Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuk, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexandre, Szuto, Anna, Liao, Meijiang, Figlewicz, Denise A., Bouhouche, Ahmed, Benomar, Ali, Yahyaoui, Mohamed, Ouazzani, Reda, Yoon, Grace, Dupré, Nicolas, Suchowersky, Oksana, Bolduc, Francois V., Parker, J. Alex, Dion, Patrick A., Drapeau, Pierre, Rouleau, Guy A., Ouled Amar Bencheikh, Bouchra
Published in American journal of human genetics (05.05.2016)
Published in American journal of human genetics (05.05.2016)
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Journal Article
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis
Leblond, Claire S, Gan-Or, Ziv, Spiegelman, Dan, Laurent, Sandra B, Szuto, Anna, Hodgkinson, Alan, Dionne-Laporte, Alexandre, Provencher, Pierre, de Carvalho, Mamede, Orrù, Sandro, Brunet, Denis, Bouchard, Jean-Pierre, Awadalla, Philip, Dupré, Nicolas, Dion, Patrick A, Rouleau, Guy A
Published in Neurobiology of aging (2016)
Published in Neurobiology of aging (2016)
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Journal Article
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuk, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexandre, Szuto, Anna, Liao, Meijiang, Figlewicz, Denise A., Bouhouche, Ahmed, Benomar, Ali, Yahyaoui, Mohamed, Ouazzani, Reda, Yoon, Grace, Dupré, Nicolas, Suchowersky, Oksana, Bolduc, Francois V., Parker, J. Alex, Dion, Patrick A., Drapeau, Pierre, Rouleau, Guy A., Ouled Amar Bencheikh, Bouchra
Published in American journal of human genetics (02.06.2016)
Published in American journal of human genetics (02.06.2016)
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Journal Article
Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies
Krohn, Lynne, Öztürk, Tuğba Nur, Vanderperre, Benoît, Ouled Amar Bencheikh, Bouchra, Ruskey, Jennifer A., Laurent, Sandra B., Spiegelman, Dan, Postuma, Ronald B., Arnulf, Isabelle, Hu, Michele T. M., Dauvilliers, Yves, Högl, Birgit, Stefani, Ambra, Monaca, Christelle Charley, Plazzi, Giuseppe, Antelmi, Elena, Ferini‐Strambi, Luigi, Heidbreder, Anna, Rudakou, Uladzislau, Cochen De Cock, Valérie, Young, Peter, Wolf, Pavlina, Oliva, Petra, Zhang, Xiaokui Kate, Greenbaum, Lior, Liong, Christopher, Gagnon, Jean‐François, Desautels, Alex, Hassin‐Baer, Sharon, Montplaisir, Jacques Y., Dupré, Nicolas, Rouleau, Guy A., Fon, Edward A., Trempe, Jean‐François, Lamoureux, Guillaume, Alcalay, Roy N., Gan‐Or, Ziv
Published in Annals of neurology (01.01.2020)
Published in Annals of neurology (01.01.2020)
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Journal Article
SMPD1 mutations, activity, and α‐synuclein accumulation in Parkinson's disease
Alcalay, Roy N., Mallett, Victoria, Vanderperre, Benoît, Tavassoly, Omid, Dauvilliers, Yves, Wu, Richard Y.J., Ruskey, Jennifer A., Leblond, Claire S., Ambalavanan, Amirthagowri, Laurent, Sandra B., Spiegelman, Dan, Dionne‐Laporte, Alexandre, Liong, Christopher, Levy, Oren A., Fahn, Stanley, Waters, Cheryl, Kuo, Sheng‐Han, Chung, Wendy K., Ford, Blair, Marder, Karen S., Kang, Un Jung, Hassin‐Baer, Sharon, Greenbaum, Lior, Trempe, Jean‐Francois, Wolf, Pavlina, Oliva, Petra, Zhang, Xiaokui Kate, Clark, Lorraine N., Langlois, Melanie, Dion, Patrick A., Fon, Edward A., Dupre, Nicolas, Rouleau, Guy A., Gan‐Or, Ziv
Published in Movement disorders (01.04.2019)
Published in Movement disorders (01.04.2019)
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Journal Article
Fine‐Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies
