User profiles for Nicolas Dupre

Nicolas Dupre

Université Laval
Verified email at fmed.ulaval.ca
Cited by 9261

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

…, PF Pradat, W Camu, V Meininger, N Dupre… - Nature …, 2008 - nature.com
Recently, TDP-43 was identified as a key component of ubiquitinated aggregates in
amyotrophic lateral sclerosis (ALS), an adult-onset neurological disorder that leads to the …

NMR studies of cathode materials for lithium-ion rechargeable batteries

CP Grey, N Dupré - Chemical reviews, 2004 - ACS Publications
Lithium intercalation or insertion materials have been widely investigated in the search for
new electrode materials for use in high-voltage rechargeable batteries. 1-6 The first …

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia

F Gros-Louis, N Dupré, P Dion, MA Fox, S Laurent… - Nature …, 2007 - nature.com
The past decade has seen great advances in unraveling the biological basis of hereditary
ataxias. Molecular studies of spinocerebellar ataxias (SCA) have extended our understanding …

Short- and Long-Range Order in the Positive Electrode Material, Li(NiMn)0.5O2:  A Joint X-ray and Neutron Diffraction, Pair Distribution Function Analysis and NMR …

J Bréger, N Dupré, PJ Chupas, PL Lee… - Journal of the …, 2005 - ACS Publications
The local environments and short-range ordering of LiNi 0.5 Mn 0.5 O 2 , a potential Li-ion
battery positive electrode material, were investigated by using a combination of X-ray and …

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis

…, PN Valdmanis, E Kabashi, P Dion, N Dupre… - Journal of medical …, 2009 - jmg.bmj.com
Aims and background: Mutations in the TARDBP gene, which encodes the TAR DNA
binding protein (TDP-43), have been described in individuals with familial and sporadic …

[PDF][PDF] Exome sequencing identifies FUS mutations as a cause of essential tremor

…, M Belouchi, M Panisset, P Cossette, N Dupré… - The American Journal of …, 2012 - cell.com
Essential tremor (ET) is a common neurodegenerative disorder that is characterized by a
postural or motion tremor. Despite a strong genetic basis, a gene with rare pathogenic …

From animal models to human disease: a genetic approach for personalized medicine in ALS

…, PN Valdmanis, PV Gould, JP Julien, N Dupré - Acta neuropathologica …, 2016 - Springer
Amyotrophic Lateral Sclerosis (ALS) is the most frequent motor neuron disease in adults.
Classical ALS is characterized by the death of upper and lower motor neurons leading to …

The classification of autosomal recessive cerebellar ataxias: a consensus statement from the society for research on the cerebellum and ataxias task force

…, M Manto, GA Rouleau, C Klein, N Dupre - The Cerebellum, 2019 - Springer
There is currently no accepted classification of autosomal recessive cerebellar ataxias, a
group of disorders characterized by important genetic heterogeneity and complex phenotypes. …

High-resolution X-ray diffraction, DIFFaX, NMR and first principles study of disorder in the Li2MnO3–Li [Ni1/2Mn1/2] O2 solid solution

J Bréger, M Jiang, N Dupré, YS Meng… - Journal of Solid State …, 2005 - Elsevier
X-ray diffraction patterns of Li[Li (1−2 x )/3 Ni x Mn 2/3− x /3 ]O 2 show reflections between
20 and 35, 2θ (CuKα) due to Li 2 MnO 3 -like ordering of the transition metal (Ni, Mn and Li) …

The failure mechanism of nano-sized Si-based negative electrodes for lithium ion batteries

Y Oumellal, N Delpuech, D Mazouzi, N Dupré… - Journal of Materials …, 2011 - pubs.rsc.org
Understanding the failure mechanism of silicon based negative electrodes for lithium ion
batteries is essential for solving the problem of low coulombic efficiency and capacity fading on …