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

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Mendelian Disorder +10

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 · 344 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

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 · 328 citations · Full text

Immunology, Immune Regulation, Cell Death +22

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 · 277 citations

K–cl Cotransporter Kcc3, Synaptic Transmission, Corpus Callosum +17

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 · 194 citations · Full text

Essential Tremor, Somatic Variant, Genetic Disorder +5