Nicolas Dupré

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

Edor Kabashi, Paul N. Valdmanis, Patrick A. Dion et al. · Nature Genetics · 2008 · 1.5K citations

Life Sciences, Genetics, Neurology +14

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

François Gros‐Louis, Nicolas Dupré, Patrick A. Dion et al. · Nature Genetics · 2006 · 347 citations

Life Sciences, Genetics, Molecular Genetics +12

Deregulation of TDP-43 in amyotrophic lateral sclerosis triggers nuclear factor κB–mediated pathogenic pathways

Vivek Swarup, Daniel J. Phaneuf, Nicolas Dupré et al. · The Journal of Experimental Medicine · 2011 · 335 citations · Full text

Life Sciences, Neurology, Neuroscience +17

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

Heidi Howard, David B. Mount, Daniel Rochefort et al. · Nature Genetics · 2002 · 278 citations

Medicine, Neurology, Neuroscience +16

Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor

Nancy D. Merner, Simon Girard, Hélène Catoire et al. · The American Journal of Human Genetics · 2012 · 195 citations · Full text

Life Sciences, Genetics, Neurology +12