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Patrick Dion

Research Profile

Disorders

Physiology

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Publications

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Shawn J Stochmanski; Martine Therrien; Don J Van Meyel; Kishanda Vyboh; Graziella Di Cristo; Patrick Dion; Claudia Gaspar; Rebecca Gaudet; Liliane Karemera; Josée Laganière; Sandra Laurent; Daniel Rochefort; Guy A Rouleau
Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron models.
Veronique V Belzil; Bernard Brais; Hussein Daoud; Patrick Dion; Jean-Sébastien Langlais; Guy A Rouleau
Novel FUS deletion in a patient with juvenile amyotrophic lateral sclerosis.
Anne Noreau; Marie-France Rioux; Anna Szuto; Pascale Thibodeau; Bernard Brais; Patrick Dion; Nicolas Dupré; Annie Levert; Guy A Rouleau
CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjects.

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All Publications

2012: Shawn J Stochmanski; Martine Therrien; Don J Van Meyel; Kishanda Vyboh; Graziella Di Cristo; Patrick Dion; Claudia Gaspar; Rebecca Gaudet; Liliane Karemera; Josée Laganière; Sandra Laurent; Daniel Rochefort; Guy A Rouleau
Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron models.
Human molecular genetics 2012;21(10):2211-8.
2012: Veronique V Belzil; Bernard Brais; Hussein Daoud; Patrick Dion; Jean-Sébastien Langlais; Guy A Rouleau
Novel FUS deletion in a patient with juvenile amyotrophic lateral sclerosis.
Archives of neurology 2012;69(5):653-6.
2012: Anne Noreau; Marie-France Rioux; Anna Szuto; Pascale Thibodeau; Bernard Brais; Patrick Dion; Nicolas Dupré; Annie Levert; Guy A Rouleau
CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjects.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2012;39(1):91-4.
2011: Hussein Daoud; Paul N Valdmanis; François Gros-Louis; Véronique Belzil; Dan Spiegelman; Edouard Henrion; Ousmane Diallo; Anne Desjarlais; Julie Gauthier; William Camu; Patrick Dion; Guy Rouleau
Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis.
Archives of neurology 2011;68(5):587-93.
2011: Veronique V Belzil; Hussein Daoud; Judith St-Onge; Anne Desjarlais; Jean-Pierre Bouchard; Nicolas Dupre; Lucette Lacomblez; François Salachas; Pierre-François Pradat; Vincent Meininger; William Camu; Patrick Dion; Guy Rouleau
Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2011;12(2):113-7.
2011: Véronique V Belzil; Judith St-Onge; Hussein Daoud; Anne Desjarlais; Jean-Pierre Bouchard; Nicolas Dupré; William Camu; Patrick Dion; Guy Rouleau
Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.
Journal of human genetics 2011;56(3):247-9.
2010: Myriam Srour; Jean-Baptiste Rivière; Jessica M T Pham; Marie-Pierre Dubé; Simon Girard; Steves Morin; Patrick Dion; Géraldine Asselin; Daniel Rochefort; Pascale Hince; Sabrina Diab; Naser Sharafaddinzadeh; Sylvain Chouinard; Hugo Théoret; Frédéric Charron; Guy Rouleau
Mutations in DCC cause congenital mirror movements.
Science (New York, N.Y.) 2010;328(5978):592.
2009: Paul N Valdmanis; Veronique V Belzil; James Lee; Patrick Dion; Judith St-Onge; Pascale Hince; Benoit Funalot; Philippe Couratier; Pierre Clavelou; William Camu; Guy Rouleau
A mutation that creates a pseudoexon in SOD1 causes familial ALS.
Annals of human genetics 2009;73(Pt 6):652-7.
2009: V V Belzil; Paul N Valdmanis; Patrick Dion; H Daoud; Edor Kabashi; A Noreau; J Gauthier; P Hince; A Desjarlais; Jean-Pierre Bouchard; Lucette Lacomblez; François Salachas; P-F Pradat; William Camu; Vincent Meininger; Nicolas Dupré; Guy Rouleau
Mutations in FUS cause FALS and SALS in French and French Canadian populations.
Neurology 2009;73(15):1176-9.
2009: Paul N Valdmanis; Hussein Daoud; Patrick Dion; Guy Rouleau
Recent advances in the genetics of amyotrophic lateral sclerosis.
Current neurology and neuroscience reports 2009;9(3):198-205.
2008: Adèle Salin-Cantegrel; Masoud Shekarabi; Sébastien Holbert; Patrick Dion; Daniel Rochefort; Janet Laganière; Sandra Dacal; Pascale Hince; Liliane Karemera; Claudia Gaspar; Jean-Yves Lapointe; Guy Rouleau
HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3.
Human molecular genetics 2008;17(17):2703-11.
2008: François Gros-Louis; Jasna Kriz; Edor Kabashi; Jonathan McDearmid; Stéphanie Millecamps; Makoto Urushitani; Li Lin; Patrick Dion; Qinzhang Zhu; Pierre Drapeau; Jean-Pierre Julien; Guy Rouleau
Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish.
Human molecular genetics 2008;17(17):2691-702.
2008: Paul N Valdmanis; Edor Kabashi; A Dyck; P Hince; J Lee; Patrick Dion; M D'Amour; F Souchon; Jean-Pierre Bouchard; François Salachas; Vincent Meininger; P M Andersen; William Camu; Nicolas Dupré; Guy Rouleau
Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden.
Neurology 2008;71(7):514-20.
2008: Edor Kabashi; Paul N Valdmanis; Patrick Dion; Dan Spiegelman; Brendan J McConkey; Christine Vande Velde; Jean-Pierre Bouchard; Lucette Lacomblez; Ksenia Pochigaeva; Francois Salachas; Pierre-Francois Pradat; William Camu; Vincent Meininger; Nicolas Dupre; Guy Rouleau
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
Nature genetics 2008;40(5):572-4.
2007: Edor Kabashi; Paul N Valdmanis; Patrick Dion; Guy Rouleau
Oxidized/misfolded superoxide dismutase-1: the cause of all amyotrophic lateral sclerosis?
Annals of neurology 2007;62(6):553-9.
2007: Lan Xiong; Patrick Dion; Jacques Montplaisir; Anastasia Levchenko; Pascale Thibodeau; Liliane Karemera; Jean-Baptiste Rivière; Judith St-Onge; Claudia Gaspar; Marie-Pierre Dubé; Alex Desautels; Gustavo Turecki; Guy Rouleau
Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(7):911-7.
2007: Inge A Meijer; Patrick Dion; Sandra Laurent; Nicolas Dupré; Bernard Brais; Annie Levert; Jack Puymirat; Marie-France Rioux; Michel Sylvain; Peng-Peng Zhu; Cynthia Soderblom; Julia Stadler; Craig Blackstone; Guy Rouleau
Characterization of a novel SPG3A deletion in a French-Canadian family.
Annals of neurology 2007;61(6):599-603.
2007: Christiane Messaed; Patrick Dion; Aida Abu-Baker; Daniel Rochefort; janet laganiere; Bernard Brais; Guy Rouleau
Soluble expanded PABPN1 promotes cell death in oculopharyngeal muscular dystrophy.
Neurobiology of disease 2007;26(3):546-57.
2007: Paul N Valdmanis; Inge A Meijer; Annie Reynolds; Adrienne Lei; Patrick MacLeod; David Schlesinger; Mayana Zatz; Evan Reid; Patrick Dion; Pierre Drapeau; Guy Rouleau
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.
American journal of human genetics 2007;80(1):152-61.
2007: François Gros-Louis; Nicolas Dupré; Patrick Dion; Michael A Fox; Sandra Laurent; Steve Verreault; Joshua R Sanes; Jean-Pierre Bouchard; Guy Rouleau
Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
Nature genetics 2007;39(1):80-5.
2006: Hitesh K Jindal; Kazumi Yoshinaga; Pil-Soo Seo; Mohini Lutchman; Patrick Dion; Guy Rouleau; Toshihiko Hanada; Athar H Chishti
Purification of the NF2 tumor suppressor protein from human erythrocytes.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2006;33(4):394-402.
2005: Qing Ling Duan; Borzoo Nikpoor; Marie-Pierre Dube; Giuseppe Molinaro; Inge A Meijer; Patrick Dion; Daniel Rochefort; Judith Saint-Onge; Leah Flury; Nancy Brown; James V Gainer; Jean-Lucien Rouleau; Angelo Agostoni; Massimo Cugno; Pierre Simon; Pierre Clavel; Jacky Potier; Bassem Wehbe; Seddik Benarbia; Julien Marc-Aurele; Jacques Chanard; Tatiana Foroud; Albert Adam; Guy Rouleau
A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors.
American journal of human genetics 2005;77(4):617-26.
2005: André Toulouse; Faith Au-Yeung; Claudia Gaspar; Julie Roussel; Patrick Dion; Guy Rouleau
Ribosomal frameshifting on MJD-1 transcripts with long CAG tracts.
Human molecular genetics 2005;14(18):2649-60.
2005: Patrick Dion; Vijayalakshmi Shanmugam; Claudia Gaspar; Christiane Messaed; Inge A Meijer; André Toulouse; janet laganiere; Julie Roussel; Daniel Rochefort; Simon Laganiere; Carol Allen; George Karpati; Jean-Pierre Bouchard; Bernard Brais; Guy Rouleau
Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice.
Neurobiology of disease 2005;18(3):528-36.
2003: Xueping Fan; Christiane Messaed; Patrick Dion; janet laganiere; Bernard Brais; George Karpati; Guy Rouleau
HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2003;30(3):244-51.
2001: Xueping Fan; Patrick Dion; janet laganiere; Bernard Brais; Guy Rouleau
Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death.
Human molecular genetics 2001;10(21):2341-51.
2001: M Jannatipour; Patrick Dion; S Khan; Hitesh K Jindal; Xiaotang Fan; Josée Laganière; Athar H Chishti; Guy Rouleau
Schwannomin isoform-1 interacts with syntenin via PDZ domains.
The Journal of biological chemistry 2001;276(35):33093-100.
2000: Vijayalakshmi Shanmugam; Patrick Dion; Daniel Rochefort; Josée Laganière; Bernard Brais; Guy Rouleau
PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophy.
Annals of neurology 2000;48(5):798-802.
2000: Claudia Gaspar; M Jannatipour; Patrick Dion; Josée Laganière; Jorge Sequeiros; Bernard Brais; Guy Rouleau
CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation.
Human molecular genetics 2000;9(13):1957-66.
2000: A Toulouse; J Morin; Patrick Dion; B Houle; W E Bradley
RARbeta2 specificity in mediating RA inhibition of growth of lung cancer-derived cells.
Lung cancer (Amsterdam, Netherlands) 2000;28(2):127-37.