Works by Dupre, Nicolas


Results: 133
    1

    Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population.

    Published in:
    2017
    By:
    • 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.;
    • Schmouth, Jean-François;
    • Dupré, Nicolas;
    • Vilariño-Güell, Carles
    Publication type:
    journal article
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    Regional Cerebral Atrophy Contributes to Personalized Survival Prediction in Amyotrophic Lateral Sclerosis: A Multicentre, Machine Learning, Deformation‐Based Morphometry Study.

    Published in:
    Annals of Neurology, 2025, v. 97, n. 6, p. 1144, doi. 10.1002/ana.27196
    By:
    • Lajoie, Isabelle;
    • Kalra, Sanjay;
    • Hanstock, Christopher;
    • Wilman, Alan;
    • Eurich, Dean;
    • Beaulieu, Christian;
    • Yang, Yee Hong;
    • Korngut, Lawrence;
    • Frayne, Richard;
    • Briemberg, Hannah;
    • Zinman, Lorne;
    • Graham, Simon;
    • Genge, Angela;
    • Dionne, Annie;
    • Dupré, Nicolas;
    • Shoesmith, Christen;
    • Benatar, Michael;
    • Welsh, Robert;
    • Dadar, Mahsa
    Publication type:
    Article
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    Standards of Fluid Biomarker Collection and Pre-analytical Processes in Humans and Mice: Recommendations by the Ataxia Global Initiative Working Group on Biomarkers.

    Published in:
    Cerebellum, 2024, v. 23, n. 3, p. 881, doi. 10.1007/s12311-023-01561-1
    By:
    • Santorelli, Filippo M.;
    • McLoughlin, Hayley S.;
    • Wolter, Justin M.;
    • Galatolo, Daniele;
    • Synofzik, Matthis;
    • Mengel, David;
    • Opal, Puneet;
    • Irina, Antonijevic;
    • Georg, Auburger;
    • Luis, Bataller;
    • Enrico, Bertini;
    • Sylvia, Boesch;
    • Samantha, Boeshore;
    • Ronald, Buijsen;
    • Edwin, Chan;
    • Giulia, Coarelli;
    • Nicolas, Dupré;
    • Alexandra, Durr;
    • Andreas, Eigentler;
    • Ewelina, Elert-Dobkowska
    Publication type:
    Article
    7

    An Exploratory Survey on the Care for Ataxic Patients in the American Continents and the Caribbean.

    Published in:
    Cerebellum, 2023, v. 22, n. 4, p. 708, doi. 10.1007/s12311-022-01442-z
    By:
    • Jardim, Laura Bannach;
    • Hasan, Ali;
    • Kuo, Sheng-han;
    • Magaña, Jonathan Javier;
    • França Jr, Marcondes;
    • Marques Jr, Wilson;
    • Camejo, Claudia;
    • Santana-da-Silva, Luiz Carlos;
    • Leão, Emília Embiruçu;
    • Espíndola, Gisele;
    • Canals, Francisca;
    • Miranda, Marcelo;
    • Salvatierra, Igor;
    • Cornejo-Olivas, Mario;
    • Fernandez-Ruiz, Juan;
    • Braga-Neto, Pedro;
    • Dávila-Ortiz de Montellano, David José;
    • Flores-Lagunes, Luis Leonardo;
    • Dupré, Nicolas;
    • Brais, Bernard
    Publication type:
    Article
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    Root resorptions induced by genetic disorders: A systematic review.

    Published in:
    Oral Diseases, 2024, v. 30, n. 6, p. 3799, doi. 10.1111/odi.14942
    By:
    • Dupre, Nicolas;
    • Riou, Margot C.;
    • Isaac, Juliane;
    • Ferre, François;
    • Cormier‐Daire, Valérie;
    • Kerner, Stéphane;
    • de La Dure‐Molla, Muriel;
    • Nowwarote, Nunthawan;
    • Acevedo, Ana Carolina;
    • Fournier, Benjamin P. J.
    Publication type:
    Article
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    Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7.

    Published in:
    Movement Disorders, 2021, v. 36, n. 7, p. 1664, doi. 10.1002/mds.28528
    By:
    • Estiar, Mehrdad A.;
    • Yu, Eric;
    • Haj Salem, Ikhlass;
    • Ross, Jay P.;
    • Mufti, Kheireddin;
    • Akçimen, Fulya;
    • Leveille, Etienne;
    • Spiegelman, Dan;
    • Ruskey, Jennifer A.;
    • Asayesh, Farnaz;
    • Dagher, Alain;
    • Yoon, Grace;
    • Tarnopolsky, Mark;
    • Boycott, Kym M.;
    • Dupre, Nicolas;
    • Dion, Patrick A.;
    • Suchowersky, Oksana;
    • Trempe, Jean‐Francois;
    • Rouleau, Guy A.;
    • Gan‐Or, Ziv
    Publication type:
    Article
    19

    Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease.

