Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids von 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

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Nuclear Receptor NR1H3 in Familial Multiple Sclerosis von Wang, Zhe, Sadovnick, A. Dessa, Traboulsee, Anthony L., Ross, Jay P., Bernales, Cecily Q., Encarnacion, Mary, Yee, Irene M., de Lemos, Madonna, Greenwood, Talitha, Lee, Joshua D., Wright, Galen, Ross, Colin J., Zhang, Si, Song, Weihong, Vilariño-Güell, Carles

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Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study von Alipour, Paria, Senkevich, Konstantin, Ross, Jay P, Spiegelman, Dan, Manousaki, Despoina, Dion, Patrick A, Rouleau, Guy A

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Investigation of the RFC1 Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations von Akçimen, Fulya, Ross, Jay P, Bourassa, Cynthia V, Liao, Calwing, Rochefort, Daniel, Gama, Maria Thereza Drumond, Dicaire, Marie-Josée, Barsottini, Orlando G, Brais, Bernard, Pedroso, José Luiz, Dion, Patrick A, Rouleau, Guy A

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Exome sequencing in genetic disease: recent advances and considerations [version 1; peer review: 2 approved] von Ross, Jay P, Dion, Patrick A, Rouleau, Guy A

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Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression von Sarayloo, Faezeh, Dionne-Laporte, Alexandre, Catoire, Helene, Rochefort, Daniel, Houle, Gabrielle, Ross, Jay P, Akçimen, Fulya, Barros Oliveira, Rachel De, Turecki, Gustavo, Dion, Patrick A, Rouleau, Guy A

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Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion von Spataro, Rossella, Kousi, Maria, Farhan, Sali M K, Willer, Jason R, Ross, Jay P, Dion, Patrick A, Rouleau, Guy A, Daly, Mark J, Neale, Benjamin M, La Bella, Vincenzo, Katsanis, Nicholas

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Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability von Schmilovich, Zoe, Bourque, Vincent-Raphaël, Douard, Elise, Huguet, Guillaume, Poulain, Cécile, Ross, Jay P, Alipour, Paria, Castonguay, Charles-Étienne, Younis, Nadine, Jean-Louis, Martineau, Saci, Zohra, Pausova, Zdenka, Paus, Tomas, Schuman, Gunter, Porteous, David, Davies, Gail, Redmond, Paul, Harris, Sarah E, Deary, Ian J, Whalley, Heather, Hayward, Caroline, Dion, Patrick A, Jacquemont, Sébastien, Rouleau, Guy A

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Nuclear Receptor NR1H3 in Familial Multiple Sclerosis von Wang, Zhe, Sadovnick, A. Dessa, Traboulsee, Anthony L., Ross, Jay P., Bernales, Cecily Q., Encarnacion, Mary, Yee, Irene M., de Lemos, Madonna, Greenwood, Talitha, Lee, Joshua D., Wright, Galen, Ross, Colin J., Zhang, Si, Song, Weihong, Vilariño-Güell, Carles

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Case-Control Studies Are Not Familial Studies von Wang, Zhe, Sadovnick, A. Dessa, Traboulsee, Anthony L., Ross, Jay P., Bernales, Cecily Q., Encarnacion, Mary, Yee, Irene M., de Lemos, Madonna, Greenwood, Talitha, Lee, Joshua D., Wright, Galen, Ross, Colin J., Zhang, Si, Song, Weihong, Vilariño-Güell, Carles

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Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor von Castonguay, Charles-Etienne, Liao, Calwing, Khayachi, Anouar, Liu, Yumin, Medeiros, Miranda, Houle, Gabrielle, Ross, Jay P., Dion, Patrick A., Rouleau, Guy A.

