., Michaud, Jacques L., Rouleau, Guy A., Campeau, Philippe M.
Published in Annals of neurology (01.06.2018)
Published in Annals of neurology (01.06.2018)
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A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia
Seixas, Ana I., Loureiro, Joana R., Costa, Cristina, Ordóñez-Ugalde, Andrés, Marcelino, Hugo, Oliveira, Cláudia L., Loureiro, José L., Dhingra, Ashutosh, Brandão, Eva, Cruz, Vitor T., Timóteo, Angela, Quintáns, Beatriz, Rouleau, Guy A., Rizzu, Patrizia, Carracedo, Ángel, Bessa, José, Heutink, Peter, Sequeiros, Jorge, Sobrido, Maria J., Coutinho, Paula, Silveira, Isabel
Published in American journal of human genetics (06.07.2017)
Published in American journal of human genetics (06.07.2017)
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Genetics of familial and sporadic amyotrophic lateral sclerosis
Gros-Louis, Francois, Gaspar, Claudia, Rouleau, Guy A.
Published in Biochimica et biophysica acta (01.11.2006)
Published in Biochimica et biophysica acta (01.11.2006)
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Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo
Kabashi, Edor, Lin, Li, Tradewell, Miranda L., Dion, Patrick A., Bercier, Valérie, Bourgouin, Patrick, Rochefort, Daniel, Bel Hadj, Samar, Durham, Heather D., Velde, Christine Vande, Rouleau, Guy A., Drapeau, Pierre
Published in Human molecular genetics (15.02.2010)
Published in Human molecular genetics (15.02.2010)
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Population‐Based Study of Age and Sex Differences in Bone Volumetric Density, Size, Geometry, and Structure at Different Skeletal Sites
Riggs, B Lawrence, Melton, L Joseph, Robb, Richard A, Camp, Jon J, Atkinson, Elizabeth J, Peterson, James M, Rouleau, Peggy A, McCollough, Cynthia H, Bouxsein, Mary L, Khosla, Sundeep
Published in Journal of bone and mineral research (01.12.2004)
Published in Journal of bone and mineral research (01.12.2004)
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Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations
Rudakou, Uladzislau, Yu, Eric, Krohn, Lynne, Ruskey, Jennifer A, Asayesh, Farnaz, Dauvilliers, Yves, Spiegelman, Dan, Greenbaum, Lior, Fahn, Stanley, Waters, Cheryl H, Dupré, Nicolas, Rouleau, Guy A, Hassin-Baer, Sharon, Fon, Edward A, Alcalay, Roy N, Gan-Or, Ziv
Published in Brain (London, England : 1878) (03.03.2021)
Published in Brain (London, England : 1878) (03.03.2021)
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KIF1A, an Axonal Transporter of Synaptic Vesicles, Is Mutated in Hereditary Sensory and Autonomic Neuropathy Type 2
Rivière, Jean-Baptiste, Ramalingam, Siriram, Lavastre, Valérie, Shekarabi, Masoud, Holbert, Sébastien, Lafontaine, Julie, Srour, Myriam, Merner, Nancy, Rochefort, Daniel, Hince, Pascale, Gaudet, Rébecca, Mes-Masson, Anne-Marie, Baets, Jonathan, Houlden, Henry, Brais, Bernard, Nicholson, Garth A., Van Esch, Hilde, Nafissi, Shahriar, De Jonghe, Peter, Reilly, Mary M., Timmerman, Vincent, Dion, Patrick A., Rouleau, Guy A.
Published in American journal of human genetics (12.08.2011)
Published in American journal of human genetics (12.08.2011)
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C9orf72 repeat expansions are a rare genetic cause of parkinsonism
LESAGE, Suzanne, LE BER, Isabelle, ROULEAU, Guy A, DÜRR, Alexandra, BRICE, Alexis, CONDROYER, Christel, BROUSSOLLE, Emmanuel, GABELLE, Audrey, THOBOIS, Stéphane, PASQUIER, Florence, MONDON, Karl, DION, Patrick A, ROCHEFORT, Daniel
Published in Brain (London, England : 1878) (01.02.2013)
Published in Brain (London, England : 1878) (01.02.2013)
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