Elodie Martin

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

Giovanni Stévanin, Filippo M. Santorelli, Hamid Azzedine et al. · Nature Genetics · 2007 · 332 citations

Medicine, Neurology, Neuroscience +8

Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

Sylvain Hanein, Elodie Martin, Amir Boukhris et al. · The American Journal of Human Genetics · 2008 · 213 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia

Elodie Martin, Rebecca Schüle, Katrien Smets et al. · The American Journal of Human Genetics · 2013 · 171 citations · Full text

Life Sciences, Genetics, Neurology +10

KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations

Stephan Klebe, Alexander Lossos, Hamid Azzedine et al. · European Journal of Human Genetics · 2012 · 157 citations

Life Sciences, Genetics, Neurology +10

Involvement of TRPV1 and TRPV4 channels in migration of rat pulmonary arterial smooth muscle cells

Elodie Martin, Diana Dahan, Guillaume Cardouat et al. · Pflügers Archiv - European Journal of Physiology · 2012 · 93 citations

Life Sciences, Cell Biology, Physiology +9