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VPS35 and DNAJC13 disease-causing variants in essential tremor von Rajput, Alex, Ross, Jay P, Bernales, Cecily Q, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra I, Ross, Owen A, van Gerpen, Jay, Uitti, Ryan J, Wszolek, Zbigniew K, Rajput, Ali H, Vilariño-Güell, Carles

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Editorial Note to:Nuclear Receptor NR1H3 in Familial Multiple Sclerosis von Wang, Zhe, Sadovnick, A. Dessa, Traboulsee, Anthony L., Ross, Jay P., Bernales, Cecily Q., Encarnacion, Mary, Yee, Irene M., de Lemos, Madonna, Greenwood, Talitha, Lee, Joshua D., Wright, Galen, Ross, Colin J., Zhang, Si, Song, Weihong, Vilariño-Güell, Carles

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Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette’s syndrome von Liao, Calwing, Vuokila, Veikko, Catoire, Hélène, Akçimen, Fulya, Ross, Jay P., Bourassa, Cynthia V., Dion, Patrick A., Meijer, Inge A., Rouleau, Guy A.

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Moyamoya Disease Susceptibility Gene RNF213 Regulates Endothelial Barrier Function von Roy, Vincent, Ross, Jay P., Pépin, Rémy, Cortez Ghio, Sergio, Brodeur, Alyssa, Touzel Deschênes, Lydia, Le-Bel, Gaëtan, Phillips, Daniel E., Milot, Geneviève, Dion, Patrick A., Guérin, Sylvain, Germain, Lucie, Berthod, François, Auger, François A., Rouleau, Guy A., Dupré, Nicolas, Gros-Louis, François

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Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project von Akçimen, Fulya, Ross, Jay P., Liao, Calwing, Spiegelman, Dan, Dion, Patrick A., Rouleau, Guy A.

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Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome von Akçimen, Fulya, Chia, Ruth, Saez‐Atienzar, Sara, Ruffo, Paola, Rasheed, Memoona, Ross, Jay P., Liao, Calwing, Ray, Anindita, Dion, Patrick A., Scholz, Sonja W., Rouleau, Guy A., Traynor, Bryan J.

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Evolution of a Human-Specific Tandem Repeat Associated with ALS von Course, Meredith M., Gudsnuk, Kathryn, Smukowski, Samuel N., Winston, Kosuke, Desai, Nitin, Ross, Jay P., Sulovari, Arvis, Bourassa, Cynthia V., Spiegelman, Dan, Couthouis, Julien, Yu, Chang-En, Tsuang, Debby W., Jayadev, Suman, Kay, Mark A., Gitler, Aaron D., Dupre, Nicolas, Eichler, Evan E., Dion, Patrick A., Rouleau, Guy A., Valdmanis, Paul N.

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The value of testing for ATXN2 intermediate repeat expansions in routine clinical practice for amyotrophic lateral sclerosis von Salmon, Kristiana, Ross, Jay P, Bertone, Vanessa, Gobbo, Maria, Anoja, Nancy, Karamchandani, Jason, Dion, Patrick A, Rouleau, Guy A, Genge, Angela

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Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis von Liao, Calwing, Castonguay, Charles-Etienne, Heilbron, Karl, Vuokila, Veikko, Medeiros, Miranda, Houle, Gabrielle, Akçimen, Fulya, Ross, Jay P, Catoire, Helene, Diez-Fairen, Monica, Kang, Jooeun, Mueller, Stefanie H, Girard, Simon L, Hopfner, Franziska, Lorenz, Delia, Clark, Lorraine N, Soto-Beasley, Alexandra I, Klebe, Stephan, Hallett, Mark, Wszolek, Zbigniew K, Pendziwiat, Manuela, Lorenzo-Betancor, Oswaldo, Seppi, Klaus, Berg, Daniela, Vilariño-Güell, Carles, Postuma, Ronald B, Bernard, Geneviève, Dupré, Nicolas, Jankovic, Joseph, Testa, Claudia M, Ross, Owen A, Arzberger, Thomas, Chouinard, Sylvain, Louis, Elan D, Mandich, Paola, Vitale, Carmine, Barone, Paolo, García-Martín, Elena, Alonso-Navarro, Hortensia, Agúndez, José A. G, Jiménez-Jiménez, Félix Javier, Pastor, Pau, Rajput, Alex, Deuschl, Günther, Kuhlenbaümer, Gregor, Meijer, Inge A, Dion, Patrick A, Rouleau, Guy A

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