Krohn, Lynne, Wu, Richard Y. J., Heilbron, Karl, Ruskey, Jennifer A., Laurent, Sandra B., Blauwendraat, Cornelis, Alam, Armaghan, Arnulf, Isabelle, Hu, Michele T. M., Dauvilliers, Yves, Högl, Birgit, Toft, Mathias, Bjørnarå, Kari Anne, Stefani, Ambra, Holzknecht, Evi, Monaca, Christelle Charley, Abril, Beatriz, Plazzi, Giuseppe, Antelmi, Elena, Ferini‐Strambi, Luigi, Young, Peter, Heidbreder, Anna, Cochen De Cock, Valérie, Mollenhauer, Brit, Sixel‐Döring, Friederike, Trenkwalder, Claudia, Sonka, Karel, Kemlink, David, Figorilli, Michela, Puligheddu, Monica, Dijkstra, Femke, Viaene, Mineke, Oertel, Wolfang, Toffoli, Marco, Gigli, Gian Luigi, Valente, Mariarosaria, Gagnon, Jean‐François, Nalls, Mike A., Singleton, Andrew B., Desautels, Alex, Montplaisir, Jacques Y., Cannon, Paul, Ross, Owen A., Boeve, Bradley F., Dupré, Nicolas, Fon, Edward A., Postuma, Ronald B., Pihlstrøm, Lasse, Rouleau, Guy A., Gan‐Or, Ziv
Published in Annals of neurology (01.04.2020)
Published in Annals of neurology (01.04.2020)
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Journal Article
LRRK2 p.M1646T is associated with glucocerebrosidase activity and with Parkinson's disease
Sosero, Yuri L., Yu, Eric, Krohn, Lynne, Rudakou, Uladzislau, Mufti, Kheireddin, Ruskey, Jennifer A., Asayesh, Farnaz, Laurent, Sandra B., Spiegelman, Dan, Fahn, Stanley, Waters, Cheryl, Sardi, S. Pablo, Bandres-Ciga, Sara, Alcalay, Roy N., Gan-Or, Ziv, Senkevich, Konstantin
Published in Neurobiology of aging (01.07.2021)
Published in Neurobiology of aging (01.07.2021)
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Journal Article
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease
Saini, Prabhjyot, Rudakou, Uladzislau, Yu, Eric, Ruskey, Jennifer A., Asayesh, Farnaz, Laurent, Sandra B., Spiegelman, Dan, Fahn, Stanley, Waters, Cheryl, Monchi, Oury, Dauvilliers, Yves, Dupré, Nicolas, Greenbaum, Lior, Hassin-Baer, Sharon, Espay, Alberto J., Rouleau, Guy A., Alcalay, Roy N., Fon, Edward A., Postuma, Ronald B., Gan-Or, Ziv
Published in Neurobiology of aging (01.04.2021)
Published in Neurobiology of aging (01.04.2021)
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Journal Article
Common and rare GCH1 variants are associated with Parkinson's disease
Rudakou, Uladzislau, Ouled Amar Bencheikh, Bouchra, Ruskey, Jennifer A., Krohn, Lynne, Laurent, Sandra B., Spiegelman, Dan, Liong, Christopher, Fahn, Stanley, Waters, Cheryl, Monchi, Oury, Fon, Edward A., Dauvilliers, Yves, Alcalay, Roy N., Dupré, Nicolas, Gan-Or, Ziv
Published in Neurobiology of aging (01.01.2019)
Published in Neurobiology of aging (01.01.2019)
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Journal Article
Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder
Mufti, Kheireddin, Yu, Eric, Rudakou, Uladzislau, Krohn, Lynne, Ruskey, Jennifer A, Asayesh, Farnaz, Laurent, Sandra B, Spiegelman, Dan, Arnulf, Isabelle, Hu, Michele T M, Montplaisir, Jacques Y, Gagnon, Jean-François, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Bernardini, Andrea, Högl, Birgit, Stefani, Ambra, Holzknecht, Evi, Sonka, Karel, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel-Döring, Friederike, Cochen De Cock, Valérie, Monaca, Christelle Charley, Heidbreder, Anna, Ferini-Strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley F, Trempe, Jean-François, Rouleau, Guy A, Postuma, Ronald B, Gan-Or, Ziv
Published in Neurology (09.03.2021)
Published in Neurology (09.03.2021)
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Journal Article
Oligogenicity, C9orf72 expansion, and variant severity in ALS
Ross, Jay P., Leblond, Claire S., Laurent, Sandra B., Spiegelman, Dan, Dionne-Laporte, Alexandre, Camu, William, Dupré, Nicolas, Dion, Patrick A., Rouleau, Guy A.
