De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia

by Leblond, Claire S., Webber, Alina, Gan-Or, Ziv, Moore, Fraser, Dagher, Alain, Dion, Patrick A., Rouleau, Guy A.
Published 2016

GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis

by Mallett, Victoria, Ross, Jay P., Alcalay, Roy N., Ambalavanan, Amirthagowri, Sidransky, Ellen, Dion, Patrick A., Rouleau, Guy A., Gan-Or, Ziv
Published 2016

SCARB2 variants and glucocerebrosidase activity in Parkinson’s disease

by Alcalay, Roy N, Levy, Oren A, Wolf, Pavlina, Oliva, Petra, Zhang, Xiaokui Kate, Waters, Cheryl H, Fahn, Stanley, Kang, Un Jung, Liong, Christopher, Ford, Blair, Mazzoni, Pietro, Kuo, Sheng, Johnson, Amelie, Xiong, Lan, Rouleau, Guy A, Chung, Wendy K, Marder, Karen S, Gan-Or, Ziv
Published 2016

Clinical and genetic study of hereditary spastic paraplegia in Canada

by Chrestian, Nicolas, Dupré, Nicolas, Gan-Or, Ziv, Szuto, Anna, Chen, Shiyi, Venkitachalam, Anil, Brisson, Jean-Denis, Warman-Chardon, Jodi, Ahmed, Sohnee, Ashtiani, Setareh, MacDonald, Heather, Mohsin, Noreen, Mourabit-Amari, Karim, Provencher, Pierre, Boycott, Kym M., Stavropoulos, Dimitri J., Dion, Patrick A., Ray, Peter N., Suchowersky, Oksana, Rouleau, Guy A., Yoon, Grace
Published 2016

GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder

by Gan-Or, Ziv, Mirelman, Anat, Postuma, Ronald B, Arnulf, Isabelle, Bar-Shira, Anat, Dauvilliers, Yves, Desautels, Alex, Gagnon, Jean-François, Leblond, Claire S, Frauscher, Birgit, Alcalay, Roy N, Saunders-Pullman, Rachel, Bressman, Susan B, Marder, Karen, Monaca, Christelle, Högl, Birgit, Orr-Urtreger, Avi, Dion, Patrick A, Montplaisir, Jacques Y, Giladi, Nir, Rouleau, Guy A
Published 2015