FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Paul Valdmanis

Research Profile

Disorders

Physiology

Chemicals & Drugs

Procedures

DNA Mutational Analysis

Concepts & Ideas

Anatomy

Occupations

Genetics

Genes & Molecular Sequences

Dominant Genes

Co-author Network

Publications

TOP 3
Edor Kabashi; Jean-Philippe Loeffler; Jonathan McDearmid; Vincent Meininger; Inge A Mejier; Frédérique René; Guy A Rouleau; Jérome Sinniger; Paul N Valdmanis; Valérie Bercier; William Camu; Patrick A Dion; Sylvie Dirrig-Grosch; Pierre Drapeau; Nicolas Dupre; Hajer El Oussini; François Gros-Louis; David Hollinger; Luc Dupuis
Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis.
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.
Paul N Valdmanis; Nicolas Dupré; Mathieu Lachance; Shawn J Stochmanski; Veronique V Belzil; Patrick A Dion; Isabelle Thiffault; Bernard Brais; Lyle Weston; Louis Saint-Amant; Mark E Samuels; Guy Rouleau
A mutation in the RNF170 gene causes autosomal dominant sensory ataxia.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Paul Valdmanis (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Edor Kabashi; Jean-Philippe Loeffler; Jonathan McDearmid; Vincent Meininger; Inge A Mejier; Frédérique René; Guy A Rouleau; Jérome Sinniger; Paul N Valdmanis; Valérie Bercier; William Camu; Patrick A Dion; Sylvie Dirrig-Grosch; Pierre Drapeau; Nicolas Dupre; Hajer El Oussini; François Gros-Louis; David Hollinger; Luc Dupuis
Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis.
Human molecular genetics 2013;22(12):2350-60.
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: Paul N Valdmanis; Nicolas Dupré; Mathieu Lachance; Shawn J Stochmanski; Veronique V Belzil; Patrick A Dion; Isabelle Thiffault; Bernard Brais; Lyle Weston; Louis Saint-Amant; Mark E Samuels; Guy Rouleau
A mutation in the RNF170 gene causes autosomal dominant sensory ataxia.
Brain : a journal of neurology 2011;134(Pt 2):602-7.
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.
2009: Paul N Valdmanis; Dominique J Verlaan; Guy Rouleau
The proportion of mutations predicted to have a deleterious effect differs between gain and loss of function genes in neurodegenerative disease.
Human mutation 2009;30(3):E481-9.
2009: H Daoud; Paul N Valdmanis; Edor Kabashi; P Dion; Nicolas Dupré; W Camu; Vincent Meininger; Guy Rouleau
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.
Journal of medical genetics 2009;46(2):112-4.
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.
2008: Paul N Valdmanis; Edor Kabashi; Patrick A Dion; Guy Rouleau
ALS predisposition modifiers: knock NOX, who's there? SOD1 mice still are.
European journal of human genetics : EJHG 2008;16(2):140-2.
2008: Paul N Valdmanis; Guy Rouleau
Genetics of familial amyotrophic lateral sclerosis.
Neurology 2008;70(2):144-52.
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: Nicolas Dupré; Paul N Valdmanis; Jean-Pierre Bouchard; Guy Rouleau
Autosomal dominant primary lateral sclerosis.
Neurology 2007;68(14):1156-7.
2007: Paul N Valdmanis; Nicolas Dupre; Jean-Pierre Bouchard; William Camu; François Salachas; Vincent Meininger; Michael Strong; Guy Rouleau
Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.
Archives of neurology 2007;64(2):240-5.
2006: Paul N Valdmanis; Denis Brunet; Judith St-Onge; L Weston; Guy Rouleau; Nicolas Dupré
A founder haplotype for autosomal dominant sensory ataxia in Eastern Canada.
Neurology 2006;67(12):2239-42.
2004: Paul N Valdmanis; A A Simões Lopes; François Gros-Louis; J D Stewart; Guy Rouleau; Nicolas Dupré
A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12-8q12.1.
Journal of medical genetics 2004;41(8):634-9.