Published in Neurogenetics (01.07.2020)
Published in Neurogenetics (01.07.2020)
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Journal Article
Variants in the Niemann–Pick type C gene NPC1 are not associated with Parkinson's disease
Ouled Amar Bencheikh, Bouchra, Senkevich, Konstantin, Rudakou, Uladzislau, Yu, Eric, Mufti, Kheireddin, Ruskey, Jennifer A., Asayesh, Farnaz, Laurent, Sandra B., Spiegelman, Dan, Fahn, Stanley, Waters, Cheryl, Monchi, Oury, Dauvilliers, Yves, Espay, Alberto J., Dupré, Nicolas, Greenbaum, Lior, Hassin-Baer, Sharon, Rouleau, Guy A., Alcalay, Roy N., Fon, Edward A., Gan-Or, Ziv
Published in Neurobiology of aging (01.09.2020)
Published in Neurobiology of aging (01.09.2020)
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Journal Article
Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder
Li, Jiao, Ruskey, Jennifer A., Arnulf, Isabelle, Dauvilliers, Yves, Hu, Michele T.M., Högl, Birgit, Leblond, Claire S., Zhou, Sirui, Ambalavanan, Amirthagowri, Ross, Jay P., Bourassa, Cynthia V., Spiegelman, Dan, Laurent, Sandra B, Stefani, Ambra, Charley Monaca, Christelle, Cochen De Cock, Valérie, Boivin, Michel, Ferini‐Strambi, Luigi, Plazzi, Giuseppe, Antelmi, Elena, Young, Peter, Heidbreder, Anna, Labbe, Catherine, Ferman, Tanis J., Dion, Patrick A., Fan, Dongsheng, Desautels, Alex, Gagnon, Jean‐François, Dupré, Nicolas, Fon, Edward A., Montplaisir, Jacques Y., Boeve, Bradley F., Postuma, Ronald B., Rouleau, Guy A., Ross, Owen A., Gan‐Or, Ziv
Published in Movement disorders (01.07.2018)
Published in Movement disorders (01.07.2018)
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Journal Article
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid‐Eye‐Movement Sleep Behavior Disorder
Mufti, Kheireddin, Rudakou, Uladzislau, Yu, Eric, Krohn, Lynne, Ruskey, Jennifer A., Asayesh, Farnaz, Laurent, Sandra B., Spiegelman, Dan, Arnulf, Isabelle, Hu, Michele T.M., Montplaisir, Jacques Y., Gagnon, Jean‐François, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Högl, Birgit, Stefani, Ambra, Holzknecht, Evi, Šonka, Karel, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel‐Döring, Friederike, Cochen De Cock, Valérie, Monaca, Christelle Charley, Heidbreder, Anna, Ferini‐Strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley F., Postuma, Ronald B., Rouleau, Guy A., Gan‐Or, Ziv
Published in Movement disorders (01.01.2021)
Published in Movement disorders (01.01.2021)
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Journal Article
Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor Cases
Schmouth, Jean-François, Houle, Gabrielle, Ambalavanan, Amirthagowri, Leblond, Claire S., Spiegelman, Dan, Laurent, Sandra B., Bourassa, Cynthia V., Panisset, Michel, Chouinard, Sylvain, Dupré, Nicolas, Vilariño-Güell, Carles, Rajput, Alex, Dion, Patrick A., Rouleau, Guy A.
