Stéphanie Millecamps

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Wouter van Rheenen, Aleksey Shatunov, Annelot M. Dekker et al. · Nature Genetics · 2016 · 628 citations · Full text

Life Sciences, Genetics, Neuroscience +17

<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

Stéphanie Millecamps, François Salachas, C. Cazeneuve et al. · Journal of Medical Genetics · 2010 · 296 citations · Full text

Life Sciences, Genetics, Neurology +17

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology

Elisa Teyssou, Takahiro Takeda, Vincent Lebon et al. · Acta Neuropathologica · 2013 · 231 citations · Full text

Life Sciences, Molecular Genetics, Neuroscience +12

Oxidation of SQSTM1/p62 mediates the link between redox state and protein homeostasis

Bernadette Carroll, Elsje G. Otten, Diego Manni et al. · Nature Communications · 2018 · 187 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +14

Phenotype difference between ALS patients with expanded repeats in <i>C9ORF72</i> and patients with mutations in other ALS-related genes

Stéphanie Millecamps, Séverine Boillée, Isabelle Le Ber et al. · Journal of Medical Genetics · 2012 · 173 citations · Full text

Life Sciences, Genetics, Neurology +16