    Published in:
    Movement Disorders, 2021, v. 36, n. 1, p. 178, doi. 10.1002/mds.28299
    By:
    • Yu, Eric;
    • Rudakou, Uladzislau;
    • Krohn, Lynne;
    • Mufti, Kheireddin;
    • Ruskey, Jennifer A.;
    • Asayesh, Farnaz;
    • Estiar, Mehrdad A.;
    • Spiegelman, Dan;
    • Surface, Matthew;
    • Fahn, Stanley;
    • Waters, Cheryl H.;
    • Greenbaum, Lior;
    • Espay, Alberto J.;
    • Dauvilliers, Yves;
    • Dupré, Nicolas;
    • Rouleau, Guy A.;
    • Hassin‐Baer, Sharon;
    • Fon, Edward A.;
    • Alcalay, Roy N.;
    • Gan‐Or, Ziv
    Publication type:
    Article
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    SYNE1 Mutations in Autosomal Recessive Cerebellar Ataxia.

    Published in:
    JAMA Neurology, 2013, v. 70, n. 10, p. 1296, doi. 10.1001/jamaneurol.2013.3268
    By:
    • Noreau, Anne;
    • Bourassa, Cynthia V.;
    • Szuto, Anna;
    • Levert, Annie;
    • Dobrzeniecka, Sylvia;
    • Gauthier, Julie;
    • Forlani, Sylvie;
    • Durr, Alexandra;
    • Anheim, Mathieu;
    • Stevanin, Giovanni;
    • Brice, Alexis;
    • Bouchard, Jean-Pierre;
    • Dion, Patrick A.;
    • Dupré, Nicolas;
    • Rouleau, Guy A.
    Publication type:
    Article
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    GCH1 mutations in hereditary spastic paraplegia.

    Published in:
    Clinical Genetics, 2021, v. 100, n. 1, p. 51, doi. 10.1111/cge.13955
    By:
    • Varghaei, Parizad;
    • Yoon, Grace;
    • Estiar, Mehrdad A.;
    • Veyron, Simon;
    • Leveille, Etienne;
    • Dupré, Nicolas;
    • Trempe, Jean‐François;
    • Rouleau, Guy A.;
    • Gan‐Or, Ziv
    Publication type:
    Article
    29
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    TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.

    Published in:
    Nature Genetics, 2008, v. 40, n. 5, p. 572, doi. 10.1038/ng.132
    By:
    • Kabashi, Edor;
    • Valdmanis, Paul N.;
    • Dion, Patrick;
    • Spiegelman, Dan;
    • McConkey, Brendan J.;
    • Velde, Christine Vande;
    • Bouchard, Jean-Pierre;
    • Lacomblez, Lucette;
    • Pochigaeva, Ksenia;
    • Salachas, Francois;
    • Pradat, Pierre-Francois;
    • Camu, William;
    • Meininger, Vincent;
    • Dupre, Nicolas;
    • Rouleau, Guy A.
    Publication type:
    Article
    31
    32

    The K–Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum.

    Published in:
    Nature Genetics, 2002, v. 32, n. 3, p. 384, doi. 10.1038/ng1002
    By:
    • Howard, Heidi C.;
    • Mount, David B.;
    • Rochefort, Daniel;
    • Byun, Nellie;
    • Dupré, Nicolas;
    • Lu, Jianming;
    • Fan, Xuemo;
    • Song, Luyan;
    • Rivière, Jean-Baptiste;
    • Prévost, Claude;
    • Horst, Jürgen;
    • Simonati, Alessandro;
    • Lemcke, Beate;
    • Welch, Rick;
    • England, Roger;
    • Zhan, Frank Q.;
    • Mercado, Adriana;
    • Siesser, William B.;
    • George, Alfred L.;
    • McDonald, Michael P.
    Publication type:
    Article
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    Glucocerebrosidase Mutations in a French-Canadian Parkinson's Disease Cohort.

    Published in:
    Canadian Journal of Neurological Sciences, 2011, v. 38, n. 5, p. 772, doi. 10.1017/S0317167100012300
    By:
    • Noreau, Anne;
    • Rivière, Jean-Baptiste;
    • Diab, Sabrina;
    • Dion, Patrick A.;
    • Panisset, Michel;
    • Soland, Valérie;
    • Jodoin, Nicolas;
    • Langlois, Mélanie;
    • Chouinard, Sylvain;
    • Dupré, Nicolas;
    • Rouleau, Guy A.
    Publication type:
    Article
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    A Novel Mutation in a Large French-Canadian Family with LGMD1B.

    Published in:
    Canadian Journal of Neurological Sciences, 2008, v. 35, n. 3, p. 331, doi. 10.1017/S031716710000891X
    By:
    • Chrestian, Nicolas;
    • Valdmanis, Paul N.;
    • Echahidi, Najmeddine;
    • Brunet, Denis;
    • Bouchard, Jean-Pierre;
    • Gould, Peter;
    • Rouleau, Guy A.;
    • Champagne, Jean;
    • Dupré, Nicolas
    Publication type:
    Article
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