Published in Molecular neurobiology (01.06.2019)
Published in Molecular neurobiology (01.06.2019)
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Journal Article
Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population
Houle, Gabrielle, Schmouth, Jean‐François, Leblond, Claire S., Ambalavanan, Amirthagowri, Spiegelman, Dan, Laurent, Sandra B., Bourassa, Cynthia V., Panisset, Michel, Chouinard, Sylvain, Dupré, Nicolas, Vilariño‐Güell, Carles, Rajput, Alex, Dion, Patrick A., Rouleau, Guy A.
Published in Movement disorders (01.02.2017)
Published in Movement disorders (01.02.2017)
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Journal Article
Rare PSAP Variants and Possible Interaction with GBA in REM Sleep Behavior Disorder
Sosero, Yuri L., Yu, Eric, Estiar, Mehrdad A., Krohn, Lynne, Mufti, Kheireddin, Rudakou, Uladzislau, Ruskey, Jennifer A., Asayesh, Farnaz, Laurent, Sandra B., Spiegelman, Dan, Trempe, Jean-François, Quinnell, Timothy G., Oscroft, Nicholas, Arnulf, Isabelle, Montplaisir, Jacques Y., Gagnon, Jean-François, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Bernardini, Andrea, Sonka, Karel, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Antelmi, Elena, Biscarini, Francesco, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel-Döring, Friederike, Cochen De Cock, Valérie, Monaca, Christelle Charley, Heidbreder, Anna, Ferini-Strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley F., Postuma, Ronald B., Rouleau, Guy A., Ibrahim, Abubaker, Stefani, Ambra, Högl, Birgit, Hu, Michele T.M., Gan-Or, Ziv
Published in Journal of Parkinson's disease (01.01.2022)
Published in Journal of Parkinson's disease (01.01.2022)
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Journal Article
Analysis of common and rare VPS13C variants in late-onset Parkinson disease
Rudakou, Uladzislau, Ruskey, Jennifer A, Krohn, Lynne, Laurent, Sandra B, Spiegelman, Dan, Greenbaum, Lior, Yahalom, Gilad, Desautels, Alex, Montplaisir, Jacques Y, Fahn, Stanley, Waters, Cheryl H, Levy, Oren, Kehoe, Caitlin M, Narayan, Sushma, Dauvilliers, Yves, Dupré, Nicolas, Hassin-Baer, Sharon, Alcalay, Roy N, Rouleau, Guy A, Fon, Edward A, Gan-Or, Ziv
Published in Neurology. Genetics (01.02.2020)
Published in Neurology. Genetics (01.02.2020)
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Journal Article
The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder
Gan-Or, Ziv, Mohsin, Noreen, Girard, Simon L, Montplaisir, Jacques Y, Ambalavanan, Amirthagowri, Strong, Stephanie, Mallett, Victoria, Laurent, Sandra B, Bourassa, Cynthia V, Boivin, Michel, Langlois, Melanie, Arnulf, Isabelle, Högl, Birgit, Frauscher, Birgit, Monaca, Christelle, Desautels, Alex, Gagnon, Jean-François, Postuma, Ronald B, Dion, Patrick A, Dauvilliers, Yves, Dupre, Nicolas, Alcalay, Roy N, Rouleau, Guy A
Published in Neurobiology of aging (01.07.2016)
Published in Neurobiology of aging (01.07.2016)
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Journal Article
No rare deleterious variants from STK32B , PPARGC1A , and CTNNA3 are associated with essential tremor
Houle, Gabrielle, Ambalavanan, Amirthagowri, Schmouth, Jean-François, Leblond, Claire S, Spiegelman, Dan, Laurent, Sandra B, Bourassa, Cynthia V, Grayson, Celene, Panisset, Michel, Chouinard, Sylvain, Dupré, Nicolas, Vilariño-Güell, Carles, Rajput, Alex, Girard, Simon L, Dion, Patrick A, Rouleau, Guy A
Published in Neurology. Genetics (01.10.2017)
Published in Neurology. Genetics (01.10.2017)
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Journal Article