Nathalie Roeckel-Trévisiol

SRPX2 mutations in disorders of language cortex and cognition

Patrice Roll, Gabrielle Rudolf, Sandrine Pereira et al. · Human Molecular Genetics · 2006 · 257 citations

Life Sciences, Genetics, Neuroscience +17

Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex

Sarah Jamali, Fabrice Bartoloméi, Andrée Robaglia‐Schlupp et al. · Brain · 2006 · 100 citations · Full text

Medicine, Neurology, Neuroscience +14

<i>PMPCA</i>mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia

Rebekah Jobling, Mirna Assoum, Oleksandr Gakh et al. · Brain · 2015 · 77 citations · Full text

Life Sciences, Genetics, Neurology +16

Functional Variant in Complement C3 Gene Promoter and Genetic Susceptibility to Temporal Lobe Epilepsy and Febrile Seizures

Sarah Jamali, Annick Salzmann, Nader Perroud et al. · PLoS ONE · 2010 · 34 citations · Full text

Life Sciences, Genetics, Neurology +16

Nuclear localization of a novel human syntaxin 1B isoform

Sandrine Pereira, Annick Massacrier, Patrice Roll et al. · Gene · 2008 · 14 citations

Life Sciences, Genetics, Molecular Biology +5