Stéphanie Millecamps

<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 · 292 citations · Full text

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

Elisa Teyssou, Takahiro Takeda, Vincent Lebon et al. · Acta Neuropathologica · 2013 · 228 citations · Full text

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Genetics +6

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 · 182 citations · Full text

Mitophagy, Molecular Biology, Cell Death +23

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 · 172 citations · Full text

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

Russell L. McLaughlin, Dick Schijven, Wouter van Rheenen et al. · Nature Communications · 2017 · 154 citations · Full text